Hennie Bikker - Concepedia

Author

Hennie Bikker

Amsterdam UMC Location University of Amsterdam

Also Known As

Bikker H, Bikker, Hennie, H Bikker, H. BIKKER, H. Bikker, Hennie Bikker

Publications

Citations

H-Index

Concepts

All Affiliations

Amsterdam UMC Location University of Amsterdam University of Amsterdam University Medical Center Groningen University of Groningen Emma Kinderziekenhuis

About

Hennie Bikker is an author at Amsterdam UMC Location University of Amsterdam specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	1.5K
2	Public Health	5	5	388
3	Natural Sciences	3	3	182
4	Health Sciences	1	1	103
5	Social Sciences	1	1	330

Hennie Bikker

Publications

4.1K

Citations

H-Index

Page 1

	Year	Citations
Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism J.C. Moreno, Hennie Bikker, Marlies Kempers, New England Journal of Medicine	2002	474
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers Aditya Bhonsale, Judith A. Groeneweg, Cynthia A. James, European Heart Journal	2015	423
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, Journal of the American College of Cardiology CardiomyopathyElectrophysiological EvaluationNeurophysiologyPhysiologyDiastolic Function	2009	330
Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury, Journal of the American College of Cardiology CardiomyopathyHeart FailureGenetic DisorderGeneticsMedicine	2011	301
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, The Journal of Clinical Endocrinology & Metabolism Mendelian DisorderExon 9Genetic DisorderIodine Deficiency DisordersGenetics	2000	182
Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia Christian van der Werf, Ineke Nederend, Nynke Hofman, Circulation Arrhythmia and Electrophysiology	2012	168
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death Roddy Walsh, Arnon Adler, Ahmad S. Amin, European Heart Journal	2021	126
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome Saskia M. Maas, Adam Shaw, Hennie Bikker, European Journal of Medical Genetics Tricho-rhino-phalangeal SyndromeGeneticsGenetic EpidemiologyGenetic Disorder	2015	119
A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy Paul A. van der Zwaag, Jan D.H. Jongbloed, Maarten P. van den Berg, Human Mutation CardiomyopathyFunctional GenomicsHereditary CardiomyopathyGeneticsGenetic Variants Database	2009	119
Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele Frank Baas, Hennie Bikker, Gert‐Jan B. van Ommen, Human Genetics Restriction Site PolymorphismUnusual ScarcityAllelic VariantAllergyGenetic Disorder	1984	118

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