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Circulation
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May 27, 2026
Association of Common Ancestry-Enriched Variants With Cardiomyopathy and Arrhythmias
Temidayo A Abe, Megan C Lancaster, Dan M Roden
Journal of Cardiovascular Electrophysiology
|
October 27, 2022
Left atrial appendage dimension predicts elevated brain natriuretic peptide in nonvalvular atrial fibrillation
Jason A Cook, Megan C Lancaster, Arvindh N Kanagasundram, et al.
Genome Biology
|
July 2, 2024
Benchmarking computational variant effect predictors by their ability to infer human traits
Daniel R Tabet, Da Kuang, Megan C Lancaster, et al.
Circulation Research
|
May 26, 2022
Arrhythmias as Presentation of Genetic Cardiomyopathy
J Lukas Laws, Megan C Lancaster, M Ben Shoemaker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Research Square
|
October 4, 2023
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Biorxiv : the Preprint Server for Biology
|
February 26, 2024
Multifocal Ectopic Purkinje Premature Contractions due to neutralization of an <i>SCN5A</i> negative charge: structural insights into the gating pore hypothesis
Andrew M Glazer, Tao Yang, Bian Li, et al.
Nature Communications
|
August 29, 2024
Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 29, 2026
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders
Temidayo A Abe, Favour E Markson, Quinn S Wells, et al.
Nature Reviews. Cardiology
|
September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine
Andrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
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Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Circulation
|
May 27, 2026
Association of Common Ancestry-Enriched Variants With Cardiomyopathy and Arrhythmias
Temidayo A Abe, Megan C Lancaster, Dan M Roden
Journal of Cardiovascular Electrophysiology
|
October 27, 2022
Left atrial appendage dimension predicts elevated brain natriuretic peptide in nonvalvular atrial fibrillation
Jason A Cook, Megan C Lancaster, Arvindh N Kanagasundram, et al.
Genome Biology
|
July 2, 2024
Benchmarking computational variant effect predictors by their ability to infer human traits
Daniel R Tabet, Da Kuang, Megan C Lancaster, et al.
Circulation Research
|
May 26, 2022
Arrhythmias as Presentation of Genetic Cardiomyopathy
J Lukas Laws, Megan C Lancaster, M Ben Shoemaker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Research Square
|
October 4, 2023
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Biorxiv : the Preprint Server for Biology
|
February 26, 2024
Multifocal Ectopic Purkinje Premature Contractions due to neutralization of an <i>SCN5A</i> negative charge: structural insights into the gating pore hypothesis
Andrew M Glazer, Tao Yang, Bian Li, et al.
Nature Communications
|
August 29, 2024
Detection of distant relatedness in biobanks to identify undiagnosed cases of Mendelian disease as applied to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 29, 2026
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders
Temidayo A Abe, Favour E Markson, Quinn S Wells, et al.
Nature Reviews. Cardiology
|
September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicine
Andrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
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of 2