Author Title Type [ Year]
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Mahadevan J, Pathak AKumar, Vemula A, Nadella RKumar, Viswanath B, Jain S, Purushottam M, Mondal M. 2021. Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes.. Sci Rep. 11(1):21088. DOI:10.1038/s41598-021-00123-x.
Sreeraj VS, Puzhakkal JC, Holla B, Nadella RKumar, Sheth S, Balachander S, Ithal D, Ali F, Viswanath B, Muralidharan K, Venkatasubramanian G, John JP, Benegal V, Murthy P, Varghese M, Reddy YJanardhan, Jain S. 2021. Cross-diagnostic evaluation of minor physical anomalies in psychiatric disorders.. J Psychiatr Res. 142:54-62. DOI:10.1016/j.jpsychires.2021.07.028.
Sreeraj VS, Holla B, Ithal D, Nadella RKumar, Mahadevan J, Balachander S, Ali F, Sheth S, Narayanaswamy JC, Venkatasubramanian G, John JP, Varghese M, Benegal V, Jain S, Reddy YJanardhan, Viswanath B. 2021. Psychiatric symptoms and syndromes transcending diagnostic boundaries in Indian multiplex families: The cohort of ADBS study.. Psychiatry Res. 296:113647. DOI:10.1016/j.psychres.2020.113647.
Someshwar A, Holla B, Agarwal PPansari, Thomas A, Jose A, Joseph B, Raju B, Karle H, Muthukumaran M, Kodancha PG, Kumar P, Reddy PV, Nadella RKumar, Naik ST, Mitra S, Mallappagiri S, Sreeraj VS, Balachander S, Ganesh S, Murthy P et al.. 2020. Adverse childhood experiences in families with multiple members diagnosed to have psychiatric illnesses.. Aust N Z J Psychiatry. 54(11):1086-1094. DOI:10.1177/0004867420931157.
Paul P, Iyer S, Nadella RKumar, Nayak R, Chellappa AS, Ambardar S, Sud R, Sukumaran SK, Purushottam M, Jain S, Viswanath B. 2020. Lithium response in bipolar disorder correlates with improved cell viability of patient derived cell lines.. Sci Rep. 10(1):7428. DOI:10.1038/s41598-020-64202-1.
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.
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.
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.
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.