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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: jain s. J Neurogenet. 2022 Mar;36(1):21-31. doi: 10.1080/01677063.2022.2064463. Epub 2022 May 2. J Neurogenet. 2022. PMID: 35499206
Serotonergic candidate genes and puerperal psychosis: an association study.
Kumar HB, Purushottam M, Kubendran S, Gayathri P, Mukherjee O, Murthy AR, Ghosh S, Chandra P, Reddy YC, Benegal V, Brahmachari SK, Jain S. Kumar HB, et al. Among authors: jain s. Psychiatr Genet. 2007 Oct;17(5):253-60. doi: 10.1097/YPG.0b013e3280ae6cc3. Psychiatr Genet. 2007. PMID: 17728663
SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.
Krishna N, Mohan S, Yashavantha BS, Rammurthy A, Kiran Kumar HB, Mittal U, Tyagi S, Mukerji M, Jain S, Pal PK, Purushottam M. Krishna N, et al. Among authors: jain s. Indian J Med Res. 2007 Nov;126(5):465-70. Indian J Med Res. 2007. PMID: 18160752 Free article.
Evolutionary analysis of PHLPP1 gene in humans and non-human primates.
Anbazhagan P, Purushottam M, Kumar HB, Kubendran S, Mukherjee O, Brahmachari SK, Jain S, Sowdhamini R. Anbazhagan P, et al. Among authors: jain s. Bioinformation. 2008 Aug 1;2(10):471-4. doi: 10.6026/97320630002471. Bioinformation. 2008. PMID: 18841245 Free PMC article.
Apolipoprotein E polymorphism and dementia: a hospital-based study from southern India.
Bharath S, Purushottam M, Mukherjee O, Bagepally BS, Prakash O, Kota L, Krishnappa SB, Sivakumar PT, Jain S, Varghese M. Bharath S, et al. Among authors: jain s. Dement Geriatr Cogn Disord. 2010;30(6):455-60. doi: 10.1159/000322093. Epub 2011 Jan 20. Dement Geriatr Cogn Disord. 2010. PMID: 21252538 Free article.
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