Search research articles
Contact Us
Filters
Showing results (171-180 of 961) with videos related to
Page
of 97
Sort By:
Circulation. Cardiovascular Genetics
|
December 15, 2017
Genome-Wide Association Studies Revealing the Heritability of Common Atrial Fibrillation: Is Bigger Always Better?
Sebastian Clauss, Moritz F Sinner, Stefan Kääb
Circulation. Cardiovascular Genetics
|
December 16, 2017
Calcific Aortic Valve Disease: Insights Into the Genetics of Vascular Ageing
Richmond W Jeremy
Circulation. Cardiovascular Genetics
|
December 17, 2017
Surviving Sudden Death: Where Does Next-Generation Sequencing Fit in the Assessment of Sudden Death Victims and Their Families
Robert M Hamilton, Kristopher S Cunningham, Elijah R Behr
Circulation. Cardiovascular Genetics
|
September 7, 2017
Insights From the Positive Association of Height With Incident Venous Thromboembolism
C Mary Schooling
Circulation. Cardiovascular Genetics
|
October 15, 2017
A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients
Allison L Cirino, Neal K Lakdawala, Barbara McDonough, et al.
Circulation. Cardiovascular Genetics
|
October 15, 2017
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Aldi T Kraja, James P Cook, Helen R Warren, et al.
Circulation. Cardiovascular Genetics
|
October 15, 2017
Sex Determines Cardiac Myocyte Stretch and Relaxation
Michael J Coronado, DeLisa Fairweather, Katelyn A Bruno
Circulation. Cardiovascular Genetics
|
October 28, 2016
Cardiovascular Risk Factors Associated With Blood Metabolite Concentrations and Their Alterations During a 4-Year Period in a Population-Based Cohort
Maria Elena Lacruz, Alexander Kluttig, Daniel Tiller, et al.
Circulation. Cardiovascular Genetics
|
December 22, 2016
Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, "Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction"
Josef Finsterer, Sinda Zarrouk-Mahjoub
Circulation. Cardiovascular Genetics
|
November 24, 2016
International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium)
Guillaume Jondeau, Jacques Ropers, Ellen Regalado, et al.
Page
of 97
Search research articles
Search
Showing results (171-180 of 961) with videos related to
Sort By:
Page
of 97
Circulation. Cardiovascular Genetics
|
December 15, 2017
Genome-Wide Association Studies Revealing the Heritability of Common Atrial Fibrillation: Is Bigger Always Better?
Sebastian Clauss, Moritz F Sinner, Stefan Kääb
Circulation. Cardiovascular Genetics
|
December 16, 2017
Calcific Aortic Valve Disease: Insights Into the Genetics of Vascular Ageing
Richmond W Jeremy
Circulation. Cardiovascular Genetics
|
December 17, 2017
Surviving Sudden Death: Where Does Next-Generation Sequencing Fit in the Assessment of Sudden Death Victims and Their Families
Robert M Hamilton, Kristopher S Cunningham, Elijah R Behr
Circulation. Cardiovascular Genetics
|
September 7, 2017
Insights From the Positive Association of Height With Incident Venous Thromboembolism
C Mary Schooling
Circulation. Cardiovascular Genetics
|
October 15, 2017
A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients
Allison L Cirino, Neal K Lakdawala, Barbara McDonough, et al.
Circulation. Cardiovascular Genetics
|
October 15, 2017
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Aldi T Kraja, James P Cook, Helen R Warren, et al.
Circulation. Cardiovascular Genetics
|
October 15, 2017
Sex Determines Cardiac Myocyte Stretch and Relaxation
Michael J Coronado, DeLisa Fairweather, Katelyn A Bruno
Circulation. Cardiovascular Genetics
|
October 28, 2016
Cardiovascular Risk Factors Associated With Blood Metabolite Concentrations and Their Alterations During a 4-Year Period in a Population-Based Cohort
Maria Elena Lacruz, Alexander Kluttig, Daniel Tiller, et al.
Circulation. Cardiovascular Genetics
|
December 22, 2016
Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, "Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction"
Josef Finsterer, Sinda Zarrouk-Mahjoub
Circulation. Cardiovascular Genetics
|
November 24, 2016
International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium)
Guillaume Jondeau, Jacques Ropers, Ellen Regalado, et al.
Page
of 97