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Discovery biology of neuropsychiatric syndromes (DBNS): a center for integrating clinical medicine and basic science.
Viswanath B, Rao NP, Narayanaswamy JC, Sivakumar PT, Kandasamy A, Kesavan M, Mehta UM, Venkatasubramanian G, John JP, Mukherjee O, Purushottam M, Kannan R, Mehta B, Kandavel T, Binukumar B, Saini J, Jayarajan D, Shyamsundar A, Moirangthem S, Vijay Kumar KG, Thirthalli J, Chandra PS, Gangadhar BN, Murthy P, Panicker MM, Bhalla US, Chattarji S, Benegal V, Varghese M, Reddy JYC, Raghu P, Rao M, Jain S. Viswanath B, et al. Among authors: kannan r. BMC Psychiatry. 2018 Apr 18;18(1):106. doi: 10.1186/s12888-018-1674-2. BMC Psychiatry. 2018. PMID: 29669557 Free PMC article.
Adverse childhood experiences in families with multiple members diagnosed to have psychiatric illnesses.
Someshwar A, Holla B, Pansari Agarwal P, Thomas A, Jose A, Joseph B, Raju B, Karle H, Muthukumaran M, Kodancha PG, Kumar P, Reddy PV, Kumar Nadella R, Naik ST, Mitra S, Mallappagiri S, Sreeraj VS, Balachander S, Ganesh S, Murthy P, Benegal V, Reddy JY, Jain S, Mahadevan J, Viswanath B; ADBS Consortium. Someshwar A, et al. Aust N Z J Psychiatry. 2020 Nov;54(11):1086-1094. doi: 10.1177/0004867420931157. Epub 2020 Jun 15. Aust N Z J Psychiatry. 2020. PMID: 32538179
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes.
Mahadevan J, Pathak AK, Vemula A, Nadella RK, Viswanath B, Jain S; Accelerator Program for Discovery in Brain disorders using Stem cells (ADBS) Consortium; Purushottam M, Mondal M. Mahadevan J, et al. Sci Rep. 2021 Oct 26;11(1):21088. doi: 10.1038/s41598-021-00123-x. Sci Rep. 2021. PMID: 34702870 Free PMC article. Clinical Trial.
Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance.
Nadella RK, Chellappa A, Subramaniam AG, More RP, Shetty S, Prakash S, Ratna N, Vandana VP, Purushottam M, Saini J, Viswanath B, Bindu PS, Nagappa M, Mehta B, Jain S, Kannan R. Nadella RK, et al. Among authors: kannan r. Hum Genomics. 2019 Oct 22;13(1):53. doi: 10.1186/s40246-019-0236-0. Hum Genomics. 2019. PMID: 31640787 Free PMC article.
Novel insights into the genetic profile of hereditary spastic paraplegia in India.
Narendiran S, Debnath M, Shivaram S, Kannan R, Sharma S, Christopher R, Seshagiri DV, Jain S, Purushottam M, Mangalore S, Bharath RD, Bindu PS, Sinha S, Taly AB, Nagappa M. Narendiran S, et al. Among authors: kannan r. J Neurogenet. 2022 Mar;36(1):21-31. doi: 10.1080/01677063.2022.2064463. Epub 2022 May 2. J Neurogenet. 2022. PMID: 35499206
765 results