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Michael F. Murray, MD
Michael F. Murray, MD
Chief, Division of Genomic Medicine & Clinical Director, Institute for Genomic Health
Verified email at mssm.edu - Homepage
Title
Cited by
Cited by
Year
Embryonic stem cell-specific MicroRNAs
HB Houbaviy, MF Murray, PA Sharp
Developmental cell 5 (2), 351-358, 2003
15402003
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
13452015
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
12682002
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
8402017
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
6522013
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
5872016
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
5322017
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
5202016
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
4482016
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
4312016
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
2522013
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
2322012
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
2152018
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
2152012
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
2012017
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
1982017
Association between titin loss-of-function variants and early-onset atrial fibrillation
SH Choi, LC Weng, C Roselli, H Lin, CM Haggerty, MB Shoemaker, ...
Jama 320 (22), 2354-2364, 2018
1842018
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
1782012
Biologic replacement for fibrin clot
M Murray, M Murray, J Marler, K Spindler, A Sawyer
US Patent App. 10/378,285, 2004
1762004
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
1752016
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