Author Title Type [ Year]
Filters: Keyword is Humans and Author is Mukherjee, Odity [Clear All Filters]
Ganesh S, P HAhmed, Nadella RK, More RP, Seshadri M, Viswanath B, Rao M, Jain S, Mukherjee O. 2019. Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.. Psychiatry Clin Neurosci. 73(1):11-19. DOI:10.1111/pcn.12788.
Iyer S, Bhatia P, Rao M, Mukherjee O. 2018. Developing two reference control samples for the Indian population.. Stem Cell Res. 30:38-42. DOI:10.1016/j.scr.2018.05.001.
Syama A, Sen S, Kota LNarayanan, Viswanath B, Purushottam M, Varghese M, Jain S, Panicker MM, Mukherjee O. 2018. Mutation burden profile in familial Alzheimer's disease cases from India.. Neurobiol Aging. 64:158.e7-158.e13. DOI:10.1016/j.neurobiolaging.2017.12.002.