आय सी एम आर - राष्ट्रीय प्रतिरक्षा रुधिर विज्ञान संस्थान

ICMR-National Institute of Immunohaematology

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2021-Till Date




Publications 2016-2020
1 Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H,Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, Ramanagoudr-Bhojappa R, Smogorzewska A, Mohan S, Rajendran A, Auerbach AD, Takata M, Chandrasekharap A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat. 2020 Jan;41(1):122-128. (IF 4.453)
2 Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y,Raicha B, Serrao E. Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
Am J Clin Pathol. 2020 Jan 1;153(1):82-87.(IF 1.962)
3 Ghosh K, Ghosh K, Agrawal R,Nadkarni AH. Recent advances in screening and diagnosis of haemoglobinopathy.
Expert Rev Hematol. 2020 Jan;13(1):13-21. (IF: 2.505)
4 Solanki A, Rajendran A, Mohan S, Raj R, Vundinti BR Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia.
PLoS One. 2020 Jan 15;15(1):e0227603.eCollection 2020 (IF:2.776)
5 Deshpande R, Shanbhag S, Jadli A,Shetty S. A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non-pathogenic gene variants.
Haemophilia. 2020 Jan;26(1):e26-e27 (IF:3.590)
6 Ghosh K, Ghosh K, Agrawal R,Nadkarni AH. Recent advances in screening and diagnosis of hemoglobinopathy.
Expert Rev Hematol. 2020 Jan;13(1):13-21.
8 Devendra R, Gupta V, Biradar SS, Bhat P, Hegde S, Hoti SL, Mukherjee MB, Hegde HV. G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India.
Ann Hum Biol. 2020 Feb;47(1):55-58(IF:1.588)
9 Bargir UA, Hule GP, Kambli P, Kulkarni M, Donta AK, Taur P, Gorakshakar A, Desai M, Madkaikar MR. "FUT2" a potential genetic modifier in NCF1 deficiency.
J Allergy Clin Immunol Pract. 2020 Mar;8(3):1097-1099. (IF:7.55)
10 Krishnan VP, Taur P, Pandrowala A,Madkaikar M, Desai M X-Linked Hyper IgM Syndrome Presenting with Recurrent Tuberculosis-a Case Report.
J Clin Immunol. 2020 Apr;40(3):531-533.(IF:6.780)
11 More TA, Dongerdiye R, Devendra R, Warang PP,Kedar PS. Mechanosensitive Piezo1 ion channel protein (PIEZO1 gene): update and extended mutation analysis of hereditary xerocytosis in India.
Ann Hematol. 2020 Apr;99(4):715-727
12 Gupta V, Kulkarni A, Warang P, Devendra R, Chiddarwar A,Kedar P. Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia.
Hum Mutat. 2020 Apr;41(4):737-748.
13 Chawla SS, Gorakshakar AC, Ghosh KK,Madkaikar MR, Devarajan PV Fabrication of gelatin functionalized silver nanoparticles for blood group profiling.
Nanotechnology. 2020 May 1;31(29):295102. doi: 10.1088/1361-6528/ab83b9.(IF:3.551)
14 More TA, Dalal B, Devendra R, Warang P,Shankarkumar A, Kedar P. Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.
Cytometry B Clin Cytom. 2020 May;98(3):238-249.
15 Purohit S, Srivastava S,Shankarkumar A, Raj A, Dalal B, Marathe N, Shende C. Prevalence of Vitamin D Deficiency Amongst Indian Orthopaedic Surgeons.
Indian J Orthop. 2020 May 14;54(Suppl 1):183-187.
16 Umare V, Pradhan V, Dadheech S, Rajadhyaksha A, Ghosh K, Nadkarni A Clinical implications of IL-10 promoter polymorphisms on disease susceptibility in Indian SLE patients.
Lupus. 2020 Jun; 29(6):587-598.(IF:2.924)
17 Bargir UA,Madkaikar MR. 2019 Update on Primary Immunodeficiency Disorders by the International Union of Immunological Societies.
Indian Pediatr. 2020 Jun 15;57(6):565-567.(IF:1.186)
18 Prabhudesai A,Sharma R,Shetty S,Phadnis A,Kulkarni B. Congenital PAI-1 deficiency results in psoas hematoma in an Indian patient.
Thromb Res.2020 Jun;190:35-38. [IF: 2.77].
19 Hariharan P, Kishnani P, Sawant P, Gorivale M, Mehta P, Kargutkar N, Colah R, Nadkarni A Genotypic-phenotypic heterogeneity of ??-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India..
