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Clinical Genetics|March 1, 2024
Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardiaCaroline Pham, Tamara T Koopmann, Jeffrey M Vinocur, et al.
Circulation. Cardiovascular Genetics|January 24, 2016
Sudden Cardiac Arrest and Rare Genetic Variants in the CommunityAnnalisa Milano, Marieke T Blom, Elisabeth M Lodder, et al.
Disease Models & Mechanisms|June 19, 2019
Genetic variation in GNB5 causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (IK,ACh)Christiaan C Veerman, Isabella Mengarelli, Charlotte D Koopman, et al.
JAMA Network Open|January 25, 2023
Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in DenmarkCharlotte Glinge, Sára Rossetti, Louise Bruun Oestergaard, et al.
Circulation Research|June 23, 2017
The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical HeterogeneityChristiaan C Veerman, Svitlana Podliesna, Rafik Tadros, et al.
Plos One|May 22, 2014
Genome-wide identification of expression quantitative trait loci (eQTLs) in human heartTamara T Koopmann, Michiel E Adriaens, Perry D Moerland, et al.
Plos One|November 17, 2020
Histological, immunohistochemical and transcriptomic characterization of human tracheoesophageal fistulasErwin Brosens, Janine F Felix, Anne Boerema-de Munck, et al.
Open Heart|February 6, 2021
Discovery of predictors of sudden cardiac arrest in diabetes: rationale and outline of the RESCUED (REcognition of Sudden Cardiac arrest vUlnErability in Diabetes) projectLaura H van Dongen, Peter P Harms, Mark Hoogendoorn, et al.
American Journal of Medical Genetics. Part A|July 14, 2019
GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumDoris Škorić-Milosavljević, Fleur V Y Tjong, Julien Barc, et al.
Heart Rhythm|July 17, 2018
Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)Svitlana Podliesna, Julian Delanne, Lindsey Miller, et al.
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