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Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US.
Vitamin D Status, Gender Differences, and Cardiometabolic Health Disparities.
PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor.
Association of APOE polymorphisms with diabetes and cardiometabolic risk factors and the role of APOE genotypes in response to anti-diabetic therapy: results from the AIDHS/SDS on a South Asian population.
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.
Carriers of a novel frame-shift insertion in WNT16a possess elevated pancreatic expression of TCF7L2.
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study.
A rare missense variant in the milk fat globule-EGF factor 8 (MFGE8) increases T2DM susceptibility and cardiovascular disease risk with population-specific effects.
The p22 phox polymorphism C242T is not associated with CHD risk in Asian Indians and Chinese.
Role of an intronic polymorphism in the PDCD1 gene with the risk of sporadic systemic lupus erythematosus and the occurrence of antiphospholipid antibodies.
TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels.
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.
Genetic variation in the paraoxonase-3 (PON3) gene is associated with serum PON1 activity.
Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes.
Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs.
Targeted sequencing of candidate genes of dyslipidemia in Punjabi Sikhs: Population-specific rare variants in GCKR promote ectopic fat deposition.
Indo-US Collaboration in Genomic Studies on Diabetes
Case Control Studies