| 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 | 121 | 2022 |
| 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 | 105 | 2020 |
| 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 | 104 | 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 | 93 | 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 | 67 | 2022 |
| Genome-wide association studies of cardiovascular disease R Walsh, SJ Jurgens, J Erdmann, CR Bezzina Physiological reviews 103 (3), 2039-2055, 2023 | 49 | 2023 |
| 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 | 43 | 2022 |
| 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 | 33 | 2023 |
| 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 | 31 | 2022 |
| 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 | 30 | 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 | 25 | 2020 |
| 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, DM West, SJ Jurgens, ... Nature Genetics, 1-9, 2025 | 20 | 2025 |
| Deep learning of left atrial structure and function provides link to atrial fibrillation risk JP Pirruccello, P Di Achille, SH Choi, JT Rämö, S Khurshid, M Nekoui, ... Nature Communications 15 (1), 4304, 2024 | 17 | 2024 |
| 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 | 17 | 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 | 15 | 2023 |
| 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 | 15 | 2020 |
| Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings SL Zheng, SJ Jurgens, KA McGurk, X Xu, C Grace, PI Theotokis, ... Nature Genetics, 1-9, 2025 | 11 | 2025 |
| 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 | 11 | 2023 |
| Selenoprotein deficiency disorder predisposes to aortic aneurysm formation E Schoenmakers, F Marelli, HF Jørgensen, WE Visser, C Moran, ... Nature Communications 14 (1), 7994, 2023 | 10 | 2023 |
| Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies A Lipov, SJ Jurgens, F Mazzarotto, M Allouba, JP Pirruccello, Y Aguib, ... Nature Cardiovascular Research 2 (11), 1078-1094, 2023 | 9 | 2023 |
