Author [ Title] Type Year
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Najar AH, Sneha KM, Ashok A, Babu S, Subramaniam AG, Kannan R, Viswanath B, Purushottam M, Varghese M, Parvez S, Panicker MM, Mukherjee O, Jain S. 2019. Derivation of iPSC lines from two patients with familial Alzheimer's disease from India.. Stem Cell Res. 34:101370. DOI:10.1016/j.scr.2018.101370.
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.
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.
Mukherjee O, Acharya S, Rao M. 2019. Making NSC and Neurons from Patient-Derived Tissue Samples.. Methods Mol Biol. 1919:9-24. DOI:10.1007/978-1-4939-9007-8_2.
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.