| Sr. No. | Title | Date | |
|---|---|---|---|
| 1 |
Dhangar S, Shanmukhaiah C, Ghatanatti J, Sawant L, Maurya N, Vundinti BR Comprehensive analysis of tyrosine kinase domain mutations and imatinib resistance in chronic myeloid leukemia patients
Leuk Res. 2025 Mar 17;152:107679. (IF:2.1)
|
2025 | |
| 2 |
Surve S, Thakor M, Madkaikar M, Kaur H, Desai S, Shanmugam R, Mohanty SS, Pandey A, Kerketta SA, Dave K, Gawit KG, Ramasamy LB, Warerkar O, Kedar P, Kulkarni R, Nair S, Rajamani N, Nadkarni A Protocol for a Multicentric Cohort Study on Neonatal Screening and Early Interventions for Sickle Cell Disease Among High-Prevalence States of India
Diagnostics (Basel). 2025 Mar 14;15(6):730. (IF:3.0)
|
2025 | |
| 3 |
Paramasivam P, Jaganathasamy N, Ramalingam S, Mahalingam V, Nagarajan S, Shaik FA, Karuppasamy S, Bhaskar A, Srinivasan P, Manoharan T, Natesan A, Chinnaiyan P An Application for Spatial Frailty Models: An Exploration with Data on Fungal Sepsis in Neonates
Diseases. 2025 Mar 14;13(3):83. (IF:2.9)
|
2025 | |
| 4 |
Gupta M, Madkaikar M Predictive Markers for Response to Immunosuppressive Therapy in Aplastic Anaemia
Scand J Immunol. 2025 Mar;101(3):e70010. (IF:4.1)
|
2025 | |
| 5 |
Augustine M, Parchure D, Kshirsagar P, Bhembre S, Mallya MV, Adsule H, Sreekumar K, Kulkarni S Alloimmunization Due to Multiple Red Cell Antibodies in a RhD Positive Pregnancy: Lessons to be Learnt
Indian J Hematol Blood Transfus. 2025 Feb 19:1-4. (IF:0.7)
|
2025 | |
| 6 |
Govindarajan R, Jaganathasamy N, Krishnamoorthi R, Kumari K, Kumar A, Paulraj PS Risk factors of scrub typhus infection in children and adults in Kerala, south India
Asian Pac J Trop Med. 2025 Feb;18(2):84-92. (IF:1.9)
|
2025 | |
| 7 |
Asokan D, Mall A, Sankhe L, Jaganathasamy N, Pardeshi G Temporal Trends of Dog Bite Cases and their Correlation with Meteorological Factors in a Metropolitan City
Indian J Community Med. 2025 Feb;:10-4103. (IF:0.9)
|
2025 | |
| 8 |
Kawankar N, Shanmukhaiah C, Kulkarni B Identification of a GFI1B variant associated with abnormal platelet function and normal platelet count
Br J Haematol. 2025 Feb;206(2):777-780.
|
2025 | |
| 9 |
Kulkarni BP, Shanmukhaiah C, Ghargi K, Pandey P, Kharat S, Pawar P, Shinde S, Kawankar N, Shanbhag S Coincidental occurrence of severe factor XII deficiency in a case of mild hemophilia A: a unique coagulation laboratory diagnostic conundrum
Blood Coagul Fibrinolysis. 2025 Jan 27. doi: 10.1097/MBC.0000000000001346.
|
2025 | |
| 10 |
Ghatanatti J, Dhangar S, Vundinti BR Variant Klinefelter Syndrome With Xq Trisomy (47,X,i(X)(q10),Y): A Case Report and Review of the Literature
Cureus. 2025 Jan 12;17(1):e77351. (IF:1.2)
|
2025 | |
| 11 |
Tomar A, Devendra R, Parchure D, Kulkarni S Weak or partial D: Importance of molecular characterization of D variants
Transfus Apher Sci. 2025 Jan 11;64(2):104069. (IF:1.4)
|
2025 | |
| 12 |
Davidovich C, Erokhina K, Gupta CL, Zhu YG, Su JQ, Djordjevic SP, Wyrsch ER, Blum SE, Cytryn E Occurrence of "under-the-radar" antibiotic resistance in anthropogenically affected produce
ISME J. 2025 Jan 2;19(1):wrae261. (IF:10.8)
|
2025 | |
| 13 |
Saptarshi AN, Subramaniam K, Nemani S, More TA, Dongerdiye R, Kedar P Hematopoietic Stem Cell Transplant of a Congenital Dyserythropoietic Anemia Type II Patient: A Rare Report from the Indian Population
Indian J Hematol Blood Transfus. 2025 Jan;41(1):194-196. (IF:0.7)
|
2025 | |
| 14 |
Jose A, Bodade A, Madkaikar MR Assessing and managing iron deficiency anemia in sickle cell disease: Insights from a systematic review and meta-analysis
J Postgrad Med. 2025 Jan–Mar;71(1):33-40.
|
2025 | |
| 15 |
Gaikwad P, Bargir UA, Jodhawat N, Dalvi A, Shinde S, Tamhankar P, Setia P, Kambli P, Dhawale A, Temkar L, Vedpathak D, Jose A, Gupta M, Yadav-Malik R, Dutta S, Bose K, Taur P, Gowri V, Iyengar V, Chougule A, Desai M, Sivasankaran M, Bhattad S, Balaji S, Mudaliar S, Kacha A, Subramanian G, Patel S, Sharma S, Sampagar A, Madkaikar M Mutational Landscape of Patients with Wiskott Aldrich Syndrome: Update from India
J Clin Immunol. 2024 Dec 17;45(1):56. (IF:7.2)
|
2024 | |
| 16 |
Snigdha A, Majumdar V, Manjunath NK, Jose A Yoga-based lifestyle intervention for healthy ageing in older adults: a two-armed, waitlist randomized controlled trial with multiple primary outcomes
Geroscience. 2024 Dec;46(6):6039-6054. (IF:5.3)
|
2024 | |
| 17 |
Roshan Shaikh, Ghosh Kanjaksha, Ajit Gorakshakar Whispers of the Genome: Unmasking SNP through Simple Modified PCR
Indian Journal of Anthropological Research. 2024 Dec;3(2):291-303.
|
2024 | |
| 18 |
Prabhakar Kedar, Rashmi Dongerdiye, Ritika Khurana, Sangeeta Mudaliar Rare red cell enzymopathies in the Indian population: A comprehensive review
Pediatric Hematology Oncology Journal. 2024 Dec;9(4):235-243.
|
2024 | |
| 19 |
Gupta M, S C, Vundinti B, Jose A, Tiwari S, Bhowmick A, Madkaikar M Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Nov 12;218(3):291-299. (IF:3.4)
|
2024 | |
| 20 |
Roshan Shaikh, Ghosh Kanjaksha, Ajit Gorakshakar Duffy Binding Protein Ligand (PvDBP) gene duplication in Indian P. Vivax Malaria isolates: implication for malaria research
Curr Genet. 2024 Nov 9;70(1):18. (IF:1.8)
|
2024 | |
| 21 |
Baysac K, Sun G, Nakano H, Schmitz EG, Cruz AC, Fisher C, Bailey AC; PLCG2-Immune Dysregulation Working Group; Mace E, Milner JD, Ombrello MJ PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants
J Allergy Clin Immunol. 2024 Jan;153(1):230-242. (IF:14.29)
|
2024 | |
| 22 |
Malhotra S, Roy M, Parchure D, Kaba M, Jain A, Kulkarni S, Bansal D, Sharma RR Autoimmune anti‐D in an RhD‐positive young infant: Learning from a rare case.
Vox Sanguinis. 2024 Jan;119(1):70-3. Short Report (IF:1.8)
|
2024 | |
| 23 |
Chougule A, Iyengar VV, Gowri V, Taur P, Madkaikar MR, Bodhanwala M, Desai MM Cleavage-resistant RIPK1-induced autoinflammatory syndrome-A report of three generations with periodic fever and clinical response to colchicine.
Int J Rheum Dis. 2024 Jan;27(1):e14837.(IF:2.4)
|
2024 | |
| 24 |
Khanna D, Shruti T, Tiwari M, Sharma P, Khan A, Ranjan S, Balasundaram P, Khargekar N, Chaturvedi P, Mishra A Prevalence of Oral Potentially Malignant Lesions, Tobacco use, and Effect of Cessation Strategies among Solid Waste Management workers in Northern India: a pre-post intervention study
BMC Oral Health. 2024 Oct 26;24(1):1292. (IF:2.6)
|
2024 | |
| 25 |
Gupta CL, Jaganathasamy N, Madkaikar M Microbiome in sickle cell disease: Pathophysiology and therapeutic insights
Br J Haematol. 2024 Oct;205(4):1279-1287. (IF:5.1)
|
2024 | |
| 26 |
Shinde-Vhatkar S, Bargir U, Madkaikar M Immunophenotypic Analysis of Patients with Pyogenic Liver Abscess for Underlying Inborn Errors of Immunity
Indian J Pediatr. 2024 Oct;91(10):1105. (IF:2.1)
|
2024 | |
| 27 |
Dongerdiye R, Kedar PS, Saptarshi A, Sampagar A, Shanmukhaiah C, Mudaliar S, Kanvinde P, Desai M, Madkaikar M Non-syndromic congenital sideroblastic anaemia; phenotype, and genotype of 15 Indian patients
Ann Hematol. 2024 Oct;103(10):3987-3998. (IF:3.0)
|
2024 | |
| 28 |
Shaikh R, Kanjaksha G, Kashivishwanath V, Kulkarni S, Jadhav S, Maru H, Gorakshakar A ACKR1 gene polymorphisms in Bombay blood group (O(h)) individuals of Indian origin
Transfus Apher Sci. 2024 Oct;63(5):103975. (IF:1.4)
|
2024 | |
| 29 |
Kumar LS, Raghavendra PR, Nair S, et al. Silver hair in a neonate: a tale of 2 fatal cases
Oxf Med Case Reports. 2024;2024(9):omae106. (IF:N/A)
|
2024 | |
| 30 |
Radhika R, Tullu MS, Karande S, Bargir UA Major Histocompatibility Complex (MHC) Class II Deficiency- A Case of Primary Immunodeficiency Disorder
Indian J Pediatr. 2024 Sep;91(9):967-969. (IF:2.1)
|
2024 | |
| 31 |
Gupta M, S C, Vundinti B, Jose A, Tiwari S, Bhowmick A, Madkaikar M Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Aug 13:uxae076. (IF:3.4)
|
2024 | |
| 32 |
Banerjee A, Farci P Fibrosis and Hepatocarcinogenesis: Role of Gene-Environment Interactions in Liver Disease Progression
Int J Mol Sci. 2024 Aug 8;25(16):8641. (IF:4.9)
|
2024 | |
| 33 |
Banerjee A, Athalye S, Shingade P, Khargekar V, Mahajan N, Madkaikar M, Khargekar N Efficacy of daily versus intermittent oral iron supplementation for prevention of anaemia among pregnant women: a systematic review and meta-analysis
EClinicalMedicine. 2024 Jul 17;74:102742. (IF:9.9)
|
2024 | |
| 34 |
Mohanty MC, Govindaraj G, Ahmad M, Varose SY, Tatkare M, Shete A, Yadav S, Joshi Y, Yadav P, Sharma D, Kumar A, Verma H, Patil AP, Edavazhipurath A, Dhanasooraj D, Othayoth Kandy S, Puthenpurayil JM, Chakyar K, Melarcode Ramanan K, Madkaikar M Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Excretion in an Infant with Severe Combined Immune Deficiency with Spillover to a Parent
Vaccines (Basel). 2024 Jul 9;12(7):759. (IF:7.8)
|
2024 | |
| 35 |
Anuradha R, Srinivas M, Satyavani M, Suresh K, Muralidhar MN, Rajender Rao K Preconceptional paternal caloric restriction of high-fat diet-induced obesity in Wistar rats dysregulates the metabolism of their offspring via AMPK/SIRT1 pathway
Lipids Health Dis. 2024 Jun 8;23(1):174. (IF:3.9)
|
2024 | |
| 36 |
Jodhawat N, Bargir UA, Rawal G, Kamble P, Shinde-Vhatkar S, Dalvi A, Kulkarni S, Madkaikar M Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features.
J Clin Immunol. 2024 Jun 7;44(6):144. (IF:7.2)
|
2024 | |
| 37 |
Yadav RM, Desai SS, Gupta M, Dalvi A, Bargir UA, Jodhawat N, Setia P, Shinde S, Parab A, Gada A, Taur P, Desai M, Madkaikar M Clinical Utility of Flow-Cytometry for Diagnosis and Genotype Phenotype Correlation in a Cohort of X-linked Agammaglobulinemia Patients.
Indian J Pediatr. 2024 Jun;91(6):638. (IF:4.3)
|
2024 | |
| 38 |
Thaker P, Mahajan N, Mukherjee MB, Colah RB Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.
Int J Lab Hematol. 2024 Jun;46(3):434-450. (IF:2.2)
|
2024 | |
| 39 |
Jain D, Gupta M, Madkaikar M, Jena RK, Khargekar N, Saraf SL, Krishnamurti L, Gupta K Sickle cell disease in India: current status and progress.
Lancet Haematol. 2024 May;11(5):e322-e323. (IF:15.4)
|
2024 | |
| 40 |
Patil R, Shanmukhaiah C, Gogtay NJ, Pandey P, Patil K, Jijina F, Madkaikar M Low-dose Emicizumab prophylaxis in severe haemophilia A patients -a retrospective study bringing new hope for our patients.
J Thromb Haemost. 2024 Apr;22(4):1024-1030. (IF:16.041)
|
2024 | |
| 41 |
Budukh AM, Pradhan S, Singh VB, Khanna D, Bagal SS, Chakravarti PS, Sharma AN, Vishwakarma RK, Shinde SS, Khargekar NC, Chaturvedi P, Dikshit RP, Shukla VK, Badwe RA Cancer pattern in Varanasi district from Uttar Pradesh state of India, a foundation for cancer control based on the first report of the population-based cancer registry.
Indian J Cancer. 2024 Apr 1;61(2):383-389. (IF:1.0)
|
2024 | |
| 42 |
Khargekar N, Takke A, Athalye S, Panale P, Rajamani N, Banerjee A Exploring factors influencing the perspective regarding HIV transmission and prevention among college students in India.
J Family Med Prim Care. 2024 Apr;13(4):1467-1472. (IF:1.1)
|
2024 | |
| 43 |
Jeffrey Pradeep Raj, Suraj Kallarakal Tomy, Amrutha Jose, Aadrika Kashyap, Joseph Varghese Kureethara, Tomy K Kallarakal Knowledge and perceptions about clinical research and its ethical conduct among college students from non-science background: a representative nation-wide survey from India.
BMJ Public Health 2024;2:e000748.
|
2024 | |
| 44 |
Asokan D, Mall A, Sankhe L, Jaganathasamy N, Pardeshi G Profile and geospatial analysis of dog bite cases attending the antirabies vaccine outpatient department at the tertiary level hospital of Mumbai.
Indian J Public Health. 2024 Apr 1;68(2):175-179. (IF:0.9)
|
2024 | |
| 45 |
Yadav RM, Gomare M, Gaikwad A, Waghmare U, Betodkar U, Vashi MD, Kamal VK, Thangaraj JWV, Bangar S, Bhatnagar T, Murhekar M Interplay of missed opportunity for vaccination and poor response to the vaccine led to measles outbreak in a slum area of Eastern Mumbai, India.
Epidemiol Infect. 2024 Mar 18;152:e56. (IF:2.5)
|
2024 | |
| 46 |
Kripa PK, Thanzeen PS, Nagaraj Jaganathasamy, Sangamithra Ravishankaran, Anupkumar R Anvikar, Alex Eapen Impact of climate change on temperature variations and extrinsic incubation period of malaria parasites in Chennai, India- Implications on its disease transmission potential.
Parasites Vectors. 2024 Mar 15;17(1):134.(IF:4.0)
|
2024 | |
| 47 |
Maurya N, Shanmukhaiah C, Dhangar S, Madkaikar M, Vundinti BR Comprehensive study of chromosomal CNVs and genomic variations predicting overall survival in Myelodysplastic syndromes.
Oncology. 2024 Mar;102(10):897-906. (IF:3.5)
|
2024 | |
| 48 |
Dalvi A, Bargir UA, Natraj G, Shah I, Madkaikar M Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease.
Pathogens. 2024 Feb 25;13(3):203.(IF:3.3)
|
2024 | |
| 49 |
Khargekar N, Banerjee A, Athalye S, Mahajan N, Kargutkar N, Tapase P, Madkaikar M Role of hydroxyurea therapy in the prevention of organ damage in sickle cell disease: a systematic review and meta-analysis.
Syst Rev. 2024 Feb 8;13(1):60. Systematic Review & Meta Analysis (IF:6.3)
|
2024 | |
| 50 |
Athalye S, Patil A, Khargekar N, Shinde S, Chavan S, Dixit A, Shankarkumar A, Madkaikar M, Banerjee A Efficacy of combined HBsAg, anti-HBc and anti-HBs screening in minimizing transfusion transmission risk of hepatitis B infection in low resource setting.
Heliyon. 2024 Feb 3;10(3):e25805 (IF:3.4)
|
2024 | |
| 51 |
Gorivale M, Sawant P, Kargutkar N, Hariharan P, Thaker P, Chiddarwar A, Nadkarni A When a synonymous mutation breaks the silence in a thalassaemia patient.
Br J Haematol. 2024 Feb;204(2):677-682. (IF:5.1)
|
2024 | |
| 52 |
Ghosh K, Kinanka Ghosh and Bipin Kulkarni. HNF1 Associated Novel Missense Mutation Associated with MODY-3 and Type 2 Diabetes in an Indian Family
Am J Biomed Sci & Res. Nov 2023: 19(2) AJBSR.MS.ID.002574, DOI: 10.34297 AJBSR.2023.19.002574 (Impact factor: 1.628).
|
2023 | |
| 53 |
Gaikwad P, Bargir UA, Shinde S, Kini P, Chaurasia R, Yadav U, Dhawale A, George M, Jodhawat N, Setia P, Vedpathak D, Dalvi A, Parab A, Gupta M, Yadav RM, Goriwale M, Vundinti B, Bhat N, Sapra BK, Otiv M, Sharma R, Madkaikar M. A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case.
J Clin Immunol. 2023 Nov;43(8):1891-1902. (IF:8.542)
|
2023 | |
| 54 |
Surve S, Chauhan S, Kulkarni R, Salvi N, Nadkarni A, Madkaikar M, Chaudhary K, Chavan A, Suryavanshi D, Thorat A, Kaur H. Challenges in screening for sickle cell disease among newborns from the tribal region of Palghar, Maharashtra during the COVID-19 pandemic.
Indian J Med Res. 2023 Oct 1;158(4):378-383. (IF:5.274)
|
2023 | |
| 55 |
Satija A, Anand T, Mukherjee A, Velamuri PS, Singh KJ, Das M, Josten K, Keche AY, Nagarkar NM, Gupta P, Himanshu D, Mistry SN, Patel JD, Rao P, Rohatgi S, Ghosh S, Hazra A, Kindo AJ, Annamalai R, Rudramurthy SM, Singh MP, Shameem M, Fatima N, Khambholja JR, Parikh S, Madkaikar M, Pradhan VD, Bhargava A, Mehata R, Arora RD, Tigga R, Banerjee G, Sonkar V, Malhotra HS, Kumar N, Patil R, Raut CG, Bhattacharyya K, Arthur P, Somu L, Srikanth P, Shah PB, Panda NK, Sharma D, Hasan W, Ahmed A, Bathla M, Solanki S, Doshi H, Kanani Y, Patel N, Shah Z, Tembhurne AK, Rajguru C, Sankhe LR, Chavan SS, Yadav RM, Panda S. Satellite Epidemic of Covid-19 Associated Mucormycosis in India: A Multi-Site Observational Study.
Mycopathologia 2023 Oct;188(5):745-753.(IF:3.785)
|
2023 | |
| 56 |
Shabrish S, Chandrakasan S, Madkaikar M Editorial: NK cell defects: diagnosis and treatment.
Front Immunol. 2023 Oct 31;14:1323793. doi: 10.3389/fimmu.2023.1323793. eCollection 2023.(IF:8.787)
|
2023 | |
| 57 |
Shah A, Kumar C, Shanmukhaiah C, Rajendran A, Mudaliar S, Idicula-Thomas S, Vundinti BR. Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia.
Ann Hematol. 2023 Oct;102(10):2683-2693.(IF:3.5)
|
2023 | |
| 58 |
Ghosh K, Shome DK, Kulkarni B, Ghosh MK, Ghosh K. Fibrosis and bone marrow: understanding causation and pathobiology
J Transl Med. 2023 Oct 9;21(1):703.(IF:8.448)
|
2023 | |
| 59 |
Venkatachari IV, Chougule A, Gowri V, Taur P, Bodhanwala M, Prabhu S, Madkaikar M, Desai M Monogenic inborn errors of immunity in autoimmune disorders
Immunol Res. 2023 Oct;71(5):771-780. (IF:4.4)
|
2023 | |
| 60 |
Saptarshi AN, More TA, Dongerdiye R, Kedar P Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.
Indian J Pediatr. 2023 Aug;90(8):840. (IF:1.136)
|
2023 | |
| 61 |
Jodhawat N, Bargir UA, Setia P, Taur P, Bala N, Madkaikar A, Yadav RM, Dalvi A, Shinde S, Gupta M, Shelar S, Kambli P, Gowri V, Lokeshwar M, Satoskar P, Desai M, Madkaikar M Normative data for paediatric lymphocyte subsets: A pilot study from western India.
Indian J Med Res. 2023 Aug;158(2):161-174. (IF:5.274)
|
2023 | |
| 62 |
Athalye S, Khargekar N, Shinde S, Parmar T, Chavan S, Swamidurai G, Pujari V, Panale P, Koli P, Shankarkumar A, Banerjee A Exploring risk factors and transmission dynamics of Hepatitis B infection among Indian families: Implications and perspective.
