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Scientific Reports|July 28, 2018
Identification of an INa-dependent and Ito-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patientDongrui Ma, Zhenfeng Liu, Li Jun Loh, et al.
Circulation|July 10, 2019
Widespread Translational Control of Fibrosis in the Human Heart by RNA-Binding ProteinsSonia Chothani, Sebastian Schäfer, Eleonora Adami, et al.
Nature Genetics|January 26, 2021
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effectRafik Tadros, Catherine Francis, Xiao Xu, et al.
Nature Communications|August 11, 2019
WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalingHuimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
Nature Communications|September 11, 2019
Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalingHuimei Chen, Aida Moreno-Moral, Francesco Pesce, et al.
Science (New York, N.Y.)|December 21, 2019
Potassium channel dysfunction in human neuronal models of Angelman syndromeAlfred Xuyang Sun, Qiang Yuan, Masahiro Fukuda, et al.
Circulation. Cardiovascular Genetics|July 16, 2015
ZBTB17 (MIZ1) Is Important for the Cardiac Stress Response and a Novel Candidate Gene for Cardiomyopathy and Heart FailureByambajav Buyandelger, Catherine Mansfield, Sawa Kostin, et al.
European Journal of Human Genetics : EJHG|September 20, 2019
The yield of postmortem genetic testing in sudden death cases with structural findings at autopsyNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.
Journal of the American College of Cardiology|April 29, 2017
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death SyndromeNajim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, et al.
Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.
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