Ann Hematol. 2020 Jul;99(7):1475-1483.(IF 3.0)
20 Shabrish S, Karnik N, Gupta V, Bhate P,Madkaikar M. Impaired NK cell activation during acute dengue virus infection: A contributing factor to disease severity.
Heliyon. 2020 Jul 4;6(7):e04320. doi: 10.1016/j.heliyon.2020.e04320. eCollection 2020
21 Kulkarni S & Harita Maru. Extended phenotyping of blood group antigens: Towards improved transfusion practices.
Global Journal of Transfusion Medicine2020 Jul-Dec, 5: 120-5. (IF:-)
22 Dhangar S, Ghatanatti J,Vundinti BR. array-CGH revealed gain of Yp11.2 in 49,XXXXY and gain of Xp22.33 in 48,XXYY karyotypes of two rare klinefelter variants.
Intractable Rare Dis Res. 2020 Aug;9(3):145-150.(IF:1.447)
23 Mehta P, Sawant P, Gorivale M, Nadkarni A, Colah R, Mukherjee MB. Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathies.
Int J Lab Hematol. 2020 Aug;42(4):482-491.(IF 2.2)
24 Mishra G, Sachan D, Krishna D, Parchure D,Madkaikar M, Kulkarni S. Characterising Indian RhD variants by serological and molecular methods.
Transfus Med. 2020 Aug;30(4):324-326.(IF:2.159)
25 Vira HJ, Pradhan VD, Umare VD, Chaudhary AK, Rajadhyksha AG, Nadkar MY, Ghosh K,Nadkarni AH. Role of MMP-2 and its inhibitor TIMP-2 as biomarkers for susceptibility to systemic lupus erythematosus.
Biomark Med. 2020 Aug;14(12):1109-1119.
26 Smvk P, M N M, D M DY, Kondeti S, Kalashikam RR. Strain specific variation underlines the disparity in stress response of rats to calorie dense diets in the pathophysiology of obesity.
Steroids. 2020 Aug;160:108653. doi: 10.1016/j.steroids.2020.108653.
27 Vira HJ, Pradhan VD, Umare VD, Chaudhary AK, Rajadhyksha AG, Nadkar MY, Ghosh K,Nadkarni AH. Expression of the matrix metalloproteinases MMP-2 and MMP-9 and their inhibitors TIMP-1 and TIMP-2 in systemic lupus erythematosus patients.
Neth J Med. 2020 Sep;78(5):261-268.
28 Soni P, Shanmukhaiah C,Patil R, Shetty S. Differential response to FEIBA is strongly associated with the prothrombotic microparticles.
Blood Cells Mol Dis. 2020 Sep;84:102441. doi: 10.1016/j.bcmd.2020.102441.
29 Talukdar D; Gogoi, A, Doley, D, Marak R, Kakati S, Pradhan V, Nadkarni A, Baruah S. The clinical and immunological profile of SLE patients from Assam, North-East India.
Ind J Rheumatol 2020 Sep;15(3):181-186(IF:0.327)
30 Kulkarni S, Choudhary B, Gogri H, Sharma J, Madkaikar M. Red cell antigen phenotypes in blood donors & thalassaemia patients for creation of red cell antigen-matched inventory.
Indian J Med Res. 2020 Sep;152(3):273-279.
31 Agarwal A, Mukherjee A, Kumar G, Chatterjee P, Bhatnagar T, Malhotra P; PLACID Trial Collaborators Convalescent plasma in the management of moderate covid-19 in adults in India: open label phase II multicentre randomised controlled trial (PLACID Trial).
BMJ. 2020 Oct 22;371:m3939. doi: 10.1136/bmj.m3939.(IF:30.223)
32 Gupta AD, Daruwalla MR, Pawar R, Sidhwa K, Hariharan P,Nadkarni A, Hb Yaizu A rare beta-globin chain variant posing diagnostic dilemma in high- performance liquid chromatography.
Ind J Pathol Microbiol 2020 Oct-Dec ;63(4) 663-665.(IF:0.663)
33 Hariharan P, Chavan V, Nadkarni A Significance of Heme oxygenase -1 (HMOX-1) gene on fetal hemoglobin induction in sickle cell anemia patients
Scientific Reports. 2020 Oct 28;10(1):18506.(IF 4.0)
34 Ukirde V, Usulumarty D, Maru H, Billa V. Are weak blood groups important to look for in kidney transplantation? A case report on interchanging blood groups.
