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Michael F Murray

Showing results (31-40 of 96) with videos related to

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Coronary Artery Disease|January 4, 2021
Genetic screening for familial hypercholesterolemia identifies patients not meeting cholesterol treatment guidelinesLaney K Jones, Celeena R Jefferson, Nan Chen, et al.
Annals of Internal Medicine|July 18, 2018
Whole-Exome Sequencing in Adults With Chronic Kidney DiseaseAlex R Chang, Jonathan Z Luo, Kevin Ho, et al.
The Journal of Applied Laboratory Medicine|June 14, 2021
An Integrated Approach to Deploy Panel-Based Pharmacogenetic Testing and Clinical Decision SupportRebecca A Pulk, Allen L Hsiao, Michael F Murray, et al.
Trends in Genetics : TIG|March 13, 2026
Just-in-time education to prepare clinicians for genomicsDanielle R Hoffman, Ayuko A Iverson, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2023
The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Aya Abu-El-Haija, Honey V Reddi, Hannah Wand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2021
The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell SymposiumSonja A Rasmussen, Noura S Abul-Husn, Jean-Laurent Casanova, et al.
Journal of Cutaneous Pathology|December 15, 2010
Erdheim-Chester disease presenting with cutaneous involvement: a case report and literature reviewElgida Radoncipi Volpicelli, Leona Doyle, Justin P Annes, et al.
Human Genetics|August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomasKamil J Cygan, Rachel Soemedi, Christy L Rhine, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2018
Trajectory of exonic variant discovery in a large clinical population: implications for variant curationUyenlinh L Mirshahi, Jonathan Z Luo, Kandamurugu Manickam, et al.
Plos Genetics|March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutationsChristy L Rhine, Kamil J Cygan, Rachel Soemedi, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Coronary Artery Disease|January 4, 2021
Genetic screening for familial hypercholesterolemia identifies patients not meeting cholesterol treatment guidelinesLaney K Jones, Celeena R Jefferson, Nan Chen, et al.
Annals of Internal Medicine|July 18, 2018
Whole-Exome Sequencing in Adults With Chronic Kidney DiseaseAlex R Chang, Jonathan Z Luo, Kevin Ho, et al.
The Journal of Applied Laboratory Medicine|June 14, 2021
An Integrated Approach to Deploy Panel-Based Pharmacogenetic Testing and Clinical Decision SupportRebecca A Pulk, Allen L Hsiao, Michael F Murray, et al.
Trends in Genetics : TIG|March 13, 2026
Just-in-time education to prepare clinicians for genomicsDanielle R Hoffman, Ayuko A Iverson, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2023
The clinical application of polygenic risk scores: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Aya Abu-El-Haija, Honey V Reddi, Hannah Wand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 13, 2021
The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell SymposiumSonja A Rasmussen, Noura S Abul-Husn, Jean-Laurent Casanova, et al.
Journal of Cutaneous Pathology|December 15, 2010
Erdheim-Chester disease presenting with cutaneous involvement: a case report and literature reviewElgida Radoncipi Volpicelli, Leona Doyle, Justin P Annes, et al.
Human Genetics|August 7, 2017
Defective splicing of the RB1 transcript is the dominant cause of retinoblastomasKamil J Cygan, Rachel Soemedi, Christy L Rhine, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 20, 2018
Trajectory of exonic variant discovery in a large clinical population: implications for variant curationUyenlinh L Mirshahi, Jonathan Z Luo, Kandamurugu Manickam, et al.
Plos Genetics|March 6, 2018
Hereditary cancer genes are highly susceptible to splicing mutationsChristy L Rhine, Kamil J Cygan, Rachel Soemedi, et al.
Pageof 10