Jain S - Search Results

1

Determinants of Onset of Huntington's Disease with Behavioral Symptoms: Insight from 92 Patients.

Lenka A, Kamble NL, Sowmya V, Jhunjhunwala K, Yadav R, Netravathi M, Kandasamy M, Moily NS, Purushottam M, Jain S, Pal PK. Lenka A, et al. Among authors: jain s. J Huntingtons Dis. 2015;4(4):319-24. doi: 10.3233/JHD-150166. J Huntingtons Dis. 2015. PMID: 26682993

2

Perspectives towards predictive testing in Huntington disease.

Nagaraja SM, Jain S, Muthane UB. Nagaraja SM, et al. Among authors: jain s. Neurol India. 2006 Dec;54(4):359-62. doi: 10.4103/0028-3886.28105. Neurol India. 2006. PMID: 17114842 Free article.

3

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

4

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.

5

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.

6

Spinocerebellar ataxias types 1, 2 and 3: age adjusted clinical severity of disease at presentation correlates with size of CAG repeat lengths.

Netravathi M, Pal PK, Purushottam M, Thennarasu K, Mukherjee M, Jain S. Netravathi M, et al. Among authors: jain s. J Neurol Sci. 2009 Feb 15;277(1-2):83-6. doi: 10.1016/j.jns.2008.10.016. Epub 2008 Dec 2. J Neurol Sci. 2009. PMID: 19049837

7

Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms.

Gupta M, Chauhan C, Bhatnagar P, Gupta S, Grover S, Singh PK, Purushottam M, Mukherjee O, Jain S, Brahmachari SK, Kukreti R. Gupta M, et al. Among authors: jain s. Pharmacogenomics. 2009 Feb;10(2):277-91. doi: 10.2217/14622416.10.2.277. Pharmacogenomics. 2009. PMID: 19207030

8

Phylogenetic analysis and selection pressures of 5-HT receptors in human and non-human primates: receptor of an ancient neurotransmitter.

Anbazhagan P, Purushottam M, Kumar HB, Mukherjee O, Jain S, Sowdhamini R. Anbazhagan P, et al. Among authors: jain s. J Biomol Struct Dyn. 2010 Apr;27(5):581-98. doi: 10.1080/07391102.2010.10508573. J Biomol Struct Dyn. 2010. PMID: 20085376

9

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

Swaminathan B, Shubha GN, Shubha D, Murthy AR, Kiran Kumar HB, Shylashree S, Gayathri N, Jamuna R, Jain S, Purushottam M, Nalini A. Swaminathan B, et al. Among authors: jain s. Neurol India. 2009 Nov-Dec;57(6):734-8. doi: 10.4103/0028-3886.59468. Neurol India. 2009. PMID: 20139501 Free article.

10

North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion.

Singh I, Faruq M, Mukherjee O, Jain S, Pal PK, Srivastav MV, Behari M, Srivastava AK, Mukerji M. Singh I, et al. Among authors: jain s. Ann Hum Genet. 2010 May;74(3):202-10. doi: 10.1111/j.1469-1809.2010.00569.x. Epub 2010 Mar 31. Ann Hum Genet. 2010. PMID: 20374234

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