Indian J Transplant 2020 Oct-Dec; 14(4):355-357.(IF:0.13)
35 Anila Mani, Garima Mishra, Kulkarni Swati, Debasish Gupta D-phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17-(Hr0) antibodies
Transfusion Medicine. 2021 Oct;31(5):383-386. (IF:2.019)
36 Kulkarni S, Mishra G, Maru H, Parchure D, Gupta D, Bajaj AK, Sindhwani SP, Chaphekar A, Shah R, Frec C,Madkaikar M, Fichou Y. Molecular characterization of rare D--/D-- variants in individuals of Indian origin.
Blood Transfus. 2020 Nov 27. doi: 10.2450/2020.0183-20.(IF:3.662)
37 Vinod Umare, Sneha Dadheech, Vandana Pradhan, Anjali Rajadhyaksha, Kanjaksha Ghosh, Anita Nadkarni* Cytokine genes multi-locus analysis reveals synergistic influence on genetic susceptibility in Indian SLE - A multifactor-dimensionality reduction approach.
Cytokine 2020 Nov;135:155240. (IF 3.5)
38 Kelkar MG, Bargir UA, Malik-Yadav R, Gupta M, Dalvi A, Jodhawat N, Shinde S, Madkaikar M T Cells Exhibit an Exhausted Phenotype in Hemophagocytic Lymphohistiocytosis
J Clin Immunol. 2021 Nov 41(8):1794-1803. (IF:8.317)
39 Yadav RM, Gupta M, Dalvi A, Bargir UA, Hule G, Shabrish S, Aluri J, Kulkarni M, Kambli P, Uppuluri R, Seshadri S, Jagadeesh S, Suresh B, Raja J, Taur P, Malaischamy S, Ghosh P, Mahalingam S, Kadam P, Lashkari HP, Tamhankar P, Tamhankar V, Mithbawkar S, Bh Prenatal Diagnosis for Primary Immunodeficiency Disorders-An Overview of the Indian Scenario.
Front Immunol. 2020 Dec 7;11:612316. doi: 10.3389/fimmu.2020.612316. eCollection 2020.(IF:6.429)
40 Dongerdiye R, Jagadeesh S, Suresh B, Rajendran A, Devendra R, Warang P,Kedar PS. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in theHK1gene causing severe haemolytic anaemia with developmental delay in an Indian family.
J Clin Pathol. 2020 Dec 25:jclinpath-2020-206960. doi: 10.1136/jclinpath-2020-206960.
41 Devendra R, Gupta V, Shanmugam R, Singh MPSS, Patel P, Valecha N, Mishra N, Ahmed N, Hoti SL, Hegde HV, Warang P, Chiddarwar A,Kedar P, Mayekar P, Mukherjee MB. Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.
Infect Genet Evol. 2020 Dec;86:104597. doi: 10.1016/j.meegid.2020.104597.
42 Kambli PM,Bargir UA, Yadav RM, Gupta MR, Dalvi AD, Hule G, Kelkar M, Sawant-Desai S, Setia P, Jodhawat N, Nambiar N, Dhawale A, Gaikwad P, Shinde S, Taur P, Gowri V, Pandrowala A, Gupta A, Joshi V, Sharma M, Arora K, Pilania RK, Chaudhary H, Agarwal A, K Clinical and Genetic Spectrum of a Large Cohort of Patients With Leukocyte Adhesion Deficiency Type 1 and 3: A Multicentric Study From India.
Front Immunol. 2020 Dec 16;11:612703. doi: 10.3389/fimmu.2020.612703. eCollection 2020.PMID:33391282
43 George M, Solanki A, Chavan N, Rajendran A, Raj R, Mohan S, Nemani S, Kanvinde S, Munirathnam D, Rao S, Radhakrishnan N, Lashkari HP, Ghildhiyal RG, Manglani M, Shanmukhaiah C, Bhat S, Ramesh S, Cherian A, Junagade P, Vundinti BR. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
Hum Mutat. 2021 Dec;42(12):1648-1665. (IF:4.878)
44 Roos D, Madkaikar M, Kuhns DB et al. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
Blood Cells Mol Dis. 2021 Dec92:102596 (IF:2.40)
45 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.
J Clin Pathol. 2019 Jan;72(1):81-85.(IF:2.894)
46 Upadhye D, Jain D, Nadkarni A,Ghosh K, Colah R. Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India.
Indian J Hematol Blood Transfus. 2019 Jan;35(1):109-113. (IF: 0.474)
47 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.
Biomark Med. 2019 Jan; 13(1):33-43.(IF:2.346)
48 Aluri J, Desai M, Gupta M, Dalvi A, Terance A, Rosenzweig SD, Stoddard JL, Niemela JE, Tamankar V, Mhatre S, Bargir U, Kulkarni M, Shah N, Aggarwal A, Lashkari HP, Krishna V, Govindaraj G, Kalra M,Madkaikar M Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India.
