Important Announcement Tender for Technical and Lab Equipment

Department of Hematogenetics


Name - Dr. Malay Biswanath Mukherjee

Degree - MSc , PhD

Designation - Scientist E

Email - malaybmukherjee@gmail.com

Degree University Subject Year
MSc University of Pune Anthropolgy 1982
PhD University of Mumbai Applied Biology 1996
  • Awarded "Dr B C Mehta Diamond Jubilee Endowment Prize in the year 1994
  • Awarded "Dr B.C.Mehta Diamond Jubilee Endowment" prize for the best article in the original article section of the Indian Journal of Hematology & Blood Transfusion, entitled "Hemoglobin S quantitation in sickle cell heterozygotes among a tribal group of Valsad and scheduled caste population of Nagpur" in the year 1994.
  • Awarded BGRC best paper prize for the young scientist in 37th Annual conference of Indian Society of Hematology and Blood Transfusion at Chandigarh in November 96. The title of the paper was "Molecular genetics of sickle cell anemia with diverse clinical expression in the two population groups in western India ".
  • Awarded "BGRC Best paper prize for the Young Scientist in the year 1996
  • Awarded ICMR BGRC Silver Jubilee Oration Award for the year 2010.
Research Teacher University Subject
MSc Mumbai Applied Biology
PhD Mumbai Applied Biology
PhD Maharashtra University of Health Sciences Genetics and Molecular Biology
  • S D'Silva, R B Colah, K Ghosh, M B Mukherjee (2013): UDP- glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults. Gene 513: 36-39.
  • K Ghosh, M B Mukherjee (2013): G6PD: A common enzyme deficiency with uncommon clinical manifestations. In S A Rathi and M B Agarwal (eds) "Haematology Today" Mumbai, pp 51 – 60.
  • S D'Silva, R B Colah, K Ghosh, M B Mukherjee (2013): Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates. Curr Sci 105: 446-447.
  • R B Colah, M B Mukherjee, K Ghosh (2014): Sickle cell disease in India. Curr Opin Hematol 21: 215-223.
  • S D'Silva, R B Colah, K Ghosh, M B Mukherjee (2014): Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates. Gene 547: 18-22.
  • P Warang, R Devendra, S D'Silva, A Chiddarwar, P Kedar, K Ghosh, R Colah, M B Mukherjee (2015): Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis? Ann Hematol 94: 169-171.
  • P Warang, R Devendra, S D'Silva, A Chiddarwar, P Kedar, K Ghosh, R Colah, M B Mukherjee (2015): Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis? Ann Hematol 94: 169-171.
  • R B Colah, M B Mukherjee, S Martin, K Ghosh (2015): Sickle cell disease in tribal populations in India. Ind J Med Res 141: 509-515.
  • M B Mukherjee, R B Colah, S Martin, K Ghosh (2015): Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India – Country scenario. Ind J Med Res 141: 516-520.
  • Epidemiology, Population Genetics and Molecular Genetics