| Embryonic stem cell-specific MicroRNAs HB Houbaviy, MF Murray, PA Sharp Developmental cell 5 (2), 351-358, 2003 | 1514 | 2003 |
| siRNA-directed inhibition of HIV-1 infection CD Novina, MF Murray, DM Dykxhoorn, PJ Beresford, J Riess, SK Lee, ... Nature medicine 8 (7), 681-686, 2002 | 1258 | 2002 |
| ClinGen—the clinical genome resource HL Rehm, JS Berg, LD Brooks, CD Bustamante, JP Evans, MJ Landrum, ... New England Journal of Medicine 372 (23), 2235-2242, 2015 | 1150 | 2015 |
| Genetic and pharmacologic inactivation of ANGPTL3 and cardiovascular disease FE Dewey, V Gusarova, RL Dunbar, C O’Dushlaine, C Schurmann, ... New England Journal of Medicine 377 (3), 211-221, 2017 | 757 | 2017 |
| Implementing genomic medicine in the clinic: the future is here TA Manolio, RL Chisholm, B Ozenberger, DM Roden, MS Williams, ... Genetics in Medicine 15 (4), 258-267, 2013 | 600 | 2013 |
| Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ... Science 354 (6319), aaf6814, 2016 | 547 | 2016 |
| Inactivating variants in ANGPTL4 and risk of coronary artery disease FE Dewey, V Gusarova, C O’Dushlaine, O Gottesman, J Trejos, C Hunt, ... New England Journal of Medicine 374 (12), 1123-1133, 2016 | 493 | 2016 |
| Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the clinical genome resource NT Strande, ER Riggs, AH Buchanan, O Ceyhan-Birsoy, M DiStefano, ... The American Journal of Human Genetics 100 (6), 895-906, 2017 | 445 | 2017 |
| Genetic identification of familial hypercholesterolemia within a single US health care system NS Abul-Husn, K Manickam, LK Jones, EA Wright, DN Hartzel, ... Science 354 (6319), aaf7000, 2016 | 419 | 2016 |
| The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research DJ Carey, SN Fetterolf, FD Davis, WA Faucett, HL Kirchner, U Mirshahi, ... Genetics in medicine 18 (9), 906-913, 2016 | 375 | 2016 |
| Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis B Coste, G Houge, MF Murray, N Stitziel, M Bandell, MA Giovanni, ... Proceedings of the National Academy of Sciences 110 (12), 4667-4672, 2013 | 239 | 2013 |
| A public resource facilitating clinical use of genomes MP Ball, JV Thakuria, AW Zaranek, T Clegg, AM Rosenbaum, X Wu, ... Proceedings of the National Academy of Sciences 109 (30), 11920-11927, 2012 | 222 | 2012 |
| The adult galactosemic phenotype SE Waisbren, NL Potter, CM Gordon, RC Green, P Greenstein, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2012 | 199 | 2012 |
| 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 |
| The impact of whole-genome sequencing on the primary care and outcomes of healthy adult patients: a pilot randomized trial JL Vassy, KD Christensen, EF Schonman, CL Blout, JO Robinson, ... Annals of internal medicine 167 (3), 159-169, 2017 | 191 | 2017 |
| Exploring concordance and discordance for return of incidental findings from clinical sequencing RC Green, JS Berg, GT Berry, LG Biesecker, DP Dimmock, JP Evans, ... Genetics in Medicine 14 (4), 405-410, 2012 | 180 | 2012 |
| Association of rare and common variation in the lipoprotein lipase gene with coronary artery disease AV Khera, HH Won, GM Peloso, C O’Dushlaine, D Liu, NO Stitziel, ... Jama 317 (9), 937-946, 2017 | 176 | 2017 |
| Biologic replacement for fibrin clot M Murray, M Murray, J Marler, K Spindler, A Sawyer US Patent App. 10/378,285, 2004 | 171 | 2004 |
| 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 | 167 | 2016 |
| Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician … BR Korf, AB Berry, M Limson, AJ Marian, MF Murray, PP O’Rourke, ... Genetics in medicine 16 (11), 804-809, 2014 | 166 | 2014 |