Front Immunol. 2019 Feb 4;10:23. eCollection 2019. (IF: 5.511)
49 Shabrish S, Desai M, Saxena V, Kelkar M,Madkaikar M. IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections.
J Clin Immunol. 2019 Feb;39(2):135-137. (IF: 4.227)
50 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.
Intractable Rare Dis Res. 2019 Feb;8(1):72-77
51 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.
Indian J Pediatr. 2019 Mar 16.doi:10.1007/s12098-019-02904-9.[Epub ahead of print] (IF: 1.046 )
52 Desai SA, Martin SL, Nanavati RN,Colah RB, Ghosh K, Kabra N, Mukherjee MB. Red Cell Distribution Width (RDW): Normative Data in Indian Neonates.
J Pediatr Hematol Oncol. 2019 Mar;41(2): e119-e-121.(IF: 1.060)
53 Shabrish S, Kelkar M, Chavan N, Desai M, Bargir U, Gupta M, Mehta P, Chichra A, S C, Taur P, Saxena V, Vundinti BR,Madkaikar M. Natural Killer Cell Degranulation Defect: A Cause for Impaired NK-Cell Cytotoxicity a and Hyperinflammation in Fanconi Anemia Patients.
Front Immunol. 2019 Mar 21;10:490. eCollection 2019 (IF: 3.35)
54 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.
Mediterr J Hematol Infect Dis. 2019 Mar 1;11(1):e2019018.
55 Gaikwad T, Deshpande R,Shetty S. Anti-factor VIII inhibitors against A2 and C2 domains in hemophilia A patients from India.
Blood Cells Mol Dis. 2018 Mar;75:11-12.(IF:1.836)
56 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.
Int J Dermatol. 2019 Mar 13. doi: 10.1111/ijd.14424. [Epub ahead of print]
57 Umare V, Pradhan V, Nath S, Rajadhyaksha A,Ghosh K, Nadkarni AH. Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients.
Lupus. 2019 Apr;28(4):545-554
58 Nadkarni AH, Gorakshakar AC, Sawant PM, Italia KY, Upadhye DS, Gorivale MS, Mehta PR, Hariharan P,Ghosh K, Colah RB. The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15years at a referral center.
Int J Lab Hematol. 2019 Apr;41(2):218-226. (IF:1.919)
59 Devendra R, Warang P, Gupta V, Chiddarwar A, Kedar P, Agarwal MB,Mukherjee MB. A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.
Indian J Hematol Blood Transfus. 2019 Apr;35(2):399-401.
60 Sidhwa K, Daruwalla MR, Pawar R, Nadkarni A,Hariharan P, Mehta P, Gupta AD. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband.
Indian J Pathol Microbiol. 2019 Apr-Jun;62(2):323-325.
61 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.
62 Bandari AK, Bhat S, Archana MV, Yadavalli S, Patel K, Rajagopalan P, Madugundu AK,Madkaikar M, Reddy K, Muthusamy B, Pandey A. Family-Based Next-Generation Sequencing Study Identifies anIL2RGVariant in an Infant with Primary Immunodeficiency.
OMICS. 2019 May;23(5):285-290. doi: 10.1089/omi.2018.0196.(IF:2.370)
63 Martin SL, Desai S, Nanavati R, Colah RB,Ghosh K, Mukherjee MB. Red cell distribution width and its association with mortality in neonatal sepsis.
J Matern Fetal Neonatal Med. 2019 Jun;32(12):1925-1930.
64 Dongerdiye R, Kamat P, Jain P,Warang P, Devendra R, Wasekar N, Sharma R, Mhaskar K, Madkaikar MR, Manglani MV, Kedar PS. Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
J Clin Pathol. 2019 Jun; 72(6): 393-398.(IF: 2.894)
65 Madkaikar MR, Shabrish S, Kulkarni M, Aluri J, Dalvi A, Kelkar M, Gupta M. Application of Flow Cytometry in Primary Immunodeficiencies: Experience From India.
Front Immunol. 2019 Jun 11;10:1248. doi: 10.3389/fimmu.2019.01248. eCollection 2019. Review.(IF:6.429)
66 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.
Pregnancy Hypertens. 2019 Jul;17:20-27.
67 Das Gupta A,Hariharan P, Daruwalla M, Sidhwa K, Pawar R, Nadkarni A. Hemoglobin Titusville [?2 Codon 94 G>A]: A Rare Alpha GlobinChain Variant Causing Low Oxygen Saturation.
