Detalhe da pesquisa
1.
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
J Hum Genet
; 61(6): 515-22, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26911350
2.
Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
Mol Vis
; 22: 1036-47, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27582626
3.
Role of inflammatory gene polymorphisms in left ventricular dysfunction (LVD) susceptibility in coronary artery disease (CAD) patients.
Cytokine
; 61(3): 856-61, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23357300
4.
Association of angiotensin I-converting enzyme gene insertion/deletion polymorphism with rheumatic heart disease in Indian population and meta-analysis.
Mol Cell Biochem
; 382(1-2): 75-82, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23749169
5.
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.
J Neurol
; 266(8): 1919-1926, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-31069529
6.
Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.
J Genet
; 95(2): 263-72, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27350668
7.
Role of angiotensin II type I (AT1 A1166C) receptor polymorphism in susceptibility of left ventricular dysfunction.
Indian Heart J
; 67(3): 214-21, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26138177
8.
Genetic predisposition to left ventricular dysfunction: a multigenic and multi-analytical approach.
Gene
; 546(2): 309-17, 2014 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24875414
9.
Matrix metalloproteinases in coronary artery disease.
Adv Clin Chem
; 64: 1-72, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24938016
10.
Significant role of ADRB3 rs4994 towards the development of coronary artery disease.
Coron Artery Dis
; 25(1): 29-34, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24201118
11.
Multi-analytic approach elucidates significant role of hormonal and hepatocanalicular transporter genetic variants in gallstone disease in North Indian population.
PLoS One
; 8(4): e59173, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23577061
12.
Impact of renin-angiotensin-aldosterone system gene polymorphisms on left ventricular dysfunction in coronary artery disease patients.
Dis Markers
; 32(1): 33-41, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22297600
13.
Association of matrix metalloproteinases (MMP2, MMP7 and MMP9) genetic variants with left ventricular dysfunction in coronary artery disease patients.
Clin Chim Acta
; 413(19-20): 1668-74, 2012 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22664146