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Stefano Duga

Showing results (131-140 of 141) with videos related to

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The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|February 18, 2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseThomas R Webb, Jeanette Erdmann, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
The New England Journal of Medicine|June 20, 2020
Genomewide Association Study of Severe Covid-19 with Respiratory Failure, David Ellinghaus, Frauke Degenhardt, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 15

Showing results (131-140 of 141) with videos related to

Sort By:
Pageof 15
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|February 18, 2017
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery DiseaseThomas R Webb, Jeanette Erdmann, Kathleen E Stirrups, et al.
Journal of the American College of Cardiology|October 12, 2010
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studiesThemistocles L Assimes, Hilma Hólm, Sekar Kathiresan, et al.
The New England Journal of Medicine|June 20, 2020
Genomewide Association Study of Severe Covid-19 with Respiratory Failure, David Ellinghaus, Frauke Degenhardt, et al.
Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.
Human Molecular Genetics|June 16, 2022
Novel genes and sex differences in COVID-19 severityRaquel Cruz, Silvia Diz-de Almeida, Miguel López de Heredia, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 15