Indian J Hematol Blood Transfus. 2019 Jul;35(3):593-595.
68 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.
Front Immunol. 2019 Jul 23;10:1567.doi:10.3389/fimmu.2019.01567. eCollection(IF:6.429).
69 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?
Front Immunol. 2019 Jul 31;10:1739. doi: 10.3389/fimmu.2019.01739. eCollection (IF:6.429).
70 Nair R, Gogri H,Kulkarni S, Gupta D. Detection of a rare subgroup of A phenotype while resolving ABO discrepancy.
Asian J Transfus Sci. 2019 Jul-Dec;13(2):129-131
71 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.
Clin Chim Acta. 2019 Aug;495:309-317.
72 Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S,Madkaikar M. 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)
73 Bandari AK, Muthusamy B, Bhat S, Govindaraj P, Rajagopalan P, Dalvi A, Shankar S, Raja R, Reddy KS,Madkaikar M, Pandey A. A Novel Splice Site Mutation inIFNGR2in Patients With Primary Immunodeficiency Exhibiting Susceptibility to Mycobacterial Diseases.
Front Immunol. 2019 Aug 21;10:1964. doi: 10.3389/fimmu.2019.01964. eCollection 2019.(IF:6.429)
74 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 Nave Systemic Sclerosis Patients from Western India.
J Assoc Physicians India. 2019 Aug;67(8):26-30.(IF:0.47)
75 Mukherjee MB, Colah RB, Mehta PR, Shinde N, Jain D, Desai S, Dave K, Italia Y, Raicha B, Serrao E. Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
Am J Clin Pathol. 2019 Aug 1. pii: aqz108. doi: 10.1093/ajcp/aqz108. [Epub ahead of print]\
76 Ghosh K, Ghosh K, Agrawal R,Nadkarni AH. Recent advances in screening and diagnosis of haemoglobinopathy.
Expert Rev Hematol. 2019 Aug 21. doi: 10.1080/17474086.2019.1656525. [Epub ahead of print]
77 Soni P, Mantri S, Prabhudesai A,Patil R, Shanmukhaiah C, Shetty S. Triple jeopardy: A case of Glanzmann's thrombasthenia with anti-GPIIb-IIIa antibodies and HPA incompatibility resulting in stillbirth.
Thromb Res. 2019 Sep;181:141-144
78 Bargir UA, Hule GP, Kambli P, Kulkarni M, Donta AK, Taur P, Gorakshakar A, Desai M, Madkaikar MR. "FUT2" a potential genetic modifier in NCF1 deficiency.
J Allergy Clin Immunol Pract. 2019 Sep 5. pii: S2213-2198(19)30758-5. doi: 10.1016/j.jaip.2019.08.035. [Epub ahead of print] No abstract available.(IF:7.550)
79 Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, Ramanagoudr-Bhojappa R, Smogorzewska A, Mohan S, Rajendran A, Auerbach AD, Takata M, Chandrasekhara A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Hum Mutat. 2019 Sep 12. doi: 10.1002/humu.23914. [Epub ahead of print]
80 Dhangar S, Shanbhag V, Shanmukhaiah C,Vundinti BR. Lack of association between functional polymorphism of DNA repair genes (XRCC1, XPD) and clinical response in Indian chronic myeloid leukemia patients.
Mol Biol Rep. 2019 Oct;46(5):4997-5003.
81 Prabhudesai A,Shetty S, Shanmukhaiah C, Kalantri S, Bhattacharyya M, Kulkarni B A rare cause of bleeding in two Indian families with congenital alpha-2-antiplasmin deficiency.
Haemophilia. 2019 Oct 2. doi: 10.1111/hae.13851. [Epub ahead of print]
82 Kedar PS, Harigae H, Ito E, Muramatsu H, Kojima S, Okuno Y, Fujiwara T, Dongerdiye R, Warang PP, Madkaikar MR. Study of pathophysiology and molecular characterization of congenital anemia in India using targeted next-generation sequencing approach.
Int J Hematol. 2019 Nov;110(5):618-626.(IF:2.245)
83 More TA, Dalal B, Devendra R, Warang P, Shankarkumar A, Kedar P Applications of imaging flow cytometry in the diagnostic assessment of red cell membrane disorders.
Cytometry B Clin Cytom. 2019 Nov 21. doi: 10.1002/cyto.b.21857. [Epub ahead of print](IF: 2.891)
84 Hariharan P, Colah R,Ghosh K, Nadkarni A. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Genomics. 2019 Dec, 111(6):1771-1776.(IF: 2.910)
85 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.