J Infect Public Health. 2023 Jul;16(7):1109-1114. (IF:7.537)
|
2023 | |
| 63 |
Saptarshi AN, Dongerdiye RK, More TA, Kedar PS. Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Ital J Pediatr. 2023 Jul 16;49(1):84.(IF:3.288)
|
2023 | |
| 64 |
Mohanty MC, Desai M, Mohammad A, Aggarwal A, Govindaraj G, Bhattad S, Lashkari HP, Rajasekhar L, Verma H, Kumar A, Sawant U, Varose SY, Taur P, Yadav RM, Tatkare M, Fernandes M, Bargir U, Majumdar S, Edavazhippurath A, Rangarajan J, Manthri R, Madkaikar MR Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I.
Vaccines (Basel). 2023 Jul 6;11(7):1211. (IF:7.8)
|
2023 | |
| 65 |
Kargutkar N, Nadkarni A Effect of hydroxyurea on erythrocyte apoptosis in hemoglobinopathy patients.
Expert Rev Hematol.2023 Jul-Dec;16(9):685-692. doi: 10.1080/17474086.2023.2231152. (IF: 2.8)
|
2023 | |
| 66 |
Gowri V, Chougule A, Gupta M, Taur P, Iyengar VV, Sivasankaran M, Munirathnam D, Krishna S, Bargir UA, Dalvi A, Setia P, Jodhawat N, Shinde S, Prabhu SS, Bodhanwala M, Madkaikar MR, Desai MM Clinical, immunological and molecular findings of patients with DOCK-8 deficiency from India
Scand J Immunol. 2023 Jul;98(1):e13276. .(IF:3.889)
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2023 | |
| 67 |
Setia P, Bargir UA, Shanmukhaiah C, Jodhawat N, Gaikwad P, Vedpathak D, Dutta S, Kulkarni R, Kambli P, Dalvi A, Shinde S, Gupta M, Nambiar N, Sawant S, Shelar S, Dhawale A, Mohanty M, Yadav RM, Bose K, Madkaikar M. Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas-mediated apoptotic pathway.
Br J Haematol. 2023 Jul;202(2):e11-e15.(IF:8.615)
|
2023 | |
| 68 |
Khadilkar P, Chougule D, Tipnis T, Khopkar U, Nadkar M, Rajadhyaksha A, Kini S, Kharkar V, Athvale A, Athvale T, Madkaikar M, Pradhan V A comparative study of modulatory interaction between cytokines and apoptotic proteins among Scleroderma patients with and without pulmonary involvement.
Cytokine 2023 Jun;166:156183.(IF:3.926)
|
2023 | |
| 69 |
Dhangar S, Shanmukhaiah C, Sawant L, Ghatanatti J, Shah A, Mathan S LP, Vundinti BR. Synergetic effect of Azacitidine and Sorafenib in treatment of a case of myeloid neoplasm with sole chromosomal abnormality t(8;22)(p11.2;q11.2)/BCR-FGFR1 rearrangement
Cancer Genet. 2023 Jun;274-275:26-29. (IF:2.169)
|
2023 | |
| 70 |
Patil R, Singh SV, Mandlik JS, Jadhav A, Handa A, Jadhav A Evaluating the Efficacy of Certain Intermediate Irrigants in Preventing Precipitate Formed Due to Sodium Hypochlorite and Chlorhexidine Within the Root Canal System: An In Vitro Study.
Cureus 2023 Jun 2;15(6):e39871.(IF:1.2)
|
2023 | |
| 71 |
Dongerdiye R, Bokde M, More TA, Saptarshi A, Devendra R, Chiddarwar A, Warang P, Kedar P. Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
Ann Hematol. 2023 May;102(5):1029-1036.(IF:4.03)
|
2023 | |
| 72 |
Mohanty MC, Mohammad A, Verma H, Kumar A, Madkaikar MR, Desai M, Varose SY, Sawant U, Yadav RM, Taur P, Kathuria R, Tatkare M, Murhekar M, Haldar P, Abraham P Poliovirus surveillance in patients with primary immunodeficiencies, India
Bull World Health Organ. 2023 May 1;101(5):346-354.(IF:11.1)
|
2023 | |
| 73 |
Shete A, Deshpande S, Sawant J, Warthe N, Thakar M, Madkaikar M, Pradhan V, Rao P, Rohatgi S, Mukherjee A, Anand T, Satija A, Sharma Velamuri P, Das M, Deasi N, Kumar Tembhurne A, Yadav R, Pawaskar S, Rajguru C, Sankhe LR, Chavan SS, Panda S. Higher proinflammatory responses possibly contributing to suppressed cytotoxicity in patients with COVID-19 associated mucormycosis
Immunobiology. 2023 May;228(3):152384.(IF:3.152)
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2023 | |
| 74 |
Maru V, Madkaikar M, Gada A, Pakhmode V, Padawe D, Bapat S. Response of stem cells derived from human exfoliated deciduous teeth to Bio-C Repair and Mineral Trioxide Aggregate Repair HP: Cytotoxicity and gene expression assessment.
Dent Res J (Isfahan). 2023 Apr 26;20:55. eCollection 2023.(IF:1.23)
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2023 | |
| 75 |
Shah I, Shetty NS, Chigari P, Pradhan V, Chougule D, Poojari VS, Jaiswal A, Madkaikar M. Vitamin D receptor genetic polymorphisms in severe and recurrent tuberculosis in children
Indian J Tuberc. 2023 Apr;70(2):239-244.(IF:1.57)
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Parchure DS, Mishra GV, Kulkarni SS. Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population
Immunohematology. 2023 Apr 5;39(1):19-31.(IF:0.268)
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Roos D, van Leeuwen K, Madkaikar M, Kambli PM, Gupta M, Mathews V, Rawat A, Kuhns DB, Holland SM, de Boer M, Kanegane H, Parvaneh N, Lorenz M, Schwarz K, Klein C, Sherkat R, Jafari M, Wolach B, den Dunnen JT, Kuijpers TW, Köker MY Hematologically important mutations: Leukocyte adhesion deficiency (second update)
Blood Cells Mol Dis. 2023 Mar;99:102726.(IF:2.3)
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| 78 |
Chougule A, Taur P, Iyengar VV, Gowri V, Kulkarni BP, Madkaikar MR, Bodhanwala, M, Desai MM. Clinical features, laboratory and molecular findings of children with leukocyte adhesion deficiency type-III from a single center in India.
Pediatric Hematology Oncology Journal Volume 8, Issue 1, March 2023, Pages 4-9 (IF : 1.969)
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| 79 |
More TA, Devendra R, Dongerdiye R, Warang P, Kedar P Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum
Mol Genet Genomics. 2023 Mar;298(2):427-439.(IF:3.1)
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2023 | |
| 80 |
Lokhande AS, Panchal F, Munshi R, Madkaikar M, Malshe VC, Devarajan PV pH-responsive microparticles of rifampicin for augmented intramacrophage uptake and enhanced antitubercular efficacy.
Int J Pharm. 2023 Mar 25;635:122729.(IF:5.8)
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Desai N, Pradhan V, Chougule D, Tiwari S, Mandke C, Yadav RM, Athvale A, Kawle J, Pai V, Pawaskar S, Kharkar H, Bhosale S, Parab A, Ansari S, Kumar KH, Mhashal S, Redkar N, Madkaikar M Perturbations of immune landscape in COVID-19 associated mucormycosis. M
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Kargutkar N, Hariharan P, Nadkarni A Dynamic interplay of microRNA in diseases and therapeutic A.
Clin Genet. 2023 Mar;103(3):268-276. (IF:3.5)
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2023 | |
| 83 |
Pandrowala A, Desai M, Madkaikar M, Kulkarni S, Shobhavat L, Mishra J, Jain S, Chandane P, Sehgal K, Chavan S, Karkera P, Bendre P, Thanky A, Rao S, Prabhu S, Bodhanwala M, Agarwal B, Hiwarkar P. Changing outcomes of stem cell transplantation in primary immunodeficiencies: Results from a tertiary-care charitable trust hospital in Mumbai.
J Allergy Clin Immunol Glob. 2023 Mar 29;2(3):100105. (IF: --)
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Chougule A, Taur P, Gowri V; C. O. E. Consortium; Desai MM SPENCD Presenting with Evans Phenotype and Clinical Response to JAK1/2 Inhibitors-a Report of 2 Cases.
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| 85 |
Banerjee A, Athalye S, Khargekar N, Shingade P, Madkaikar M. Chronic Hepatitis B and Related Liver Diseases Are Associated with Reduced 25-Hydroxy-Vitamin D Levels: A Systematic Review and Meta-Analysis.
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Maurya N, Mohanty P, Panchal P, Shanmukhaiah C, Vundinti BR. Over expression of mTOR gene predicts overall survival in myelodysplastic syndromes
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Kulkarni V, Chellasamy SK, Dhangar S, Ghatanatti J, Vundinti BR Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
Mol Hum Reprod. 2023 Jan 31;29(2):gaad001.(IF:4.0)
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Khargekar N, Shinde N, Banerjee A, Madkaikar M, Nadkarni A Impact of COVID-19 infection among indian sickle cell disease patients.A.
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Vundinti BR, Korgaonkar S, Dhangar S, Jijina F, Shanmukhaiah C Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective study
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Kargutkar N, Sawant-Mulay M, Hariharan P, Chandrakala S, Nadkarni A Role of microRNA in hydroxyurea mediated HbF induction in sickle cell anaemia patients.
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Gupta A, Jain M, Sheety T, Salunkhe L, Gorivale M, Nadkarni A Hemoglobin Reims- a rare alphgaglobin chain varinay and its interaction with beta thalassemia
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Anand T, Mukherjee A, Satija A, Sharma Velamuri P, Singh J, Das M, Josten K, Yadav P, Sahay RR, Keche AY, Nagarkar NM, Gupta P, Himanshu D, Mistry SN, Pate JD, Rao P, Rohatgi S, Ghosh S, Hazra A, Kindo AJ, Annamalai R, Rudramurthy SM, Singh MP, Fatima MS, Khambholja JR, Parikh S, Madkaikar MR, Pradhan VD, Kataria S, Sharma P, Panda S, ICMR Mucormycosis group A case control investigation of Covid-19 associated mucormycosis in India.
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Reetika Malik Yadav, Neha Jodhawat, Maya Gupta et al. Utility of HLA-DR in screening panel for errors of immunity.
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Takke A, Zarekar M, Muthuraman V, Ashar A, Patil K, Badhavkar A, Trivedi J, Khargekar N, Madkaikar M, Banerjee A. Comparative study of clinical features and vaccination status in Omicron and non-Omicron infected patients during the third wave in Mumbai, India.
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Hariharan P, Sawant P, Sheth J, Nadkarni A. Rapid molecular identification of a rare β-globin gene deletion & its clinical implication.
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Shanmukhaiah C, Jijina F, Kannan S, Pai NG, Kulkarni B, Khuba SV, Shaikh M, Joshi A, Phatale R, Apte S. Efficacy of emicizumab in von Willebrand disease (VWD) patients with and without alloantibodies to von Willebrand factor (VWF): Report of two cases and review of literature.
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Kelkar MG, Bargir UA, Malik-Yadav R, Gupta M, Dalvi A, Jodhawat N, Shinde S, Madkaikar MR. CD8 T Cells Exhibit an Exhausted Phenotype in Hemophagocytic Lymphohistiocytosis.
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Roos D, van Leeuwen K, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, de Boer M, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Garcia-Morato MB, Shephard JLV, Cagdas D, Tezcan I, Sherkat R, Mortaz E Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
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Zian Z, Berry SPD, Bahmaie N, Ghotbi D, Kashif A, Madkaikar M, Bargir UA, Abdullahi H, Khan H, Azizi G. The clinical efficacy of Rituximab administration in autoimmunity disorders, primary immunodeficiency diseases and malignancies.
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Afroz T, Mishra G, Saleh AJM, Madkaikar M, Kulkarni S Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent.
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Thakar M, Saxena V, Janakiram N, Ravi V, Desai A, Singh S, Shivanna N, Minz RY, Singh A, Chatterjee M, Madkaikar M, Bembalkar S, Mukherjee A, Mahesh V. Reference Ranges of Different Lymphocyte Subsets in Indian Children: A Multi-Centric Study.
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Sane M, Dighe V, Patil R, Hassan PA, Gawali S, Patravale V. Bivalirudin and sirolimus co-eluting coronary stent: Potential strategy for the prevention of stent thrombosis and restenosis.
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Khadilkar PV, Khopkar US, Nadkar MY, Rajadhyaksha AG, Chougule DA, Deshpande SD, Madkaikar MR, Pradhan VD. Fibrotic Cytokine Interplay in Evaluation of Disease Activity in Treatment Naïve Systemic Sclerosis Patients from Western India.
J Assoc Physicians India. 2019 Aug;67(8):26-30.(IF:0.47)
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Bandari AK, Muthusamy B, Bhat S, Govindaraj P, Rajagopalan P, Dalvi A, Shankar S, Raja R, Reddy KS, Madkaikar MR, Pandey A. A Novel Splice Site Mutation in IFNGR2 in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases.
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Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar MR. Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.
Indian J Pediatr. 2019 Aug;86(8):692-699.(IF:1.181)
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Dalal K, Dalal B, Bhatia S, Shukla A, Shankarkumar A Analysis of serum Haptoglobin using glycoproteomics and lectin immunoassay in liver diseases in Hepatitis B virus infection.
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Jadli A, Ghosh K, Damania K, Satoskar P, Bansal V, Shetty S. Prediction of preeclampsia using combination of biomarkers at 18-23?weeks of gestation: A nested case-control study.
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Hule GP, Bargir UA, Kulkarni M, Kambli P, Taur P, Desai M, Madkaikar MR. Does Pioglitazone Lead to Neutrophil Extracellular Traps Formation in Chronic Granulomatous Disease Patients?
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Mohanty MC, Madkaikar MR, Desai M, Aluri J, Varose SY, Taur P, Sharma DK, Nalavade UP, Rane SV, Gupta M, Shabarish S, Dalvi A, Deshpande JM. Natural Clearance of Prolonged VDPV Infection in a Child With Primary Immunodeficiency Disorder.
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Madkaikar MR, Shabrish S, Kulkarni M, Aluri J, Dalvi A, Kelkar M, Gupta M. Application of Flow Cytometry in Primary Immunodeficiencies: Experience From India.
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Korgaonkar S, Dhangar S, Kulkarni V, Kerketta L, Vundinti BR. Chromosomal Aberrations in Primary Amenorrhea: A Retrospective Study.
J Hum Reprod Sci. 2019 Apr-Jun;12(2):92-97.
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Indian J Pathol Microbiol. 2019 Apr-Jun;62(2):323-325.
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Aluri J, Gupta MR, Dalvi A, Mhatre S, Kulkarni M, Desai M, Shah NK, Madkaikar Lymphopenia and Severe Combined Immunodeficiency (SCID) - Think Before You Ink.
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Ghosh K, Mishra K, Shah A, Patel P, Shetty S. Novel Deleterious Sequence Change in the NLRP12 Gene in a Child with the Autoinflammatory Syndrome, Joint Hypermobility and Cutis Laxa from India.
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Mohanty P, Jadhav P, Shanmukhaiah C, Kumar S, Vundinti BR. A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.
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Front Immunol. 2019 Mar 21;10:490. eCollection 2019 (IF: 3.35)
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Gaikwad T, Deshpande R, Shetty S. Anti-factor VIII inhibitors against A2 and C2 domains in hemophilia A patients from India.
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Shabrish S, Desai M, Saxena V, Kelkar M, Madkaikar MR. IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections.
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Dhangar S, Korgaonkar S, Vundinti BR. Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.
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Vira H, Pradhan V, Umare V, Chaudhary A, Rajadhyksha A, Nadkar M, Ghosh K, Nadkarni A. Role of polymorphisms in MMP-9 and TIMP-1 as biomarkers for susceptibility to systemic lupus erythematosus patients.
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Kedar PS, Gupta V, Dongerdiye R, Chiddarwar A, Warang P, Madkaikar MR Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.
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Indian J Hematol Blood Transfus. 2019 Jan;35(1):109-113. (IF: 0.474)
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Hariharan P, Colah R, Ghosh K, Nadkarni A. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
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Chiddarwar AS, D'Silva SZ, Colah RB, Ghosh K, Mukherjee MB. Genetic lesions in the UGT1A1 genes among Gilberts syndrome patients from India.
Mol Biol Rep. 2018 Dec; 45(6):2733-2739.(IF:1.889)
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Kulkarni S, Choudhary B, Gogri H, Patil S, Manglani M, Sharma R, Madkaikar MR. Molecular genotyping of clinically important blood group antigens in patients with thalassaemia.
Indian J Med Res. 2018 Dec;148(6):713-720. (IF: 1.508)
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Hockham C, Bhatt S, Colah R, Mukherjee MB, Penman BS, Gupta S, Piel FB. The spatial epidemiology of sickle-cell anaemia in India.
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Patil R, S C, Parihar A, Mohite A, Shetty S. Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients.
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Rambhia KD, Kharkar V, Pradhan V, Patwardhan M, Ghosh K, Khopkar US. A study of prevalence of autoantibodies in patients with lichen planus from Mumbai, India.
Indian J Dermatol Venereol Leprol. 2018 Nov-Dec;84(6):667-671.(IF: 2.229)
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Cytokine. 2018 Nov;111:20-27 (IF:3.514)
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Gorakshakar AC, Breganza PV, Colaco SP, Shaikh RF, Bohra MY, Sawant PM, Nadkarni AH, Colah RB, Ghosh KK. Rare ?- and ?-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India.
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Shukla P, Korgaonkar S, Kerketta L, Vundinti BR. Prevalence and Association of Dermatological Manifestations with Fanconi Anemia: A Retrospective Study.
Indian Dermatol Online J. 2018 Sep-Oct;9(5):341-342.(IF: --)
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Warang P & Kedar PS. Hereditary elliptocytosis: A rare red cell membrane disorder.
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Dhangar S, C SK, S C, Vundinti BR. Imatinib resistance due to a novel and rare class of mutation at position S348 (1043nt C?A) of Bcr/Abl gene in a chronic myeloid leukemia patient.
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Pradhan V, Pandit P, Surve P, Lecerf M, Rajadhyaksha A, Nadkar M, Khadilkar PV, Chougule DA, Naigaonkar AA, Lacroix-Desmazes S, Bayry J, Ghosh K, Kaveri SV. Catalytic antibodies in patients with systemic lupus erythematosus.
Eur J Rheumatol. 2018 Sep;5(3):173-178. (IF: --)
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Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar MR. Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
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Hule GP, Kanvinde PR, Kulkarni MA, van Leeuwen K, de Boer M, Bargir UA, Taur PD, Desai MM, Madkaikar MRR p47phox-/- Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.
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Warang P, Homma T, Pandya R, Sawant A, Shinde N, Pandey D, Fujii J, Madkaikar MR, Mukherjee MB Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
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Infect Genet Evol. 2018 Aug;62:205-210.(IF:2.545)
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Colah R, Nadkarni A, Gorakshakar A, Sawant P, Italia K, Upadhye D, Gaikwad H, Ghosh K. Prenatal Diagnosis of HbE-?-Thalassemia: Experience of a Center in Western India.
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Yabaji PM, Shankarkumar A, Shukla A, Bhatia S Hepatitis C virus infection in a tertiary care hospital in Mumbai, India: Identification of a mixed and novel genotype.
Indian J Med Microbiol. 2018 Jul-Sep;36(3):352-356.(IF: 1.157)
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Lad H, Yadav M, Mehta P, Patel P, Sawant P, Colah RB, Mukherjee MB, Shanmugam R. First Observation of Hb Lepore Hollandia in the Baiga Tribal Family.
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Swati Yardi, Mehul Rajpurkar, Aruna Shankarkumar. A retrospective study of quality management system at National Reference Laboratory in Mumbai- highlighting quality in HIV testing.
International J Med Sci Public Health 2018 June; 7(10):1-6. Online First (IF:)
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Deshpande R, Pathare A, Alkindi S, Al Zadjali S, Ghosh K, Shetty S. A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.
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Fichou Y, Parchure D, Gogri H, Gopalkrishnan V, Le Maréchal C, Chen JM, Férec C, Madkaikar MR, Ghosh K, Kulkarni S. Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
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Acta Trop. 2018 May;181:21-24. (IF: 2.509)
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Chougule D, Nadkar M, Rajadhyaksha A, Pandit-Shende P, Surve P, Dawkar N, Khadilkar P, Patwardhan M, Kaveri S, Ghosh K, Pradhan V. Association of clinical and serological parameters of systemic lupus erythematosus patients with Epstein-Barr virus antibody profile.
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Prabhudesai A, Shetty S, Ghosh K, Kulkarni B. Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein Occlusion.
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Gaikwad T, Ghosh K, Avery P, Kamali F, Shetty S. Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.
Clin Appl Thromb Hemost. 2018 Mar;24(2):353-359.(IF: 2.096)
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Gogri H, Ray S, Agrawal S, Aruna S, Ghosh K, Gorakshakar A Heterogeneity of O blood group in India: Peeping through the window of molecular biology.
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Patil RK, Ghosh K, Chandrakala S, Shetty S. A possible need for routine screening for Strongyloides stercoralis infection in Indian haemophilia patients.
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Kulkarni S, Parchure DS, Gopalkrishnan V, Madkaikar MR. Screening for DEL phenotype in RhD negative Indians.
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Pathak V, Colah R, Ghosh K Plasmodium falciparum malaria skews globin gene expression balance in in-vitro haematopoietic stem cell culture system: Its implications in malaria associated anemia.
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Gene 2018 Jan 30;641:41-45.(IF: 3.191)
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2017 | |
| 302 |
Pranatharthiharan S, Patel MD, Malshe VC, Pujari V, Gorakshakar A, Madkaikar MR, Ghosh K, Devarajan PV. Asialoglycoprotein receptor targeted delivery of doxorubicin nanoparticles for hepatocellular carcinoma.
Drug Deliv. 2017 Nov;24(1):20-29(IF: 6.402)
|
2017 | |
| 303 |
Mohanty MC, Madkaikar MR, Desai M, Taur P, Nalavade UP, Sharma DK, Gupta M. Dalvi A, Shabrish S, Kulkarni M, Aluri J, Deshpande JM Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India.
Emerg Infect Dis. 2017 Oct;23(10):1664-1670. (IF: 8.222)
|
2017 | |
| 304 |
Jadli A, Ghosh K, Satoskar P, Damania K, Bansal V, Shetty S. Combination of copeptin, placental growth factor and total annexin V microparticles for prediction of preeclampsia at 10-14 weeks of gestation.
Placenta. 2017 Oct;58:67-73. (IF: 2.759)
|
2017 | |
| 305 |
Shanbhag S, Ghosh K, Shetty S. Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories.
