A
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.
C
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.
D
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.
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.
E
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.
G
Giri S, Purushottam M, Viswanath B, Muddashetty RS.
2019. Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing.. Stem Cell Res. 39:101494. DOI:10.1016/j.scr.2019.101494.
I
P HAhmed, V V, More RPrabhakar, Viswanath B, Jain S, Rao MS, Mukherjee O.
2019. INDEX-db: The Indian Exome Reference Database (Phase I).. J Comput Biol. 26(3):225-234. DOI:10.1089/cmb.2018.0199.
L
M
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.
P
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.