Hennie Bikker

Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism

J.C. Moreno, Hennie Bikker, Marlies Kempers et al. · New England Journal of Medicine · 2002 · 474 citations · Full text

Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers

Aditya Bhonsale, Judith A. Groeneweg, Cynthia A. James et al. · European Heart Journal · 2015 · 423 citations · Full text

The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

Argelia Medeiros‐Domingo, Zahurul A. Bhuiyan, David J. Tester et al. · Journal of the American College of Cardiology · 2009 · 330 citations · Full text

Cardiomyopathy, Electrophysiological Evaluation, Neurophysiology +7

Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury et al. · Journal of the American College of Cardiology · 2011 · 301 citations · Full text

Cardiomyopathy, Heart Failure, Genetic Disorder +6

Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)

Hennie Bikker, Thomas Vulsma, Janine S. E. de Randamie et al. · The Journal of Clinical Endocrinology & Metabolism · 2000 · 182 citations

Mendelian Disorder, Exon 9, Genetic Disorder +13