Int J Dermatol. 2019 Dec;58(12):1468-1471.(IF:1.794)
86 Pathak V, Colah R,Ghosh K Effect of inherited red cell defects on growth ofPlasmodium falciparum: Anin vitrostudy.
Indian J Med Res. 2018 Jan;147(1):102-109.(IF: 1.508)
87 Kerketta LS, Ghosh K. Circulating microfilariae in haematological malignancies: do they have a role in pathogenesis?
J Helminthol.2018Jan;92(1):125-127.(IF: 1.61)
88 Umare V, Pradhan V, Rajadhyaksha A, Ghosh K, Nadkarni A. Predisposition of IL-1? (-511 C/T) polymorphism to renal and hematologic disorders in Indian SLE patients.
Gene 2018Jan 30;641:41-45.(IF: 3.191)
89 Patil R, Bajpai S, Ghosh K, Shetty S. Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop.2018Jan 31;181:21-24.(IF: 2.509)
90 Martin SL, Desai S, Nanavati R, Colah RB, Ghosh K, Mukherjee MB. Red cell distribution width and its association with mortality in neonatal sepsis.
J Matern Fetal Neonatal Med.2018Jan 8:1-6.(IF: 1.493)
91 Upadhye D, Das RS, Ray J, Acharjee S, Ghosh K, Colah RB, Mukherjee MB. Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
Hemoglobin.2018 Jan;42(1):43-46. (IF: 0.67)
92 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.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68.(IF: 1.06)
93 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.
Exp Parasitol.2018Feb;185:29-38.(IF: 1.821)
94 Aluri J, Gupta M, Dalvi A, Mhatre S, Kulkarni M, Hule G, Desai M, Shah N, Taur P, Vedam R,Madkaikar M. Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India.
Front Immunol. 2018 Feb 16;9:188.(IF: 5.511)
95 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.
J Med Virol.2018Mar;90(3):559-563.(IF: 1.988)
96 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.2018Mar;24(2):353-359.(IF: 2.096)
97 Patil RK, Ghosh K, Chandrakala S,Shetty S. A possible need for routine screening forStrongyloides stercoralisinfection in Indian haemophilia patients.
Indian J Med Res. 2018 Mar;147(3):315-317 (IF: 1.508)
98 Kulkarni S, Parchure DS, Gopalkrishnan V,Madkaikar M. Screening for DEL phenotype in RhD negative Indians.
J Clin Lab Anal. 2018 Mar;32(3). doi: 10.1002/jcla.22288. Epub 2017 Jun 23 (IF:1.303)
99 Prabhudesai A, Shetty S,Ghosh K, Kulkarni B. Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein Occlusion.
J Assoc Physicians India. 2018 Mar;66(3):76-78.(IF:0.37)
100 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.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68. (IF: --)
101 Kulkarni SS, Gogri H, Parchure D, Mishra G,Ghosh K, Rajadhyaksha S, Madkaikar M, Frec C, Fichou Y. RHD-Positive Alleles among D- C/E+ Individuals from India.
Transfus Med Hemother. 2018 May;45(3):173-177. (IF: 2.152)
102 Patil R, Bajpai S, Ghosh K,Shetty S. Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop. 2018 May;181:21-24. (IF: 2.509)
103 Fichou Y, Parchure D, Gogri H, Gopalkrishnan V, Le Marchal C, Chen JM, Frec C, Madkaikar M, Ghosh K, Kulkarni S. Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Transfusion.2018Jun;58(6):1540-1549. (IF: 3.423)
104 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.
Int J Lab Hematol. 2018 Jun;40(3):e49-e51. (IF: 1.919)
105 Gogri H, Pitale P,Madkaikar M, Kulkarni S. Molecular genotyping of Indian blood group system antigens in Indian blood donors.
Transfus Apher Sci. 2018 Jun;57(3):388-390. (IF: --)
106 Gupta M,Aluri J,Desai M,Lokeshwar M,Taur P,Lenardo M,Bergerson J,Dalvi A,Mhatre S,Kulkarni M,Kambli P,Madkaikar M. Clinical, Immunological, and Molecular Findings in Four Cases of B Cell Expansion With NF-?B and T Cell Anergy Disease for the First Time From India.
