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Dan M Roden

Showing results (501-510 of 593) with videos related to

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Heart Rhythm|December 3, 2014
Progress toward the prevention and treatment of atrial fibrillation: A summary of the Heart Rhythm Society Research Forum on the Treatment and Prevention of Atrial Fibrillation, Washington, DC, December 9-10, 2013David R Van Wagoner, Jonathan P Piccini, Christine M Albert, et al.
Annual Review of Biomedical Data Science|August 10, 2023
The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical ResearchKelsey R Mayo, Melissa A Basford, Robert J Carroll, et al.
Plos One|November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesElijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.
Clinical Pharmacology and Therapeutics|February 21, 2018
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and ProjectsSimona Volpi, Carol J Bult, Rex L Chisholm, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
Science (New York, N.Y.)|October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
JAMA Oncology|April 21, 2022
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple DiseasesChenjie Zeng, Lisa A Bastarache, Ran Tao, et al.
Pageof 60

Showing results (501-510 of 593) with videos related to

Sort By:
Pageof 60
Heart Rhythm|December 3, 2014
Progress toward the prevention and treatment of atrial fibrillation: A summary of the Heart Rhythm Society Research Forum on the Treatment and Prevention of Atrial Fibrillation, Washington, DC, December 9-10, 2013David R Van Wagoner, Jonathan P Piccini, Christine M Albert, et al.
Annual Review of Biomedical Data Science|August 10, 2023
The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical ResearchKelsey R Mayo, Melissa A Basford, Robert J Carroll, et al.
Plos One|November 14, 2013
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizesElijah R Behr, Marylyn D Ritchie, Toshihiro Tanaka, et al.
Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.
Clinical Pharmacology and Therapeutics|February 21, 2018
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and ProjectsSimona Volpi, Carol J Bult, Rex L Chisholm, et al.
Communications Biology|October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
Science (New York, N.Y.)|October 30, 2025
The functional landscape of coding variation in the familial hypercholesterolemia gene <i>LDLR</i>Daniel R Tabet, Atina G Coté, Megan C Lancaster, et al.
JAMA Oncology|April 21, 2022
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple DiseasesChenjie Zeng, Lisa A Bastarache, Ran Tao, et al.
Pageof 60