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American Journal of Preventive Cardiology
|
November 28, 2022
Earlier treatment in adults with high lifetime risk of cardiovascular diseases: What prevention trials are feasible and could change clinical practice? Report of a National Heart, Lung, and Blood Institute (NHLBI) Workshop
Ann Marie Navar, Lawrence J Fine, Walter T Ambrosius, et al.
Circulation. Genomic and Precision Medicine
|
April 10, 2026
Development of an Integrated Monogenic and Polygenic Risk Assessment Tool for Coronary Artery Disease and Its Application in a Community-Based Health Care Biobank
Jianfeng Xu, Zhuqing Shi, Sumeet A Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 12, 2021
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test
Deanna G Brockman, Christina A Austin-Tse, Renée C Pelletier, et al.
Circulation. Genomic and Precision Medicine
|
October 1, 2021
Rare, Damaging DNA Variants in <i>CORIN</i> and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses
Minxian Wang, Vivian S Lee-Kim, Deepak S Atri, et al.
Nature Communications
|
May 9, 2020
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
James P Pirruccello, Alexander Bick, Minxian Wang, et al.
Cell
|
April 20, 2019
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood
Amit V Khera, Mark Chaffin, Kaitlin H Wade, et al.
JACC. Advances
|
July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and Management
W H Wilson Tang, Quan M Bui, Allison L Cirino, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2023
Rare penetrant mutations confer severe risk of common diseases
Petko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Cell Reports. Medicine
|
November 29, 2021
Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease
Nooshin Ghodsian, Erik Abner, Connor A Emdin, et al.
Science (New York, N.Y.)
|
June 1, 2023
Rare penetrant mutations confer severe risk of common diseases
Petko P Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
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of 14
Search research articles
Search
Showing results (81-90 of 140) with videos related to
Sort By:
Page
of 14
American Journal of Preventive Cardiology
|
November 28, 2022
Earlier treatment in adults with high lifetime risk of cardiovascular diseases: What prevention trials are feasible and could change clinical practice? Report of a National Heart, Lung, and Blood Institute (NHLBI) Workshop
Ann Marie Navar, Lawrence J Fine, Walter T Ambrosius, et al.
Circulation. Genomic and Precision Medicine
|
April 10, 2026
Development of an Integrated Monogenic and Polygenic Risk Assessment Tool for Coronary Artery Disease and Its Application in a Community-Based Health Care Biobank
Jianfeng Xu, Zhuqing Shi, Sumeet A Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 12, 2021
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test
Deanna G Brockman, Christina A Austin-Tse, Renée C Pelletier, et al.
Circulation. Genomic and Precision Medicine
|
October 1, 2021
Rare, Damaging DNA Variants in <i>CORIN</i> and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses
Minxian Wang, Vivian S Lee-Kim, Deepak S Atri, et al.
Nature Communications
|
May 9, 2020
Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy
James P Pirruccello, Alexander Bick, Minxian Wang, et al.
Cell
|
April 20, 2019
Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood
Amit V Khera, Mark Chaffin, Kaitlin H Wade, et al.
JACC. Advances
|
July 4, 2025
Cardiologists' Perceptions of Cardiogenetic Testing and Management
W H Wilson Tang, Quan M Bui, Allison L Cirino, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2023
Rare penetrant mutations confer severe risk of common diseases
Petko Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Cell Reports. Medicine
|
November 29, 2021
Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease
Nooshin Ghodsian, Erik Abner, Connor A Emdin, et al.
Science (New York, N.Y.)
|
June 1, 2023
Rare penetrant mutations confer severe risk of common diseases
Petko P Fiziev, Jeremy McRae, Jacob C Ulirsch, et al.
Page
of 14