Front Immunol.2018 Jun 14;9:1049. eCollection 2018. (IF: 3.35)
107 Vinod Gupta, Rati Devendra, Aruna Rajendran, Neeraj Sidharthan, Prashant Warang,Prabhakar Kedar. Two Novel C-Terminal Frame shift Mutations in the CYB5R3 Gene Lead to Global Growth and Methemoglobinemia Type II. Developmental Delay associated with Recessive Congenital
Journal of Medical Science and Clinical Research 2018 June;6(6):626-636.(IF:6.379)
108 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.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):474-479 (IF:0.474)
109 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.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):581-584.(IF:0.474)
110 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)
111 Martin SL,Desai S,Nanavati R,Colah RB,Ghosh K,Mukherjee MB. Innate immune gene polymorphisms and their association with neonatal sepsis.
Infect Genet Evol. 2018 Aug;62:205-210.(IF:2.545)
112 Hule GP, Kanvinde PR, Kulkarni MA, van Leeuwen K, de Boer M, Bargir UA, Taur PD, Desai MM, Madkaikar MR p47phox-/-Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.
J Clin Immunol. 2018 Aug;38(6):638-641.(IF:4.227)
113 Warang P, Homma T, Pandya R, Sawant A, Shinde N, Pandey D, Fujii J,Madkaikar M, Mukherjee MB Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
Br J Haematol. 2018 Aug;182(4):559-566. (IF: 5.128)
114 Kedar PS, Gupta V, Warang P, Chiddarwar A, Madkaikar M. Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
Hematology. 2018 Sep;23(8):567-573.(IF: 1.315)
115 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.
Leuk Res. 2018 Sep;72:96-98.(IF:2.319)
116 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: --)
117 Warang P &Kedar P. Hereditary elliptocytosis: A rare red cell membrane disorder.
IndianJ Hematol Blood Transfus 2018 Oct;34(4):754-755.(IF:0.474)
118 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: --)
119 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.
Hemoglobin. 2018 Sep - Nov;42(5-6):297-301. (IF: 0.462)
120 Dash PM, Sahu PK, Patel S, Mashon RS, Kharat KR,Mukherjee MB. Effect of Assorted Globin Haplotypes and ?-Thalassemia on the Clinical Heterogeneity of Hb S-?-Thalassemia.
Hemoglobin. 2018 Nov 29:1-7.(IF:0.462)
121 Chougule D, Nadkar M, Venkataraman K, Rajadhyaksha A, Hase N, Jamale T, Kini S, Khadilkar P, Anand V,Madkaikar M, Pradhan V Adipokine interactions promote the pathogenesis of systemic lupus erythematosus.
Cytokine. 2018 Nov;111:20-27 (IF:3.514)
122 Kulkarni M, Hule G, de Boer M, van Leeuwen K, Kambli P, Aluri J, Gupta M, Dalvi A, Mhatre S, Taur P, Desai M,Madkaikar M Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
J Clin Immunol. 2018 Nov;38(8):898-916. (IF: 4.227)
123 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)
124 Kulkarni S, Choudhary B, Gogri H, Patil S, Manglani M, Sharma R, Madkaikar M. 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)
125 Chiddarwar AS, D'Silva SZ, Colah RB,Ghosh K, Mukherjee MB. Genetic lesions in the UGT1A1 genes among Gilbert's syndrome patients from India.
Mol Biol Rep. 2018 Dec; 45(6):2733-2739.(IF:1.889)
126 Dalal K, Khorate P, Dalal B, Chavan R, Bhatia S, Kale A, Shukla P,Shankarkumar A. Differentially expressed serum host proteins in hepatitis B and C viral infections.
Virusdisease. 2018 Dec;29(4):468-477.(IF:0.364)
127 Patil R, S C, Parihar A, Mohite A,Shetty S. Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients.
Thromb Res. 2018 Dec;172:29-35.(IF:2.779)
128 Hariharan P, Colah R,Ghosh K, Nadkarni A. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Genomics. 2018 Dec 5. pii: S0888-7543(18)30542-1. doi: 10.1016/j.ygeno.2018.11.032.[Epub ahead of print] (IF: 2.910)
129 Hockham C, Bhatt S, Colah R,Mukherjee MB, Penman BS, Gupta S, Piel FB. The spatial epidemiology of sickle-cell anaemia in India.
Sci Rep. 2018 Dec 6;8(1):17685.(IF:4.122)
130 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)
131 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)
132 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)
133 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)
134 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)
135 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)
136 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)
137 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 Tcells (LAT) lead to a novel form of severe combined immunodeficiency.
J Allergy Clin Immunol. 2017 Feb;139(2):634-642.e5. (IF: 13.081)
138 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)
139 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)
140 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)
141 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)
142 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.
