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Nature Communications
|
November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
Circulation. Genomic and Precision Medicine
|
May 13, 2018
Common Coding Variants in <i>SCN10A</i> Are Associated With the Nav1.8 Late Current and Cardiac Conduction
Vincenzo Macri, Jennifer A Brody, Dan E Arking, et al.
Journal of the American College of Cardiology
|
April 22, 2026
Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study
Nicholas Sunderland, Geraldine Asselin, Albert Henry, et al.
European Heart Journal
|
March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Sophie Garnier, Magdalena Harakalova, Stefan Weiss, 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.
Nature Communications
|
January 11, 2020
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia Shah, Albert Henry, Carolina Roselli, et al.
ESC Heart Failure
|
September 4, 2021
The genomics of heart failure: design and rationale of the HERMES consortium
R Thomas Lumbers, Sonia Shah, Honghuang Lin, et al.
Nature Genetics
|
March 4, 2025
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Albert Henry, Xiaodong Mo, Chris Finan, et al.
Nature Genetics
|
June 13, 2018
Multi-ethnic genome-wide association study for atrial fibrillation
Carolina Roselli, Mark D Chaffin, Lu-Chen Weng, et al.
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Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Nature Communications
|
November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
Circulation. Genomic and Precision Medicine
|
May 13, 2018
Common Coding Variants in <i>SCN10A</i> Are Associated With the Nav1.8 Late Current and Cardiac Conduction
Vincenzo Macri, Jennifer A Brody, Dan E Arking, et al.
Journal of the American College of Cardiology
|
April 22, 2026
Body Mass Index, Clinical Outcomes, and Mortality in Heart Failure: A Mendelian Randomization Study
Nicholas Sunderland, Geraldine Asselin, Albert Henry, et al.
European Heart Journal
|
March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Sophie Garnier, Magdalena Harakalova, Stefan Weiss, 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.
Nature Communications
|
January 11, 2020
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia Shah, Albert Henry, Carolina Roselli, et al.
ESC Heart Failure
|
September 4, 2021
The genomics of heart failure: design and rationale of the HERMES consortium
R Thomas Lumbers, Sonia Shah, Honghuang Lin, et al.
Nature Genetics
|
March 4, 2025
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Albert Henry, Xiaodong Mo, Chris Finan, et al.
Nature Genetics
|
June 13, 2018
Multi-ethnic genome-wide association study for atrial fibrillation
Carolina Roselli, Mark D Chaffin, Lu-Chen Weng, et al.
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of 8