| Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel AC Sturm, JW Knowles, SS Gidding, ZS Ahmad, CD Ahmed, ... Journal of the American College of Cardiology 72 (6), 662-680, 2018 | 470 | 2018 |
| Reappraisal of reported genes for sudden arrhythmic death: evidence-based evaluation of gene validity for Brugada syndrome SM Hosseini, R Kim, S Udupa, G Costain, R Jobling, E Liston, SM Jamal, ... Circulation 138 (12), 1195-1205, 2018 | 294 | 2018 |
| An international, multicentered, evidence-based reappraisal of genes reported to cause congenital long QT syndrome A Adler, V Novelli, AS Amin, E Abiusi, M Care, EA Nannenberg, ... Circulation 141 (6), 418-428, 2020 | 287 | 2020 |
| Homocysteine and MTHFR mutations: relation to thrombosis and coronary artery disease EA Varga, AC Sturm, CP Misita, S Moll Circulation 111 (19), e289-e293, 2005 | 237 | 2005 |
| Genetic testing for inherited cardiovascular diseases: a scientific statement from the American Heart Association K Musunuru, RE Hershberger, SM Day, NJ Klinedinst, AP Landstrom, ... Circulation: Genomic and Precision Medicine 13 (4), e000067, 2020 | 232 | 2020 |
| Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ... JAMA Network Open 1 (5), e182140-e182140, 2018 | 197 | 2018 |
| A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort MLB Schwartz, CZ McCormick, AL Lazzeri, ML D’Andra, MLG Hallquist, ... The American Journal of Human Genetics 103 (3), 328-337, 2018 | 150 | 2018 |
| Delivery of cascade screening for hereditary conditions: a scoping review of the literature MC Roberts, WD Dotson, CS DeVore, EM Bednar, DJ Bowen, TG Ganiats, ... Health Affairs 37 (5), 801-808, 2018 | 136 | 2018 |
| Genomics-first evaluation of heart disease associated with titin-truncating variants CM Haggerty, SM Damrauer, MG Levin, D Birtwell, DJ Carey, AM Golden, ... Circulation 140 (1), 42-54, 2019 | 119 | 2019 |
| Patient assessment of chatbots for the scalable delivery of genetic counseling T Schmidlen, M Schwartz, K DiLoreto, HL Kirchner, AC Sturm Journal of genetic counseling 28 (6), 1166-1177, 2019 | 110 | 2019 |
| Predictive utility of polygenic risk scores for coronary heart disease in three major racial and ethnic groups O Dikilitas, DJ Schaid, ML Kosel, RJ Carroll, CG Chute, JC Denny, ... The American Journal of Human Genetics 106 (5), 707-716, 2020 | 105 | 2020 |
| Clinical outcomes of a genomic screening program for actionable genetic conditions AH Buchanan, HL Kirchner, MLB Schwartz, MA Kelly, T Schmidlen, ... Genetics in Medicine 22 (11), 1874-1882, 2020 | 101 | 2020 |
| Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders MT Oetjens, MA Kelly, AC Sturm, CL Martin, DH Ledbetter Nature communications 10 (1), 4897, 2019 | 100 | 2019 |
| convened by the Familial Hypercholesterolemia Foundation AC Sturm, JW Knowles, SS Gidding, ZS Ahmad, CD Ahmed, ... Clinical genetic testing for familial hypercholesterolemia: JACC scientific …, 2018 | 99 | 2018 |
| Patient-centered precision health in a learning health care system: Geisinger’s genomic medicine experience MS Williams, AH Buchanan, FD Davis, WA Faucett, MLG Hallquist, ... Health Affairs 37 (5), 757-764, 2018 | 95 | 2018 |
| Genetic testing in dyslipidemia: a scientific statement from the National Lipid Association EE Brown, AC Sturm, M Cuchel, LT Braun, PB Duell, JA Underberg, ... Journal of clinical lipidology 14 (4), 398-413, 2020 | 87 | 2020 |
| Tools for assessing readability and quality of health‐related web sites R Shedlosky‐Shoemaker, AC Sturm, M Saleem, KM Kelly Journal of genetic counseling 18 (1), 49-59, 2009 | 77 | 2009 |
| American Heart Association Council on Genomic and Precision Medicine; Council on Arteriosclerosis, Thrombosis and Vascular Biology; Council on Cardiovascular and Stroke Nursing … K Musunuru, RE Hershberger, SM Day, NJ Klinedinst, AP Landstrom, ... Genetic testing for inherited cardiovascular diseases: a scientific …, 2020 | 71 | 2020 |
| Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death R Walsh, A Adler, AS Amin, E Abiusi, M Care, H Bikker, S Amenta, ... European heart journal 43 (15), 1500-1510, 2022 | 67 | 2022 |
| SCN5A variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmia H Musa, CF Kline, AC Sturm, N Murphy, S Adelman, C Wang, H Yan, ... Proceedings of the National Academy of Sciences 112 (40), 12528-12533, 2015 | 66 | 2015 |
Marc S. WilliamsProfessor and Director Emeritus, Genomic Medicine Institute, GeisingerVerified email at geisinger.edu
