Detalhe da pesquisa
1.
Epigenome-wide methylation study identified two novel CpGs associated with T2DM risk and a network of co-methylated CpGs capable of patient's classifications.
Hum Mol Genet
; 32(16): 2576-2586, 2023 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37184252
2.
A novel antisense lncRNA, ARBAG harboring an RNA destabilizing GWAS variant for C-peptide dictates the transcript isoforms of GABRA6 in cerebellum.
Hum Mol Genet
; 32(19): 2929-2939, 2023 09 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37498167
3.
Renin-Angiotensin System in Pathogenesis of Atherosclerosis and Treatment of CVD.
Int J Mol Sci
; 22(13)2021 Jun 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-34206708
4.
Anti-Inflammatory Therapy for Atherosclerosis: Focusing on Cytokines.
Int J Mol Sci
; 22(13)2021 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34209109
5.
Role of Tmem163 in zinc-regulated insulin storage of MIN6 cells: Functional exploration of an Indian type 2 diabetes GWAS associated gene.
Biochem Biophys Res Commun
; 522(4): 1022-1029, 2020 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31813547
6.
Multifaceted genome-wide study identifies novel regulatory loci in SLC22A11 and ZNF45 for body mass index in Indians.
Mol Genet Genomics
; 295(4): 1013-1026, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32363570
7.
Comparison of plasma adipocytokines & C-reactive protein levels in healthy schoolgoing adolescents from private & government-funded schools of Delhi, India.
Indian J Med Res
; 151(1): 47-58, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32134014
8.
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
J Hum Genet
; 64(6): 573-587, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30911093
9.
Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.
Hum Mol Genet
; 25(10): 2070-2081, 2016 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26911676
10.
DNA methylation profiling reveals the presence of population-specific signatures correlating with phenotypic characteristics.
Mol Genet Genomics
; 292(3): 655-662, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28271161
11.
Authors' response.
Indian J Med Res
; 156(1): 155-156, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36510909
12.
Strong influence of variants near MC4R on adiposity in children and adults: a cross-sectional study in Indian population.
J Hum Genet
; 58(1): 27-32, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23151679
13.
Systematic analysis and functional annotation of variations in the genome of an Indian individual.
Hum Mutat
; 33(7): 1133-40, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22461382
14.
Common variants of SLAMF1 and ITLN1 on 1q21 are associated with type 2 diabetes in Indian population.
J Hum Genet
; 57(3): 184-90, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22277902
15.
Identification of genetic effects underlying type 2 diabetes in South Asian and European populations.
Commun Biol
; 5(1): 329, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35393509
16.
Protein molecular function influences mutation rates in human genetic diseases with allelic heterogeneity.
Biochem Biophys Res Commun
; 412(4): 716-22, 2011 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21867677
17.
No association of TNFRSF1B variants with type 2 diabetes in Indians of Indo-European origin.
BMC Med Genet
; 12: 110, 2011 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21849023
18.
Association of variants in genes involved in pancreatic ß-cell development and function with type 2 diabetes in North Indians.
J Hum Genet
; 56(10): 695-700, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21814221
19.
Common variants of FTO and the risk of obesity and type 2 diabetes in Indians.
J Hum Genet
; 56(10): 720-6, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21814223
20.
Harnessing the Potential of Long Non-coding RNAs to Manage Metabolic Diseases.
Curr Pharm Des
; 27(35): 3668-3685, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33719960