Rai E - Search Results

1

Review: Understanding Rare Genetic Diseases in Low Resource Regions Like Jammu and Kashmir - India.

Angural A, Spolia A, Mahajan A, Verma V, Sharma A, Kumar P, Dhar MK, Pandita KK, Rai E, Sharma S. Angural A, et al. Among authors: rai e. Front Genet. 2020 Apr 30;11:415. doi: 10.3389/fgene.2020.00415. eCollection 2020. Front Genet. 2020. PMID: 32425985 Free PMC article. Review.

2

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

3

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

4

Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.

Darvishi K, Sharma S, Bhat AK, Rai E, Bamezai RN. Darvishi K, et al. Among authors: rai e. Cancer Lett. 2007 May 8;249(2):249-55. doi: 10.1016/j.canlet.2006.09.005. Epub 2006 Nov 1. Cancer Lett. 2007. PMID: 17081685

5

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

6

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

7

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.

8

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

9

mtDNA G10398A variation provides risk to type 2 diabetes in population group from the Jammu region of India.

Sharma V, Sharma I, Singh VP, Verma S, Pandita A, Singh V, Rai E, Sharma S. Sharma V, et al. Among authors: rai e. Meta Gene. 2014 Apr 13;2:269-73. doi: 10.1016/j.mgene.2014.02.003. eCollection 2014 Dec. Meta Gene. 2014. PMID: 25606409 Free PMC article.

10

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.

Rai E, Mahajan A, Kumar P, Angural A, Dhar MK, Razdan S, Thangaraj K, Wise CA, Ikegawa S, Pandita KK, Sharma S. Rai E, et al. Sci Rep. 2016 Jun 13;6:27684. doi: 10.1038/srep27684. Sci Rep. 2016. PMID: 27291587 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

76 results

Search Page

Filters