| Genetics of congenital heart disease: the glass half empty AC Fahed, BD Gelb, JG Seidman, CE Seidman Circulation research 112 (4), 707-720, 2013 | 751 | 2013 |
| Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions AC Fahed, M Wang, JR Homburger, AP Patel, AG Bick, CL Neben, C Lai, ... Nature communications 11 (1), 3635, 2020 | 383 | 2020 |
| Familial hypercholesterolemia: the lipids or the genes? AC Fahed, GM Nemer Nutrition & Metabolism 8, 1-12, 2011 | 133 | 2011 |
| Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study TR Tromp, ML Hartgers, GK Hovingh, AJ Vallejo-Vaz, KK Ray, H Soran, ... The Lancet 399 (10326), 719-728, 2022 | 115 | 2022 |
| Plaque erosion and acute coronary syndromes: phenotype, molecular characteristics and future directions AC Fahed, IK Jang Nature Reviews Cardiology 18 (10), 724-734, 2021 | 111 | 2021 |
| Diet, genetics, and disease: a focus on the Middle East and North Africa region AC Fahed, AKM El-Hage-Sleiman, TI Farhat, GM Nemer Journal of Nutrition and Metabolism 2012 (1), 109037, 2012 | 111 | 2012 |
| A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease AP Patel, M Wang, Y Ruan, S Koyama, SL Clarke, X Yang, C Tcheandjieu, ... Nature Medicine 29 (7), 1793-1803, 2023 | 101 | 2023 |
| Association of rare pathogenic DNA variants for familial hypercholesterolemia, hereditary breast and ovarian cancer syndrome, and lynch syndrome with disease risk in adults … AP Patel, M Wang, AC Fahed, H Mason-Suares, D Brockman, R Pelletier, ... JAMA network open 3 (4), e203959-e203959, 2020 | 95 | 2020 |
| Heart failure in congenital heart disease: a confluence of acquired and congenital AC Fahed, AE Roberts, S Mital, NK Lakdawala Heart failure clinics 10 (1), 219-227, 2014 | 78 | 2014 |
| UBQLN2 mutation causing heterogeneous X‐linked dominant neurodegeneration AC Fahed, B McDonough, CM Gouvion, KL Newell, LS Dure, M Bebin, ... Annals of neurology 75 (5), 793-798, 2014 | 71 | 2014 |
| Homozygous familial hypercholesterolemia in Lebanon: a genotype/phenotype correlation AC Fahed, RM Safa, FF Haddad, FF Bitar, RR Andary, MT Arabi, ST Azar, ... Molecular genetics and metabolism 102 (2), 181-188, 2011 | 69 | 2011 |
| Primary carnitine deficiency: novel mutations and insights into the cardiac phenotype K Shibbani, AC Fahed, L Al‐Shaar, M Arabi, G Nemer, F Bitar, ... Clinical genetics 85 (2), 127-137, 2014 | 68 | 2014 |
| NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity OK Abou Hassan, AC Fahed, M Batrawi, M Arabi, MM Refaat, ... Scientific reports 5 (1), 8848, 2015 | 46 | 2015 |
| Connecting the lines between hypogonadism and atherosclerosis AC Fahed, JM Gholmieh, ST Azar International Journal of Endocrinology 2012 (1), 793953, 2012 | 45 | 2012 |
| Translational medicine in the era of big data and machine learning WS Weintraub, AC Fahed, JS Rumsfeld Circulation Research 123 (11), 1202-1204, 2018 | 44 | 2018 |
| Design and user experience testing of a polygenic score report: a qualitative study of prospective users DG Brockman, L Petronio, JS Dron, BC Kwon, T Vosburg, L Nip, A Tang, ... BMC Medical Genomics 14, 1-20, 2021 | 42 | 2021 |
| Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis G Hindy, DJ Tyrrell, A Vasbinder, C Wei, F Presswalla, H Wang, P Blakely, ... The Journal of clinical investigation 132 (24), 2022 | 40 | 2022 |
| The potential of polygenic scores to improve cost and efficiency of clinical trials AC Fahed, AA Philippakis, AV Khera Nature communications 13 (1), 2922, 2022 | 39 | 2022 |
| Students’ perceptions of peer-organized extra-curricular research course during medical school: a qualitative study B Nazha, RH Salloum, AC Fahed, M Nabulsi PloS one 10 (3), e0119375, 2015 | 38 | 2015 |
| Transethnic transferability of a genome-wide polygenic score for coronary artery disease AC Fahed, KG Aragam, G Hindy, YDI Chen, K Chaudhary, A Dobbyn, ... Circulation: Genomic and Precision Medicine 14 (1), e003092, 2021 | 35 | 2021 |