Michael F Murray

发表

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge

Daniel Nilsson, Peter Szolovits, Karen Eilbeck, 2014, Genome Biology.

A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health

Muin J Khoury, Sheri D Schully, Laura Lyman Rodriguez, 2018, PLoS medicine.

A public resource facilitating clinical use of genomes

Euan A Ashley, Jong Bhak, Leonid Peshkin, 2012, Proceedings of the National Academy of Sciences.

Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis

Alexander Hoischen, Gunnar Houge, Matthew S. Lebo, 2013, Proceedings of the National Academy of Sciences.

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.

Matthew S. Lebo, Heidi L Rehm, Danielle R Azzariti, 2017, Annals of internal medicine.

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

Isaac S Kohane, Sek Won Kong, Heidi L Rehm, 2014, Trials.

Health-care referrals from direct-to-consumer genetic testing.

David Veenstra, Robert C Green, Monica A Giovanni, 2010, Genetic testing and molecular biomarkers.

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

Matthew S. Lebo, Isaac S Kohane, Heidi L Rehm, 2014, BMC Medical Genetics.

The Application of Computer‐Based Tools in Obtaining the Genetic Family History

Monica A Giovanni, Michael F Murray, M. Murray, 2010, Current protocols in human genetics.

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Gonçalo Abecasis, Dan M Roden, Christopher M Haggerty, 2018, JAMA.