Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs

Diabetologia. 2012 Feb;55(2):349-57. doi: 10.1007/s00125-011-2355-6. Epub 2011 Nov 4.

2012

Analysis of 32 common susceptibility genetic variants and their combined effect in predicting risk of Type 2 diabetes and related traits in Indians

Diabet Med. 2012 Jan;29(1):121-7. doi: 10.1111/j.1464-5491.2011.03438.x.

2012

Mutations in the ?-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities

Cell Rep. Dec 12 [Epub ahead of print]

2012

The phylogeography of Y-chromosome haplogroup H1a1a-M82 reveals the likely Indian origin of the European Romani populations.

PLoS One 7:e48477

2012

IL-4 Haplotype -590T, -34T and Intron-3 VNTR R2 Is Associated with Reduced Malaria Risk among Ancestral Indian Tribal Populations

PLoS One. 7(10):e48136

2012

Complex genetic origin of Indian populations and its implications

J Biosci. Nov;37(5):911-9

2012

Genomic view on the peopling of India

Investig Genet. Oct 1;3(1):20. [Epub ahead of print]

2012

Novel mutations in calcium/calmodulin-dependent protein kinase IV (CAMK4) gene in infertile men.

Int J Androl. Aug 17 [Epub ahead of print]

2012

High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians.

BMC Med Genet. Aug 10;13(1):69. [Epub ahead of print]

2012

Association of SNP41, SNP56 and a novel SNP in PDE4D gene with stroke and its subtypes.

Gene. Jul 3. [Epub ahead of print]

2012

Dopamine Transporter (DAT1) VNTR Polymorphism and Alcoholism in Two Culturally Different Populations of South India

Am J Addict. 21: 343-347

2012

Genetic and functional evaluation of the role of DLL1 in susceptibility to visceral leishmaniasis in India.

Inf. Genet. Evol. 24 April

2012

Comprehensive DNA copy number profile and BAC library construction of an Indian individual

Gene (21 March)

2012

Genetic affinities of the central Indian tribal populations.

PLoS One. 7: e32546

2012

Complete Androgen Insensitivity Syndrome Despite Partial Loss of Androgen Function Due to L712V Mutation in the Androgen Receptor Gene.

J Androl. Feb 23. [Epub ahead of print]

2012