Erwin van Wijk

5.2k citations

76 papers · 2.7k · h-index 27

Impact in

Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 5%
- Vestibular and auditory disorders

Papers in

Molecular Biology 52
- Retinal Development and Disorders 24
- RNA regulation and disease 9
- RNA Research and Splicing 8
- Connexins and lens biology 7
- Advanced biosensing and bioanalysis techniques 7
Sensory Systems 27
- Hearing, Cochlea, Tinnitus, Genetics 27

Co-authors: Hannie Kremer (40 shared papers)Ronald Roepman (15 shared papers)Uwe Wolfrum (14 shared papers)Tina Märker (9 shared papers)Frans P.M. Cremers (14 shared papers)Cor W. R. J. Cremers (11 shared papers)Theo Peters (17 shared papers)J. J. M. Meulenberg (3 shared papers)
Journals: Human Molecular Genetics (9 papers)Investigative Ophthalmology & Visual Science (6 papers)Molecular Therapy — Nucleic Acids (5 papers)International Journal of Molecular Sciences (4 papers)The American Journal of Human Genetics (3 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Erwin van Wijk

74 papers receiving 2.7k citations

Peers

Countries citing papers authored by Erwin van Wijk

Since Specialization

Citations

This map shows the geographic impact of Erwin van Wijk'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 Erwin van Wijk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erwin van Wijk more than expected).

Fields of papers citing papers by Erwin van Wijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erwin van Wijk. 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 Erwin van Wijk. The network helps show where Erwin van Wijk may publish in the future.

