| ACMG SF v3. 0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG) DT Miller, K Lee, WK Chung, AS Gordon, GE Herman, TE Klein, ... Genetics in medicine 23 (8), 1381-1390, 2021 | 441 | 2021 |
| Adaptations to climate in candidate genes for common metabolic disorders AM Hancock, DB Witonsky, AS Gordon, G Eshel, JK Pritchard, G Coop, ... PLoS genetics 4 (2), e32, 2008 | 350 | 2008 |
| Design and anticipated outcomes of the eMERGE‐PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems LJ Rasmussen‐Torvik, SC Stallings, AS Gordon, B Almoguera, ... Clinical Pharmacology & Therapeutics 96 (4), 482-489, 2014 | 254 | 2014 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 236 | 2014 |
| Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ... Jama 315 (1), 47-57, 2016 | 189 | 2016 |
| Genetic variation among 82 pharmacogenes: the PGRNseq data from the eMERGE network WS Bush, DR Crosslin, A Owusu‐Obeng, J Wallace, B Almoguera, ... Clinical Pharmacology & Therapeutics 100 (2), 160-169, 2016 | 182 | 2016 |
| Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and … DT Miller, K Lee, AS Gordon, LM Amendola, K Adelman, SJ Bale, ... Genetics in Medicine 23 (8), 1391-1398, 2021 | 181 | 2021 |
| Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ... The American Journal of Human Genetics 98 (6), 1051-1066, 2016 | 168 | 2016 |
| ACMG SF v3. 1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) DT Miller, K Lee, NS Abul-Husn, LM Amendola, K Brothers, WK Chung, ... Genetics in Medicine 24 (7), 1407-1414, 2022 | 139 | 2022 |
| Large-scale genome-wide association study of coronary artery disease in genetically diverse populations C Tcheandjieu, X Zhu, AT Hilliard, SL Clarke, V Napolioni, S Ma, KM Lee, ... Nature medicine 28 (8), 1679-1692, 2022 | 121 | 2022 |
| PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation AS Gordon, RS Fulton, X Qin, ER Mardis, DA Nickerson, S Scherer Pharmacogenetics and genomics 26 (4), 161-168, 2016 | 108 | 2016 |
| Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results HK Tabor, PL Auer, SM Jamal, JX Chong, JH Yu, AS Gordon, TA Graubert, ... The American Journal of Human Genetics 95 (2), 183-193, 2014 | 97 | 2014 |
| Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 93 | 2019 |
| Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset AS Gordon, HK Tabor, AD Johnson, BM Snively, TL Assimes, PL Auer, ... Human molecular genetics 23 (8), 1957-1963, 2014 | 86 | 2014 |
| Frequency of genomic secondary findings among 21,915 eMERGE network participants AS Gordon, H Zouk, E Venner, CM Eng, BH Funke, LM Amendola, ... Genetics in Medicine 22 (9), 1470-1477, 2020 | 76 | 2020 |
| The eMERGE genotype set of 83,717 subjects imputed to~ 40 million variants genome wide and association with the herpes zoster medical record phenotype IB Stanaway, TO Hall, EA Rosenthal, M Palmer, V Naranbhai, R Knevel, ... Genetic epidemiology 43 (1), 63-81, 2019 | 75 | 2019 |
| Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families JH Kim, GP Jarvik, BL Browning, R Rajagopalan, AS Gordon, MJ Rieder, ... Anesthesiology 119 (5), 1054-1065, 2013 | 72 | 2013 |
| Pharmacogenetics in American Indian populations: analysis of: CYP2D6:: CYP3A4:: CYP3A5:, and: CYP2C9: in the Confederated Salish and Kootenai Tribes A Fohner, LAI Muzquiz, MA Austin, A Gaedigk, A Gordon, T Thornton, ... Pharmacogenetics and genomics 23 (8), 403-414, 2013 | 67 | 2013 |
| ACMG SF v3. 2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG) DT Miller, K Lee, NS Abul-Husn, LM Amendola, K Brothers, WK Chung, ... Genetics in Medicine 25 (8), 100866, 2023 | 51 | 2023 |
| Variation in genes controlling warfarin disposition and response in American Indian and Alaska Native people: CYP2C9:: VKORC1:: CYP4F2:: CYP4F11:: GGCX AE Fohner, R Robinson, J Yracheta, DA Dillard, B Schilling, B Khan, ... Pharmacogenetics and genomics 25 (7), 343-353, 2015 | 46 | 2015 |
