| Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease D Fatkin, C MacRae, T Sasaki, MR Wolff, M Porcu, M Frenneaux, ... New England Journal of Medicine 341 (23), 1715-1724, 1999 | 1583 | 1999 |
| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1387 | 2021 |
| Relations between left atrial appendage blood flow velocity, spontaneous echocardiographic contrast and thromboembolic risk in vivo D Fatkin, RP Kelly, MP Feneley Journal of the American College of Cardiology 23 (4), 961-969, 1994 | 960 | 1994 |
| Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes SG Priori, AA Wilde, M Horie, Y Cho, ER Behr, C Berul, N Blom, ... Europace 15 (10), 1389-1406, 2013 | 797 | 2013 |
| Multi-ethnic genome-wide association study for atrial fibrillation C Roselli, MD Chaffin, LC Weng, S Aeschbacher, G Ahlberg, CM Albert, ... Nature genetics 50 (9), 1225-1233, 2018 | 614 | 2018 |
| Transesophageal echocardiography before and during direct current cardioversion of atrial fibrillation: evidence for “atrial stunning” as a mechanism of thromboembolic … D Fatkin, DL Kuchar, CW Thorburn, MP Feneley Journal of the American College of Cardiology 23 (2), 307-316, 1994 | 583 | 1994 |
| Molecular mechanisms of inherited cardiomyopathies D Fatkin, RM Graham Physiological reviews 82 (4), 945-980, 2002 | 495 | 2002 |
| Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C–deficient mice V Nikolova, C Leimena, AC McMahon, JC Tan, S Chandar, D Jogia, ... The Journal of clinical investigation 113 (3), 357-369, 2004 | 468 | 2004 |
| Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease AM Roberts, JS Ware, DS Herman, S Schafer, J Baksi, AG Bick, ... Science translational medicine 7 (270), 270ra6-270ra6, 2015 | 456 | 2015 |
| Exclusion of atrial thrombus by transesophageal echocardiography does not preclude embolism after cardioversion of atrial fibrillation. A multicenter study. IW Black, D Fatkin, KB Sagar, BK Khandheria, DY Leung, JM Galloway, ... Circulation 89 (6), 2509-2513, 1994 | 447 | 1994 |
| Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy EP Kirk, M Sunde, MW Costa, SA Rankin, O Wolstein, ML Castro, ... The American Journal of Human Genetics 81 (2), 280-291, 2007 | 418 | 2007 |
| A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022 | 346 | 2022 |
| Cardiac homeobox gene NKX2-5mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome DA Elliott, EP Kirk, T Yeoh, S Chandar, F McKenzie, P Taylor, P Grossfeld, ... Journal of the American College of Cardiology 41 (11), 2072-2076, 2003 | 312 | 2003 |
| Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice BK McConnell, KA Jones, D Fatkin, LH Arroyo, RT Lee, O Aristizabal, ... The Journal of clinical investigation 104 (9), 1235-1244, 1999 | 308 | 1999 |
| Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation FA Stennard, MW Costa, D Lai, C Biben, MB Furtado, MJ Solloway, ... Oxford University Press for The Company of Biologists Limited 132 (10), 2451 …, 2005 | 276 | 2005 |
| An abnormal Ca2+ response in mutant sarcomere protein–mediated familial hypertrophic cardiomyopathy D Fatkin, BK McConnell, JO Mudd, C Semsarian, IGP Moskowitz, ... The Journal of clinical investigation 106 (11), 1351-1359, 2000 | 276 | 2000 |
| Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype DB Sparrow, G Chapman, MA Wouters, NV Whittock, S Ellard, D Fatkin, ... The American Journal of Human Genetics 78 (1), 28-37, 2006 | 267 | 2006 |
| Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression BG Bruneau, ZZ Bao, D Fatkin, J Xavier-Neto, D Georgakopoulos, ... Molecular and cellular biology 21 (5), 1730-1736, 2001 | 206 | 2001 |
| Analysis of protein sequence and interaction data for candidate disease gene prediction RA George, JY Liu, LL Feng, RJ Bryson-Richardson, D Fatkin, ... Nucleic acids research 34 (19), e130-e130, 2006 | 187 | 2006 |
| Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection D Adlam, TM Olson, N Combaret, JC Kovacic, SE Iismaa, A Al-Hussaini, ... Journal of the American College of Cardiology 73 (1), 58-66, 2019 | 186 | 2019 |
