Detalhe da pesquisa
1.
Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India.
BMC Genomics
; 25(1): 31, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38178039
2.
Mutation screening in autosomal dominant congenital cataract families from North India.
Mol Genet Genomics
; 298(6): 1279-1288, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37458831
3.
A nonsense mutation in C8orf37 linked with retinitis pigmentosa, early macular degeneration, cataract, and myopia in an arRP family from North India.
BMC Ophthalmol
; 23(1): 210, 2023 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37170250
4.
A missense mutation in TTC8/BBS8 affecting mRNA splicing in patients with non-syndromic retinitis pigmentosa.
Mol Genet Genomics
; 297(5): 1439-1449, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939099
5.
Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Coronary Artery Disease in North Indian Punjabi Population.
Biochem Genet
; 60(6): 2120-2136, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35260951
6.
A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans.
Nutr J
; 20(1): 71, 2021 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34315477
7.
APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups.
Lipids Health Dis
; 20(1): 113, 2021 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34548093
8.
Novel mutation in MKKS/BBS6 linked with arRP and polydactyly in a family of North Indian origin.
Clin Exp Ophthalmol
; 48(3): 343-355, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31989739
9.
A novel mutation in the PRPF31 in a North Indian adRP family with incomplete penetrance.
Doc Ophthalmol
; 137(2): 103-119, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30099644
10.
Genetics of diabetes.
World J Diabetes
; 14(6): 656-679, 2023 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37383588
11.
Assessment of Cardiovascular Parameters on Submaximal Treadmill Exercise in Obese versus Nonobese Adults.
Int J Appl Basic Med Res
; 13(4): 212-217, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38229726
12.
Molecular diagnosis of autosomal dominant congenital cataract in two families from North India reveals a novel and a known variant in GJA8 and GJA3.
Front Pediatr
; 10: 1003909, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36533234
13.
Genetic and Non-genetic Determinants of Cardiovascular Disease in South Asians.
Curr Diabetes Rev
; 17(9): e011721190373, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33461471
14.
Association of TNF-α gene alterations (c.-238G>A, c.-308G>A, c.-857C>T, c.-863C>A) with primary glaucoma in north Indian cohort.
Gene
; 709: 25-35, 2019 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31132515