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Nature Genetics
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December 5, 2024
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Sean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature
|
August 10, 2021
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans
Sanna Gudmundsson, Konrad J Karczewski, Laurent C Francioli, et al.
Nature Genetics
|
February 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Rafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics
|
January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Rafik Tadros, Catherine Francis, Xiao Xu, et al.
Nature
|
August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Annals of Neurology
|
April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
Emily C Oates, Kristi J Jones, Sandra Donkervoort, et al.
Nature Genetics
|
November 21, 2024
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Sean L Zheng, Albert Henry, Douglas Cannie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
European Heart Journal
|
August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
Renee Johnson, Robert A Fletcher, Stacey Peters, et al.
Nucleic Acids Research
|
November 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the world
Michael A Gargano, Nicolas Matentzoglu, Ben Coleman, et al.
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of 73
Search research articles
Search
Showing results (711-720 of 721) with videos related to
Sort By:
Page
of 73
Nature Genetics
|
December 5, 2024
Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Sean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.
Nature
|
August 10, 2021
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans
Sanna Gudmundsson, Konrad J Karczewski, Laurent C Francioli, et al.
Nature Genetics
|
February 18, 2025
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Rafik Tadros, Sean L Zheng, Christopher Grace, et al.
Nature Genetics
|
January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Rafik Tadros, Catherine Francis, Xiao Xu, et al.
Nature
|
August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
Annals of Neurology
|
April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
Emily C Oates, Kristi J Jones, Sandra Donkervoort, et al.
Nature Genetics
|
November 21, 2024
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Sean L Zheng, Albert Henry, Douglas Cannie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
European Heart Journal
|
August 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
Renee Johnson, Robert A Fletcher, Stacey Peters, et al.
Nucleic Acids Research
|
November 12, 2023
The Human Phenotype Ontology in 2024: phenotypes around the world
Michael A Gargano, Nicolas Matentzoglu, Ben Coleman, et al.
Page
of 73