Hennie Bikker

5.0k citations

70 papers · 3.0k indexed · h-index 28

Cardiology and Cardiovascular Medicine top 1%
- Cardiac electrophysiology and arrhythmias 14
- Cardiovascular Effects of Exercise 13
- Cardiomyopathy and Myosin Studies 8
Endocrinology, Diabetes and Metabolism top 1%
- Thyroid Disorders and Treatments 21
Endocrine and Autonomic Systems top 5%
Orthopedics and Sports Medicine top 5%
- Sports injuries and prevention 8
Molecular Biology top 5%
- Ion channel regulation and function 11
- Congenital heart defects research 5
Pediatrics, Perinatology and Child Health
- Neonatal Health and Biochemistry 6

Co-authors: Jan J. M. de Vijlder Frank Baas Thomas Vulsma Carrie Ris‐Stalpers J. Peter van Tintelen Arthur A.M. Wilde Michael J. Ackerman A S Paul van Trotsenburg
Cited by: Cardiology and Cardiovascular Medicine Endocrinology, Diabetes and Metabolism Endocrine and Autonomic Systems
Journals: New England Journal of Medicine (1 paper)Nucleic Acids Research (2 papers)Circulation (1 paper)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Hennie Bikker

68 papers receiving 2.9k citations

Peers

Countries citing papers authored by Hennie Bikker

Since Specialization

Citations

This map shows the geographic impact of Hennie Bikker's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hennie Bikker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hennie Bikker more than expected).

