Hennie Bikker

5.0k citations

70 papers · 3.0k indexed · h-index 28

Molecular Biology top 5%
Cardiology and Cardiovascular Medicine top 1%
Endocrinology, Diabetes and Metabolism top 1%
Genetics top 5%
Physiology top 10%

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
Topics: Thyroid Disorders and Treatments (21 papers)Cardiac electrophysiology and arrhythmias (14 papers)Cardiovascular Effects of Exercise (13 papers)
Cited by: Cardiology and Cardiovascular Medicine Endocrinology, Diabetes and Metabolism Endocrine and Autonomic Systems
Journals: New England Journal of Medicine Nucleic Acids Research Circulation
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 of co-authors of Hennie Bikker

This figure shows the co-authorship network connecting the top 25 collaborators of Hennie Bikker. A scholar is included among the top collaborators of Hennie Bikker based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hennie Bikker. Hennie Bikker is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical and preclinical insights into high-dose ambroxol therapy for Gaucher disease type 2 and 3: A comprehensive systematic review 2024 ·Molecular Genetics and Metabolism ·(unknown),(unknown),Eleonora L. Swart,Hennie Bikker,Carla E. M. Hollak,Marion M. Brands	4
2	Mild Isolated Congenital Central Hypothyroidism Due to a Novel Homozygous Variant in TSHB : A Case Report 2022 ·Thyroid ·(unknown),Hennie Bikker,Anita Boelen,(unknown),A S Paul van Trotsenburg,Nitash Zwaveling‐Soonawala	0
3	Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance 2022 ·Human Molecular Genetics ·(unknown),Marianne Bootsma,Chai‐Ann Ng,Arthur A.M. Wilde,(unknown),Hennie Bikker,Imke Christiaans,Saskia N. van der Crabben,Janna A. Hol,Tamara T. Koopmann,Jeroen Knijnenburg,(unknown),Jasper J. van der Smagt,Connie R. Bezzina,Jamie I. Vandenberg,Arie O. Verkerk,Daniela Q.C.M. Barge‐Schaapveld,Elisabeth M. Lodder	2
4	A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome 2021 ·Heart Rhythm ·(unknown),(unknown),(unknown),John R. Giudicessi,Dan Ye,Hennie Bikker,Ram K. Rohatgi,David J. Tester,J. Martijn Bos,Arthur A.M. Wilde,Michael J. Ackerman	10
5	Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 2021 ·European Heart Journal ·Roddy Walsh,Arnon Adler,Ahmad S. Amin,Emanuela Abiusi,Melanie Care,Hennie Bikker,(unknown),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	71
6	Defective Levothyroxine Response in a Patient with Dyshormonogenic Congenital Hypothyroidism Caused by a Concurrent Pathogenic Variant in Thyroid Hormone Receptor-β 2021 ·Thyroid ·(unknown),Hennie Bikker,(unknown),Jacquelien J Hillebrand,(unknown),Nitash Zwaveling‐Soonawala,A S Paul van Trotsenburg	3
7	Early Lethal Noncompaction Cardiomyopathy in Siblings With Compound Heterozygous RYR2 Variant 2021 ·Canadian Journal of Cardiology ·(unknown),Annette F. Baas,Catharina M.L. Volker‐Touw,Hennie Bikker,Christian Schroer,Johannes M. P. J. Breur	1
8	Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance 2019 ·Netherlands Heart Journal ·Freyja H.M. van Lint,Olaf R.F. Mook,Mariëlle Alders,Hennie Bikker,Ronald H. Lekanne Deprez,Imke Christiaans	41
9	Long QT Syndrome 2015 ·Mariëlle Alders,Hennie Bikker,Imke Christiaans	13
10	Characterization and treatment of persistent hepatocellular secretory failure 2014 ·Liver International ·Remco van Dijk,Andreas E. Kremer,Wouter L. Smit,(unknown),Thomas van Gulik,Dirk J. Gouma,Johan S. Laméris,Hennie Bikker,(unknown),Pieter Stokkers,(unknown),Piter J. Bosma,Peter L. M. Jansen,Ulrich Beuers	27
11	Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers 2013 ·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	39
12	Genetics and phenomics of hypothyroidism and goiter due to TPO mutations 2010 ·Molecular and Cellular Endocrinology ·Carrie Ris‐Stalpers,Hennie Bikker	92
13	Haplotype sharing test maps genes for familial cardiomyopathies† 2010 ·Clinical Genetics ·(unknown),(unknown),Frans Gerbens,(unknown),(unknown),(unknown),(unknown),Irene M. van Langen,Hennie Bikker,(unknown),Maarten P. van den Berg,Robert M.W. Hofstra,(unknown)	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 2009 ·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	244
15	Maternal Isodisomy for Chromosome 2p Causing Severe Congenital Hypothyroidism 2001 ·The Journal of Clinical Endocrinology & Metabolism ·Egbert Bakker,Hennie Bikker,Raoul C. M. Hennekam,(unknown),(unknown),Thomas Vulsma,Jan J. M. de Vijlder	42
16	Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update) 2000 ·The Journal of Clinical Endocrinology & Metabolism ·Egbert Bakker,Hennie Bikker,Thomas Vulsma,(unknown),Brenda M. Wiedijk,Jan J. M. de Vijlder	120
17	A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect 1999 ·Clinical Endocrinology ·Cecília L. S. Santos,Hennie Bikker,(unknown),(unknown),Marcos Antônio Tambascia,Jan J. M. de Vijlder,Geraldo Medeiros‐Neto	40
18	Congenital hypothyroidism caused by a premature termination signal in exon 10 of the human thyroid peroxidase gene. 1996 ·The Journal of Clinical Endocrinology & Metabolism ·Hennie Bikker,J. J. J. Waelkens,Bert Bravenboer,J J de Vijlder	45
19	Structure and characterization of a 50 bp repeat in intron 10 of the human thyroid peroxidase gene 1992 ·Molecular and Cellular Endocrinology ·Hennie Bikker,Frank Baas,Jan J. M. de Vijlder	4
20	Regional localization of the gene for thyroid peroxidase to human chromosome 2pter→p12 1988 ·Cytogenetic and Genome Research ·Jan J. M. de Vijlder,Christiane Dinsart,Frédérick Libert,(unknown),Hennie Bikker,P. A. Bolhuis,Gilbert Vassart	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) and Cardiovascular Effects of Exercise (13 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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