Jain S - Search Results

1

Common psychiatric diseases and human genetic variation.

Mukherjee O, Saleem Q, Purushottam M, Anand A, Brahmachari SK, Jain S. Mukherjee O, et al. Among authors: jain s. Community Genet. 2002;5(3):171-7. doi: 10.1159/000066332. Community Genet. 2002. PMID: 14960887

2

Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation.

Saleem Q, Choudhry S, Mukerji M, Bashyam L, Padma MV, Chakravarthy A, Maheshwari MC, Jain S, Brahmachari SK. Saleem Q, et al. Among authors: jain s. Hum Genet. 2000 Feb;106(2):179-87. doi: 10.1007/s004390051026. Hum Genet. 2000. PMID: 10746559

3

Association analysis of 5HT transporter gene in bipolar disorder in the Indian population.

Saleem Q, Ganesh S, Vijaykumar M, Reddy YC, Brahmachari SK, Jain S. Saleem Q, et al. Among authors: jain s. Am J Med Genet. 2000 Apr 3;96(2):170-2. Am J Med Genet. 2000. PMID: 10893491

4

Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia.

Saleem Q, Sreevidya VS, Sudhir J, Savithri JV, Gowda Y, B-Rao C, Benegal V, Majumder PP, Anand A, Brahmachari SK, Jain S. Saleem Q, et al. Among authors: jain s. Am J Med Genet. 2000 Dec 4;96(6):744-8. doi: 10.1002/1096-8628(20001204)96:6<744::aid-ajmg9>3.0.co;2-z. Am J Med Genet. 2000. PMID: 11121173

5

The polyglutamine motif is highly conserved at the Clock locus in various organisms and is not polymorphic in humans.

Saleem Q, Anand A, Jain S, Brahmachari SK. Saleem Q, et al. Among authors: jain s. Hum Genet. 2001 Aug;109(2):136-42. doi: 10.1007/s004390100550. Hum Genet. 2001. PMID: 11511917

6

A clinical study of patients with genetically confirmed Huntington's disease from India.

Murgod UA, Saleem Q, Anand A, Brahmachari SK, Jain S, Muthane UB. Murgod UA, et al. Among authors: jain s. J Neurol Sci. 2001 Sep 15;190(1-2):73-8. doi: 10.1016/s0022-510x(01)00593-7. J Neurol Sci. 2001. PMID: 11574110

7

Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder.

Saleem Q, Dash D, Gandhi C, Kishore A, Benegal V, Sherrin T, Mukherjee O, Jain S, Brahmachari SK. Saleem Q, et al. Among authors: jain s. Mol Psychiatry. 2001 Nov;6(6):694-700. doi: 10.1038/sj.mp.4000924. Mol Psychiatry. 2001. PMID: 11673798

8

CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.

Choudhry S, Mukerji M, Srivastava AK, Jain S, Brahmachari SK. Choudhry S, et al. Among authors: jain s. Hum Mol Genet. 2001 Oct 1;10(21):2437-46. doi: 10.1093/hmg/10.21.2437. Hum Mol Genet. 2001. PMID: 11689490

9

Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population.

Saleem Q, Roy S, Murgood U, Saxena R, Verma IC, Anand A, Muthane U, Jain S, Brahmachari SK. Saleem Q, et al. Among authors: jain s. Acta Neurol Scand. 2003 Oct;108(4):281-6. doi: 10.1034/j.1600-0404.2003.00133.x. Acta Neurol Scand. 2003. PMID: 12956863

10

Evidence of linkage and association on 18p11.2 for psychosis.

Mukherjee O, Meera P, Ghosh S, Kubendran S, Kiran K, Manjunath KR, Subhash MN, Benegal V, Brahmachari SK, Majumder PP, Jain S. Mukherjee O, et al. Among authors: jain s. Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):868-73. doi: 10.1002/ajmg.b.30363. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16941653

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