Thromb Res. 2017 Oct;158:138-139. (IF: 2.65)
|
2017 | |
| 306 |
Priya Hariharan, Madhavi Sawant, Manju Gorivale, Ruma Manchanda, Roshan Colah, Ghosh, Anita Nadkarni. Synergistic effect of two ??globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Mol Biol Rep 2017 Oct;44(5):413-417. (IF: 1.828)
|
2017 | |
| 307 |
Prabhudesai A, Shanbhag S, Mirgal D, Kawankar N, Shetty S. A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.
Haemophilia. 2017 Sep;23(5):e477-e479. (IF: 3.569)
|
2017 | |
| 308 |
Gorakshakar A, Gogri H, Ghosh K. Evolution of technology for molecular genotyping in blood group systems.
Indian J Med Res. 2017 Sep;146(3):305-315.(IF:1.532)
|
2017 | |
| 309 |
Kedar PS. Next-generation sequencing: emerging technology in the area of hematology and blood disorder.
Hematol Blood Disord 2017 Sep;1(1):1-2. (IF: )
|
2017 | |
| 310 |
Prabhudesai A, Shetty S, Ghosh K, Kulkarni B Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.
Eur J Haematol. 2017 Sep; 99(3):249-254. (IF: 2.653)
|
2017 | |
| 311 |
Vira H, Pradhan V, Umare V, Chaudhary A, Rajadhyksha A, Nadkar M, Ghosh K, Nadkarni A. Role of MMP-7 in the pathogenesis of systemic lupus erythematosus (SLE).
Lupus. 2017 Aug;26(9):937-943. (IF: 2.454)
|
2017 | |
| 312 |
Patil R, Ghosh K, Shetty S. Mortality caused by intracranial bleeding in non-severe hemophilia A patients: comment.
J Thromb Haemost. 2017 Aug; 15(8):1709-10. (IF: 5.287)
|
2017 | |
| 313 |
Umare VD, Pradhan VD, Rajadhyaksha AG, Ghosh K, Nadkarni AH. A functional SNP MCP-1 (-2518A/G) predispose to renal disorder in Indian Systemic Lupus Erythematosus patients.
Cytokine. 2017 Aug;96:189-194. (IF: 3.488)
|
2017 | |
| 314 |
Gaikwad T, Ghosh K, Shetty S. Dosing algorithms for vitamin K antagonists across VKORC1 and CYP2C9 genotypes: comment.
J Thromb Haemost. 2017 Aug; 15(8):1708. (IF: 5.287)
|
2017 | |
| 315 |
Kulkarni SS, Vasantha K, Gogri H, Parchure D, Madkaikar M, Férec C, Fichou Y. First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms.
Transfusion. 2017 Aug;57(8):1944-1948 (IF: 3.386)
|
2017 | |
| 316 |
Das S, Chiddarwar A, Warang P and Kedar P. Association of Heme Oxygenase-1 (Number of GT Repeats) with the methemoglobin levels in recessive congenital methemoglobinemia in Indian population.
J Molecular Genet Medicine 2017 Jul; 11(3):1-5 (IF: 2.20)
|
2017 | |
| 317 |
Warang P, Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M. Does novel P5N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
Blood Cells Mol Dis. 2017 Jul;66:8-10. (IF: 1.882)
|
2017 | |
| 318 |
Prabhudesai A, Shetty S, Ghosh K, Kulkarni B. Dysfunctional fibrinolysis and cerebral venous thrombosis.
Blood Cells Mol Dis. 2017 Jun;65:51-55. (IF: 1.882)
|
2017 | |
| 319 |
Aluri J, Italia K, Gupta M, Dalvi A, Bavdekar A, Madkaikar M. Low T cell receptor excision circles (TRECs) in a case of ZAP 70 deficient severe combined immunodeficiency (SCID) with a novel mutation from India.
Blood Cells Mol Dis. 2017 Jun;65:95-96. (IF: 1.882)
|
2017 | |
| 320 |
Hariharan P, Gorivale M, Colah R, Ghosh K, Nadkarni A. Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?
Ann Hum Genet. 2017 May;81(3):125-128. (IF: 1.659)
|
2017 | |
| 321 |
Kedar P, Desai A, Warang P, Colah R. A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia.
Hematology. 2017 May;22(4):252-257 (IF: )
|
2017 | |
| 322 |
Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K. Effect of the Hemochromatosis Mutations on Iron Overload among the Indian ? Thalassemia Carriers.
J Clin Lab Anal. 2017 May;31(3).(IF: 1.521)
|
2017 | |
| 323 |
Umare V, Nadkarni A, Nadkar M, Rajadhyksha A, Khadilkar P, Ghosh K, Pradhan VD Do high sensitivity C-reactive protein and serum interleukin-6 levels correlate with disease activity in systemic lupus erythematosuspatients?
J Postgrad Med. 2017 Apr-Jun;63(2):92-95. (IF: 0.912)
|
2017 | |
| 324 |
Warang P, Roshan Colah , Kedar PS. Lead poisoning induced severe hemolytic anemia, basophilic stippling, mimicking erythrocyte pyrimidine 5’-nucleotidase deficiency in Beta thalassemia minor.
J Clin Toxicol 2017 Apr; 7(2):1-3. (IF: 3.677)
|
2017 | |
| 325 |
Mehta P, Upadhye D, Hariharan P, Italia K, Sawant P, Nadkarni A, Subramanian G,Mukherjee MB. Identification of high oxygen affinity hemoglobin (Hb Andrew-Minneapolis) in an Indian family.
|
2017 | |
| 326 |
Kerketta LS, Ghosh K, Nadkarni A, Madkaikar M, Vundinti BR. Centrosome Aberration Frequency and Disease Association in B-Acute Lymphoblastic Leukemia.
In Vivo. 2017 Mar-Apr;31(2):215-220. (IF: 0.953)
|
2017 | |
| 327 |
R Devendra, R Shanmugam, MPSS Singh, CP Vishwakarma, S Godbhole, N Singh, V Gupta, P Kedar, MB Mukherjee. Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, India.
Meta Gene, 2017 Mar; 12:130-133. (IF: 1.27)
|
2017 | |
| 328 |
Doley D, Kakati S, Saikia L, Rajadhyaksha A, Nadkar M, Khadilkar P, Patwardhan M, Pradhan V. A Comparitive Study of Anticardiolipin Antibodies among Systemic Lupus Erythematosus Patients from Western and Eastern India.
J Assoc Physicians India. 2017 Mar;65(3):14-19. (IF: 0.37)
|
2017 | |
| 329 |
Madkaikar M, Gupta M, Dixit A, Patil V. Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W).
J Pediatr Hematol Oncol. 2017 Mar;39(2):143-146. (IF: 1.076)
|
2017 | |
| 330 |
Umare VD, Pradhan VD, Rajadhyaksha AG, Patwardhan MM, Ghosh K, Nadkarni AH. Impact of TNF-? and LT? gene polymorphisms on genetic susceptibility in Indian SLE patients.
Hum Immunol. 2017 Feb;78(2):201-208. (IF: 2.311)
|
2017 | |
| 331 |
Solanki A, Kumar Selvaa C, Sheth F, Radhakrishnan N, Kalra M, Vundinti BR. Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.
Leuk Res. 2017 Feb;53:50-56. (IF: 2.501)
|
2017 | |
| 332 |
Bacchelli C, Moretti FA, Carmo M, Adams S, Stanescu HC, Pearce K, Madkaikar M, Gilmour KC, Nicholas AK, Woods CG, Kleta R, Beales PL, Qasim W, Gaspar HB. Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency.
J Allergy Clin Immunol. 2017 Feb;139(2):634-642.e5. (IF: 13.081)
|
2017 | |
| 333 |
Deshpande R, Ghosh K, Shetty S. Synergistic effect of factor VII gene polymorphisms causing mild factor VII deficiency in a case of severe factor X deficiency.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):105-106.(IF: 1.367)
|
2017 | |
| 334 |
Ali S, Shetty S, Ghosh K. A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):94-95.(IF: 1.367)
|
2017 | |
| 335 |
Patil R, Mukaddam A, Ghosh K, Shetty S. Management of pregnancy in dysfibrinogenemia cases: a dilemma.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):91-93. (IF: 1.367)
|
2017 | |
| 336 |
Chiddarwar AS, D'Silva SZ, Colah RB, Ghosh K, Mukherjee MB. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults.
Ann Hum Genet. 2017 Jan;81(1):11-19.(IF: 1.659)
|
2017 | |
| 337 |
Gupta AD, Nadkarni A, Mehta P, Goriwale M, Ramani M, Chaudhary P, Mehrotra V, Colah R. Phenotypic expression of HbO Indonesia in two Indian families and its interaction with sickle hemoglobin.
Indian J Pathol Microbiol. 2017 Jan-Mar;60(1):79-83.(IF: 0.616)
|
2017 | |
| 338 |
P Hariharan, S Colaco, R Colah, K Ghosh A Nadkarni Do b-globin gene variants contribute in substantial reduction in HbA2 levels?
Int. J. Lab Hematol 2016 Dec;38(6):610-615.(IF: 2.03)
|
2016 | |
| 339 |
Patil R, Ghosh K, Shetty S. Betrixaban in Acutely Ill Medical Patients.
N Engl J Med. 2016 Dec 15;375(24):e50.(IF: 72.406)
|
2016 | |
| 340 |
Kulkarni M, Desai M, Gupta M, Dalvi A, Taur P, Terrance A, Bhat S, Manglani M, RajR, Shah I, Madkaikar M. Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families.
J Clin Immunol. 2016 Nov;36(8):774-784. (IF: 3.253)
|
2016 | |
| 341 |
Kawankar N, Rathi J, Ghosh K, Shetty S. Clinical and molecular epidemiology of factor XI deficiency in India.
Thromb Res. 2016 Nov;147:85-87.(IF: 2.65)
|
2016 | |
| 342 |
Garg S, Shanmukhaiah C, Ghosh K, Madkaikar MR. Cell signaling in putative leukemic stem cells and blast population in acute myeloid leukemia.
Leuk Lymphoma. 2016 Sep;57(9):2195-8. (IF: 2.755)
|
2016 | |
| 343 |
Ghosh K Management of Haemophilia in Developing Countries: Challenges and Options.
Indian J Hematol Blood Transfus. 2016 Sep;32(3):347-55.(IF: 0.403)
|
2016 | |
| 344 |
Ali S, Shetty S, Ghosh K. Bengal macrothrombocytopenia is not totally an innocuous condition.
Blood Cells Mol Dis. 2016 Sep;60:3-6.(IF: 1.882)
|
2016 | |
| 345 |
Shanbhag S, Ghosh K, Shetty S. First trimester prenatal diagnosis of severe FXIII deficiency.
Haemophilia. 2016 Sep;22(5):e443-4. (IF: 3.569)
|
2016 | |
| 346 |
Italia K, Dabke P, Sawant P, Nadkarni A, Ghosh K, Colah RB. Hb E-?-Thalassemia in Five Indian States.
Hemoglobin. 2016 Sep;40(5):310-315.(IF: 0.77)
|
2016 | |
| 347 |
Kulkarni SS, Vasantha K, Ghosh K. Antigen negative red blood cell inventory of Indian blood donors.
Transfus Apher Sci. 2016 Aug;55(1):131-5. (IF: 1.3)
|
2016 | |
| 348 |
Gupta M, Aluri J, Terrance A, Madkaikar MR. Adenosine Deaminase Deficiency with a Novel Gene Mutation.
Indian J Pediatr. 2016 Aug;83(8):875-6. (IF: 0.945)
|
2016 | |
| 349 |
Mohanty P, Korgaonkar S, Shanmukhaiah C, Ghosh K, Vundinti BR. Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.
Blood Cells Mol Dis. 2016 Jul;59:52-7.(IF: 1.882)
|
2016 | |
| 350 |
Ali S, Ghosh K, Daly ME, Hampshire DJ, Makris M, Ghosh M, Mukherjee L, Bhattacharya M, Shetty S. Congenital macrothrombocytopenia is a heterogeneous disorder in India.
Haemophilia. 2016 Jul; 2(4):570-82.(IF: 3.569)
|
2016 | |
| 351 |
Chaudhary AK, Chaudhary S, Ghosh K, Nadkarni A. Pleiotropic Roles of Metalloproteinases in Hematological Malignancies: an Update.
Asian Pacific J. of Cancer Prevention 2016 Jul; 17(7):3043-51.(IF: 2.39)
|
2016 | |
| 352 |
Deshpande R, Kulkarni B, Ghosh K, Shetty S. A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis.
Thromb Res. 2016 Jul;143:1-2.(IF: 2.65)
|
2016 | |
| 353 |
Patil R, Ghosh K, Shetty S. Comment on Salomon et al. Gestational Diabetes Mellitus Is Associated With Changes in the Concentration and Bioactivity of Placenta-Derived Exosomes in Maternal Circulation Across Gestation. Diabetes 2016;65:598-609.
Diabetes. 2016 Jul;65(7):e24-5.(IF: 8.684)
|
2016 | |
| 354 |
Italia K, Chandrakala S, Ghosh K, Colah R. Can hydroxyurea serve as a free radical scavenger and reduce iron overload in ?-thalassemia patients?
Free Radic Res. 2016 Jul; 27:1-7.(IF: 3.188)
|
2016 | |
| 355 |
Sawant M, Chandrakala S, Colah R, Ghosh K, Nadkarni A. Does HbF induction by hydroxycarbamide work through MIR210 in sickle cell anaemia patients?
Br J Haematol. 2016 Jun;173(5):801-3. (IF: 5.67)
|
2016 | |
| 356 |
Colah RB, Nadkarni A, Gorakshakar A, Sawant P, Gorivale M, Mehta P, Sawant M, Ghosh K. Five Rare ? Globin Chain Hemoglobin Variants in India.
Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):282-6.(IF: 0.403
|
2016 | |
| 357 |
Patil R, Ghosh K, Shetty S. Could procoagulant cell-derived microparticles have a more crucial role in pregnancy complications rather than exosomes?
Am J Obstet Gynecol. 2016 Jun;214(6):765-6. (IF: 5.574)
|
2016 | |
| 358 |
Gogri H, Kulkarni SS, Vasantha K, Jadhav S, Ghosh K, Gorakshakar A. Partial matching of blood group antigens to reduce alloimmunization in Western India.
Transfus Apher Sci. 2016 Jun;54(3):390-5.(IF: 1.3)
|
2016 | |
| 359 |
Shabrish S, Gupta M, Madkaikar MR A Modified NK Cell Degranulation Assay Applicable for Routine Evaluation of NK Cell Function.
J Immunol Res. 2016;2016:3769590.(IF: 4.856)
|
2016 | |
| 360 |
Upadhye D, Jain D, Trivedi Y, Nadkarni A, Ghosh K, Colah R. Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients.
Ann Hematol. 2016 Jun;95(7):1201-3.(IF: 3.083)
|
2016 | |
| 361 |
Disha S Parchure, Kulkarni SS Noninvasive fetal RHD genotyping from maternal plasma
Global Journal of Transfusion Science 2016 Jan-Jun;1(1): 21-28.(IF:--)
|
2016 | |
| 362 |
Kulkarni B, Gorakshakar A, Singh V, Parihar A, Donta A, Gogri H, Jadhav S, Ghosh K, Shetty S. Indian Bombay phenotype: it is different!
Blood Transfus. 2016 Jun 24;15(1):74-76. (IF: 1.607)
|
2016 | |
| 363 |
Pathak V, Colah R, Ghosh K. Correlation between 'H' blood group antigen and Plasmodium falciparum invasion.
Ann Hematol. 2016 Jun;95(7):1067-75.(IF: 3.083)
|
2016 | |
| 364 |
Patil R, Ghosh K, Shetty S. Annexin A5 levels or circulating microparticles: what we see depends mainly on what we look for.
J Intern Med. 2016 Jun;279(6):608. (IF: 7.598)
|
2016 | |
| 365 |
Madkaikar MR, Shabrish S, Desai M. Current Updates on Classification, Diagnosis and Treatment of Hemophagocytic Lymphohistiocytosis (HLH).
Indian J Pediatr. 2016 May;83(5):434-43.(IF: 0.945)
|
2016 | |
| 366 |
Fleisher TA, Madkaikar MR, Rosenzweig SD. Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies.
Indian J Pediatr. 2016 May;83(5):444-9.(IF: 0.945)
|
2016 | |
| 367 |
Mirgal D, Ghosh K, Mahanta J, Dutta P, Shetty S. Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.
Trans R Soc Trop Med Hyg. 2016 May;110(5):294-8.(IF: --)
|
2016 | |
| 368 |
Shetty S, Ghosh K. Why should hemophilia B be milder than hemophilia A?
Haematologica. 2016 May;101(5):e213. (IF: 7.702)
|
2016 | |
| 369 |
Jadli AS, Ghosh K, Shetty S. Preeclampsia: simplified or still miles to go?
Am J Obstet Gynecol. 2016 May;214(5):668-9.(IF: 5.574)
|
2016 | |
| 370 |
Mohapatra R, Warang P, Ghosh K, Colah R. Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye.
Cytometry B Clin Cytom. 2016 May;90(3):279-84.(IF: 2.474)
|
2016 | |
| 371 |
Pradhan V, Pandit P, Rajadhyaksha A, Patwardhan M, Surve P, Kamble P, Lecerf M, Bayry J, Kaveri S, Ghosh K, Nadkar MY. Association of Serum Ferritin Levels with Hematological Manifestations in Systemic Lupus Erythematosus Patients from Western India.
J Assoc Physicians India. 2016 May;64(5):14-18.(IF: 0.37)
|
2016 | |
| 372 |
Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2016 May;2(4):381-5.(IF: 2.096)
|
2016 | |
| 373 |
Garg S, Ghosh K, Madkaikar MR. Antigen expression on a putative leukemic stem cell population and AML blast.
Int J Hematol. 2016 May;103(5):567-71.(IF: 1.61)
|
2016 | |
| 374 |
Madkaikar MR, Aluri J, Gupta S. Guidelines for Screening, Early Diagnosis and Management of Severe Combined Immunodeficiency (SCID) in India.
Indian J Pediatr. 2016 May;83(5):455-62 (IF: 0.945)
|
2016 | |
| 375 |
Patil R, Ghosh K, Shetty S. Re: Does low-molecular-weight heparin influence fetal growth or uterine and umbilical arterial Doppler in women with a history of early-onset uteroplacental insufficiency and an inheritable thrombophilia? Secondary randomised controlled trial results LMWH
BJOG. 2016 Apr;123(5):844.(IF: 5.051)
|
2016 | |
| 376 |
Jacob S, Nayak S, Kakar R, Chaudhari UK, Joshi D, Vundinti BR, Fernandes G, Barai RS, Kholkute SD, Sachdeva G. A triad of telomerase, androgen receptor and early growth response 1 in prostate cancer cells.
Cancer Biol Ther. 2016 Apr 2;1(4):439-48.(IF: 3.294)
|
2016 | |
| 377 |
Patil R, Ghosh K, Shetty S. A simple clot based assay for detection of procoagulant cell-derived microparticles.
Clin Chem Lab Med. 2016 Apr 1;54(5):799-803.(IF: 3.432)
|
2016 | |
| 378 |
Pinto P, Ghosh K, Shetty S. F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association.
Mutat Res. 2016 Apr;786:27-33.(IF: 5.5)
|
2016 | |
| 379 |
Shanbhag S, Ghosh K, Shetty S. Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.
Blood Cells Mol Dis. 2016 Mar;57:81-4.(IF: 1.882)
|
2016 | |
| 380 |
Patil R, Ghosh K, Mukherjee S, Shetty S. Does consumption of platelet-derived microparticles in the fibrin clot explain the decrease in their percentage during pregnancy?
Blood Cells Mol Dis. 2016 Mar;57:115-7.(IF: 1.882)
|
2016 | |
| 381 |
Shetty S, Sharma N, Ghosh K. Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.
Crit Rev Oncol Hematol. 2016 Mar;99:129-33.(IF: 4.971)
|
2016 | |
| 382 |
Jadli A, Ghosh K, Shetty S. Prediction of small-for-gestational-age at 35-37 weeks of gestation: too late for management?
Ultrasound Obstet Gynecol. 2016 Mar;47(3):385.(IF: 4.71)
|
2016 | |
| 383 |
Garg S, Shanmukhaiah C, Marathe S, Mishra P, Babu Rao V, Ghosh K, Madkaikar MR. Differential antigen expression and aberrant signaling via PI3/AKT, MAP/ERK, JAK/STAT, and Wnt/? catenin pathways in Lin-/CD38-/CD34+ cells in acute myeloid leukemia.
Eur J Haematol. 2016 Mar;96(3):309-17.(IF: 2.653)
|
2016 | |
| 384 |
Chaudhary AK, Chaudhary S, Ghosh K, Shanmukaiah C, Nadkarni AH. Secretion and Expression of Matrix Metalloproteinase-2 and 9 from Bone Marrow Mononuclear Cells in Myelodysplastic Syndrome and Acute Myeloid Leukemia.
Asian Pac J Cancer Prev. 2016 Mar;17(3):1519-29.(IF: 2.39 )
|
2016 | |
| 385 |
Mahadik K, Shaikh R, Mahajan N, Pandit A, Shinde S, Kanjaksha Ghosh, Ajit C.Gorakshakar. Analysis of Complement Recepter Type I(CR1) Polymorphisms and Its Association with Malaria in Rural Population of Maharashtra.
World J Res Review. 2016 Mar;2(3):13-17.(IF: )
|
2016 | |
| 386 |
Patil R, Ghosh K, Shetty S. Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.
Ann Hematol. 2016 Feb;95(3):533-4.(IF: 3.083)
|
2016 | |
| 387 |
Pathak VA, Ghosh K. Erythropoiesis in Malaria Infections and Factors Modifying the Erythropoietic Response.
Anemia. 2016;2016:9310905. Epub 2016 Feb 29. Review. (IF: 3.00)
|
2016 | |
| 388 |
Upadhye DS, Jain DL, Trivedi YL, Nadkarni AH, Ghosh K, Colah RB Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.
PLoS One. 2016 Jan 19;11(1):e0147081.(IF: 2.806)
|
2016 | |
| 389 |
Solanki A, Mohanty P, Shukla P, Rao A, Ghosh K, Vundinti BR. FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients.
