| Mutations in NOTCH1 cause aortic valve disease V Garg, AN Muth, JF Ransom, MK Schluterman, R Barnes, IN King, ... Nature 437 (7056), 270-274, 2005 | 1773 | 2005 |
| GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5 V Garg, IS Kathiriya, R Barnes, MK Schluterman, IN King, CA Butler, ... Nature 424 (6947), 443-447, 2003 | 1444 | 2003 |
| Genetic basis for congenital heart disease: revisited: a scientific statement from the American Heart Association ME Pierpont, M Brueckner, WK Chung, V Garg, RV Lacro, AL McGuire, ... Circulation 138 (21), e653-e711, 2018 | 490 | 2018 |
| A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects H Yamagishi, V Garg, R Matsuoka, T Thomas, D Srivastava Science 283 (5405), 1158-1161, 1999 | 346 | 1999 |
| Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development V Garg, C Yamagishi, T Hu, IS Kathiriya, H Yamagishi, D Srivastava Developmental biology 235 (1), 62-73, 2001 | 331 | 2001 |
| Spectrum of heart disease associated with murine and human GATA4 mutation SK Rajagopal, Q Ma, D Obler, J Shen, A Manichaikul, A Tomita-Mitchell, ... Journal of molecular and cellular cardiology 43 (6), 677-685, 2007 | 283 | 2007 |
| Genetics of congenital heart disease A A Richards, V Garg Current cardiology reviews 6 (2), 91-97, 2010 | 253 | 2010 |
| Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development M Maitra, MK Schluterman, HA Nichols, JA Richardson, CW Lo, ... Developmental biology 326 (2), 368-377, 2009 | 243 | 2009 |
| GATA4 sequence variants in patients with congenital heart disease A Tomita-Mitchell, CL Maslen, CD Morris, V Garg, E Goldmuntz Journal of medical genetics 44 (12), 779-783, 2007 | 236 | 2007 |
| Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease K Bosse, CP Hans, N Zhao, SN Koenig, N Huang, A Guggilam, S LaHaye, ... Journal of molecular and cellular cardiology 60, 27-35, 2013 | 179 | 2013 |
| The congenital heart disease genetic network study: rationale, design, and early results Pediatric Cardiac Genomics Consortium, Writing Committee:, B Gelb, ... Circulation research 112 (4), 698-706, 2013 | 170 | 2013 |
| Molecular genetics of aortic valve disease V Garg Current opinion in cardiology 21 (3), 180-184, 2006 | 161 | 2006 |
| Identification of GATA6 sequence variants in patients with congenital heart defects M Maitra, SN Koenig, D Srivastava, V Garg Pediatric Research 68 (4), 281-285, 2010 | 147 | 2010 |
| Inhibitory role of Notch1 in calcific aortic valve disease A Acharya, CP Hans, SN Koenig, HA Nichols, CL Galindo, HR Garner, ... PloS one 6 (11), e27743, 2011 | 146 | 2011 |
| Percutaneous patent ductus arteriosus (PDA) closure in very preterm infants: feasibility and complications CH Backes, SL Cheatham, GM Deyo, S Leopold, MK Ball, CV Smith, ... Journal of the American Heart Association 5 (2), e002923, 2016 | 133 | 2016 |
| Cryptic chromosomal abnormalities identified in children with congenital heart disease AA Richards, LJ Santos, HA Nichols, BP Crider, FF Elder, NS Hauser, ... Pediatric research 64 (4), 358-363, 2008 | 132 | 2008 |
| Insights into the genetic basis of congenital heart disease V Garg Cellular and Molecular Life Sciences CMLS 63, 1141-1148, 2006 | 129 | 2006 |
| A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data H Hu, JC Roach, H Coon, SL Guthery, KV Voelkerding, RL Margraf, ... Nature biotechnology 32 (7), 663-669, 2014 | 113 | 2014 |
| Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms M Basu, V Garg Birth defects research 110 (20), 1504-1516, 2018 | 111 | 2018 |
| Congenital Heart Disease–Causing Gata4 Mutation Displays Functional Deficits In Vivo C Misra, N Sachan, CR McNally, SN Koenig, HA Nichols, A Guggilam, ... PLoS genetics 8 (5), e1002690, 2012 | 100 | 2012 |
