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Plos Genetics|December 14, 2012
Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conductionElisabeth M Lodder, Brendon P Scicluna, Annalisa Milano, et al.
The Journal of Pathology|February 10, 2022
The earliest events in BRAF-mutant colorectal cancer: exome sequencing of sessile serrated lesions with a tiny focus dysplasia or cancer reveals recurring mutations in two distinct progression pathwaysArne Gc Bleijenberg, Joep Eg IJspeert, Jos Bg Mulder, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|December 16, 2020
Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencingJohannes Steinfurt, Connie R Bezzina, Jürgen Biermann, et al.
International Journal of Cardiology|March 7, 2017
Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillationKrystien V Lieve, Arie O Verkerk, Svitlana Podliesna, et al.
Journal of the American Heart Association|July 26, 2017
Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease-Causing MutationChristiaan C Veerman, Isabella Mengarelli, Elisabeth M Lodder, et al.
BMC Public Health|May 12, 2007
Referral patterns of children with poor growth in primary health careFloor K Grote, Wilma Oostdijk, Sabine M P F De Muinck Keizer-Schrama, et al.
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.
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