PLoS One. 2016 Jan 22;11(1):e0147016.(IF: 2.806)
|
2016 | |
| 390 |
Gorakshakar AC, Ghosh K. Use of lectins in immunohematology.
Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF: 1.06)
|
2016 | |
| 391 |
Joshi D, Korgaonkar S, Shanmukhaiah C, Vundinti BR. Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome.
Ann Hematol. 2016 Jan;95(1):79-85.(IF: 3.083)
|
2016 | |
| 392 |
Pinto P, Shetty S, Lacroix-Desmazes S, Bayry J, Kaveri S, Ghosh K. Antibody profile in Indian severe haemophilia A patients with and without FVIII inhibitors
Immunol Lett. 2016 Jan;169:93-7.(IF: 2.86)
|
2016 | |
| 393 |
Kulkarni B, Ghosh K, Shetty S. Second trimester prenatal diagnosis in Glanzmanns Thrombasthenia.
Haemophilia. 2015 Dec 28. [Epub ahead of print] (IF: 2.673)
|
2015 | |
| 394 |
Gorivale M, Sawant P, Mehta P, Nadkarni A, Ghosh K, Colah R. Challenges in Prenatal Diagnosis of Beta Thalassaemia: Couples with Normal HbA2 in One Partner.
Prenat Diagn. 2015 Dec;35(13):1353-7. (IF: 3.043)
|
2015 | |
| 395 |
Ali S, Ghosh K, Shetty S. Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP).
Blood Cells Mol Dis. 2015 Dec;5(4):410-4. (IF: 2.731)
|
2015 | |
| 396 |
Mehta PR, Upadhye DS, Sawant PM, Gorivale MS, Nadkarni AH, Shanmukhaiah C, Ghosh K, Colah RB. Diverse phenotypes and transfusion requirements due to interaction of ?-thalassemias with triplicated ?-globin genes.
Ann Hematol. 2015 Dec;94(12):1953-8. (IF: 3.022)
|
2015 | |
| 397 |
Nadkarni A, Dabke P, Colah R, Ghosh K. Molecular understanding of Indian untransfused thalassemia intermedia.
Int J Lab Hematol. 2015 Dec;37(6):791-6. (IF: 2.401)
|
2015 | |
| 398 |
Patil R, Ghosh K, Damania K, Bansal V, Satoskar P, Darekar A, Shetty S. Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss.
Br J Haematol. 2015 Dec;171(5):892-6. (IF: 5.812)
|
2015 | |
| 399 |
Kasatkar P, Ghosh K, Shetty S. Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
Indian J Med Res. 2015 Dec;142(6):759-62. (IF: 1.446)
|
2015 | |
| 400 |
Dalal B, Shankarkumar A, Ghosh K. Individualization of antiretroviral therapy Pharmacogenomic aspect.
Indian J Med Res. 2015 Dec;142(6):663-74. (IF: )
|
2015 | |
| 401 |
Mukaddam A, Kulkarni B, Jadli A, Ghosh K, Shetty S. Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families.
Haemophilia. 2015 Nov;21(6):e519-23. (IF: 2.673)
|
2015 | |
| 402 |
Pradhan V, Patwardhan M, Rajadhyksha A, Umare V, Khadilkar P, Kaveri SV, Ghosh K Association of clinical presentation with anti-nuclear antibody specificities among patients with systemic lupus erythematosus.
Indian J Nephrol. 2015 Nov-Dec;25(6):391-2 (IF: 0.55)
|
2015 | |
| 403 |
Gorakshakar A, Donta A, Jadhav S, Vasantha K, Ghosh K. Molecular analysis of Bombay phenotype cases seen in India.
ISBT Science Series 2015 Nov; 10(2):100-105. (IF: 0.39)
|
2015 | |
| 404 |
Patil A and Shankar Kumar A. Hepatitis B screening accuracy in blood bank.
Intl J Recent Scient Res 2015 Nov; 6(11): 7345-7357 (IF: 0.13)
|
2015 | |
| 405 |
Italia K, Colah R, Ghosh K. Experimental animal model to study iron overload and iron chelation and review of other such models.
Blood Cells Mol Dis. 2015 Oct;55(3):194-9. (IF: 2.731)
|
2015 | |
| 406 |
Sonawane Patil A, Shankarkumar Pawar A. Blood donation in Maharashtra: Prevalence of transfusion transmitted infections in blood donors.
Int J Pharm Bio Sci 2015 Oct; (4): (B) 981-987. (IF: 0.36)
|
2015 | |
| 407 |
Patil R, Ghosh K, Vora S, Shetty S. Inherited and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss.
Blood Cells Mol Dis. 2015 Oct;55(3):200-5. (IF: 2.731)
|
2015 | |
| 408 |
Vaidya S, Ghosh K, Shanmukhaiah C, Vundinti BR Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Oct 15;765:124-30. (IF: 2.73)
|
2015 | |
| 409 |
Pradhan V, Kemp EH, Nadkar M, Rajadhyaksha A, Lokhandwala K, Patwardhan M, Weetman AP, Nadkarni A, Ghosh K. Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to systemic lupus erythematosus in an Indian population.
Scand J Rheumatol. 2015 Oct;44(5):425-7. (IF: 2.307)
|
2015 | |
| 410 |
Korgaonkar S, Vundinti BR. Trisomy 8 Mosaicism in a Boy with Dysmorphic Features.
Indian Pediatr. 2015 Sep;52(9):812-3. (IF: 0.972)
|
2015 | |
| 411 |
Priya Madan Yabaji, Aruna Shankarkumar, and Kanjaksha Ghosh. A silent killer HCV (Hepatitis C virus) in India : A Review of prevalence from all available data
Intl J Curr Res, 2015 Sep; 7(9): 20193-20203. (IF: 0.08)
|
2015 | |
| 412 |
Jadli A, Ghosh K, Shetty S. Is peripheral blood corin level clinically relevant for prediction of pre-eclampsia?
Ultrasound Obstet Gynecol. 2015 Sep;46(3):380. (IF: 4.254)
|
2015 | |
| 413 |
Patil R, Ghosh K, Shetty S. Tissue factor expressed by circulating cancer cell-derived microparticles drastically increases the incidence of deep vein thrombosis in mice: comment.
J Thromb Haemost. 2015 Sep;13(9):1737-8. (IF: 5.565)
|
2015 | |
| 414 |
Patil R, Ghosh K, Shetty S. Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss.
Ann Intern Med. 2015 Sep 15;163(6):483-4. (IF: 16.593)
|
2015 | |
| 415 |
Kasatkar P, Kulkarni B, Ghosh K, Shetty S. Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.
Ann Hematol. 2015 Aug;94(8):1409-10. (IF: 3.022)
|
2015 | |
| 416 |
Vaidya S, Ghosh K, Shanmukhaiah C, Vundinti BR. Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Aug 21;765:124-130. (IF: 2.73 )
|
2015 | |
| 417 |
Pathak V, Colah R, Ghosh K. Tyrosine kinase inhibitors: New class of antimalarials on the horizon?
Blood Cells Mol Dis. 2015 Aug;55(2):119-26. (IF: 2.18)
|
2015 | |
| 418 |
Jadli A, Sharma N, Damania K, Satoskar P, Bansal V, Ghosh K, Shetty S. Promising prognostic markers of preeclampsia: new avenues in waiting.
Thromb Res. 2015 Aug;136(2):189-95. Review. (IF: 2.32)
|
2015 | |
| 419 |
Dalal K., Shankarkumar A. Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma.
Intl J Res Engg Applied Sci 2015Aug; 5(8): 76-89. (IF:)
|
2015 | |
| 420 |
Lobo V, Shetty S, Kulkarni B, Butera D, Magalhaes GS, Ghosh K Erratum to: A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2015 Jul;94(7):1259. (IF: 3.022)
|
2015 | |
| 421 |
Jadli A, Kulkarni B, Ghosh K, Shetty S. High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.
Indian J Med Res. 2015 Jul;142(1):85-7. (IF: 1.446)
|
2015 | |
| 422 |
Merchant R, Italia K, Ahmed J, Ghosh K, Colah RB. A successful twin pregnancy in a patient with HbE-?-thalassemia in western India.
J Postgrad Med. 2015 Jul-Sep;61(3):203-5. (IF: 0.87)
|
2015 | |
| 423 |
Ghosh K. Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Indian J Hematol Blood Transfus. 2015 Jun;31(2):314-6. (IF: 0.232)
|
2015 | |
| 424 |
Ghosh K Factors Modulating Blood HbA1C Level and Diabetic Retinopathy.
J Assoc Physicians India. 2015 May;63(5):95-6. (IF: 0.37)
|
2015 | |
| 425 |
Korgaonkar S, Vundinti BR. Tetrasomy X in a Child with Upper Limb Deformity.
Indian Pediatr. 2015 May;52(5):439. (IF: 0.972 )
|
2015 | |
| 426 |
Shanbhag S, Lulla C, Ghosh K, Shetty S. Prenatal diagnosis in a haemophilia carrier with triplet pregnancy.
Haemophilia. 2015 May;21(3):e228-30. (IF: 2.673 )
|
2015 | |
| 427 |
Mukherjee MB, Colah RB, Martin S, Ghosh K. Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario.
Indian J Med Res. 2015 May;141(5):516-20. (IF: 1.446)
|
2015 | |
| 428 |
Mukaddam A, Patil R, Jadli A, Chandrakala S, Ghosh K, Shetty S Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
Am J Clin Pathol. 2015 May;143(5):755-. (IF: 2.278)
|
2015 | |
| 429 |
Madkaikar MR, Italia K, Gupta M, Desai M, Aggarwal A, Singh S, Suri D, Mishra A, Chavan S, Ghosh K, Sarangal R, Dogra S. Leukocyte adhesion deficiency-I with a novel intronic mutation presenting with pyoderma gangrenosum- like lesions.
J Clin Immunol. 2015 May;3(4):431-4. (IF: 3.094 )
|
2015 | |
| 430 |
Ghosh K, Colah RB, Mukherjee MB. Haemoglobinopathies in tribal populations of India.
Indian J Med Res. 2015 May;141(5):505-8. (IF: 1.446)
|
2015 | |
| 431 |
Colah RB, Mukherjee MB, Martin S, Ghosh K. Sickle cell disease in tribal populations in India.
Indian J Med Res. 2015 May;141(5):509-15. (IF: 1.446 )
|
2015 | |
| 432 |
Ghosh K. Sickle cell anaemia: The need for new approaches in management.
Natl Med J India. 2015 Mar-Apr;28(2):90-3. (IF: 0.907)
|
2015 | |
| 433 |
Shanbhag S, Pai N, Ghosh K, Shetty S. Prenatal diagnosis in a family with purfura fulminans.
Blood Coagul Fibrinolysis. 2015 Apr;26(3):350. (IF: 1.242 )
|
2015 | |
| 434 |
Upadhye D, Koduri P, Tarakeshwari S, Mehta P, Surve R, Warang P, Kedar PS, Nadkarni A, Ghosh K, Colah R. Hb M Hyde Park and Hb M Boston in two Indian families - a rare cause of methaemoglobinemia.
Int J Lab Hematol. 2015 Apr;37(2):e40-3. (IF: 2.401)
|
2015 | |
| 435 |
Patil AS, Shankarkumar A. Hepatitis B Diagnosis in Blood Bank: Evaluation and Challenges
MGM J Med Sci 2015 Apr-Jun; 2 (2) : 83-89 (IF: )
|
2015 | |
| 436 |
Deb S, Ghosh K, Shetty SD. Nanoimaging in cardiovascular diseases: Current state of the art.
Indian J Med Res. 2015 Mar;141(3):285-98. (IF: 1.446 )
|
2015 | |
| 437 |
Mishra A, Italia K, Gupta M, Desai M, Madkaikar MR Syndrome due to CD40 Deficiency: Possibly the first case from India.
Journal of Postgraduate Medicine. 2015 Jan-Mar; 61:41-48. (IF: 0.87 )
|
2015 | |
| 438 |
Italia K, Krishnamurti L, Mehta V, Raicha B, Italia K, Mehta P, Ghosh K, Colah R. Feasibility of a Newborn screening and follow-up programme for sickle cell disease among South Gujarat (India) tribal populations.
J Med Screen 2015 Mar;22(1):1-7 (IF: 1.75)
|
2015 | |
| 439 |
Kangne HK, Jijina FF, Italia YM, Jain DL, Nadkarni AH, Ghosh KK, Colah RB. The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Sickle Cell Disease in Western India. Mutations in
Clin Appl Thromb Hemost. 2015 Mar;21(2):186-9.(IF: 1.973)
|
2015 | |
| 440 |
Warang P, Kedar PS, Ghosh K, Colah RB. Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience.
Clin Chem Lab Med 2015 Mar1;53(4):e105-8. (IF: 3.017 )
|
2015 | |
| 441 |
Shetty S, Ghosh K Challenges and open issues in the management of acquired hemophilia A (AHA).
Blood Cells Mol Dis. 2015 Mar;54(3):275-80.Review.(IF: 2.731)
|
2015 | |
| 442 |
Mhatre S, Madkaikar MR, Desai M, Ghosh K. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India
Blood Cells Mol Dis. 2015 Mar;54(3):250-7. (IF: 2.731 )
|
2015 | |
| 443 |
Mohanty D, Mukherjee MB, Colah RB, Wadia M, Ghosh K, Chottray GP, Jain D, Italia Y, Ashokan KS, Kaul R, Shukla DK, Muthuswamy V. Spectrum of Hemoglobinopathies Among the Primitive Tribes: A Multicentric Study in India.
Asia Pac J Public Health. 2015 Mar;27(2):NP562-71 (IF: 1.05)
|
2015 | |
| 444 |
Vandana VP, Patwardhan M, Rajadhyaksha A, Dhawale N, Ghosh K Neuropsychiatric manifestations and associated autoantibodies in systemic lupus erythematosus patients from Western India.
Rheumatol Int. 2015 Mar;35(3):541-5. (IF: 1.702)
|
2015 | |
| 445 |
Koduri PR, Kedar PS, Warang P. Erythrocytosis, methemoglobinemia, and the saturation gap.
Ann Hematol. 2015 Mar;94(3):509-10.(IF: 3.022)
|
2015 | |
| 446 |
Madkaikar MR, Italia K, Gupta M, Chavan S, Mishra A, Rao M, Mhatre S, Desai M, Manglani M, Singh S, Suri D, Agrawal A, Ghosh K Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.
Blood Cells Mol Dis. 2015 Mar;54(3):217-23. (IF: 2.731)
|
2015 | |
| 447 |
Shetty S, Ghosh K Novel therapeutic approaches for haemophilia.
Haemophilia 2015 Mar;21(2):152-61. (IF: 2.673 )
|
2015 | |
| 448 |
Warang P, Devendra R, DSilva S, Chiddarwar A, Kedar PS, Ghosh K, Colah R, Mukherjee MB Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
Ann Hematol. 2015 Jan;94(1):169-71. (IF: 3.022)
|
2015 | |
| 449 |
Vandana VP, Surve P, Rajadhyaksha A, Rajendran V, Patwardhan M, Umare V, Ghosh K, Nadkarni A Mannose binding lectin (MBL) 2 gene polymorphism & its association with clinical manifestations in systemic lupus erythematosus (SLE) patients from western India.
Indian J Med Res. 2015 Feb;141(2):199-204. (IF: 1.446)
|
2015 | |
| 450 |
Vaidya S, Vundinti BR, Shanmukhaiah C, Chakrabarti P, Ghosh K. Evolution of BCR/ABL gene mutation in CML is time dependent and dependent on the pressure exerted by tyrosine kinase inhibitor
PLoS One. 2015 Jan 28;10(1):e0114828. eCollection 2015. (IF: 3.057)
|
2015 | |
| 451 |
Italia K, Kangne H, Shanmukaiah C, Nadkarni AH, Ghosh K, Colah RB. Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype.
Br J Haematol. 2015 Jan;168(1):156-9. (IF: 5.812)
|
2015 | |
| 452 |
Warang PP, Kedar PS, Shanmukaiah C, Ghosh K, Colah RB Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
Clin Genet. 2015 Jan;87(1):62-7. (IF: 3.892)
|
2015 | |
| 453 |
Umare V, Vandana VP, Nadkar M, Rajadhyaksha A, Patwardhan M, Ghosh K, Nadkarni AH Effect of proinflammatory cytokines (IL-6, TNF-?, and IL-1?) on clinical manifestations in Indian SLE patients.
Mediators Inflamm. 2014;2014:385297.Epub 2014 Dec 7.
|
2014 | |
| 454 |
Kedar PS, Warang P, Sanyal S, Devendra R, Ghosh K, Colah R Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.
Clin Chim Acta 2014 Nov1; 437:103-5.(IF:2.764)
|
2014 | |
| 455 |
Mhatre S, Madkaikar MR, Jijina F, Ghosh K Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis Type-2.
J Pediat Hematol Oncol 2014 Nov; 36(8):e524-7.(iF:0.973)
|
2014 | |
| 456 |
Mohapatra R, Warang P, Ghosh K, Colah R. Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye
Cytometry B Clin Cytom. 2014 Nov 24. [Epub ahead of print](IF:2.824)
|
2014 | |
| 457 |
Colaco S, Surve R, Sawant P, Nadkarni A, Ghosh K, Colah R. HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association.
Mediterr J Hematol Infect Dis. 2014 Nov 1;6(1):e2014072. eCollection 2014.(IF:-)
|
2014 | |
| 458 |
Mhatre S, Madkaikar MR, Ghosh K, Desai M, Pujari V, Gupta M. Rapid flow cytometry based cytotoxicity assay for evaluation of NK cell function
Indian J Exp Biol 2014 Oct; 52(10):983-8.(IF:0.835)
|
2014 | |
| 459 |
Kulkarni B, Nair SB, Vijapurkar M, Mota L, Shanbhag S, Ali S, Shetty SD, Ghosh K. Molecular pathology of rare bleeding disorders (RBDs) in India: A systematic review.
PLos One 2014 Oct 2; 9(9):e108683.(IF:3.534)Review
|
2014 | |
| 460 |
Shetty S, Ghosh K Paternal factor V Leiden and recurrent pregnancy loss: a new concept behind fetal genetics?: comment
J Thromb Haemost. 2014 Oct; 12(10):1758-9.(IF:5.72)
|
2014 | |
| 461 |
Dabke PS, Colah RB, Ghosh K, Nadkarni AH. Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients
Hematology 2014 Oct; 19(7):388-92.(IF:1.393)
|
2014 | |
| 462 |
Vandana VP, Rajadhyaksha A, Nadkar M, Pandit P, Surve P, Lecerf M, Bayry J, Kaveri S, Ghosh K Clinical and autoimmune profile of scleroderma patients from Western India
Int J Rheumatol. 2014;2014:983781. Epub 2014 Oct 19.(IF:1.469)
|
2014 | |
| 463 |
Pinto P, Ghosh K, Shetty S Analysis of F8 inversions as risk factors for FVIII inhibitor development in Indian severe haemophilia A patients
Blood Cells Mol Dis 2014 Sep; 53(3):161-3.(IF:2.331)
|
2014 | |
| 464 |
Gaikwad T, Ghosh K, Shetty S VKORC1 and CYP2C9 genotype distribution in Asian countries.
Thromb Res. 2014 Sep; 134(3):537-44.(IF:3.133)
|
2014 | |
| 465 |
Pai N, Ghosh K, Shetty S Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).
Clin Appl Thromb Hemost. 2014 Sep;20(6):573-6 (IF: 1.332)
|
2014 | |
| 466 |
Madkaikar MR, Gupta M, Chavan S, Italia K, Desai M, Merchant R, Radhakrishnan N, Ghosh K X-linked hyper IgM syndrome: Clinical, immunological and molecular features in patients from India
Blood Cells Mol Dis. 2014 Sep; 53(3):99-104.(IF:2.331)
|
2014 | |
| 467 |
Pinto P, Parasannanavar D, Ghosh K, Shetty S The association of HLA-DRB1 and HLA-DQB1 alleles with the development of factor VIII inhibitors in severe haemophilia A patients in India.
Tissue Antigens 2014 Aug; 84(2):235-7.(IF:2.35)
|
2014 | |
| 468 |
Ghosh K, Shetty S, Patil R. Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study: comment
J Thromb Haemost. 2014 Aug; 12(8):1377-8.(IF:5.72)
|
2014 | |
| 469 |
Maiti AK, Kim-Howard X, Motghare P, Vandana VP, Chua KH, Sun C, Arango-Guerrero MT, Ghosh K,Niewold TB, Harley JB, Anaya JM, Looger LL, Nath SK. Combined protein and nucleic acid-level effects of rs1143679(R77H), a lupus-predisposing variant within ITGAM.
Hum Mol Genet 2014 Aug 1; 23(15):4161-76.(IF:6.393)
|
2014 | |
| 470 |
D'Silva S, Colah RB, Ghosh K, Mukherjee MB Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates
Gene. 2014 Aug 15;547(1):18-22.(IF:2.443)
|
2014 | |
| 471 |
Shetty S, Shelar T, Mirgal D, Nawadkar V, Pinto P, Shabhag S, Mukaddam A, Kulkarni B, Ghosh K Rare coagulation factor deficiencies: a countrywide screening data from India.
Haemophilia. 2014 Jul; 20(4):575-81.(IF:3.170)
|
2014 | |
| 472 |
Vundinti BR, Kerketta L, Korgaonkar S, Vaidya S, Ghosh K Isodicentric Philadelphia [idic(Ph)] chromosome in a case of CML at chronic phase
Indian J Cancer. 2014 July-September;51(3):383-384.(IF:0.802)
|
2014 | |
| 473 |
Solanki A, Vundinti BR. Prenatal detection of Fanconi anemia.
Indian Pediatr. 2014 Jun;51(6):501
|
2014 | |
| 474 |
Joshi D, Chandrakala S, Korgaonkar S, Ghosh K, Vundinti BR. Down-regulation of miR-199b associated with imatinib drug resistance in 9q34.1 deleted BCR/ABL positive CML patients.
Gene. 2014 Jun 1;542(2):109-12.(IF:2.082)
|
2014 | |
| 475 |
Warang P, Nair S, Nadkarni A, Kedar PS, Bhave A, Ghosh K, Colah R. Hb Koln [?98(FG5) [GTG ? ATG, Val ? Met]]: the first report from India.
