Michael Troup
Sydney, NSW, Australia
Last Updated: 09/26/2026
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Found 29 publications
Haploinsufficient variants in SMAD5 are associated with isolated congenital heart disease.
Journal: HGG advances
Published: April 28, 2025
Spontaneous Coronary Artery Dissection and a Family History of Aortic Dissection: A Genetic Association Study.
Journal: Journal of the American Heart Association
Published: April 07, 2025
Systematic evaluation of de novo mutation calling tools using whole genome sequencing data.
Journal: Briefings in bioinformatics
Published: January 23, 2025
Polygenic Risk in Families With Dilated Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: September 26, 2024
Polygenic Inheritance for Common Comorbidities Associated With Congenital Heart Disease.
Journal: JACC. Advances
Published: September 04, 2024
Polygenic Risk in Families With Spontaneous Coronary Artery Dissection.
Journal: JAMA cardiology
Published: January 24, 2024
Whole-Brain Electrophysiology and Calcium Imaging in Drosophila during Sleep and Wake.
Journal: Cold Spring Harbor protocols
Published: December 26, 2023
Whole-Brain Calcium Imaging in Drosophila during Sleep and Wake.
Journal: Cold Spring Harbor protocols
Published: December 26, 2023
Neural Ensemble Fragmentation in the Anesthetized Drosophila Brain.
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: August 31, 2022
Insights into the genetic architecture underlying complex, critical congenital heart disease.
Journal: American heart journal
Published: June 29, 2022
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing.
Journal: Circulation. Genomic and precision medicine
Published: May 18, 2022
Last Updated: 09/26/2026