Michael F. Murray

发表

Genetic identification of familial hypercholesterolemia within a single U.S. health care system

Marylyn D. Ritchie, Alan R. Shuldiner, Laney K. Jones, 2016, Science.

A One-Page Summary Report of Genome Sequencing for the Healthy Adult

Robert C. Green, Isaac S. Kohane, Heidi L. Rehm, 2015, Public Health Genomics.

Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource

J. Michael Cherry, Heidi L. Rehm, Erin Rooney Riggs, 2017, bioRxiv.

Comparing Electronic Health Record Portals to Obtain Patient-Entered Family Health History in Primary Care

David W. Bates, E. John Orav, Elissa V. Klinger, 2013, Journal of General Internal Medicine.

Exploring concordance and discordance for return of incidental findings from clinical sequencing

Robert C. Green, Heidi L. Rehm, Jonathan S. Berg, 2012, Genetics in Medicine.

Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

Marylyn D. Ritchie, Scott Mellis, Alan R. Shuldiner, 2016, Science.

Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the Clinical Genome Resource

J. Michael Cherry, Avni Santani, Heidi L. Rehm, 2017, bioRxiv.

Implementing genomic medicine in the clinic: The future is here

Dan M. Roden, Alan R. Shuldiner, Rex L. Chisholm, 2013 .

Finding missed cases of familial hypercholesterolemia in health systems using machine learning

Nigam H. Shah, Kenneth Jung, Juan M. Banda, 2019, npj Digital Medicine.

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics

Gregory J. Tsongalis, Bruce R. Korf, John Tooker, 2014, Genetics in Medicine.

Profiling copy number variation and disease associations from 50,726 DiscovEHR Study exomes

Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey Staples, 2017, bioRxiv.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Genome-first findings require precision phenotyping

M. Murray, Monica A. Giovanni, Michael F. Murray, 2018, Genetics in Medicine.

Implementing genomic medicine in the clinic: the future is here

Dan M. Roden, Alan R. Shuldiner, Rex L. Chisholm, 2013, Genetics in Medicine.