MichaelFMurrayMD

Medical Genetics • New York, NY

Clinical Genetics

Instructor in Medicine, Brigham and Women's Hospital

Join to view full profile

Are you Dr. Murray?

Join over one million U.S. Physicians, Nurse Practitioners and PAs, already on Doximity.

Connect with colleagues in the same hospital or clinic
You already have 45 invites waiting!
Search all U.S. specialist profiles and refer a patient
Read the latest clinical news and earn CME/CEU credits

Claim this profile

Not you? Find your profile

Office
5 E 98th St
New York, NY 10029
Phone+1 212-241-4353
Is this information wrong?

Summary

Dr. Michael Murray, MD is a board certified medical geneticist in New York, New York. He is currently licensed to practice medicine in New York, Connecticut, and Massachusetts. He is affiliated with Yale-New Haven Hospital and is an Instructor in Medicine at Brigham and Women's Hospital.

Education & Training

Children's Hospital/Harvard Medical SchoolResidency, Medical Genetics and Genomics, 2000 - 2003
University of Pennsylvania Health SystemFellowship, Infectious Disease, 1991 - 1995
Cleveland Clinic FoundationResidency, Internal Medicine, 1988 - 1991
Pennsylvania State University College of MedicineClass of 1988

Certifications & Licensure

NH State Medical License 1996 - Present
NY State Medical License 2024 - 2025
CT State Medical License 2018 - 2025
MA State Medical License 1996 - 2019
PA State Medical License 1991 - 2018
OH State Medical License 1990 - 1992
American Board of Internal Medicine Internal Medicine
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Clinical Trials

Identification of Undiagnosed Gaucher Disease Start of enrollment: 2012 Aug 01
Unknown status
Not Applicable

