Author Title Type [ Year]
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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.
Viswanath B, Rao NP, Narayanaswamy JC, Sivakumar PT, Kandasamy A, Kesavan M, Mehta UMeherwan, Venkatasubramanian G, John JP, Mukherjee O, Purushottam M, Kannan R, Mehta B, Kandavel T, Binukumar B, Saini J, Jayarajan D, Shyamsundar A, Moirangthem S, Kumar KGVijay et al.. 2018. Discovery biology of neuropsychiatric syndromes (DBNS): a center for integrating clinical medicine and basic science.. BMC Psychiatry. 18(1):106. DOI:10.1186/s12888-018-1674-2.