Michael F. Murray, MD
Michael F. Murray, MD
Director for Clinical Operations in the Center for Genomic Health at Yale
Email verificata su yale.edu - Home page
TitoloCitata daAnno
Embryonic stem cell-specific MicroRNAs
HB Houbaviy, MF Murray, PA Sharp
Developmental cell 5 (2), 351-358, 2003
13262003
siRNA-directed inhibition of HIV-1 infection
CD Novina, MF Murray, DM Dykxhoorn, PJ Beresford, J Riess, SK Lee, ...
Nature medicine 8 (7), 681, 2002
11512002
siRNA-directed inhibition of HIV-1 infection
CD Novina, MF Murray, DM Dykxhoorn, PJ Beresford, J Riess, SK Lee, ...
Nature medicine 8 (7), 681, 2002
11512002
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
4452015
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, 2013
4052013
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
2302016
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
2202017
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
1992016
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
1672012
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, 2012
1602012
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
1582016
HIV therapeutic
P Beresford, J Lieberman, M Murray, C Novina, P Sharp
US Patent App. 10/393,411, 2004
1422004
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
1412013
Biologic replacement for fibrin clot
M Murray, M Murray, J Marler, K Spindler, A Sawyer
US Patent App. 10/378,285, 2004
1382004
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, 2016
1322016
Tryptophan depletion and HIV Tryptophan depletion and HIV infection: a metabolic link to pathogenesis
MF Murray
The Lancet infectious diseases 3 (10), 644-652, 2003
1292003
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
1192016
Biologic replacement for fibrin clot
MM Murray, MF Murray, J Marler
US Patent 6,964,685, 2005
1192005
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
1152017
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
1152012
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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