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Human mtDNA hypervariable regions, HVR I and II, hint at deep common maternal founder and subsequent maternal gene flow in Indian population groups.
Sharma S, Saha A, Rai E, Bhat A, Bamezai R. Sharma S, et al. Among authors: rai e. J Hum Genet. 2005;50(10):497-506. doi: 10.1007/s10038-005-0284-2. Epub 2005 Oct 5. J Hum Genet. 2005. PMID: 16205836
The possible role of 10398A and 16189C mtDNA variants in providing susceptibility to T2DM in two North Indian populations: a replicative study.
Bhat A, Koul A, Sharma S, Rai E, Bukhari SI, Dhar MK, Bamezai RN. Bhat A, et al. Among authors: rai e. Hum Genet. 2007 Feb;120(6):821-6. doi: 10.1007/s00439-006-0272-4. Epub 2006 Oct 26. Hum Genet. 2007. PMID: 17066297
PGC-1alpha Thr394Thr and Gly482Ser variants are significantly associated with T2DM in two North Indian populations: a replicate case-control study.
Bhat A, Koul A, Rai E, Sharma S, Dhar MK, Bamezai RN. Bhat A, et al. Among authors: rai e. Hum Genet. 2007 Jun;121(5):609-14. doi: 10.1007/s00439-007-0352-0. Epub 2007 Mar 28. Hum Genet. 2007. PMID: 17390150
Interaction between the UCP2-866G/A, mtDNA 10398G/A and PGC1alpha p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population.
Rai E, Sharma S, Koul A, Bhat AK, Bhanwer AJ, Bamezai RN. Rai E, et al. Hum Genet. 2007 Dec;122(5):535-40. doi: 10.1007/s00439-007-0421-4. Epub 2007 Aug 14. Hum Genet. 2007. PMID: 17701054
A novel subgroup Q5 of human Y-chromosomal haplogroup Q in India.
Sharma S, Rai E, Bhat AK, Bhanwer AS, Bamezai RN. Sharma S, et al. Among authors: rai e. BMC Evol Biol. 2007 Nov 19;7:232. doi: 10.1186/1471-2148-7-232. BMC Evol Biol. 2007. PMID: 18021436 Free PMC article.
Interestingly, we further observed a novel 4 bp deletion/insertion polymorphism (ss4 bp, rs41352448) at 72,314 position of human arylsulfatase D pseudogene, defining a novel sub-lineage Q5 (in 5/15 individuals, i.e., 33.3 % of the observed Y-HG Q) with distributions indepe …
Interestingly, we further observed a novel 4 bp deletion/insertion polymorphism (ss4 bp, rs41352448) at 72,314 position of human arylsulfata …
The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system.
Sharma S, Rai E, Sharma P, Jena M, Singh S, Darvishi K, Bhat AK, Bhanwer AJ, Tiwari PK, Bamezai RN. Sharma S, et al. Among authors: rai e. J Hum Genet. 2009 Jan;54(1):47-55. doi: 10.1038/jhg.2008.2. Epub 2009 Jan 9. J Hum Genet. 2009. PMID: 19158816
The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population.
Rai E, Sharma S, Kaul S, Jain K, Matharoo K, Bhanwer AS, Bamezai RN. Rai E, et al. PLoS One. 2012;7(11):e48621. doi: 10.1371/journal.pone.0048621. Epub 2012 Nov 1. PLoS One. 2012. PMID: 23133645 Free PMC article.
Understanding Genetic Heterogeneity in Type 2 Diabetes by Delineating Physiological Phenotypes: SIRT1 and its Gene Network in Impaired Insulin Secretion.
Ali S, Nafis S, Kalaiarasan P, Rai E, Sharma S, Bamezai RN. Ali S, et al. Among authors: rai e. Rev Diabet Stud. 2016 Spring;13(1):17-34. doi: 10.1900/RDS.2016.13.17. Epub 2016 May 10. Rev Diabet Stud. 2016. PMID: 27563694 Free PMC article. Review.
Replication of newly identified type 2 diabetes susceptible loci in Northwest Indian population.
Sharma V, Sharma I, Sethi I, Mahajan A, Singh G, Angural A, Bhanwer AJS, Dhar MK, Singh V, Rai E, Sharma S. Sharma V, et al. Among authors: rai e. Diabetes Res Clin Pract. 2017 Apr;126:160-163. doi: 10.1016/j.diabres.2017.02.013. Epub 2017 Feb 16. Diabetes Res Clin Pract. 2017. PMID: 28258026
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