Publications & Presentations

PubMed

12 citations
Improved provider preparedness through an 8-part genetics and genomic education program
Catherine Hajek, Allison M. Hutchinson, Lauren N. Galbraith, Robert C. Green, Michael F. Murray, Natasha Petry, Charlene L. Preys, Carrie L.B. Zawatsky, Emilie S Zolti...> ;Genetics in Medicine. 2021 Nov 1
1 citations
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.
Adam H. Buchanan, Kandamurugu Manickam, Michelle N. Meyer, Jennifer K. Wagner, Miranda L.G. Hallquist, Janet L. Williams, Alanna Kulchak Rahm, Marc S. Williams, Zong M...> ;Genetics in Medicine. 2021 Oct 13
An Integrated Approach to Deploy Panel-Based Pharmacogenetic Testing and Clinical Decision Support.
Rebecca Pulk, Allen L. Hsiao, Michael F. Murray, Lisa S. Stump, Wade L. Schulz> ;The Journal of Applied Laboratory Medicine. 2021 Jul 7
12 citations
DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Gen...
Lora J. H. Bean, Maren T. Scheuner, Michael F. Murray, Leslie G. Biesecker, Robert C. Green, Kristin G. Monaghan, Glenn E. Palomaki, Richard R. Sharp, Tracy L. Trotter...> ;Genetics in Medicine. 2021 Mar 31
37 citations
DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and G...
Michael F. Murray, Monica A. Giovanni, Debra Lochner Doyle, Steven M. Harrison, Elaine Lyon, Kandamurugu Manickam, Kristin G. Monaghan, Sonja A. Rasmussen, Maren T. Sc...> ;Genetics in Medicine. 2021 Mar 16
6 citations
The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium.
Sonja A. Rasmussen, Noura S. Abul-Husn, Jean-Laurent Casanova, Mark J. Daly, Heidi L. Rehm, Michael F. Murray> ;Genetics in Medicine. 2021 Mar 12
21 citations
A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype.
Uyenlinh L. Mirshahi, Jung Kim, Ana F. Best, Zongming E. Chen, Ying Hu, Jeremy S. Haley, Alicia Golden, Richard Stahl, Kandamurugu Manickam, Ann G. Carr, Laura A. Harn...> ;JAMA Network Open. 2021 Feb 1
1 citations
Genetic screening for familial hypercholesterolemia identifies patients not meeting cholesterol treatment guidelines.
Laney K. Jones, Celeena R Jefferson, Nan Chen, Michael F. Murray> ;Coronary Artery Disease. 2021 Sep 1
5 citations
Bringing monogenic disease screening to the clinic.
Michael F. Murray, Monica A. Giovanni> ;Nature Medicine. 2020 Jul 30
33 citations
COVID-19 outcomes and the human genome.
Michael F. Murray, Eimear E. Kenny, Marylyn D. Ritchie, Daniel J. Rader, Allen E. Bale, Monica A. Giovanni, Noura S. Abul-Husn> ;Genetics in Medicine. 2020 May 12
15 citations
Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program
Jing Hao, Dina Hassen, Kandamurugu Manickam, Michael F. Murray, Dustin N. Hartzel, Yirui Hu, Kunpeng Liu, Alanna Kulchak Rahm, Marc S. Williams, Amanda L. Lazzeri, Ada...> ;Journal of Personalized Medicine. 2020 Feb 3
35 citations
Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.
Claudia Gonzaga-Jauregui, Wenzhen Ge, Jeffrey Staples, Cristopher V. Van Hout, Ashish Yadav, Ryan Colonie, Joseph B. Leader, H. Lester Kirchner, Michael F. Murray, Jef...> ;Diabetes. 2020 Feb 1
27 citations
DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps.
Michael F. Murray, James P. Evans, Muin J. Khoury> ;JAMA. 2020 Jan 28
29 citations
Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter data.
Kelly D. Myers, Joshua W. Knowles, David Staszak, Michael D. Shapiro, William James Howard, Mrinal Yadava, David Zuzick, Latoya Williamson, Nigam H. Shah, Juan M. Band...> ;The Lancet. Digital Health. 2019 Dec 1
3 citations
Predictive value of genomic screening: cross-sectional study of cystic fibrosis in 50,788 electronic health records
Jaya Prakash Sugunaraj, H M Brosius, Michael F. Murray, Kandamurugu Manickam, Jason Stamm, David J. Carey, Uyenlinh L. Mirshahi> ;NPJ Genomic Medicine. 2019 Sep 4
76 citations
Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.
Christopher M. Haggerty, Scott M. Damrauer, Michael G. Levin, David Birtwell, David J. Carey, Alicia Golden, Dustin N. Hartzel, Yirui Hu, Renae Judy, Melissa A. Kelly,...> ;Circulation. 2019 Jul 2
52 citations
Finding missed cases of familial hypercholesterolemia in health systems using machine learning.
Juan M. Banda, Ashish Sarraju, Fahim Abbasi, Justin Parizo, Mitchel Pariani, Hannah Ison, Elinor Briskin, Hannah Wand, Sebastien Dubois, Kenneth Jung, Seth A. Myers, D...> ;NPJ Digital Medicine. 2019 Apr 11
51 citations
Blockade of MCU-Mediated Ca2+ Uptake Perturbs Lipid Metabolism via PP4-Dependent AMPK Dephosphorylation
Dhanendra Tomar, Fabián Jaña, Zhiwei Dong, William J. Quinn, Pooja Jadiya, Sarah L. Breves, Cassidy C. Daw, Subramanya Srikantan, Santhanam Shanmughapriya, Neeharika N...> ;Cell Reports. 2019 Mar 26
115 citations
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.
Seung Hoan Choi, Lu-Chen Weng, Carolina Roselli, Honghuang Lin, Christopher M. Haggerty, M. Benjamin Shoemaker, John Barnard, Dan E. Arking, Daniel I. Chasman, Christi...> ;JAMA. 2018 Dec 11
9 citations
Trajectory of exonic variant discovery in a large clinical population: implications for variant curation
Uyenlinh L. Mirshahi, Jonathan Z. Luo, Kandamurugu Manickam, Amr H. Wardeh, Tooraj Mirshahi, Michael F. Murray, David J. Carey> ;Genetics in Medicine. 2019 Jun 1
8 citations
Obtaining a Genetic Family History Using Computer-Based Tools
Weilong Li, Michael F. Murray, Monica A. Giovanni> ;Current Protocols in Human Genetics. 2019 Jan 1
9 citations
The Path to Routine Genomic Screening in Health Care.
Michael F. Murray> ;Annals of Internal Medicine. 2018 Sep 18
105 citations
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L.B. Schwartz, Cara Zayac McCormick, Amanda L. Lazzeri, D’Andra M. Lindbuchler, Miranda L.G. Hallquist, Kandamurugu Manickam, Adam H. Buchanan, Alanna Kulchak Ra...> ;American Journal of Human Genetics. 2018 Sep 6
137 citations
Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H. Buchanan, Marci L.B. Schwartz, Miranda L.G. Hallquist, Janet L. Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M. Savatt, Alyson E...> ;JAMA Network Open. 2018 Sep 7
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.
Khoury, M. J.,Feero, W. G.,Chambers, D. A.,Brody, L. E.,Aziz, N.,Green, R. C.,Janssens, ACJW.,Murray, M. F.,Rodriguez, L. L.,Rutter, J. L.,Schully, S. D.,Winn, D. M.,M...> ;PLoS Med.. 2018 Aug 03
Join now to see all

Hospital Affiliations

Yale-New Haven HospitalNew Haven, Connecticut