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Michael Troup

Showing results (21-30 of 28) with videos related to

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JACC. Advances|March 22, 2025
Polygenic Inheritance for Common Comorbidities Associated With Congenital Heart DiseaseJamie-Lee M Thompson, Ingrid S Tarr, Emma M Rath, et al.
JAMA Cardiology|January 24, 2024
Polygenic Risk in Families With Spontaneous Coronary Artery DissectionIngrid Tarr, Stephanie Hesselson, Michael Troup, et al.
Journal of the American Heart Association|April 7, 2025
Spontaneous Coronary Artery Dissection and a Family History of Aortic Dissection: A Genetic Association StudyLucy McGrath-Cadell, Stephanie Hesselson, Ingrid Tarr, et al.
American Heart Journal|October 20, 2021
Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genesGillian M Blue, Mauk Mekel, Debjani Das, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
HGG Advances|July 7, 2025
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart diseaseDimuthu Alankarage, Iryna Leshchynska, Stephanie Portelli, et al.
Nature Communications|June 9, 2021
Maternal iron deficiency perturbs embryonic cardiovascular development in miceJacinta I Kalisch-Smith, Nikita Ved, Dorota Szumska, et al.
Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
JACC. Advances|March 22, 2025
Polygenic Inheritance for Common Comorbidities Associated With Congenital Heart DiseaseJamie-Lee M Thompson, Ingrid S Tarr, Emma M Rath, et al.
JAMA Cardiology|January 24, 2024
Polygenic Risk in Families With Spontaneous Coronary Artery DissectionIngrid Tarr, Stephanie Hesselson, Michael Troup, et al.
Journal of the American Heart Association|April 7, 2025
Spontaneous Coronary Artery Dissection and a Family History of Aortic Dissection: A Genetic Association StudyLucy McGrath-Cadell, Stephanie Hesselson, Ingrid Tarr, et al.
American Heart Journal|October 20, 2021
Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genesGillian M Blue, Mauk Mekel, Debjani Das, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
HGG Advances|July 7, 2025
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart diseaseDimuthu Alankarage, Iryna Leshchynska, Stephanie Portelli, et al.
Nature Communications|June 9, 2021
Maternal iron deficiency perturbs embryonic cardiovascular development in miceJacinta I Kalisch-Smith, Nikita Ved, Dorota Szumska, et al.
Circulation. Genomic and Precision Medicine|May 18, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome SequencingIngrid Tarr, Stephanie Hesselson, Siiri E Iismaa, et al.
Pageof 3