| Monogenic and polygenic contributions to atrial fibrillation risk: results from a national biobank SH Choi, SJ Jurgens, LC Weng, JP Pirruccello, C Roselli, M Chaffin, ... Circulation research 126 (2), 200-209, 2020 | 85 | 2020 |
| Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank SJ Jurgens, SH Choi, VN Morrill, M Chaffin, JP Pirruccello, JL Halford, ... Nature genetics 54 (3), 240-250, 2022 | 83 | 2022 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 64 | 2022 |
| Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots S Agrawal, M Wang, MDR Klarqvist, K Smith, J Shin, H Dashti, N Diamant, ... Nature communications 13 (1), 3771, 2022 | 52 | 2022 |
| Genetic analysis of right heart structure and function in 40,000 people JP Pirruccello, P Di Achille, V Nauffal, M Nekoui, SF Friedman, ... Nature genetics 54 (6), 792-803, 2022 | 46 | 2022 |
| Rare and common genetic variation underlying the risk of hypertrophic cardiomyopathy in a national biobank KJ Biddinger, SJ Jurgens, D Maamari, L Gaziano, SH Choi, VN Morrill, ... JAMA cardiology 7 (7), 715-722, 2022 | 28 | 2022 |
| LMNA Variants and Risk of Adult-Onset Cardiac Disease J Lazarte, SJ Jurgens, SH Choi, S Khurshid, VN Morrill, LC Weng, ... Journal of the American College of Cardiology 80 (1), 50-59, 2022 | 19 | 2022 |
| Genome-wide association studies of cardiovascular disease R Walsh, SJ Jurgens, J Erdmann, CR Bezzina Physiological Reviews 103 (3), 2039-2055, 2023 | 18 | 2023 |
| Monogenic and polygenic contributions to QTc prolongation in the population V Nauffal, VN Morrill, SJ Jurgens, SH Choi, AW Hall, LC Weng, JL Halford, ... Circulation 145 (20), 1524-1533, 2022 | 18 | 2022 |
| Genetic determinants of electrocardiographic P-wave duration and relation to atrial fibrillation LC Weng, AW Hall, SH Choi, SJ Jurgens, J Haessler, NA Bihlmeyer, ... Circulation: Genomic and Precision Medicine 13 (5), 387-395, 2020 | 18 | 2020 |
| Rare genetic variation underlying human diseases and traits: results from 200,000 individuals in the UK Biobank SJ Jurgens, SH Choi, VN Morrill, M Chaffin, JP Pirruccello, JL Halford, ... bioRxiv, 2020.11. 29.402495, 2020 | 14 | 2020 |
| Adjusting for common variant polygenic scores improves yield in rare variant association analyses SJ Jurgens, JP Pirruccello, SH Choi, VN Morrill, M Chaffin, SA Lubitz, ... Nature Genetics 55 (4), 544-548, 2023 | 13 | 2023 |
| The genetic determinants of aortic distention JP Pirruccello, JT Rämö, SH Choi, MD Chaffin, S Kany, M Nekoui, ... Journal of the American College of Cardiology 81 (14), 1320-1335, 2023 | 12 | 2023 |
| Association of rare protein-truncating DNA variants in APOB or PCSK9 with low-density lipoprotein cholesterol level and risk of coronary heart disease JS Dron, AP Patel, Y Zhang, SJ Jurgens, DJ Maamari, M Wang, ... JAMA cardiology 8 (3), 258-267, 2023 | 9 | 2023 |
| Deep learning of left atrial structure and function provides link to atrial fibrillation risk JP Pirruccello, P Di Achille, SH Choi, S Khurshid, M Nekoui, SJ Jurgens, ... MedRxiv, 2021.08. 02.21261481, 2021 | 8 | 2021 |
| Rare coding variants associated with electrocardiographic intervals identify monogenic arrhythmia susceptibility genes: a multi-ancestry analysis SH Choi, SJ Jurgens, CM Haggerty, AW Hall, JL Halford, VN Morrill, ... Circulation: Genomic and Precision Medicine 14 (4), e003300, 2021 | 7 | 2021 |
| Associations between alcohol intake and genetic predisposition with atrial fibrillation risk in a National Biobank JL Halford, LC Weng, SH Choi, SJ Jurgens, VN Morrill, S Khurshid, ... Circulation: Genomic and Precision Medicine 13 (6), e003111, 2020 | 7 | 2020 |
| Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy L Curran, A de Marvao, P Inglese, KA McGurk, PR Schiratti, A Clement, ... Circulation: Genomic and Precision Medicine 16 (6), e004200, 2023 | 4 | 2023 |
| Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy R Tadros, SL Zheng, C Grace, P Jordà, C Francis, SJ Jurgens, ... medRxiv, 2023 | 4 | 2023 |
| Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes JL Halford, VN Morrill, SH Choi, SJ Jurgens, G Melloni, NA Marston, ... Nature communications 13 (1), 5106, 2022 | 4 | 2022 |
