Department of Cytogenetics

Name : Dr. Lily S. Kerketta

Degree: MBBS Designation: Scientist E

Email: lskerketta@rediffmail.com

Education:- MBBS - Sambalpur University. Year:1979

Fields of Interest: Clinical Cytogenetics, Epigenetics

Publications:

International Journals: 12

National Journals: 10

International abstracts: 2

National abstracts: 23

Latest 10 Publications:

  1. V. Babu Rao, L Kerketta, M. Madkaikar, J. Fahah, K. Ghosh. Hybrid Cytogenetics of Chronic Lymphotic Leukemia and follicular Cell Lymhoma in a Case of Non-Hodgkin’s Lymhoma. Acta Haematologica (in press).

  2. Baburao Vhundinti, Lily Kerketta, Farah Jijina, K. Ghosh. Cytogenetic study of myelodysplastic syndrome from India . Indian journal of medical research 2009.

  3. Suchitra Swaminathan, Manisha Madkaikar, Kanjaksha Ghosh, Baburao Vhundinti, Lily Kerketta, Maya Gupta. Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation. European journal of haematoloty 2009.84:180-182

  4. Vunditi BR, Kerketta L, Madgaikar M, Jijina F, Ghosh K. Three way translocation in a new variant of t(8;21) acute myeloid leukemia involving Xp22. Indian Journal of Cancer, January-March 2008, vol 45, Issue 1, P 30-32

  5. Korgaonkar S, Baburao V, Kerketta L, Ghosh K. Chromosomal breakage in mylodisplastic syndrome. Asian Pacific J. Cancer Preview, 2007, 8: 151-4

  6. Lily Kerketta, Babu Rao Vunditi, Kanjaksha Ghosh. Transloction (2;14) (p13;q32) in a case of ph positive acute lymphoblastic leukeamia. Indian Journal of Human Genetics, September-December, 2007, Vol.13, issue 3.

  7. V. Babu Rao, L Kerketta, S. Kogaonkar, K. Ghosh. Differentiation of Nijmegen breakage syndrome from Fanconi anaemia. Genetic and Molecular research 6(3): 622-626(2007)

  8. V. Baburao, L. Kerketta, K. Seema, K. Ghosh. Dandy Walker malformations in the case of Partial Trisomy 9p(p12.1-> pter) due to maternal translocation (9;12) (p12.1;p13.3) Indian Journal of Human Genetics, Jan-Apr, 2007; 13(1):33-5

  9. Babu V. Rao, Lily Kerketta, Seema Korgaonkar, Kanjaksha Ghosh Pericentric Inversion of Chromosome 9[inv(9)(p12q13)]: Its association with genetic diseases. Indian Journal of Human Genetics, 2006, Vol 12, 3:129-132.

  10. Babu Rao V, Kerketta L, Kargaonkar S, Ghosh K, Mohanty D. Maternal origin of extra marker chromosome lq31.1-qter and 13pter-q12.2 in a child with dysomorpic eatures. Genet Counsel. Vol. 16, No. 2, 2005, pp 139-143.