Hematology. 2014 Jun;19(4):199-201.(IF:1.393)
|
2014 | |
| 476 |
Nair PS, Shetty S, Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2014 May;22(4):381-5.
|
2014 | |
| 477 |
Gaikwad T, Ghosh K, Kulkarni B, Shetty S Factor V Leiden mutation modulates the bleeding phenotype in warfarin sensitive patients.
Thromb Res. 2014 May;133(5):955-6(IF:2.427)
|
2014 | |
| 478 |
Nair PS, Shetty SD, Chandrakala S, Ghosh K Mutations in intron 1 and intron 22 inversion negative haemophilia a patients from Western India
PLoS One. 2014 May 20;9(5):e97337. eCollection 2014.(IF:3.534)
|
2014 | |
| 479 |
Colah R, Mukherjee M, Ghosh K Sickle cell disease in India.
Curr Opin Hematol. 2014 May;21(3):215-23.(IF:4.053)
|
2014 | |
| 480 |
Prasannavar DJ, Yeola A, Vandana VP, Patwardhan M, Rajadhyaksha A, Ghosh K Distribution of HLA-DR?1 alleles among well-characterized rheumatoid arthritis patients from Western India.
Rheumatol Int. 2014 May;34(5):705-8.(IF:1.516)
|
2014 | |
| 481 |
Nadkarni A, Dabke P, Colah RB, Ghosh K Fetal hemoglobin in sickle cell anemia
Blood Cells Mol Dis. 2014 Apr;52(4):175.(IF:2.331)
|
2014 | |
| 482 |
Ghosh K, Colah R, Manglani M, Choudhry VP, Verma I, Madan N, Saxena R, Jain D, Marwaha N, Das R, Mohanty D, Choudhary R, Agarwal S, Ghosh M, Ross C Guidelines for screening, diagnosis and management of hemoglobinopathies
Indian J Hum Genet. 2014 Apr;20(2):101-19. Review.
|
2014 | |
| 483 |
Vundinti BR. Methylenetetrahydrofolatereductase C677T polymorphism and folate metabolism in
Indian J Hum Genet. 2014 Apr;20(2):99-100
|
2014 | |
| 484 |
Kasatkar P, Shetty S, Ghosh K Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays
Prenat Diagn 2014 Apr; 34(4):377-81.(IF:3.296)
|
2014 | |
| 485 |
Swaminathan S, Garg S, Madkaikar MR, Gupta M, Jijina F, Ghosh K. FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from
Indian J Hum Genet. 2014 Apr;20(2):160-5.
|
2014 | |
| 486 |
Italia K, Upadhye D, Dabke P, Kangane H, Colaco S, Sawant P, Nadkarni A, Gorakshakar A, Jain D, Italia Y, Ghosh K, Colah R Clinical and hematological presentation among Indian patients with common hemoglobin variants.
Clin Chim Acta 2014 Apr 20; 431:46-51.(IF:2.824)
|
2014 | |
| 487 |
Mishra A, Gupta M, Dalvi A, Ghosh K, Madkaikar MR Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID)
J Clin Immunol 2014 Apr; 34(3):316-22.(IF:3.184)
|
2014 | |
| 488 |
Gaikwad T, Jadli A, Ghosh K, Shetty S Delayed Vitamin K deficiency related bleeding: is it genetically linked?
Indian J Pediatr. 2014 Mar;81(3):310-1. (IF:0.919)
|
2014 | |
| 489 |
Pinto P, Ghosh K, Shetty S A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII inhibitor screening assay
Clin Chem.Lab Med. 2014 Mar;52(3):e39-41.(IF:2.955)
|
2014 | |
| 490 |
46 Kasatkar P, Shetty S, Ghosh K. Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients
PLoS One. 2014 Mar 27;9(3):e92575. (IF:3.534)
|
2014 | |
| 491 |
Ali S, Ghosh K, Shetty S Novel genetic abnormalities in Bernard-Soulier syndrome in India
Ann Hematol. 2014 Mar;93(3):381-4. (IF:2.396)
|
2014 | |
| 492 |
Shetty S, Ghosh K. Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within
Haematologica. 2014 Mar;99(3):e30. (IF:5.868)
|
2014 | |
| 493 |
Colaco S, Trivedi A, Colah RB, Ghosh K, Nadkarni AH. Masking of a ?-thalassemia determinant by a novel ??globin gene defect [Hb A2-Saurashtra or ?????G2)Pro®Ser; HBD: C.301C>T] in Cis
Hemoglobin 2014 Jan-Feb; 38(1):24-7. .(IF:0.955)
|
2014 | |
| 494 |
Bhukhanvala DS, Sorathiya S, Surve R, Nair S, Italia K, Colah R, Ghosh K, Gupte SC Hemoglobin variants in Muslim community in South Gujarat, Western India.
Int J Lab Hematol. 2014 Feb;36(1):e15-7 (IF: 1.176)
|
2014 | |
| 495 |
Ray S, Gorakshakar AC, Vasantha K, Agarwal S, Nadkarni A, Ghosh K Molecular characterization of weaker variants of A and B in Indian population- the first report.
Tranf Apheresis Sci 2014 Feb; 50(1): 118-22.(IF:1.072)
|
2014 | |
| 496 |
Kerketta LS, Rao VB, Ghosh K Chimeric Fusion Karyotypes in Childhood B-cell Acute Lymphoblastic Leukemia
Indian Pediatr. 2014 Feb 8;51(2):152-3.(IF:1.036)
|
2014 | |
| 497 |
Ray S, Gorakshakar AC, Vasantha K, Nadkarni A, Italia Y, Ghosh K. Molecular genotyping of ABO blood groups in some population groups from India.
Indian J Med Res 2014 Jan; 139(1): 105-111. (IF: 1.661)
|
2014 | |
| 498 |
Kasatkar P, Ghosh K, Shetty S. An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).
Ann Hematol. 2014 Jan; 93(1): 173-5. (IF:2.396)
|
2014 | |
| 499 |
Parasannanavar DJ, Rajadhyaksha A, Ghosh K. Role of hla-B alleles and clinical presentation of b27 negative spondyarthritis patients from Mumbai, Western India
Autoimmune Dis. 2014;2014:327315. Epub 2014 Mar 6. (IF:--)
|
2014 | |
| 500 |
Devadathan K, Sreedharan M, Sarasam S, Colah RB, Kunju Mohammed PA. Neurometabolic Disorder with Microcephaly, Dystonia and Central Cyanosis Masquerading as Cerebral Palsy
J Child Neurol 2014 Jan 1-4.(IF:1.717)
|
2014 | |
| 501 |
Kerketta LS, Baburao V, Ghosh K Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymphoblastic leukemia cases from India
Indian J Hum Genet. 2014 Jan;20(1):32-6. .(IF:--)
|
2014 | |
| 502 |
Colah R Thalassemias: can we reduce the national burden ?
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I43. (IF:2.66)
|
2014 | |
| 503 |
Shetty S. Haemophilia- diagnosis and management challenges
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I44. .(IF:2.66)
|
2014 | |
| 504 |
Ghosh K. Familial Mediterranean fever: An unusal disease enlightening the inflammation biology
Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--)
|
2014 | |
| 505 |
Merchant RH, Parekh D, Ahmed N, Madkaikar MR, Ahmed J X linked agammaglobulinemia: a single centre experience from India
Indian J Pediatr 2014 Jan; 81(1):92-4. (IF:0.919)
|
2014 | |
| 506 |
Ghosh K, Gorakshakar A. Dr. Bhatias legacy in the development of immunohematology research in the country
Asian J Transfus Sci. 2014;8(Suppl 1):S1-2.
|
2014 | |
| 507 |
Vundinti BR. Chromosomal instability and molecular mutations in multi spectrum disease of Fanconi anemia
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I47. .(IF:2.66)
|
2014 | |
| 508 |
Parasannanavar DJ, Rajadhyaksha A, Ghosh K. Application of a Simple In-House PCR-SSP Technique for HLA-B* 27 Typing in Spondyloarthritis Patients.
Arthritis. 2013;2013:504109. doi: 10.1155/2013/504109. Epub 2013 Dec 19.
|
2013 | |
| 509 |
Ghosh K, Ghosh K. Pulmonary hydatidosis, strongyloidiasis and paragonimiasis in India.
J Assoc Physicians India. 2013 Dec;61(12):954-5
|
2013 | |
| 510 |
Ghosh K, Madkaikar MR, Gupta M, Jijina F. Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination
Turk J Haematol. 2013 Dec;30(4):366-70.(IF:0.34)
|
2013 | |
| 511 |
Bhukhanvala DS, Italia K, Sawant P, Colah R, Ghosh K, Gupte SC. Molecular characterization of ?-thalassemia in four communities in South Gujarat-codon
Ann Hematol. 2013 Nov;92(11):1473-6. (IF:2.615)
|
2013 | |
| 512 |
Vandana VP, Rajadhyaksha A, Yadav K, Surve P, Patwardhan M, Dhavale N, Pandit P, Ghosh K Anti-C reactive protein antibodies in Indian patients with systemic lupus erythematosus
Indian J Nephrol 2013 Nov; 23(6): 434-7.
|
2013 | |
| 513 |
Shukla P, Solanki A, Ghosh K, Vundinti BR DNA interstrand cross-link repair: understanding role of Fanconi anemia pathway and
Eur J Haematol. 2013 Nov;91(5):381-93 (IF:2.066)
|
2013 | |
| 514 |
Ali S, Ghosh K, Shetty S. Molecular pathology of Bernard-Soulier syndrome in Indian patients
Platelets. 2013 Nov; 24(7):571-3.(IF: 2.391)
|
2013 | |
| 515 |
Garg S, Madkaikar MR, Ghosh K. Investigating cell surface markers on normal hematopoietic stem cells in three different
Int J Stem Cells. 2013 Nov;6(2):129-33.(IF:0.625)
|
2013 | |
| 516 |
Lugade AA, Bharali DJ, Vandana VP, Elkin G, Mousa SA, Thanavala Y Single low-dose un-adjuvanted HBsAg nanoparticle vaccine elicits robust , durable immunity.
Nanomedicine 2013 Oct; 9(7):923-34. (IF: 5.26)
|
2013 | |
| 517 |
Jain DL, Apte M, Colah R, Sarathi V, Desai S, Gokhale A, Bhandarwar A, Jain HL, Ghosh K. Efficacy of Fixed Low Dose Hydroxyurea in Indian Children with Sickle Cell Anemia: A
Indian Pediatr. 2013 Oct;50(10):929-33 (IF :)
|
2013 | |
| 518 |
Warang P, Kedar PS, Ghosh K, Colah R. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
Blood Cells Mol Dis. 2013 Oct;51(3): 133-7.(IF: 2.361)
|
2013 | |
| 519 |
Gaikwad T, Shetty S, Ghosh K Polymorphisms of warfarin metabolizing enzymes in an Indian population
Blood Cells Mol Dis. 2013 Oct; 51(3):203.(IF: 2.361)
|
2013 | |
| 520 |
Vaidya S, Joshi D, Ghosh K, Chakrabarti P, Vundinti BR A novel 5-way translocation t(9;11;13;19;22) in a case of chronic-phase chronic myeloid
Hum Pathol. 2013 Oct; 44(10):2365-9.(IF: 3.077)
|
2013 | |
| 521 |
Pinto P, Ghosh K, Shetty S. A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII
Clin Chem Lab Med. 2013 Oct 2:1-3.(2.955)
|
2013 | |
| 522 |
Gorakshakar AC, Ghosh K. Transfusion transmitted infections in Indian thalassemics: a perspective
Indian J Hematol Blood Transfus. 2013 Sep;29(3):189-90.
|
2013 | |
| 523 |
Kasatkar P, Ghosh K, Shetty S. The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal.
J Thromb Haemost. 2013 Sep; 11(9): 1784-5.(IF: 5.731)
|
2013 | |
| 524 |
Chaudhary AK, Pandya S, Ghosh K, Nadkarni A. Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: An overview.
Mutat Res. 2013 Jul-Sep; 753(1):7-23.(IF: 3.680)
|
2013 | |
| 525 |
Ghosh K Multifactorial aetiology for bone disease in patients with haemophilia.
Eur J Haematol. 2013 May;90(5):435(IF:2.066)
|
2013 | |
| 526 |
Kasatkar P, Ghosh K, Shetty S. A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families
Ann Hematol. 2013 Aug; 92(8):1147-9. (IF: 2.615)
|
2013 | |
| 527 |
D Silva S, Colah RB, Ghosh K, Mukherjee MB. Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates
Curr Sci 2013 Aug; 105(4): 446-7. (IF: 0.933 )
|
2013 | |
| 528 |
Gupta M, Madkaikar MR, Rao VB, Mishra A, Govindaraj P, Thangaraj K, Ghosh K Mitochondrial DNA variations in myelodysplastic syndrome
Ann Hematol. 2013 Jul;92(7): 871-6. (IF: 2.615)
|
2013 | |
| 529 |
Pai N, Ghosh K, Shetty S Hereditary thrombophilia in cerebral venous thrombosis: a study from India.
Blood Coagul Fibrinolysis. 2013 Jul; 24(5):540-3.(IF:1.238)
|
2013 | |
| 530 |
Shetty S, Patil R, Ghosh K. Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review.
Eur J Obstet Gynecol Reprod Biol. 2013 Jul; 169(2):123-9.(IF:1.974)
|
2013 | |
| 531 |
Gorakshakar AC, Kulkarni SS, Ghosh K. Molecular organization of Rh gene is likely to be heterogeneous across the world.
Asian J Transfus Sci. 2013 Jul;7(2):103-4.
|
2013 | |
| 532 |
Pinto P, Ghosh K, Shetty S. Factor VIII haplotypes in severe hemophilia A patients in India
Ann Hematol. 2013 Jul; 92(7): 999-1000.(IF: 2.615)
|
2013 | |
| 533 |
Patil R, Ghosh K, Shetty S Profibrinolytic microparticles are not adequately produced to compensate their
Haematologica. 2013 Jul;98(7):e69.(IF:5.868)
|
2013 | |
| 534 |
Kasatkar P, Ghosh K, Shetty S Acquired von Willebrand syndrome: A rare disorder of heterogeneous etiology.
J Postgrad Med. 2013 Apr-Jun;59(2):98-101.(IF: 1.389)
|
2013 | |
| 535 |
Vandana VP, Mahant G, Rajadhyaksha A, Surve P, Rajendran V, Patwardhan M, Nadkarni A, Dighe S, Ghosh K. A study on anti-mannose binding lectin (anti-MBL) antibodies and serum MBL levels in
Rheumatol Int 2013 Jun; 33(6): 1533-9.(IF: 1.885)
|
2013 | |
| 536 |
Patwardhan M, Vandana VP, Taylor LH, Thakkar V, Kharkar V, Khopkar U, Ghosh K, Gawkrodger DJ, Teare MD, Weetman AP, Kemp EH. The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian vitiligo patients: a case-control study and meta-analysis
Br J Dermatol. 2013 Jun; 168(6): 1195-1204.(IF: 3.666)
|
2013 | |
| 537 |
Nair SB, Nadkarni AH, Ghosh K, Colah RB Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal a TIndian (AATAAA>AATA- -) Mutation in Four Indian Families.
Hemoglobin. 2013 May-Jun; 37(3): 277-84.(IF: 1.304)
|
2013 | |
| 538 |
Gaikwad T, Ghosh K, Kulkarni B, Kulkarni V, Ross C, Shetty S Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over
Eur J Pharmacol. 2013 Jun 15;710(1-3):80-4.(IF:2.684)
|
2013 | |
| 539 |
Madkaikar MR, Mishra A, Ghosh K. Diagnostic approach to primary immunodeficiency disorders.
Indian Pediatr. 2013 Jun 8;50(6):579-86.(IF:1.044)
|
2013 | |
| 540 |
Warang P, Kedar PS, Kar R, Ghosh K, Colah R New missense homozygous mutation (Q270Ter) in the pyrimidine 5 nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia
Ann Hematol. 2013 May;92(5):715-7. (IF: 2.615)
|
2013 | |
| 541 |
Ankolkar M, Salvi V, Warke H, Vundinti BR, Balasinor NH. Methylation status of imprinted genes DLK1-GTL2, MEST (PEG1), ZAC (PLAGL1),
Fertil Steril. 2013 May;99(6):1668-73.
|
2013 | |
| 542 |
Ghosh S,Ghosh K Maternal and neonatal outcomes in gestational diabetes mellitus
J Indian Med Assoc. 2013 May;111(5):330-1, 336.
|
2013 | |
| 543 |
Madkaikar MR, Mishra A, Desai M, Gupta M, Mhatre S, Ghosh K Comprehensive Report of Primary Immunodeficiency Disorders from a Tertiary Care Center in India
J Clin Immunol. 2013 Apr; 33(3):507-12.(IF:3.077)
|
2013 | |
| 544 |
Vandana VP, Ghosh K Immunological disturbances associated with malarial infection
J Parasitic Dis 2013 Apr;37(1):11-15. Review.
|
2013 | |
| 545 |
Italia K, Jijina F, Merchant R, Swaminathan S, Nadkarni A, Gupta M,Ghosh K, Colah R. Comparison of in-vitro and in-vivo response to fetal hemoglobin production and ?-mRNA expression by hydroxyurea in Hemoglobinopathies
Indian J Hum Genet. 2013 Apr;19(2):251-8.
|
2013 | |
| 546 |
Vandana VP,Patwardhan M, Rajadhyaksha A and Ghosh K Clinical and Immunological profile of systemic lupus erythematosus
Indian Pediatr 2013 Apr 8; 50(4): 405-7.(IF: 1.048)
|
2013 | |
| 547 |
Bhukhanvala DS, Sorathiya SM, Sawant P, Colah R,Ghosh K, Gupte SC Antenatal screening for identification of couples for prenatal diagnosis of severe
J Obstet Gynaecol India. 2013 Apr;63(2):123-7.
|
2013 | |
| 548 |
Parasannanavar DJ, Yeola A, Vandana VP, Rajyadhaksha A,Ghosh K HLA-DR?1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients.
Rheumatol Int. 2013 Apr; 33(4): 867-70.(IF: 2.200)
|
2013 | |
| 549 |
Shukla P, Rao A, Ghosh K, Vundinti BR. Identification of a novel large intragenic deletion in a family with Fanconi Anemia: First
Gene. 2013 Apr 15; 518(2): 470-5. (IF:2.443)
|
2013 | |
| 550 |
Vandana VP, Patwardhan M, Thakkar V, Kharkar V, Khopkar U, Ghosh K, Weetman AP, Gawkrodger DJ, Kemp EH. Vitiligo patients from India (Mumbai) show differences in clinical, demographic and autoantibody profiles compared to patients in western countries
J Eur Acad Dermatol Venereol. 2013 Mar;27(3):279-86.
|
2013 | |
| 551 |
Ghosh K. Cytogenetics in paediatric aplastic anaemia: does it give an insight on the evolution of the disease?
Indian J Med Res. 2013 Mar;137(3):445-6.(IF: 1.837).
|
2013 | |
| 552 |
Dabke P, Colah RB,Ghosh K, Nadkarni A. Effect of a group of genetic markers around the 5 regulatory regions of the ? globin gene cluster linked to high HbF on the clinical severity of ? thalassemia.
Blood Cells Mol Dis. 2013 Mar;50(3):156-60.(IF:2.361)
|
2013 | |
| 553 |
D Souza E, Sawant PM, Nadkarni AH, Gorakshakar A,Ghosh K, Colah RB. Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal
J Postgrad Med. 2013 Jan-Mar;59(1):15-20. (IF: 1.389)
|
2013 | |
| 554 |
Nair S, Ghosh K. The myriad effects of cigarette smoke.
J Thromb Haemost. 2013 Feb;11(2):387-8.(IF: 5.731)
|
2013 | |
| 555 |
Magerus-Chatinet A, Stolzenberg MC, Lanzarotti N, Neven B, Daussy C, Picard C, Neveux N, Desai M, Rao M, Ghosh K, Madkaikar MR, Fischer A, Rieux-Laucat F Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation
J Allergy Clin Immunol. 2013 Feb;131(2):486-90.(IF: 11.003)
|
2013 | |
| 556 |
Gaikwad T, Ghosh K, Shetty S Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy
Eur J Clin Pharmacol. 2013 Feb;69(2):293-4.(IF: 2.845)
|
2013 | |
| 557 |
Patil A, Poudyal BS, Kapali SM, Ghosh K, Shetty S Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
Ann Hematol. 2013 Jan;92(2):261-2. (IF: 2.615)
|
2013 | |
| 558 |
Kulkarni SS, Kasiviswanathan V, Ghosh K A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population
Blood Transfus. 2013 Jan;11(1):37-42. (IF: 2.099).
|
2013 | |
| 559 |
D Silva S, Colah RB, Ghosh K, Mukherjee MB. UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.
Gene. 2013 Jan 15;513(1):36-9.(IF:2.443)
|
2013 | |
| 560 |
Mohanty D, Colah RB, Gorakshakar AC, Patel RZ, Master DC, Mahanta J, Sharma SK, Chaudhari U, Ghosh M, Das S, Britt RP, Singh S, Ross C, Jagannathan L, Kaul R, Shukla DK, Muthuswamy V. Prevalence of ?-thalassemia and other haemoglobinopathies in six cities in India: a
J Community Genet. 2013 Jan;4(1):33-42.
|
2013 | |
| 561 |
Pooja Dabke, Roshan Colah, Kanjaksha Ghosh, Anita Nadkarni Effect of Cis Acting Potential Regulators in the ? Globin Gene Cluster on the Production of HbF in Thalassemia Patients.
Mediterr J Hematol Infect Dis. 2013; 5(1): e2013012. Published online 2013 February 16.(IF: )
|
2013 | |
| 562 |
Nair S, Nadkarni AH, Ghosh K, Colah R. Hemoglobin variants and high-performance liquid chromatography.
Int J Lab Hematol. 2013 Jan 11. [Epub ahead of print] .(IF: 1.176)
|
2013 | |
| 563 |
Kedar PS, Warang P, Ghosh K, Colah R. Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family
Ann Hematol. 2012 Dec;91(12):1985-6. (IF: 2.615)
|
2012 | |
| 564 |
Madkaikar MRR, Gupta M, Rao M,Ghosh K Prenatal Diagnosis of LAD-I on Cord Blood by Flowcytometry.
