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International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Sickle Cell Disease: Indian ExperienceRoshan B Colah, Pallavi Mehta, Malay B Mukherjee
Indian Journal of Pediatrics|July 1, 2004
Glucose-6-phosphate dehydrogenase deficiency in IndiaDipika Mohanty, Malay B Mukherjee, Roshan B Colah
The Indian Journal of Medical Research|July 4, 2015
Haemoglobinopathies in tribal populations of IndiaKanjaksha Ghosh, Roshan B Colah, Malay B Mukherjee
Gene|November 14, 2012
UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adultsSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Gene|May 29, 2014
Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonatesSelma D'Silva, Roshan B Colah, Kanjaksha Ghosh, et al.
Blood Cells, Molecules & Diseases|August 19, 2004
Molecular basis of G6PD deficiency in IndiaSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
The Indian Journal of Medical Research|July 4, 2015
Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenarioMalay B Mukherjee, Roshan B Colah, Snehal Martin, et al.
The Indian Journal of Medical Research|July 4, 2015
Sickle cell disease in tribal populations in IndiaRoshan B Colah, Malay B Mukherjee, Snehal Martin, et al.
Blood Cells, Molecules & Diseases|July 6, 2005
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutationSridevi Sukumar, Malay B Mukherjee, Roshan B Colah, et al.
International Journal of Laboratory Hematology|March 20, 2024
Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A reviewPallavi Thaker, Namrata Mahajan, Malay B Mukherjee, et al.
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