143 Prashant Warang, Roshan Colah and Prabhakar Kedar. 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)
144 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)
145 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: )
146 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)
147 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)
148 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)
149 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)
150 Warang P,Devendra R, Chiddarwar A, Gupta V, Mirgal D, Jadli A, Mohite A, Kedar P, Mukherjee M. Does novel P5'N-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)
151 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)
152 Kulkarni SS, Vasantha K, Gogri H, Parchure D,Madkaikar M, Frec C, Fichou Y. First report of Rhnullindividuals in the Indian population and characterization of the underlying molecular mechanisms.
153 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)
154 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)
155 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)
156 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)
157 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)
158 Kedar P. Next-generation sequencing: emerging technology in the area of hematology and blood disorder.
Hematol Blood Disord 2017 Sep;1(1):1-2. (IF: )
159 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)
160 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)
161 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)
162 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)
163 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)
164 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)
165 Pranatharthiharan S, Patel MD, Malshe VC, Pujari V, Gorakshakar A, Madkaikar M,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)
166 Yadav S,Shetty S, Kulkarni B A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.
Transfusion. 2017 Nov;57(11):2712-2714. (IF: 3.386)
167 Kedar P, Parmar V,Devendra R, Gupta V, Warang P, Madkaikar M Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
Ann Hematol. 2017 Dec;96(12):2135-2139. (IF: 3.083)
168 Kulkarni M, Gupta M,Madkaikar M Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in The Absence Of Molecular Diagnosis.
Scand J Immunol. 2017 Dec;86(6):486-490. (IF: 2.314)
169 Zaidi AU,Kedar P, Koduri PR, Goyette GW Jr, Buck S, Paglia DE, Ravindranath Y Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.
Pediatr Hematol Oncol. 2017 Dec 11:1-6. (IF: 1.12)
170 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)
171 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)
172 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)
173 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)
174 Gorakshakar AC,Ghosh K. Use of lectins in immunohematology.
Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF: 1.06)
175 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)
176 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)
177 Garg S, Shanmukhaiah C, Marathe S, Mishra P, Babu Rao V,Ghosh K, Madkaikar M. 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)
178 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)
179 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)
180 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)
181 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)
182 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: )
183 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 )
184 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)
185 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;17(4):439-48.(IF: 3.294)
186 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)
187 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)
188 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)
189 Garg S,Ghosh K, Madkaikar M. Antigen expression on a putative leukemic stem cell population and AML blast.
Int J Hematol. 2016 May;103(5):567-71.(IF: 1.61)
190 Nair PS, Shetty S,Ghosh K. Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2016 May;22(4):381-5.(IF: 2.096)
191 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)
192 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: --)
193 Shetty S,Ghosh K. Why should hemophilia B be milder than hemophilia A?
Haematologica. 2016 May;101(5):e213.(IF: 7.702)
194 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)
195 Madkaikar M, 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)
196 Fleisher TA,Madkaikar M, Rosenzweig SD. Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies.
Indian J Pediatr. 2016 May;83(5):444-9.(IF: 0.945)
197 Madkaikar M, 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)
198 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:--)
199 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)
200 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)
201 Gogri H, Kulkarni S, 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)
202 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)
203 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)
204 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)
205 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)
206 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)
207 Shabrish S, Gupta M,Madkaikar M A Modified NK Cell Degranulation Assay Applicable for Routine Evaluation of NK Cell Function.
J Immunol Res. 2016;2016:3769590.(IF: 4.856)
208 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)
209 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)
210 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)
211 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)
212 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; 22(4):570-82.(IF: 3.569)
213 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)
214 Kulkarni S,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)
215 Gupta M, Aluri J, Terrance A,Madkaikar M. Adenosine Deaminase Deficiency with a Novel Gene Mutation.
Indian J Pediatr. 2016 Aug;83(8):875-6.(IF: 0.945)
216 Ghosh K, 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)
217 Garg S, Shanmukhaiah C,Ghosh K, Madkaikar M. 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)
218 Shanbhag S,Ghosh K, Shetty S. First trimester prenatal diagnosis of severe FXIII deficiency.
Haemophilia. 2016 Sep;22(5):e443-4.(IF: 3.569)
219 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)
220 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)
221 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)
222 Kulkarni M, Desai M, Gupta M, Dalvi A, Taur P, Terrance A, Bhat S, Manglani M, Raj R, Shah I,Madkaikar M. Clinical, Immunological, and Molecular Findings of Patients with p47phoxDefect Chronic Granulomatous Disease (CGD) in Indian Families.
J Clin Immunol. 2016 Nov;36(8):774-784.(IF: 3.253)
223 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)
224 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)

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