Indian J Pediatr. 2012 Dec;79(12):1605-9.(IF: 0.521)
|
2012 | |
| 565 |
Patwardhan M, Vandana VP, Rajadhyaksha A, Umare V, Rajendran V, Surve P, Ghosh K Clinical and serological features of male Systemic Lupus Erythematosus patients from Western India
Indian J Rhematol 2012 Dec; 7(4):204-8.
|
2012 | |
| 566 |
Ghosh K, Swaminathan S, Madkaikar MR, Gupta M, Kerketta L, Vundinti B. FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India.
Ann Hematol. 2012 Nov;91(11):1703-12. (IF: 2.615)
|
2012 | |
| 567 |
Adlbrecht C, Aigner E, Bellon JM, Bouloukaki I, Bouzas-Mosquera A, Carrilho AJ, Chang KC, Chattipakorn N, Chattipakorn SC, Chen YJ, Chung YC, Colah R,Datz C, Frokjaer JB, Fujimori S, Georgiadou P, Grion CM, Hsu CP, Hulsmann M, Hung MJ, Hung MY, Iliodromit Research update for articles published in EJCI in 2010
Eur J Clin Invest 2012 Nov; 42(11):1149-64.(If: 3.365)
|
2012 | |
| 568 |
Shetty S,Ghosh K. APTT reagents for different coagulation tests: one size does not fit all
Am J Clin Pathol. 2012 Nov;138(5):757; author reply 757-8.
|
2012 | |
| 569 |
Jadli A, Kulkarni B, Ghosh K, Shetty S. Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases
Liver Int. 2012 Nov;32(10):1596-7.(IF: 3.824)
|
2012 | |
| 570 |
Jain D, Italia K, Sarathi V,Ghosh K, Colah R. Sickle Cell Disease from Central India: A Retrospective Analysis.
Indian Pediatr. 2012 Nov;49(11):911-3. (IF:1.048)
|
2012 | |
| 571 |
Kerketta LS, Rao VB, Ghosh K. Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection
Trop Med Int Health. 2012 Oct;17(10):1222-6.(IF: 2.795)
|
2012 | |
| 572 |
Kulkarni B, Kanakia S,Ghosh K, Shetty S. Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.
Ann Hematol. 2012 Oct;91(10):1667-8.(IF: 2.615)
|
2012 | |
| 573 |
Colaco S, Colah R,Ghosh K, Nadkarni A Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases
Clin Chim Acta. 2012 Oct 9;413(19-20):1705-7.(IF:2.661)
|
2012 | |
| 574 |
Pinto P,Ghosh K, Shetty S. Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients
Haemophilia. 2012 Sep;18(5):794-7.(IF: 2.597)
|
2012 | |
| 575 |
D Silva S, Colah RB,Ghosh K, Mukherjee MB G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India.
J Matern Fetal Neonatal Med. 2012 Sep; 25(9):1833-4.(IF: 1.592)
|
2012 | |
| 576 |
Vandana VPD, Dalvi H, Parsannavar D, Rajadhyaksha A, Patwardhan M, Ghosh K. Study of PTPN22 1858C/T polymorphism in rheumatoid arthritis patients from Western India.
Indian J Rheumatol 2012 Sep; 7(3):130-134.(IF: )
|
2012 | |
| 577 |
Pai N, Ghosh K, Shetty S Hereditary protein C deficiency in Indian patients with venous thrombosis.
Ann Hematol. 2012 Sep;91(9):1471-6.(IF: 2.615)
|
2012 | |
| 578 |
Vandana VP, Rajadhyaksha A, Mahant G, Surve P, Patwardhan M, Dighe S,Ghosh K Anti-C1q antibodies and their association with complement components in Indian systemic lupus erythematosus patients
Indian J Nephrol. 2012 Sep;22(5):353-7.
|
2012 | |
| 579 |
Vandana VPD APO1/F as promoter polymorphism in systemic lupus erythematosus (SLE): significance in clinical expression of the disease
J Assoc Physicians India. 2012 Sep; 60:34-7.(IF:)
|
2012 | |
| 580 |
Ghosh K, Shetty S. Bone health in persons with haemophilia (PWH): A review.
Eur J Haematol.2012 Aug;89(2):95-102.(IF: 2.614)
|
2012 | |
| 581 |
Gorakshakar AC, Ghosh K. Subclinical iron deficiency is a silent epidemic amongst voluntary blood donors.
Transfus Med. 2012 Aug;22(4):300-1. (IF:1.14)
|
2012 | |
| 582 |
Jain DL, Sarathi V, Upadhye D, Gulhane R, Nadkarni AH, Ghosh K, Colah RB. Newborn screening shows a high incidence of sickle cell anemia in Central India.
Hemoglobin. 2012 Jul-Aug; 36(4):316-22.(IF: 1.304)
|
2012 | |
| 583 |
Ghosh K, Shetty S Malignancies in persons with haemophilia: 25-year data from India.
Natl Med J India. 2012 Jul-Aug;25(4):251.(IF: 0.595)
|
2012 | |
| 584 |
Vandana VP, Das S, Surve P, Ghosh K Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus
Indian J Hum Genet 2012 May-Aug; 18(2): 155-60.
|
2012 | |
| 585 |
Warang P, Kedar P, Ghosh K, Colah RB Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
Int J Hematol. 2012 Aug;96(2):263-7. (IF: 1.268)
|
2012 | |
| 586 |
Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R. Variable haematological and clinical presentation of ?-thalassaemia carriers and homozygotes with the Poly A (T?C) mutation in the Indian population.
Eur J Haematol. 2012 Aug;89(2):160-4. (IF: 2.614)
|
2012 | |
| 587 |
Italia K, Sheth J, Sawant P, Nadkarni A, Ghosh K, Colah R. Prenatal diagnosis of HbE-Lepore and Hb Lepore-?-thalassemia: the importance of accurate genotyping of the couple at risk.
Prenat Diagn. 2012 Jul;32(7):703-7.(IF: 2.106)
|
2012 | |
| 588 |
Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional ? gene variants identified in neonates during newborn screening for sickle cell disorders.
J Clin Pathol. 2012 Jul;65(7):654-9.(IF: 2.306)
|
2012 | |
| 589 |
Kulkarni SS, K Vasantha, Ghosh K A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.
Blood Transfus 2012 Jul; 12: 1-6. (IF: 2.099)
|
2012 | |
| 590 |
Joshi SR, Vasantha K A profile of rare bloods in India and its impact in blood transfusion service.
Asian J Transf Sci 2012 Jan-Jun; 6(1): 42-43.
|
2012 | |
| 591 |
Shetty S, Ghosh K. Cancers in patients with hemophilia: a retrospective study from the Italian Association of Hemophilia Centers: a rebuttal.
J Thromb Haemost. 2012 Jun;10(6):1200-1; author reply 1201-2. (IF: 5.731)
|
2012 | |
| 592 |
Lobo V, Shetty S, Kulkarni B, Ghosh K. A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2012 Jun; 91(6):917-21.(IF: 2.615)
|
2012 | |
| 593 |
Pai N, Ghosh K, Shetty S Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups.
Blood Coagul Fibrinolysis. 2012 Jun;23(4):257-61.(IF: 1.25)
|
2012 | |
| 594 |
Warang P, Kedar PS, Ghosh K, Colah R. A new simple approach for the determination of pyrimidine 5-nucleotidase activity in human erythrocytes using an ELISA reader.
Int J Lab Hematol. 2012 Jun; 34(2): 232-4.(IF: 1.176)
|
2012 | |
| 595 |
Ghosh K. Haematology research in India: past, present and future.
Indian J Hematol Blood Transfus. 2012 Jun;27(2):55-64. (IF: 0.056)
|
2012 | |
| 596 |
Vaidya S, Sonawani A, Idicula-Thomas S, Vundinti BR, Ghosh K. Imatinib resistance due to a novel tri-nucleotide insertion in the SH2/C lobe interface of BCR/ABL kinase domain between position K357 and N358.
Leuk Res. 2012 May;36(5):e110-2.(2.472)
|
2012 | |
| 597 |
Nair PS, Shetty S, Ghosh K A homozygous female hemophilia A.
Indian J Hum Genet 2012 Jan-Apr; 18(1): 134-6.
|
2012 | |
| 598 |
Ghosh K, Ghosh K, Shetty S. Hemostasis Research in India: Past, Present, and Future.
Clin Appl Thromb Hemost. 2012 Mar-Apr;18(2):128-33.(IF: 1.332)
|
2012 | |
| 599 |
Mukherjee MB, Ghosh Kanjaksha Explaining anthropometric variations in sickle cell disease requires a multidimensional approach
Indian J Hum Genet. 2012 Jan-Apr;18(1): 1-2.
|
2012 | |
| 600 |
Vundinti BR, Korgaonkar S, Ghosh K. De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Gene. 2012 Apr 25; 498(1):128-30.(IF: 2.443)
|
2012 | |
| 601 |
Vandana VP, Hire H and Ghosh K MicroRNA profile in understanding pathogenesis of systemic lupus erythematosus
Indian J Biotechnol 2012 Apr; 11:129-33.(IF: 0.55)
|
2012 | |
| 602 |
Shetty S, Ghosh K. Malignancies in Indian haemophiliacs are mainly non viral associated
J Thromb Haemost. 2012 Apr 12.[Epub ahead of print](IF: 5.731)
|
2012 | |
| 603 |
Kawankar N, Korgaonkar S, Kerketta L, Madkaikar MR, Jijina F, Ghosh K, Vundinti BR. DNA Copy Number Changes and Immunophenotype Pattern in Karyotypically Normal Acute Myeloid Leukemia Patients from Indian Population.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 265-70.(IF: 1.110)
|
2012 | |
| 604 |
D Souza E, Nair S, Nadkarni A, Ghosh K, Colah RB SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India
Indian J Hum Genet 2012 Jan-Apr; 18(1): 87-90.
|
2012 | |
| 605 |
Nadkarni A, Italia K, Sawant P, Ghosh K, Colah R. Hemoglobin Lepore Hollandia in India.
Int J Lab Hematol. 2012 Apr;34(2):148-53. (IF: 1.176)
|
2012 | |
| 606 |
Gorakshakar A, Sathe P, Colah R, Nadkarni A, Ghosh K Hemoglobin Showa-Yakushiji: A Common ? Thalassemia Mutation Among the Agri Community from Western India.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 302-5.(IF; 1.110)
|
2012 | |
| 607 |
Shukla P, Ghosh K and Vundinti BR Current and emerging therapeutic strategies for Fanconi anemia.
The Hugo J 2012 Mar; 6:1.(IF: )
|
2012 | |
| 608 |
Kanani P, Poudyal BS, Shetty S, Kapali SM, Ghosh K. Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population.
Haemophilia. 2012 Mar;18(2):e44-5.(IF: 2.597)
|
2012 | |
| 609 |
Gupta S, Madkaikar MR, Singh S, Sehgal S. Primary immunodeficiencies in India: a perspective.
Ann N Y Acad Sci. 2012 Feb;1250:73-9.(IF: 3.155)
|
2012 | |
| 610 |
Italia KY, Sawant PM, Nadkarni AH, Ghosh K, Colah RB Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of ?-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?
Hemoglobin. 2012 Feb; 36(2):114-23. (IF: 1.304)
|
2012 | |
| 611 |
Madkaikar MR, Currimbhoy Z , Gupta M, Desai M, Rao M, Ghosh K. Clinical Profile of Leukocyte Adhesion Deficiency Type I.
Indian Pediatr 2012 Jan; 49(1): 43-45.(IF:1.048)
|
2012 | |
| 612 |
Datta S, Chowdhury A, Ghosh M, Das K, Jha P, Colah R, Mukherjee M, Majumder PP. A Genome wide search for Non-UGT1A1 markers associated with unconjugated bilirubin levels revelas significant association with a polymorphic marker near a gene of the Nucleoporin family
Ann.Hum.Genet. 2012 Jan; 76(1):33-41.(IF: 2.565)
|
2012 | |
| 613 |
Kundu T, Shaikh A, Kutty A, Nalvade A, Kulkarni SS, Kulkarni R, Ghosh K. Homeopathic medicines substantially reduce the need for clotting factor concentrates in haemophilia patients: results of a blinded placebo controlled cross over trial.
Homeopathy. 2012 Jan;101(1):38-43.(IF: 1.141)
|
2012 | |
| 614 |
Vandana VP, Patwardhan M, Athavale A, Taushid S, Ghosh K. Mycobacterium tuberculosis triggers autoimmunity?
Indian J Tuberc. 2012 Jan;59(1):49-51.
|
2012 | |
| 615 |
Vijver Edith van de, Maddelena A, Sanal O, Holland SM, Uzel G, Madkaikar MR, Martin de Boer, Karin van Leeuwen, Koker MY, Parvaneh N, Fischer A, Law SK Alex, Klein N, Tezcan F IIhan, Unal E, Patiroglu T, Belohradsky BH, Schwartz K, Somech R, Kuijpers TW, R Hematologically important mutations: Leukocyte adhesion deficiency (first update)
Blood Cells Mol Dis 2012 Jan 15; 48(1):53-61.(IF: 2.351)
|
2012 | |
| 616 |
Umapathy S, Pawar A, Mitra R, Khuperkar D, Devaraj JP, Ghosh K, Khopkar U. Hla-a and hla-B alleles associated in psoriasis patients from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct;56(5):497-500.(IF: 0.979)
|
2011 | |
| 617 |
Colah RB, Gorakshakar AC & Nadkarni AH Invasive and non-invasive approaches for prenatal diagnosis of haemoglobinopathies: Experiences from India.
Ind. J. Med. Res. 2011 Oct; 134(4): 552-60.(IF: 1.837)
|
2011 | |
| 618 |
Ghosh K, Ghosh K, Chowdhury JR. Tuberculosis and female reproductive health.
J Postgrad Med. 2011 Oct-Dec;57(4):307-13.(IF: 1.389)
|
2011 | |
| 619 |
Vundinti BR, Ghosh K Incidence of down syndrome: Hypotheses and reality
Indian J Hum Genet. 2011 Sep;17(3):117-9.
|
2011 | |
| 620 |
Shankarkumar U, Pawar A, Mitra R, Khuperkar D, Devaraj JP, Ghosh K, Khopkar U HLA-A and HLA-B alleles associated in psoriasis patient’s from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct; 56(5): 510-13.(IF: 0.979)
|
2011 | |
| 621 |
Vaidya S, Ghosh K, Vundinti BR. Recent developments in drug resistance mechanism in chronic myeloid leukemia: A review.
Eur J Haematol. 2011 Nov; 87(5):381-93. (IF 2.785)
|
2011 | |
| 622 |
Shanbhag S, Shetty S, Ghosh K Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5. (IF 2.597)
|
2011 | |
| 623 |
Vundinti BR, Korgaonkar S, Kerketta L, Ghosh K. A rare case of B-cell chronic lymphocytic leukemia with t(2;14)(p13;q32), +X, +11, +12, +13,+der(1p) karyotype.
Indian J Cancer. 2011 Jul-Sep;48(3):387-8.(IF: 0.961)
|
2011 | |
| 624 |
A Shankarkumar and U Shankarkumar HIV and Malaria co-infection in Mumbai Western India.
J Vector Borne Dis. 2011 Sep; 48(3):155-58.(IF: 1.177)
|
2011 | |
| 625 |
Shankarkumar U, Shankarkumar A, Chedda Z, Ghosh K Role of 14-bp deletion/insertion polymorphism in exon 8 of the HLA-G gene in recurrent spontaneous abortion patients.
J Hum Reprod Sci. 2011 Sep;4(3):143-6. (IF:)
|
2011 | |
| 626 |
Shanbhag S, Shetty S, Ghosh K Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5.(IF: 2.597)
|
2011 | |
| 627 |
Ghosh K. Haematology research in India: past, present and future
Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)
|
2011 | |
| 628 |
Desai –Gorakshakar K, Padwal V, Ghosh K. Women scientists in India are marching ahead.
Curr Sci 2011 Aug; 101: 3. (IF: 0.935)
|
2011 | |
| 629 |
Shetty S, Kasatkar P, Ghosh K. Pathophysiology of acquired von Willebrand disease: a concise review
Eur J Haematol. 2011 Aug;87(2):99-106. Review. (IF 2.785).
|
2011 | |
| 630 |
Kawankar N, Jijina F, Ghosh K, Vundinti BR Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.
Cancer Epidemiol. 2011 Aug;35(4):e1-5.(IF: 2.010)
|
2011 | |
| 631 |
Vandana VP, Patwardhan M, Nadkarni A, Ghosh K. Fc ? R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients.
Indian J Med Res. 2011 Aug;134(2):181-5.(IF: 1.837)
|
2011 | |
| 632 |
Ghosh K, Shetty S Epidemiology, diagnosis, and management of von Willebrand disease in India.
Semin Thromb Hemost. 2011 Jul;37(5):595-601. (IF: 4.524)
|
2011 | |
| 633 |
Shankarkumar U, Sridharan B. Glioma Indian Scenario: Is there a Human Leukocyte Antigen association?
J Nat Sci Biol Med 2011 Jul; 2(2):205-8.
|
2011 | |
| 634 |
Shanbhag S, Shetty S, Kulkarni B, Ghosh K. An improved, semi quantitative clot based assay for factor XIII
Haemophilia. 2011 Jul;17(4):718-20. (IF 2.597)
|
2011 | |
| 635 |
Shankarkumar U, Vandana VPD, Patwardhan M, Pawar A, Ghosh K. Autoantibody profile and immunological parameters in Recurrent Spontaneous Abortion patients.
Nigerian Med J 2011 Jul; 52(3):163-66.
|
2011 | |
| 636 |
Shetty S, Ghosh K. Response to the letter of Casserta et al. Acquired hemophilia a following influenza vaccination.
Autoimmun Rev. 2011 Jul 23. [Epub ahead of print](IF: 6.624)
|
2011 | |
| 637 |
Madkaikar MR, Mhatre S, Gupta M, Ghosh K. Advances in Autoimmune Lymphoproliferative Syndromes (ALPS).
Eur J Haematol. 2011 Jul; 87(1): 1-9. Review (IF 2.785)
|
2011 | |
| 638 |
Basu A, Jain P, Sarkar P, Gangodkar S, Deshpande D, Ganti K, Shetty S, Ghosh K Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein
FEMS Immunol Med Microbiol. 2011 Jul; 62(2):140-7. (IF: 2.441)
|
2011 | |
| 639 |
Shankarkumar A, Shankarkumar U, Ghosh K CCR5 chemokine receptor polymorphism in patients with HIV-1 from Western India.
J Acquir Immune Defic Syndr. 2011 Jun 1;57(2):e21. (IF: 4.570)
|
2011 | |
| 640 |
Saravanan S, Madhavan B, Murugavel KG, Balakrishnan P, Solomon SS, Umapathy S, Kantor R, Kumarasamy N, Yepthomi T, Smith DM, Mayer KH, Solomon S The association between HIV-1 subtype C antiretroviral resistance and HLA prevalence in southern India.
J Acquir Immune Defic Syndr. 2011 May;57(1):e17-19. (IF: 4.570)
|
2011 | |
| 641 |
Shetty S, Ghosh K Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review.
Thromb Res. 2011 Jun;127(6):505-12. Epub 2010 Oct 20. Review.(IF: 2.44)
|
2011 | |
| 642 |
Vandana VP, Gorakshakar A Are mannose-binding lectin gene 2 (MBL2) polymorphisms and MBL deficiency associated with infections?
Indian J Hum Genet 2011 May; 17(2):45-47.
|
2011 | |
| 643 |
Vundinti BR, Ghosh K. Chromosomal aberrations in hematological malignancies: A guide to the identification of novel oncogenes.
Indian J Hum Genet. 2011 May;17(2):43-4
|
2011 | |
| 644 |
Warang P, Gupta M, Kedar PS, Ghosh K, Colah R Flow cytometric osmotic fragility-An effective screening approach for red cell membranopathies.
Cytometry Part B Clin Cytom 2011 May; 80(3):186-90.(IF: 2.525)
|
2011 | |
| 645 |
Vaidya S, Madkaikar MR, Ghosh K, Vundinti BR. Deletion of ABL/BCR on der(9) associated with severe basophilia.
Indian J Hum Genet. 2011 May;17(2):100-3.
|
2011 | |
| 646 |
Shankarkumar U, Shankarkumar A, Ghosh K. Human immunodeficiency virus therapeutics and pharmacogenomics.
Indian J Hum Genet. 2011 May;17 Suppl 1:S22-6.
|
2011 | |
| 647 |
Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Glader B, Rivera A, Brugnara C, Alper SL Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Am J Physiol Cell Physiol 2011 May; 300(5):C1034-C1046.(IF: 3.817)
|
2011 | |
| 648 |
Shetty S, Bhave M, Ghosh K Acquired hemophilia A: diagnosis, aetiology, clinical spectrum and treatment options.
Autoimmun Rev. 2011 Apr;10(6):311-6. Review.(IF: 6.624)
|
2011 | |
| 649 |
D Silva S, Borse V, Colah RB, Ghosh K, Mukherjee MB. Association of (GT)n Repeats Promoter Polymorphism of Heme Oxygenase-1 Gene with Serum Bilirubin Levels in Healthy Indian Adults.
Genet Test Mol Biomarkers. 2011 Apr; 15(4):215-18. (IF: 1.110)
|
2011 | |
| 650 |
Ghosh K, Shetty S Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands?
Blood Coagul Fibrinolysis. 2011 Apr;22(3):241-2. (IF 1.549)
|
2011 | |
| 651 |
Umapathy S, Pawar A, Bajpai S, Pazare AR, Ghosh K HLA involvement in nevirapine-induced dermatological reaction in antiretroviral-treated HIV-1 patients.
J Pharmacol Pharmacother. 2011 Apr;2(2):114-5.
|
2011 | |
| 652 |
Shetty S, Bhave M, Ghosh K. Challenges of multiple mutations in individual patients with haemophilia.
Eur J Haematol. 2011 Mar; 86(3): 185-90. (IF 2.785)
|
2011 | |
| 653 |
Kedar PS, Warang P, Ghosh K, Colah RB. Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH-cytochrome b5 reductase gene mutations.
Am J Hematol. 2011 Mar;86(3):327-9.(IF 3.476).
|
2011 | |
| 654 |
Shankarkumar U, Shankarkumar A, Ghosh K. Involvement of HLA in serum BETA-2 Microglobin levels among Mumbai HIV-1 patients
J Adv Lab Res Biol 2011; I(III):133-35.
|
2011 | |
| 655 |
Kanjaksha Ghosh, Roshan Colah. Phenotypic diversity of sickle cell disorders: a rebuttal
Curr Sci 2011 Jan; 100(2):149.(IF:0.897)
|
2011 | |
| 656 |
Shankarkumar U and Shankarkumar A. HLA-B17 Prevalence in HIV-1 infected patients under Antiretroviral treatment.