Fields of papers citing papers by Hennie Bikker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hennie Bikker. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hennie Bikker. The network helps show where Hennie Bikker may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hennie Bikker, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hennie Bikker Line = papers co-authored together Hennie Bikker links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical and preclinical insights into high-dose ambroxol therapy for Gaucher disease type 2 and 3: A comprehensive systematic review Molecular Genetics and Metabolism ·Bibiche den Hollander,Hoang Lan Le,Eleonora L. Swart,Hennie Bikker,Carla E. M. Hollak,Marion M. Brands	2024	4
2	Mild Isolated Congenital Central Hypothyroidism Due to a Novel Homozygous Variant in TSHB : A Case Report Thyroid ·Peter Lauffer,Hennie Bikker,Anita Boelen,Jasper J. Jöbsis,A S Paul van Trotsenburg,Nitash Zwaveling‐Soonawala	2022	0
3	Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance Human Molecular Genetics ·Jaël S. Copier,Marianne Bootsma,Chai‐Ann Ng,Arthur A.M. Wilde,Robin A. Bertels,Hennie Bikker,Imke Christiaans,Saskia N. van der Crabben,Janna A. Hol,Tamara T. Koopmann,Jeroen Knijnenburg,Aafke A J Lommerse,Jasper J. van der Smagt,Connie R. Bezzina,Jamie I. Vandenberg,Arie O. Verkerk,Daniela Q.C.M. Barge‐Schaapveld,Elisabeth M. Lodder	2022	2
4	A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome Heart Rhythm ·Sahej Bains,Steven M. Dotzler,Christian Krijger,John R. Giudicessi,Dan Ye,Hennie Bikker,Ram K. Rohatgi,David J. Tester,J. Martijn Bos,Arthur A.M. Wilde,Michael J. Ackerman	2021	10
5	Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death European Heart Journal ·Roddy Walsh,Arnon Adler,Ahmad S. Amin,Emanuela Abiusi,Melanie Care,Hennie Bikker,Simona Amenta,Harriet Feilotter,Eline A. Nannenberg,Francesco Mazzarotto,Valentina Trevisan,John Garcia,Ray E. Hershberger,Marco Pérez,Amy C. Sturm,James S. Ware,Wojciech Zaręba,Valeria Novelli,Arthur A.M. Wilde,Michael H. Gollob	2021	71
6	Defective Levothyroxine Response in a Patient with Dyshormonogenic Congenital Hypothyroidism Caused by a Concurrent Pathogenic Variant in Thyroid Hormone Receptor-β Thyroid ·Peter Lauffer,Hennie Bikker,Mark R. Garrelfs,Jacquelien J Hillebrand,Marie-Louise C.S. de Sonnaville,Nitash Zwaveling‐Soonawala,A S Paul van Trotsenburg	2021	3
7	Early Lethal Noncompaction Cardiomyopathy in Siblings With Compound Heterozygous RYR2 Variant Canadian Journal of Cardiology ·Jantiene C. Duvekot,Annette F. Baas,Catharina M.L. Volker‐Touw,Hennie Bikker,Christian Schroer,Johannes M. P. J. Breur	2021	1
8	Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance Netherlands Heart Journal ·Freyja H.M. van Lint,Olaf R.F. Mook,Mariëlle Alders,Hennie Bikker,Ronald H. Lekanne Deprez,Imke Christiaans	2019	41
9	Long QT Syndrome Mariëlle Alders,Hennie Bikker,Imke Christiaans	2015	13
10	Characterization and treatment of persistent hepatocellular secretory failure Liver International ·Remco van Dijk,Andreas E. Kremer,Wouter L. Smit,Bram van den Elzen,Thomas van Gulik,Dirk J. Gouma,Johan S. Laméris,Hennie Bikker,Valentine Enemuo,Pieter Stokkers,Mark Feist,Piter J. Bosma,Peter L. M. Jansen,Ulrich Beuers	2014	27
11	Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers The American Journal of Cardiology ·Judith A. Groeneweg,Paul A. van der Zwaag,Louise R.A. Olde Nordkamp,Hennie Bikker,Jan D.H. Jongbloed,Roselie Jongbloed,Ans C.P. Wiesfeld,Moniek G.P.J. Cox,Jeroen F. van der Heijden,Douwe E. Atsma,Karin Boer,Pieter A. Doevendans,Aryan Vink,Toon A.B. van Veen,Dennis Dooijes,Maarten P. van den Berg,Arthur A.M. Wilde,J. Peter van Tintelen,Richard N.W. Hauer	2013	39
12	Genetics and phenomics of hypothyroidism and goiter due to TPO mutations Molecular and Cellular Endocrinology ·Carrie Ris‐Stalpers,Hennie Bikker	2010	92
13	Haplotype sharing test maps genes for familial cardiomyopathies† Clinical Genetics ·P. van der Zwaag,JP van Tintelen,Frans Gerbens,JDH Jongbloed,LG Boven,JJ van der Smagt,WP van der Roest,Irene M. van Langen,Hennie Bikker,RNW Hauer,Maarten P. van den Berg,Robert M.W. Hofstra,GJ te Meerman	2010	7
14	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 Journal of the American College of Cardiology ·Argelia Medeiros‐Domingo,Zahurul A. Bhuiyan,David J. Tester,Nynke Hofman,Hennie Bikker,J. Peter van Tintelen,Marcel M. A. M. Mannens,Arthur A.M. Wilde,Michael J. Ackerman	2009	244
15	Maternal Isodisomy for Chromosome 2p Causing Severe Congenital Hypothyroidism The Journal of Clinical Endocrinology & Metabolism ·Egbert Bakker,Hennie Bikker,Raoul C. M. Hennekam,Ed J. P. Lommen,M. Schipper,Thomas Vulsma,Jan J. M. de Vijlder	2001	42
16	Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update) The Journal of Clinical Endocrinology & Metabolism ·Egbert Bakker,Hennie Bikker,Thomas Vulsma,Janine S. E. de Randamie,Brenda M. Wiedijk,Jan J. M. de Vijlder	2000	120
17	A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect Clinical Endocrinology ·Cecília L. S. Santos,Hennie Bikker,Katia G. M. Rego,Antonio C. Nascimento,Marcos Antônio Tambascia,Jan J. M. de Vijlder,Geraldo Medeiros‐Neto	1999	40
18	Congenital hypothyroidism caused by a premature termination signal in exon 10 of the human thyroid peroxidase gene. The Journal of Clinical Endocrinology & Metabolism ·Hennie Bikker,J. J. J. Waelkens,Bert Bravenboer,J J de Vijlder	1996	45
19	Structure and characterization of a 50 bp repeat in intron 10 of the human thyroid peroxidase gene Molecular and Cellular Endocrinology ·Hennie Bikker,Frank Baas,Jan J. M. de Vijlder	1992	4
20	Regional localization of the gene for thyroid peroxidase to human chromosome 2pter→p12 Cytogenetic and Genome Research ·Jan J. M. de Vijlder,Christiane Dinsart,Frédérick Libert,Geurts van Kessel,Hennie Bikker,P. A. Bolhuis,Gilbert Vassart	1988	27

About Hennie Bikker

Hennie Bikker is a scholar working on Endocrinology, Diabetes and Metabolism, Cardiology and Cardiovascular Medicine and Orthopedics and Sports Medicine, having authored 70 papers that have together received 3.0k indexed citations. Recurring topics across this work include Thyroid Disorders and Treatments (21 papers), Cardiac electrophysiology and arrhythmias (14 papers), Cardiovascular Effects of Exercise (13 papers), Ion channel regulation and function (11 papers), Cardiomyopathy and Myosin Studies (8 papers), Sports injuries and prevention (8 papers), Neonatal Health and Biochemistry (6 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.3k citations), Endocrinology, Diabetes and Metabolism (943 citations) and Endocrine and Autonomic Systems (185 citations). Hennie Bikker has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Jan J. M. de Vijlder, Frank Baas, Thomas Vulsma, Carrie Ris‐Stalpers, J. Peter van Tintelen, Arthur A.M. Wilde, Michael J. Ackerman, A S Paul van Trotsenburg, Marlies Kempers and J.C. Moreno. Their work appears in journals such as New England Journal of Medicine, Nucleic Acids Research and Circulation.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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