Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michael F Murray

Showing results (41-50 of 96) with videos related to

Pageof 10
Sort By:
Blood|November 15, 2003
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr)David C Yao, Dean R Tolan, Michael F Murray, et al.
Genetic Testing and Molecular Biomarkers|October 29, 2010
Health-care referrals from direct-to-consumer genetic testingMonica A Giovanni, Matthew R Fickie, Lisa S Lehmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2020
COVID-19 outcomes and the human genomeMichael F Murray, Eimear E Kenny, Marylyn D Ritchie, et al.
Translational Behavioral Medicine|February 1, 2018
Parental attitudes and expectations towards receiving genomic test results in healthy childrenAlanna Kulchak Rahm, Lindsay Bailey, Kara Fultz, et al.
Journal of Cardiovascular Translational Research|February 5, 2026
PAD-associated Genetic Variants are More Strongly Associated with Surgical Intervention than Premature OnsetJiaqi Hu, Dana Alameddine, He Wang, et al.
BMC Genomics|July 1, 2016
A loss of function variant in CASP7 protects against Alzheimer's disease in homozygous APOE ε4 allele carriersKristin L Ayers, Uyenlinh L Mirshahi, Amr H Wardeh, et al.
Nature Medicine|June 4, 2002
siRNA-directed inhibition of HIV-1 infectionCarl D Novina, Michael F Murray, Derek M Dykxhoorn, et al.
Journal of General Internal Medicine|April 17, 2013
Comparing electronic health record portals to obtain patient-entered family health history in primary careMichael F Murray, Monica A Giovanni, Elissa Klinger, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial HypercholesterolemiaLaney K Jones, Alanna Kulchak Rahm, Kandamurugu Manickam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Improved provider preparedness through an 8-part genetics and genomic education programCatherine Hajek, Allison M Hutchinson, Lauren N Galbraith, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Blood|November 15, 2003
Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr)David C Yao, Dean R Tolan, Michael F Murray, et al.
Genetic Testing and Molecular Biomarkers|October 29, 2010
Health-care referrals from direct-to-consumer genetic testingMonica A Giovanni, Matthew R Fickie, Lisa S Lehmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2020
COVID-19 outcomes and the human genomeMichael F Murray, Eimear E Kenny, Marylyn D Ritchie, et al.
Translational Behavioral Medicine|February 1, 2018
Parental attitudes and expectations towards receiving genomic test results in healthy childrenAlanna Kulchak Rahm, Lindsay Bailey, Kara Fultz, et al.
Journal of Cardiovascular Translational Research|February 5, 2026
PAD-associated Genetic Variants are More Strongly Associated with Surgical Intervention than Premature OnsetJiaqi Hu, Dana Alameddine, He Wang, et al.
BMC Genomics|July 1, 2016
A loss of function variant in CASP7 protects against Alzheimer's disease in homozygous APOE ε4 allele carriersKristin L Ayers, Uyenlinh L Mirshahi, Amr H Wardeh, et al.
Nature Medicine|June 4, 2002
siRNA-directed inhibition of HIV-1 infectionCarl D Novina, Michael F Murray, Derek M Dykxhoorn, et al.
Journal of General Internal Medicine|April 17, 2013
Comparing electronic health record portals to obtain patient-entered family health history in primary careMichael F Murray, Monica A Giovanni, Elissa Klinger, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Healthcare Utilization and Patients' Perspectives After Receiving a Positive Genetic Test for Familial HypercholesterolemiaLaney K Jones, Alanna Kulchak Rahm, Kandamurugu Manickam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Improved provider preparedness through an 8-part genetics and genomic education programCatherine Hajek, Allison M Hutchinson, Lauren N Galbraith, et al.
Pageof 10