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Author Details

Michael F Murray
Yale School of Medicine
1999
94
37
Wade Schulz (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36920474The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
36920474The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
35115087Can We Manage Presymptomatic TTR V142I Related Risk?JACC Heart Fail2022
35672798Addressing the routine failure to clinically identify monogenic cases of common disease.Genome Med2022
34906462Improved provider preparedness through an 8-part genetics and genomic education program.Genet Med2022
35115087Can We Manage Presymptomatic TTR V142I Related Risk?JACC Heart Fail2022
35672798Addressing the routine failure to clinically identify monogenic cases of common disease.Genome Med2022
34906462Improved provider preparedness through an 8-part genetics and genomic education program.Genet Med2022
33394692Genetic screening for familial hypercholesterolemia identifies patients not meeting cholesterol treatment guidelines.Coron Artery Dis2021
34125206An Integrated Approach to Deploy Panel-Based Pharmacogenetic Testing and Clinical Decision Support.J Appl Lab Med2021
33630087A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype.JAMA Netw Open2021
33790423DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
33727704DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
33712732The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium.Genet Med2021
33394692Genetic screening for familial hypercholesterolemia identifies patients not meeting cholesterol treatment guidelines.Coron Artery Dis2021
34646007Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2021
33630087A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype.JAMA Netw Open2021
33790423DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
33712732The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium.Genet Med2021
33727704DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
34646007Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2021
34125206An Integrated Approach to Deploy Panel-Based Pharmacogenetic Testing and Clinical Decision Support.J Appl Lab Med2021
32393819COVID-19 outcomes and the human genome.Genet Med2020
32028596Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program.J Pers Med2020
31836692Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.Diabetes2020
32393819COVID-19 outcomes and the human genome.Genet Med2020
31808788DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps.JAMA2020
32733075Bringing monogenic disease screening to the clinic.Nat Med2020
32028596Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program.J Pers Med2020
31808788DNA-Based Population Screening: Potential Suitability and Important Knowledge Gaps.JAMA2020
31836692Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort.Diabetes2020
32733075Bringing monogenic disease screening to the clinic.Nat Med2020
30335217Obtaining a Genetic Family History Using Computer-Based Tools.Curr Protoc Hum Genet2019
33323221Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter data.Lancet Digit Health2019
30449888Trajectory of exonic variant discovery in a large clinical population: implications for variant curation.Genet Med2019
30335217Obtaining a Genetic Family History Using Computer-Based Tools.Curr Protoc Hum Genet2019
31508243Predictive value of genomic screening: cross-sectional study of cystic fibrosis in 50,788 electronic health records.NPJ Genom Med2019
31216868Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.Circulation2019
31304370Finding missed cases of familial hypercholesterolemia in health systems using machine learning.NPJ Digit Med2019
33323221Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter data.Lancet Digit Health2019
31216868Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants.Circulation2019
31508243Predictive value of genomic screening: cross-sectional study of cystic fibrosis in 50,788 electronic health records.NPJ Genom Med2019
31304370Finding missed cases of familial hypercholesterolemia in health systems using machine learning.NPJ Digit Med2019
30449888Trajectory of exonic variant discovery in a large clinical population: implications for variant curation.Genet Med2019
29261187Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.Genet Med2018
30073309The Path to Routine Genomic Screening in Health Care.Ann Intern Med2018
30071015A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.PLoS Med2018
30114233Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.PLoS Med2018
29884840Genome-first findings require precision phenotyping.Genet Med2018
30354341Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial Hypercholesterolemia.Circ Genom Precis Med2018
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Collaborators

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Joseph B Leader
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Alanna Kulchak Rahm
Research Institute
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Uyenlinh L Mirshahi
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William A Faucett
Genomic Medicine Institute
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Colm O'Dushlaine
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Amy C Sturm
Genomic Medicine Institute, USA Heart and Vascular Institute
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Ingrid B Borecki
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Janet L Williams
Genomic Medicine Institute
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Alexander Lopez
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Kurt D Christensen
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Omri Gottesman
Icahn School of Medicine at Mount Sinai
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John Penn
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Release 1.2