Int J Hum Genet 2011 Jan; 11(1):59-62.(IF:0.306)
|
2011 | |
| 657 |
Umapathy S, Shankarkumar A, Ramrakhiyani V, Ghosh K. Role of anti-human lymphocyte culture cytotoxic antibodies in recurrent spontaneous pregnancy loss women.
J Hum Reprod Sci. 2011 Jan;4(1):17-9. (IF)
|
2011 | |
| 658 |
Korgaonkar S, Ghosh K, Vundinti BR. A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotype.
J Hum Reprod Sci. 2011 Jan;4(1):53-5. (IF )
|
2011 | |
| 659 |
Chalvam R, Colah RB,Mohanty D, Ghosh K, Mukherjee MB Restriction fragmentlength polymorphism (RFLP) of the X chromosome linked glucose-6- phosphate dehydrogenase (G6PD) locus in India.
Ann Hum Biol. 2011 Jan;38(1):106-9.(IF: 1.975)
|
2011 | |
| 660 |
Shankarkumar U, Devraj JP, Ghosh K. Molecular characterization of HLA B*07 alleles in HLA B27 negative seronegative spondarthritis patients from India
IUP J Genet Evolution 2011; IV(3):1-8.
|
2011 | |
| 661 |
Ghosh K, Gorakshakar A. Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?
Indian J Hum Genet. 2011 Jan;17(1):1-2.
|
2011 | |
| 662 |
Pai N, Shetty S, Kulkarni B, Ghosh K. Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700.(IF:1.476)
|
2010 | |
| 663 |
Nair PS, Shetty S, Kulkarni B, Ghosh K. Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.
Clin Chim Acta 2010 Dec 14; 411(23-24):2004-8.(IF:2.661)
|
2010 | |
| 664 |
Vundinti BR, Korgaonkar S, Ghosh K. Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.
Indian J Cancer. 2010 Oct-Dec;47(4):397-9. (IF: 0.961)
|
2010 | |
| 665 |
Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, Bellgard M, Bittles AH. Profiling ?-Thalassaemia mutations in India at state and regional levels: implications genetic education, screening and counseling programmes.
Hugo J. 2009 Dec; 3(1-4): 51–62.
|
2010 | |
| 666 |
Vandana VP, Surve P, Ghosh K. Mannose Binding Lectin (MBL) in Autoimmunity and its role in systemic lupus erythematosus (SLE).
J Assoc Physicians India 2010 Nov; 58(11):688-90.
|
2010 | |
| 667 |
Nair PS, Shetty S and Ghosh K. Double mutations in haemophilia: muddling strangers or indifferent partners in crime?
Haemophilia 2010 Nov;16(6):970-1. (IF 2.394)
|
2010 | |
| 668 |
Italia KY, Jijina FF, Jain D, Merchant R, Nadkarni AH, Mukherjee M, Kanjaksha G, Colah RB The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies
Clin Biochem 2010 Nov;43(16-17):1329-1332.(IF: 2.079)
|
2010 | |
| 669 |
Korgaonkar S, Ghosh K, Jijina F and Vundinti BR. Chromosomal breakage study in children suspected with fanconi anemia in the Indian population.
J Pediatr Hematol Oncol 2010 Nov;32(8):606-10.(IF: 0.998)
|
2010 | |
| 670 |
Chandrakala S, Jijina F and Ghosh K Diffuse alveolar haemorrhage with severe haemophilia.
Haemophilia 2010 Nov;16(6): 962-4. (IF 2.394)
|
2010 | |
| 671 |
Shmukler BE, Kedar PS, Warang P, Desai M, Madkaikar MR, Ghosh K, Colah RB, Alper SL. Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
Am J Hematol 2010 Oct;85(10):824-8.(IF 3.576)
|
2010 | |
| 672 |
Burdrukkar A, Shahid T, Murthy V, Hussain T, Mulherkar R, Babu Rao V, Deshpande M, Sengar M, Ghosh Laskar S, Agarwal JP: Squamous cell carcinoma of tongue in a patient with fanconi’s anemia treated with radiation therapy: Case Report and review of literature.
Head & Neck 2010 Oct;32(10):1422-27.(IF: 2.4)
|
2010 | |
| 673 |
Black ML, Sinha S, Agarwal S, Colah R, Das R, Bellgard M, Bittles AH. A descriptive profile of ?-Thalassaemia mutations in India, Pakistan and Sri Lanka
J Community Genet. 2010 Oct 10.
|
2010 | |
| 674 |
Vandana VP, Borse V, Ghosh K. PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.
J Postgrad Med. 2010 Jul-Sep;56(3):239-42. Review. (IF:1.389)
|
2010 | |
| 675 |
Shankarkumar U. Complexities and similarities of HLA antigen distribution in Asian subcontinent.
Indian J Hum Genet. 2010 Sep;16(3):108-10.
|
2010 | |
| 676 |
Kasatkar P, Shetty S, Ghosh K. Delayed vitamin K deficiency as a cause of bleeding : still a concern in the 21st century!
Blood Coagul Fibrinolysis. 2010 Sept; 21(6):608-10. (IF 1.506)
|
2010 | |
| 677 |
Mukherjee MB, Nadkarni AH, Gorakshakar AC, Ghosh K, Mohanty D, Colah RB. Clinical, hematologic and molecular variability of sickle cell-? thalassemia in western India
Indian J Hum Genet. 2010 Sep;16(3):154-8.
|
2010 | |
| 678 |
Ghosh K, Ghosh K Sequential serologic testing for common viral markers in blood units in India is probably not cost effective.
Transfusion 2010 Aug;50(8): 1854-55. (IF 3.3)
|
2010 | |
| 679 |
Pai N, Shetty S, Ghosh K Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Aug; 89(8): 835-6. (IF: 2.688)
|
2010 | |
| 680 |
Ghosh K Bachelor of rural health care: cutting the root and watering the stem!
Natl Med J India. 2010 Jul-Aug;23(4):250. (IF 0.541)
|
2010 | |
| 681 |
Shetty S, Kulkarni B, Pai N, Mukundan P, Kasatkar P, Ghosh K. JAK2 mutations across a spectrum of venous thrombosis cases.
Am. J. Clin. Pathol 2010 Jul; 134(1):82-5. (IF 2.47)
|
2010 | |
| 682 |
Mota L, Shetty S, Idicula-Thomas S, Ghosh K. Molecular basis of factor X deficiency cases from India
Haemophilia 2010 Jul 1; 16(4): 693-7. ( IF 2.394)
|
2010 | |
| 683 |
Gangodkar S, Jain P, Dixit N, Ghosh K, Basu A Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure
J Electron Microsc (Tokyo). 2010 Jun;59(6):503-11. (IF 1.77)
|
2010 | |
| 684 |
Kanjaksha Ghosh, Kinjalka Ghosh Advances in Haematological Pharmacotherapy in 21st Century.,
Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40.
|
2010 | |
| 685 |
Colah R, Gorakshakar A, Phanasgaonkar S, D Souza E, Nadkarni A, Surve R, Sawant P, Master D, Patel R, Ghosh K, Mohanty D. Epidemiology of beta – thalassemia in Western India:mapping the frequencies and mutations in sub – regions of Maharashtra and Gujarat
Br J Haematol. 2010. Jun; 149(5): 739-47.(IF 4.942)
|
2010 | |
| 686 |
Shankarkumar U, Pawar A, Ghosh K, Bajpai S and Pazare A. Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus-infected patients of Mumbai, India
Intl J Immunogenet 2010 Jun; 37(3): 199-204.(IF: 1.62)
|
2010 | |
| 687 |
Muranjan M, Chaudhari T and Babu Rao V. Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down Syndrome.
Indian Pediatrics 2010 May 17; 47(5): 429-432. (IF: 0.9)
|
2010 | |
| 688 |
Ghosh K, Gorakshakar A Integration of modern genetic knowledge and technology into public health in India.
Indian J Hum Genet. 2010 May;16(2):45-6.
|
2010 | |
| 689 |
Vaswani RK, Dharaskar PG, Kulkarni SS, Ghosh K. \ Iron deficiency as a risk factor for first febrile seizure.
Indian Pediatr. 2010 May;47(5):437-9. (IF: 0.9)
|
2010 | |
| 690 |
Vandana VP, Deshpande N, Nadkarni A, Patwardhan M, Surve P, Ghosh K. Fc gamma R IIIBpolymorphisms:their association with clinical manifestation and autoantibodies in SLE patients from western India
Int J Rheum Dis. 2010 May; 13 (2): 138-43.(IF:0.205)
|
2010 | |
| 691 |
Kasatkar P. Shetty S, Ghosh K. VWF pseudogene; Mimics, masks and spoils.
Clin Chim Acta. 2010 Apr 2;411(7-8):607-9.(IF: 2.661)
|
2010 | |
| 692 |
Vandana VPD, Patwardhan MM, Ghosh K Anti-nucleosome antibodies as a disease marker in systemic lupus erythematosus and its correlation with disease activity and other autoantibodies
Indian J Dermatol Venereol Leprol. 2010 Mar-Apr;76(2):145-9.(IF: 0.976)
|
2010 | |
| 693 |
Madan N, Sharma S, Sood SK, Colah R, Bhatia HM Frequency of B-thalassemia trait and other hemoglobinopathies in northern and western India.
Indian J Hum Genet. Jan-Apr 2010; 16(1): 16-25.
|
2010 | |
| 694 |
Jain A, Shetty S, Kulkarni B, Ghosh K. Association of factor VII gene polymorphisms with Budd Chiari syndrome
Blood Coagul Fibrinolysis. 2010 Apr; 21(3):296-7. (IF 1.506)
|
2010 | |
| 695 |
Nadkarni AH, Nair SB, Italia KY, Warang P, Dalvi M, Ghosh K, Colah RB. Molecular diversity of hemoglobin H disease in India.
Am J Clin Pathol. 2010 Mar;133(3):491-4. (IF 3.576)
|
2010 | |
| 696 |
Nair S, Nadkarni A, Warang P, Bhave A, Ghosh K, Colah R. Five alpha globin chain variants identified during screening for haemoglobinopathies.
Eur J Clin Invest. 2010 Mar; 40(3):226-32. (IF:2.784)
|
2010 | |
| 697 |
Shetty S, Mota L, Ghosh K. Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency
Clin Chim Acta. 2010 Feb;411(3-4):291. (IF:2.960)
|
2010 | |
| 698 |
Vandana VP, Patwardhan M, Nadkarni A, Ghosh K Fc ? RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India
Autoimmune Dis 2010 Feb 9;2010.
|
2010 | |
| 699 |
Italia KY, Jijina FF, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study
J Clin Pathol. 2010 Feb;63(2):147-50. (IF 1.78)
|
2010 | |
| 700 |
Swaminathan S, Madkaikar MR, Ghosh K, Vundinti BR, Kerketta L, Gupta M. Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation.
Eur J Haematol. 2010 Feb 1;84(2):180-2.(IF:1.478)
|
2010 | |
| 701 |
Ghosh K Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
Indian J Hum Genet. 2010 Jan;16(1):6-7.
|
2010 | |
| 702 |
Colah R, Gorakshakar A, and Nadkarni A Global burden, distribution and prevention of ?-Thalassemia and hemoglobin E disorders.
Expert Rev. Hematol 2010 Mar, 3(1):103-117.(IF:1.161)
|
2010 | |
| 703 |
Vandana VPD, Deshpande NR, Ghosh K. Proteomic approach to autoimmune disorders : A review
Indian J Biotechnol 2010 Jan;9 : 13-7.(IF:--)
|
2010 | |
| 704 |
Shankarkumar U, Pawar A, Devraj JP, Bhupali K, Ghosh K. The HLA system- A review.
Anthopologist, 2010;Special Vol.6:183-97.
|
2010 | |
| 705 |
Korgaonkar S, Ghosh K and Babu Rao V. Clinical, Genetic and Cytogenetic study of Fanconi anemia in an Indian population
Hematology 2010 Jan;15(1):58-62. (IF:--) .
|
2010 | |
| 706 |
Warang P, Nair S, Nadkarni A, Ghosh K, Colah RB Hb H disease due to homozygosity for a rare alpha2-Globin Variant, Hb Sallanches
Hemoglobin 2010 Jan; 34(1): 45-48.(IF:1.106)
|
2010 | |
| 707 |
Pai N, Shetty S, Ghosh K. Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Jan 14. [Epub ahead of print](IF: 1.496)
|
2010 | |
| 708 |
Kanjaksha Ghosh ??Thalassemia- What is it ?
Physician’ s Digest 2010; Pg: 63-69.
|
2010 | |
| 709 |
Italia K, Jijina F, Chandrakala S, Nadkarni A, Sawant P, Ghosh K, Colah R. Exposure to hydroxyurea during pregnancy in sickle ?-thalassemia - A report of 2 cases.
J.Clin. Pharmacol 50; 231-4; 2010.(IF:3.59)
|
2010 | |
| 710 |
Mukherjee MB, Tripathy V, Colah RB, Solanki PK, Ghosh K, Reddy BM, Mohanty D Microsatellite diversity among the primitive tribes of India
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 114-120.
|
2009 | |
| 711 |
Singh R, Vandana VP, Patwardhan M, Ghosh K APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases.
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 98-102.
|
2009 | |
| 712 |
Ghosh K, Ghosh K. Private practice in India.
Natl Med J India. 2008 Nov-Dec;21(6):328-9.(IF:0.911)
|
2009 | |
| 713 |
Vundinti BR, Korgaonkar S, Ghosh K. Familial small supernumerary marker chromosome (sSMC) (14)(:P(11)-q(11):) In a child with translocation down syndrome
Indian J Pediatr. 2009 Dec; 76(12):1265-7. (IF:0.646)
|
2009 | |
| 714 |
Vandana VP, Ghosh K. Development of Anti-neutrophil Cytoplasmic antibodies (ANCA) and Vasculitis in BALB/c Mice: A Prototype of human ANCA associated disease.
J. Appl. Anim. Res. 2009 Dec;36:297-302.(IF:0.178)
|
2009 | |
| 715 |
Misri R, Khopkar U, Shankarkumar U, Ghosh K. Comparative case control study of clinical features and human leukocyte antigen susceptibility between familial and nonfamilial vitiligo
Indian J Dermatol Venereol Leprol. 2009 Nov-Dec;75(6):583-7.(IF:0.588)
|
2009 | |
| 716 |
Tripathy AS, Shankarkumar U, Chadha MS, Ghosh K, Arankalle VA. Association of HLA alleles with hepatitis C infection in Maharashtra, Western India
Indian J Med Res. 2009 Nov;130(5):550-5. (IF: 1.883)
|
2009 | |
| 717 |
Pai N, Shetty S, Kulkarni B, Ghosh K. Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2009 Nov 10. [Epub ahead of print] (IF: 1.286).
|
2009 | |
| 718 |
Mota L, Shetty S, Idicula-Thomas S, Ghosh K Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
Clin Chim Acta. 2009 Nov;409(1-2):106-11.Epub 2009 Sep 13. (IF:2.960)
|
2009 | |
| 719 |
Ajit Gorakshakar, Colah RB. Cascade screening for ?-thalassemia; A practical approach for identifying and counseling carriers in India.
Indian J. Comm. Med. 2009;Oct 34(4) :354-56.
|
2009 | |
| 720 |
Chalvam R, Colah RB, Mohanty D, Ghosh K, Mukherjee MB. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Blood Cells Mol Dis. 2009 Sep-Oct;43(2):156-7.(IF: 2.549)
|
2009 | |
| 721 |
Italia KY, Jijina FJ, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB. Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India
Clin Chim Acta. 2009 Sep;407(1-2):10-5. (IF:2.960)
|
2009 | |
| 722 |
Shetty S, Vora S, Kulkarni B, Mota L, Ghosh K Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency cause, consequence or a consequential cause?
Haemophilia. 2009 Sep;15(5):1104-8. (IF 2.394)
|
2009 | |
| 723 |
Ghosh K, Shetty S, Sahu D. Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI).
Haemophilia. 2009 Sep 23. [Epub ahead of print] (IF: 2.394)
|
2009 | |
| 724 |
Vaswani RK, Dharaskar PG, Kulkarni SS, Ghosh K. Iron Deficiency as a Risk Factor for First Febrile Seizure
Indian Pediatr. 2009 Sep 3. [Epub ahead of print](IF:0.956)
|
2009 | |
| 725 |
Madkaikar MR, Gupta M, Jijina F, Ghosh K. Paroxysmal Nocturnal Haemoglobinuria (PNH): diagnostic tests, advantages & limitations.
Eur J Haematol. 2009 Aug ; 83:503-511.(IF 1.478).
|
2009 | |
| 726 |
Ghosh K. Geographical heterogeneity of immigration and career paths of medical graduates in India.
Natl Med J India. 2009 Jul-Aug;22(4):218.(IF:0.911)
|
2009 | |
| 727 |
Shankarkumar U, Pawar A, Prabu G, Ghosh K. Role of HLA class I (HLA-A, B) and HLA class II (HLA-DRB, DQB) in HIV-1 patients with and without pulmonary tuberculosis.
J Acquir Immune Defic Syndr. 2009 Aug 15;51(5):640-1.(IF 4.570)
|
2009 | |
| 728 |
Prabu G, Iyer YS, Shankarkumar U, Ghosh K, Nachiappan V Monoclonal antibody produced against calf thymus histone.
Hybridoma (Larchmt). 2009 Aug;28(4):277-80.(IF 0.559)
|
2009 | |
| 729 |
Budrukkar A, Shahid T, Murthy V, Hussain T, Mulherkar R, Babu Rao V, Deshpande M, Sengar M, Ghosh-Laskar S, Agarwal JP Squamous cell carcinoma of base of tongue in a patient with Fanconi’s anemia treated with radiation therapy: case report and review of literature.
Head & Neck 2009; Aug 11 (E-pub ahead of print)(IF: 2.01).
|
2009 | |
| 730 |
Vundinti BR, Kerketta L, Jijina F, Ghosh K. Cytogenetic study of myelodysplastic syndrome from India.
Indian J Med Res. 2009 Aug;130(2):155-9. (IF: 1.883)
|
2009 | |
| 731 |
Ghosh K, Quadros L, Shetty S Spectrum of factor IX gene mutations causing haemophilia B from India.
Blood Coagul Fibrinolysis. 2009 Jul; 20(5):333-336.(IF:1.506)
|
2009 | |
| 732 |
Shetty S, Ghosh K Anti-phospholipid antibodies and other immunological causes of recurrent foetalloss--areview of literature of various therapeutic protocols.
Am J Reprod Immunol. 2009 Jul;62(1):9-24. Review.(IF 2.172)
|
2009 | |
| 733 |
Ghosh K Challenges of haemophilia care in India: lest we forget.
Indian J Med Res. 2009 Jul;130(1):87-8. (IF 1.883)
|
2009 | |
| 734 |
Umapathy Shankar kumar, Krishna kumar N Shah, Kanjaksha Ghosh HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India.
Epilepsia 2009 Jul; 50(7): 1837-38.(IF:3.733)
|
2009 | |
| 735 |
Kanjaksha Ghosh, Manisha Patwardhan, Vandana VP Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas
Rheumatol Int 2009 Jul;29(9):1047-50.(IF:1.327)
|
2009 | |
| 736 |
Ghosh K, Shetty S, Vora S Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss.
Int J Gynaecol Obstet. 2009 Jul 21. [Epub ahead of print] (IF: 1.228)
|
2009 | |
| 737 |
Vandana VPD, Ghosh K. Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
Indian J Dermatol. 2009 Jul;54(3):258-62.
|
2009 | |
| 738 |
Mamta Muranjan, Tejasvi Choudhary and Baburao Vundinti. Phenotypic heterogencity and parental origin of extrachromosome 21 in down syndrome.
Indian Pediat. 2009 July 1; [Epub ahead of print] (IF:0.956)
|
2009 | |
| 739 |
Shankarkumar U, Vandana VPD, Patwardhan M, Pawar A, Almeida A and Ghosh K HLA alleles in anti-endothelial cell antibody positive Indian SLE patients
Int J Hum Genet 2009 Apr-Jun; 9(2): 127-30. (IF: Nil)
|
2009 | |
| 740 |
Colah R, Gorakshakar A, Nadkarni A, Phanasgaonkar S, Surve R, Sawant P, Mohanty D, Ghosh K. Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
Blood Cells Mol Dis. 2009 May-Jun;42(3):241-6.(IF: 2.549)
|
2009 | |
| 741 |
Ghosh K, Ross C The teacher and the taught: medical education in India at the crossroads.
Natl Med J India. 2009 May-Jun:22(3):147-9.(IF:0.911)
|
2009 | |
| 742 |
Ghosh K, Shetty S, Tulsiani M Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia.
Clin Appl Thromb Hemost. 2009 May-Jun;15(3):277-82. Review. (IF: 1.286)
|
2009 | |
| 743 |
Ghosh K, Shetty S, Quadros L, Kulkarni B. Double mutations causing haemophilia B: a double whammy!
Br J Haematol. 2009 May;145(3):433-5. (IF: 3.195)
|
2009 | |
| 744 |
D Souza E, Ghosh K, Colah R A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies
Cytometry B Clin Cytom. 2009 May 76(B)(3): 175-80. (IF:1.439)
|
2009 | |
| 745 |
Pai N, Shetty S, Idicula-Thomas S, Kulkarni B, Ghosh K. Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First
Thromb Haemost 2009 Apr;101(4):785-87.(IF:3.413)
|
2009 | |
| 746 |
Pai N, Shetty SD, Ghosh K Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis.
Clin Appl Thromb Hemost. 2009 Apr 28. [Epub ahead of print] (IF: 1.286)
|
2009 | |
| 747 |
Devraj JP, Shankarkumar U, Ghosh K. Increased frequency of HLA-B7 among B27 – negative, seronegative spondarthritis patients from Mumbai, Western India.
