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Frederick E Dewey

Showing results (31-40 of 57) with videos related to

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Circulation. Genomic and Precision Medicine|April 3, 2019
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart DiseaseGina M Peloso, Akihiro Nomura, Amit V Khera, et al.
American Journal of Human Genetics|May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 ExomesJeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Early somatic mosaicism is a rare cause of long-QT syndromeJames Rush Priest, Charles Gawad, Kristopher M Kahlig, et al.
Circulation. Genomic and Precision Medicine|June 7, 2022
Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac HypertrophyHannah N De Jong, Frederick E Dewey, Pablo Cordero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Lancet (London, England)|May 4, 2010
Clinical assessment incorporating a personal genomeEuan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Plos Genetics|September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequenceFrederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Circulation. Genomic and Precision Medicine|April 3, 2019
Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart DiseaseGina M Peloso, Akihiro Nomura, Amit V Khera, et al.
American Journal of Human Genetics|May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 ExomesJeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine|March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery DiseaseFrederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 30, 2016
Early somatic mosaicism is a rare cause of long-QT syndromeJames Rush Priest, Charles Gawad, Kristopher M Kahlig, et al.
Circulation. Genomic and Precision Medicine|June 7, 2022
Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac HypertrophyHannah N De Jong, Frederick E Dewey, Pablo Cordero, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Lancet (London, England)|May 4, 2010
Clinical assessment incorporating a personal genomeEuan A Ashley, Atul J Butte, Matthew T Wheeler, et al.
Plos Genetics|September 22, 2011
Phased whole-genome genetic risk in a family quartet using a major allele reference sequenceFrederick E Dewey, Rong Chen, Sergio P Cordero, et al.
Pageof 6