PubRank

Vidu Garg

Author PubWeight™ 23.21‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Spectrum of heart disease associated with murine and human GATA4 mutation. J Mol Cell Cardiol 2007 1.71
2 Chromosomal haplotypes by genetic phasing of human families. Am J Hum Genet 2011 1.58
3 Cryptic chromosomal abnormalities identified in children with congenital heart disease. Pediatr Res 2008 1.31
4 Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development. Dev Biol 2008 1.29
5 Genetics of congenital heart disease. Curr Cardiol Rev 2010 1.23
6 Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease. Am J Med Genet A 2007 1.13
7 Inhibitory role of Notch1 in calcific aortic valve disease. PLoS One 2011 1.13
8 Identification of GATA6 sequence variants in patients with congenital heart defects. Pediatr Res 2010 1.10
9 Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease. J Mol Cell Cardiol 2013 1.09
10 Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. PLoS Genet 2012 1.03
11 Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome. Pediatr Cardiol 2012 0.98
12 Etiology of valvular heart disease-genetic and developmental origins. Circ J 2014 0.93
13 Inhibition of Notch1 signaling reduces abdominal aortic aneurysm in mice by attenuating macrophage-mediated inflammation. Arterioscler Thromb Vasc Biol 2012 0.89
14 Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve. BMC Med Genomics 2014 0.86
15 A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death. Heart Rhythm 2009 0.86
16 Heredity of bicuspid aortic valve: is family screening indicated? Heart 2011 0.85
17 Genetic abnormalities in FOXP1 are associated with congenital heart defects. Hum Mutat 2013 0.84
18 Fetal and postnatal lung defects reveal a novel and required role for Fgf8 in lung development. Dev Biol 2010 0.81
19 A rare human sequence variant reveals myocardin autoinhibition. J Biol Chem 2008 0.80
20 Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Circ Cardiovasc Genet 2016 0.80
21 Impact of Mendelian inheritance in cardiovascular disease. Ann N Y Acad Sci 2010 0.80
22 Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development. Eur J Hum Genet 2011 0.80
23 Genetics of valvular heart disease. Curr Cardiol Rep 2014 0.77
24 Genetic basis of aortic valvular disease. Curr Opin Cardiol 2017 0.77
25 Compacting the heart with Notch. Nat Med 2013 0.75