Br J Biomed Sci 2009 Jan-Mar; 66(1): 25-27.(0.590)
|
2009 | |
| 748 |
Nadkarni A, Gorakshakar A, Surve R, Sawant P, Phanasgaonkar S, Nair S, Ghosh K, Colah RB Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009 Jan-Mar; 33(1):59-65.(IF: 1.106)
|
2009 | |
| 749 |
Quadros L, Ghosh K, Shetty S Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes
J Pediatr Hematol Oncol. 2009 Mar;31(3):157-60.(IF:1.176)
|
2009 | |
| 750 |
Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R. Hydroxyurea in sickle cell disease - A study of clinico-pharmacological efficacy in the Indian haplotype
Blood Cells Mol Dis. 2009 Jan-Feb; 42(1): 25-31.(IF: 2.549)
|
2009 | |
| 751 |
Vijapurkar M, Ghosh K, Shetty S. Novel mutations in GP IIb gene in Glanzmann’s thrombasthenia from India.
Platelets. 2009 Feb;20(1):35-40.(IF: 2.271)
|
2009 | |
| 752 |
Vora S, Shetty S, Khare M, Ghosh K Placental histomorphology in unexplained foetal loss with thrombophilia.
Indian J Med Res 2009 Feb; 129(2): 144-49.(1.883) (IF 1.826)
|
2009 | |
| 753 |
Kedar PS, Hamada T, Warang P, Nadkarni A, Shimizu K, Fujji H, Ghosh K,Kanno H, Colah R. Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes
Clin Genet. 2009 Feb;75(2):157-62.(IF: 3.18)
|
2009 | |
| 754 |
Iyer YS, Vasantha K, Pujari V, Jadhav S, Ghosh K Murine monoclonal anti-H as typing reagent.
Indian J Med Res 2009 Jan; 129(1): 72-74. (IF: 1.883)
|
2009 | |
| 755 |
Ghosh K, Shetty S Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors.
Clin Rev Allergy Immunol. 2009 Oct;37(2):58-66. (IF: 2.080)
|
2009 | |
| 756 |
Roshan Colah. Antenatal Diagnosis of Thalasssemias-Diagnostic technology suitable for the country
Journal of the Asiatic Society 2009 Vol 51 (2):69-72(IF:--)
|
2009 | |
| 757 |
Shankarkumar U, Pawar A, Ghosh K HIV-1 evolution drug resistance, and host genetics: The Indian scenario.
Virus Adaption and Treatment 2009; 1:1-4.(IF: open access)
|
2009 | |
| 758 |
Vijapurkar M, Mota L, Shetty S, Ghosh K. Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
Haemophilia. 2009 Jan;15(1):199-202. (IF: 2.394)
|
2009 | |
| 759 |
Kanjaksha Ghosh. Molecular evolution of Globin Gene Pathology-Its Driver, Challenges and
Journal of the Asiatic Society 2009 Vol. 51(20):73-8.(IF:--)
|
2009 | |
| 760 |
Anita Nadkarni, Marukh Wadia, Ajit Gorakshakar, Ryoiti Kiyama, Roshan B.Colah, Dipika Mohanty Molecular Characterization of ??-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population
Hemoglobin Sep-Oct 2008, Vol. 32, No. 5: 425–433.(IF: 1.00)
|
2008 | |
| 761 |
Meera V, Jijina F, Shrikande M, Madkaikar MR, Ghosh K Twin pregnancy in a patient of chronic myeloid leukemia on imatinib therapy
Leuk Res 2008 Oct; 32(10) : 1620-2. (IF 2.555)
|
2008 | |
| 762 |
Edna DSouza, Pratibha M. Sawant, Anita H. Nadkarni, Ajit Gorakshakar, Dipika Mohanty, Kanjaksha Ghosh, Roshan B. Colah Evaluation of the Use of Monoclonal Antibodies and Nested PCR for Noninvasive Prenatal Diagnosis of Hemoglobinopathies in India
AJCP Aug 2008; 130(2):202-209.(If: 2.89)
|
2008 | |
| 763 |
Prabhu R, Jijina F, Shetty S, Ghosh K Successful surgery in severe haemophilia – a two stage replacement therapy in resource poor countries.
Haemophilia 2008 Jul 3. (IF 2.394)
|
2008 | |
| 764 |
Ghosh K, Shetty S antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
Blood Coagul Fibrinolysis 2008 Jul;19(5):464-65.[18600102] (IF 1.506)
|
2008 | |
| 765 |
Shetty S, Ghosh K Reduced clinical severity in a mutationally well – characterized cohort of severe hemophilia with associated thrombophilia
Am. J. Clin Pathol 2008 Jul; 130(1) 84-7. (IF 2.18)
|
2008 | |
| 766 |
Shankarkumar U, Pawar A, Gaonkar P, Parsannawar D, Salvi V, Ghosh K. HLA allele associations in idiopathic recurrent spontaneous abortion patients from India.
J. Hum Reprod. Sci, 2008 Jan-Jun;1(1):19-24.
|
2008 | |
| 767 |
Ghosh K, Shetty S, Mota L Aspirin resistance in patients with coronary artery disease- which test to use in routine management?
Blood Coagul Fibrinolysis .2008 Jun: 19(4) : 324-6. (IF 1.506)
|
2008 | |
| 768 |
Kedar PS, Warang P, Nadkarni AH, Colah RB, Ghosh K. A novel G143D mutation in the NADH-cytochrome b(5) reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood Cells Mol Dis 2008 May-Jun; 40(3):323-7. [17964195] (IF 2.549)
|
2008 | |
| 769 |
Nadkarni A, Phanasgaonkar S, Colah R, Mohanty D, Ghosh K. Prevalence and molecular characterization of alpha thalassemia syndromes among Indians
Genet Test. 2008 Jun; 12(2) : 177-80. (IF 1.7)
|
2008 | |
| 770 |
Ghosh K, Gangodkar S, Jain P, Shetty S, Ramjee S, Poddar P,Basu A Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy
J Electron Microsc(Tokyo) 2008 Jun; 57(3):113-8. (IF 1.05)
|
2008 | |
| 771 |
Colah R, Surve R. Wadia M, Solanki P, Mayekar P, Thomas M, Gorakshakar A, Dastur A, Mohanty D. Carrier screening for ?-thalassemia during pregnancy in India: a 7 year evaluation.
Genet Test. 2008 Jun : 12(2): 181-5. (IF 1.7).
|
2008 | |
| 772 |
Basu A, Jain P, Gangodkar SV, Shetty S, Ghosh K. Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.
FEMS Immunol Med Microbiol. 2008 June ; 53 (1):46-51 (IF 2.494)
|
2008 | |
| 773 |
Colah R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Sawant P, Surve R, Mohanty D, Ghosh K Hb Showa Yakushi [beta 110(612) Leu?Pro ] in three families from Western India:First report on homozygous Hb showa Yakushiji.
Blood Cells Mol Dis. 2008 May 19. (IF 2.549)
|
2008 | |
| 774 |
Quadros L, Ghosh K, Shetty S Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India.
Haemophilia. 2008 May; 14 (3) : 628-9. (IF 2.394)
|
2008 | |
| 775 |
Vijapurkar M, Ghosh K, Shetty S, McLane MA, Moura da Silva AM,Butera D. A simple, novel and robust test to diagnose type I glanzmann thrombasthenia
Haematologica. 2008 May; 93 (5) :797-8. (IF 6.416)
|
2008 | |
| 776 |
Ghosh K, Shetty S, Vora S, Salvi V. Successful pregnancy outcome in women with bad obstetric history and recurrent fetal loss due to thrombophilia: effect of unfractionated heparin and low--molecular weight heparin.
Clin Appl Thromb Hemost. 2008 Apr;14(2):174-9. [18160603] (IF 1.286)
|
2008 | |
| 777 |
Kulkarni SS, Colah R, Gorakshakar A, Gupte S, Vasantha K, Mohanty D,Ghosh K. Frequency of Partial D in Western India.
Transf Med 2008 Apr; 18(2):91-6.(IF 2.155)
|
2008 | |
| 778 |
Mohanty D, Mukherjee MB, Colah RB, Wadia M, Ghosh K, Chottray GP, Jain D, Italia Y, Ashokan K, Kaul R, Shukla DK & Muthuswamy V Iron deficiency anaemia in sickle cell disorders in India.
Indian J Med Res 2008 Apr; 127(4):366-9. [18577791](IF 1.826)
|
2008 | |
| 779 |
Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K. A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss.
Eur J Obstet Gynecol Reprod Biol 2008 Apr;137(2):136-40. (IF 1.736)
|
2008 | |
| 780 |
Ghosh K, Shetty S Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia.
Haemophilia. 2008 Mar;14(2):392-3. [18179571](IF 2.394)
|
2008 | |
| 781 |
Ghosh K, Shetty S. Blood coagulation in falciparum malaria-a review.
Parasitol Res. 2008 Mar;102(4):571-6. [18066597] (IF 3.938)
|
2008 | |
| 782 |
Vundinti BR, Kerketta L, Madkaikar MR, Jijina F, Ghosh K translocation in a new variant of +(8;21) acute myeloid leukemia involving Xp22.
Indian J Cancer. 2008 Jan-Mar; 45(1):30-2.
|
2008 | |
| 783 |
Shankarkumar U, Pawar A, Ghosh K. Implications of HLA sequence-based typing in transplantation.
J PostGrad Med. 2008 Jan-Mar;54(1):41-4. (IF 1.589)
|
2008 | |
| 784 |
Ghosh K, Vandana VP Background noise of infection for using ANCA as a diagnostic tool for vasculitis in tropical and developing countries.
Parasitol Res. 2008 Apr;102(5):1093-5. Epub 2008 Feb 24. (IF 3.938)
|
2008 | |
| 785 |
Ghosh K, Madkaikar MR, Jijina F Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage
Acta Haematol. 2008 Feb 20;119(2):69-72 (IF 1.316)
|
2008 | |
| 786 |
Kedar PS, Kazuyuki Shimizu, Kanjaksha Ghosh, Hisaichi Fujji, Roshan A proteomic analysis of CBA-Pk-1slc/Pk-1slc mice with Red Blood Cell Type Pyruvate Kinase deficiency using 2DE together with MALDI-TOF-MF analysis
FASEB J 2008;22:1025. (IF 6.721)
|
2008 | |
| 787 |
Konkankar S, Shankarkumar U HLA DRB1 alleles in chronic hepatitis B infected patients
Intl J Hum Genet 2008; 72: 275.
|
2008 | |
| 788 |
Sadawarte S, Jijina F, Nair CK, Seth S, Ghosh K. An unusual presentation of pediatric acute leukemia
Ind J Hematol Blood Transf 2008; 24:16-22.
|
2008 | |
| 789 |
Shadaan Abid, Anurupa Maitra, Pervin Meherji, Zareen Patel, Seema Kadam, Jatin Shah, Rupin Shah, Vijay Kulkarni, V BabuRao and Jyotsna Gokral. Clinical and Laboratory evaluation of idiopathic Male infertility in a secondary referral center in India.
J Clin Lab Analysis 2008; 22: 29-38.
|
2008 | |
| 790 |
Ghosh K, Shetty S and Ghosh K A high cost low volume disease: suitable preventive strategies for developing and developed countries.
The Open Hematol J 2008; 2: 20-4.
|
2008 | |
| 791 |
Ghosh K, Vandana VP, Patwardhan M and Gupta M. Antiendothelial cell antibodies in systemic lupus erytematosus.
Intl J Rheumatol Dis 2008; 11:121-6.(IF 0.205)
|
2008 | |
| 792 |
Malay Mukherjee. Laboratory diagnosis of sickle cell syndrome.
J Community Med 2008 Jan; 4(1): 11-14.
|
2008 | |
| 793 |
Kanjaksha Ghosh, Shrimati Shetty and Kinjalka Ghosh Hemophilia: A High Cost Low Volume Disease:Suitable preventive strategies for developing and developed countries.
The Open Hematology Journal, 2008; 2:20-24.
|
2008 | |
| 794 |
Shetty S, Ghosh K, Quadros L. Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
Eur J Haematol. 2008 Jan;80(1):87-9. [18028421] (IF 1.478)
|
2008 | |
| 795 |
Chalvam R, Kedar PS, Colah RB, Ghosh K, Mukherjee MB A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
J Hum Genet. 2008;53(2):181-4. [18043863] (IF: 2.431)
|
2008 | |
| 796 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Ind. J. of Hum Genet. 2007 Sep –Dec; 13(3):79-85. (IF 0.11 )3
|
2007 | |
| 797 |
Italia KY, Colah R, Mohanty D Evaluation of F cells in sickle cell disorders by flow cytometry – comparison with theKleihouer- Betke’s slide method
Int J Lab Hematol 2007 Dec: 29 (6): 409-14. (IF 1.304)
|
2007 | |
| 798 |
Ghosh K, Shetty S, Tulsiani M Evolution ofprenatal diagnosis techniques from phenotypic diagnosis to gene arrays : Its likely impact on prenatal diagnosis of hemophilia
Clin Appl Thromb Hemost first published on December 26
|
2007 | |
| 799 |
Ghosh K, Ghosh K. Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia:report of three cases.
Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26.(IF 2.615)
|
2007 | |
| 800 |
Ghosh K, Shetty S, Kulkarni B Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients
Haemophilia
|
2007 | |
| 801 |
Ghosh K, Ghosh K Pathogenesis of anemia in malaria: a concise review
Parasitol Res
|
2007 | |
| 802 |
Shankarkumar U, Ghosh K MHC non-HLA gene polymorphisms in transplantation
Indian J Pathol Microbiol
|
2007 | |
| 803 |
Phanasgaonkar S, Colah R, Ghosh K, Mohanty D, Gupte S Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India
Br J Biomed Sci
|
2007 | |
| 804 |
Nadkarni A, Surve R, Colah R, Ghosh K, Holay M, Dani A, Shrikhande A, Bharti V, Suryawanshi S. Thalassemia intermedia due to homozygosity for an Asian Indian(Agammadeltabeta) degrees deletional inversion.
Clin Chim Acta. 2007 Oct;385(1-2):81-3. Epub 2007 Jul 19. (IF 2.960)
|
2007 | |
| 805 |
Ernest Beutler, Duparc S, Doumbo O, Ghosh K, Vinicious M, de Lacerda G, Lapierre D, Looareesuwan S, Premji Z,Vulliamy T, Vhitty C. Lapierre D, Looareesuwan S, Premji Z,Vulliamy T, Vhitty C. Glucose-6- phosphate dehydrogenase deficiency and antimalarial drug development.
Am J Trop Med Hyg 2007 Oct;77(4):779-89. Rev. [17978087]. (IF 2.8)
|
2007 | |
| 806 |
Gorakshakar AC, Das MK, Phanasgaonkar SP, Nadkarni AH, Colah RB,Mohanty D Origin of the Codon 47(+A) ?-thalassemia mutation among the Nicobarese of the Andaman & Nicobar islands in India.
Br J Haematol 2007 Oct;139 (2):345-6. [17897314]. (IF 3.195)
|
2007 | |
| 807 |
Rao VB, Korgaonkar S, Kerketta L, Ghosh K Differentiation of Nijmegen breakage syndrome from Fanconi anemia
Genet Mol Res
|
2007 | |
| 808 |
Vora S, Shetty S, Ghosh K Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
Blood Coagul Fibrinolysis
|
2007 | |
| 809 |
Kulkarni SS, Gupte SC, Vasantha K, Mohanty D, Ghosh K Varied distribution of RhD epitopes in the Indian population
Natl Med J India
|
2007 | |
| 810 |
Shetty S, Vora S, Kulkarni B, Mota L, Vijapurkar M, Quadros L, Ghosh K Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.
Br J Haematol. 2007 Aug;138(4):541-4.(IF 3.195)
|
2007 | |
| 811 |
Vora S, Ghosh K, Shetty S, Salvi V, Satoskar P. Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
Thromb J. 2007 Jul 4;5:9. (IF 1.0)
|
2007 | |
| 812 |
Colah RB, Surve R, Sawant P, D’Souza E, Italia K, Phanasgaonkar S, Nadkarni AH,Gorakshakar AC HPLC studies in hemoglobinopathies
Indian J Pediatr. 2007 Jul:74(7):657-62 Review. (IF 0.9)
|
2007 | |
| 813 |
Kedar PS, Nampoothiri S, Sreedhar S, Ghosh K, Shimizu K, Kanno H, Colah RB First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation
Genet Mol Res
|
2007 | |
| 814 |
Ghosh K, Madkaikar MR, Shrikhande M Osteoporosis in young haemophiliacs from western India.
Am J Hematol. 2007 Jun;82(6):453-7. [17278114] (IF 3.576)
|
2007 | |
| 815 |
Kulkarni SS, Gorakshakar AC, Colah RB, Gupte SC, Mohanty D Usefulness of prenatal detection of Rh D typing by molecular analysis in Indians
J PostGrad Med. 2007 Apr-Jun; 53(2): 149. (IF 1.589)
|
2007 | |
| 816 |
Kulkarni SS, Vasantha K, Gupte SC, Mohanty D, Ghosh K. Potential of commercial anti-D reagents in the identification of partial D variants in Indian population.
Indian J Med Res. 2007 May;125(5):641-4. [17642499] (IF 1.823)
|
2007 | |
| 817 |
Ghosh K, Vora S, Shetty S. Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis.
Br J Haematol. 2007 Aug;138(4):555-7. [17590183] (IF 3.195)
|
2007 | |
| 818 |
Ghosh K, Madkaikar MR, Jijina F, Shetty S Fractures of long bones in severe haemophilia.
Haemophilia. 2007 May;13(3):337-9. (IF 2.394).
|
2007 | |
| 819 |
Quadros L, Ghosh K, Shetty S. A common G10430A mutation (Gly 60 Ser) in the factor IX gene presence of moderate and mild hemophilia B in the majority describes the presence of moderate and mild hemophilia B in the majority of the Gujarat population.
Ann Hematol. 2007 May;86(5):377-9. [17308903] (IF 2.688)
|
2007 | |
| 820 |
Varla-Leftherioti M, Keramitsoglou T, Spyropoulou-Vlachou M,Papadimitropoulos M, Kontopoulou-Antonopoulou V, Tsekoura C, Sankarkumar U, Paparistidis N, Ghosh K, Pawar A, Vrani V, Daniilidis M, Parapanissiou E, Diler AS, Carin M, Stavropoulos-Giokas C 14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component.
Tissue Antigens. 2007 Apr; 69 Suppl 1:297-303. (IF 3.024)
|
2007 | |
| 821 |
Umapathy S, Pawar A, Ghosh K. Specific human leukocyte antigen alleles associated with HIV-1 infection in an Indian population.
J Acquir Immune Defic Syndr. 2007 Apr 1;44(4):489-90. [17353719]. (IF 4.262)
|
2007 | |
| 822 |
Ghosh K, Ghosh K. Microarray genetic screening: the other side of the coin.
Lancet. 2007 Mar 24;369(9566):992. [17382825] (IF 33.63)
|
2007 | |
| 823 |
Mota L, Ghosh K, Shetty S Second trimester antenatal diagnosis in rare coagulation factor deficiencies.
J Pediatr Hematol Oncol. 2007 Mar;29(3):137-9. [17356389] (IF 1.176)
|
2007 | |
| 824 |
Shetty S, Ghosh K. Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
Haemophilia. 2007 Mar;13(2):172-7. [17286770] (IF 2.394)
|
2007 | |
| 825 |
Chalvam R, Mukherjee MB, Colah RB, Mohanty D, Ghosh K G6PD Namoru (208 T C) is the major polymorphic variant in the tribal populations in southern India.
Br J Haematol. 2007 Feb;136(3):512-3. No abstract available. (IF 3.195)
|
2007 | |
| 826 |
Ghosh K, Khare A, Shetty S, Kulkarni B. Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern of response to oral folic acid, vitamin B12, B6 therapy
Clin Chim Acta. 2007 Feb;377(1-2):281-2. Epub 2006 Sep 22. (IF 2.960)
|
2007 | |
| 827 |
Gupta N, Bianchi P, Fermo E, Kabra M. Warang P, Kedar PS, Gupta N, Colah R Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family
Prenat Diagn. 2007 Feb; 27(2): 117-8. (IF 2.152)
|
2007 | |
| 828 |
Madkaikar MR, Gupta M, Ghosh K, Swaminathan S, Sonawane L, Mohanty D Optimizing methods of red cell sedimentation from cord blood to maximize nucleated cell recovery prior to cryopreservation
Br J Biomed Sci
|
2007 | |
| 829 |
Madkaikar MR, Ghosh K, Gupta M, Swaminathan S, Mohanty D Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells
Acta Haematol
|
2007 | |
| 830 |
Ghosh K,Khare A, Shetty S Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India.
Indian Heart J 2007: 59(3):242-5.
|
2007 | |
| 831 |
Korgaonkar Seema, Babu Rao V, Kerketta L, Ghosh K. Chromosomal breakage in myelodysplatic syndrome.
Asian Pacific J Cancer Preview 2007; 8:151-4. (IF: 1.11)
|
2007 | |
| 832 |
Shankarkumar U, Pawar A, and Ghosh K Human leukocyte antigenpolymorphism and association: a review
Anthropologist 2007;Special Vol. No.3: 367-72.
|
2007 | |
| 833 |
Rao VB, Kerketta L, Korgaonkar S, Ghosh K. Dandy – Walker malformation in a case of partial trisomy 9p (p12.1àpter) due to maternal translocation
Indian J Hum Genet 2007;13(1): 33-5.
|
2007 | |
| 834 |
Colah R, Thomas M, Mayekar P Assessing the impact of screening and counseling high school children for b-thalassemia in India.
J Med Screen 2007; 14(3): 158. [17925089]. (IF 1.493)
|
2007 | |
| 835 |
Nadkarni A, Gorakshakar A, Colah R, Mohanty D, Ghosh K Evaluation of the clinical severity of ?-thalassemia homozygous patients using a phenotypic scoring system
J Chinese Clin Med 2007; 2(8): 439-447
|
2007 | |
| 836 |
Ghosh K Coagulation disorders seen through the window of molecular biology
Indian J Hum Genet 2007; 13(3) 79-85.
|
2007 | |
| 837 |
D”Souza E, Kulkarni SS, Colah RB, Mohanty D An improved flowcytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathies
Hemoglobin, 2007; 31(1): 39-48. (IF 1.106)
|
2007 | |
| 838 |
Dhurandhar PS, Shankarkumar U HLA association in seronegative spondyloarthritis patients from Mumbai, India.
Int. J Hum Genet. 2007; 7(3): 235-9. (IF 0.238)
|
2007 |
