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Michael F Murray

Showing results (61-70 of 96) with videos related to

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The European Respiratory Journal|August 21, 2025
Genetics of Interstitial Lung Diseases: A State-of-the-Art ReviewNicole Ng, Maria Molina-Molina, Ayodeji Adegunsoye, et al.
Plos Medicine|August 17, 2018
Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos Medicine|August 3, 2018
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
BMC Medical Genetics|February 26, 2015
A systematic approach to the reporting of medically relevant findings from whole genome sequencingHeather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, et al.
Diabetes|December 15, 2019
Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care CohortClaudia Gonzaga-Jauregui, Wenzhen Ge, Jeffrey Staples, et al.
NPJ Digital Medicine|July 16, 2019
Finding missed cases of familial hypercholesterolemia in health systems using machine learningJuan M Banda, Ashish Sarraju, Fahim Abbasi, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2013
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal ArthrogryposisBertrand Coste, Gunnar Houge, Michael F Murray, et al.
HGG Advances|December 7, 2025
Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE studySabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, et al.
The Lancet. Digital Health|December 16, 2020
Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter dataKelly D Myers, Joshua W Knowles, David Staszak, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
The European Respiratory Journal|August 21, 2025
Genetics of Interstitial Lung Diseases: A State-of-the-Art ReviewNicole Ng, Maria Molina-Molina, Ayodeji Adegunsoye, et al.
Plos Medicine|August 17, 2018
Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
Plos Medicine|August 3, 2018
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve healthMuin J Khoury, W Gregory Feero, David A Chambers, et al.
BMC Medical Genetics|February 26, 2015
A systematic approach to the reporting of medically relevant findings from whole genome sequencingHeather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, et al.
Diabetes|December 15, 2019
Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care CohortClaudia Gonzaga-Jauregui, Wenzhen Ge, Jeffrey Staples, et al.
NPJ Digital Medicine|July 16, 2019
Finding missed cases of familial hypercholesterolemia in health systems using machine learningJuan M Banda, Ashish Sarraju, Fahim Abbasi, et al.
Circulation. Arrhythmia and Electrophysiology|May 13, 2018
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the <i>KCNH2</i>-Encoded Kv11.1 ChannelJennifer L Smith, David J Tester, Allison R Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2013
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal ArthrogryposisBertrand Coste, Gunnar Houge, Michael F Murray, et al.
HGG Advances|December 7, 2025
Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE studySabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, et al.
The Lancet. Digital Health|December 16, 2020
Precision screening for familial hypercholesterolaemia: a machine learning study applied to electronic health encounter dataKelly D Myers, Joshua W Knowles, David Staszak, et al.
Pageof 10