Co-authors

The 25 scholars most cited alongside Erwin van Wijk, 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 Erwin van Wijk Line = papers co-authored together Erwin van Wijk links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 76 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells Human Molecular Genetics ·Tina Maerker, Erwin van Wijk, Nora Overlack, Ferry F.J. Kersten, JoAnn McGee, Tobias Goldmann, Elisabeth Sehn, Ronald Roepman, Edward J. Walsh, Hannie Kremer, Uwe Wolfrum	2007	194
2	Usher syndrome: molecular links of pathogenesis, proteins and pathways Human Molecular Genetics ·Hannie Kremer, Erwin van Wijk, Tina Märker, Uwe Wolfrum, Ronald Roepman	2006	192
3	Envelope Protein Requirements for the Assembly of Infectious Virions of Porcine Reproductive and Respiratory Syndrome Virus Journal of Virology ·E. H. J. Wissink, M. V. Kroese, Erwin van Wijk, F.A.M. Rijsewijk, J. J. M. Meulenberg, Peter J. M. Rottier	2005	172
4	Identification of 51 Novel Exons of the Usher Syndrome Type 2A (USH2A) Gene That Encode Multiple Conserved Functional Domains and That Are Mutated in Patients with Usher Syndrome Type II The American Journal of Human Genetics ·Erwin van Wijk, Ronald J. E. Pennings, Heleen te Brinke, Annemarie Claassen, Helger G. Yntema, Lies H. Hoefsloot, Frans P.M. Cremers, Cor W. R. J. Cremers, Hannie Kremer	2004	164
5	The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1 Human Molecular Genetics ·Erwin van Wijk, Bert van der Zwaag, Theo Peters, Ulrike Zimmermann, Heleen te Brinke, Ferry F.J. Kersten, Tina Märker, Elena Aller, Lies H. Hoefsloot, Cor W. R. J. Cremers, Frans P.M. Cremers, Uwe Wolfrum, Marlies Knipper, Ronald Roepman, Hannie Kremer	2006	147
6	OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin The American Journal of Human Genetics ·Karlien L. M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock Hock Ngu, Bartłomiej Budny, Erwin van Wijk, Nicholas T. Gorden, Malika Azhimi, Christel Thauvin‐Robinet, Joris A. Veltman, Mireille Boink, Tjitske Kleefstra, Frans P.M. Cremers, Hans van Bokhoven, Arjan P.M. de Brouwer	2009	137
7	Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2 Human Molecular Genetics ·Jan Reiners, Erwin van Wijk, Tina Märker, Ulrike Zimmermann, Karin Jürgens, Heleen te Brinke, Nora Overlack, Ronald Roepman, Marlies Knipper, Hannie Kremer, Uwe Wolfrum	2005	134
8	The major envelope protein, GP5, of a European porcine reproductive and respiratory syndrome virus contains a neutralization epitope in its N-terminal ectodomain Journal of General Virology ·E. H. J. Wissink, Erwin van Wijk, M. V. Kroese, E. Weiland, J. J. M. Meulenberg, Peter J. M. Rottier, Piet A. van Rijn	2003	108
9	Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation Molecular Therapy — Nucleic Acids ·Radulfus WN Slijkerman, Christel Vaché, Margo Dona, Gema García‐García, Mireille Claustres, Lisette Hetterschijt, Theo Peters, Bas P. Hartel, Ronald J. E. Pennings, José M Millan, Elena Aller, Alejandro Garanto, Rob W.J. Collin, Hannie Kremer, Anne‐Françoise Roux, Erwin van Wijk	2016	106
10	A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26) Journal of Medical Genetics ·Erwin van Wijk, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2003	100
11	CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia PLoS Genetics ·Francisco J. Arjona, Jeroen H. F. de Baaij, Karl P. Schlingmann, Anke L. Lameris, Erwin van Wijk, Gert Flik, Sabrina Regele, Georg Christoph Korenke, Birgit Neophytou, Stephan Rust, Nadine Reintjes, Martin Konrad, René J.M. Bindels, Joost G.J. Hoenderop	2014	93
12	The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies Progress in Retinal and Eye Research ·Ralph Slijkerman, Fei Song, Galuh Astuti, Martijn A. Huynen, Erwin van Wijk, Knut Stieger, Rob W.J. Collin	2015	82
13	Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa Ophthalmology ·Laurence Pierrache, Bas P. Hartel, Erwin van Wijk, Magda A. Meester‐Smoor, Frans P.M. Cremers, (unknown), Julie De Zaeytijd, Mary J. van Schooneveld, Cor W. R. J. Cremers, Gislin Dagnelie, Carel B. Hoyng, Arthur A. Bergen, Bart P. Leroy, Ronald J. E. Pennings, L. Ingeborgh van den Born, Caroline C. W. Klaver	2016	67
14	Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction The American Journal of Human Genetics ·Margit Schraders, Jaap Oostrik, P.L.M. Huygen, Tim M. Strom, Erwin van Wijk, Henricus P. M. Kunst, Lies H. Hoefsloot, Cor W. R. J. Cremers, R.J.C. Admiraal, Hannie Kremer	2010	64
15	The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking PLoS Genetics ·Ruxandra Bachmann‐Gagescu, Margo Dona, Lisette Hetterschijt, E.L.G.M. Tonnaer, Theo Peters, Erik de Vrieze, Dorus A. Mans, Sylvia E. C. van Beersum, Ian G. Phelps, Heleen H. Arts, Jan E.E. Keunen, Marius Ueffing, Ronald Roepman, Karsten Boldt, Dan Doherty, Cecilia B. Moens, Stephan C. F. Neuhauss, Hannie Kremer, Erwin van Wijk	2015	59
16	Usherin defects lead to early-onset retinal dysfunction in zebrafish Experimental Eye Research ·Margo Dona, Ralph Slijkerman, Kimberly Lerner, Sanne Broekman, Jeremy Wegner, Taylor Howat, Theo Peters, Lisette Hetterschijt, Nanda Boon, Erik de Vrieze, Nasrin Sorusch, Uwe Wolfrum, Hannie Kremer, Stephan C. F. Neuhauss, Jingjing Zang, Maarten Kamermans, Monte Westerfield, Jennifer B. Phillips, Erwin van Wijk	2018	53
17	Association of Whirlin with Ca_v1.3 (α_1D) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network Investigative Ophthalmology & Visual Science ·Ferry F.J. Kersten, Erwin van Wijk, Jeroen van Reeuwijk, Bert van der Zwaag, Tina Märker, Theo Peters, Nicholas Katsanis, Uwe Wolfrum, Jan E.E. Keunen, Ronald Roepman, Hannie Kremer	2010	47
18	Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11) Human Genetics ·Mirjam W.J. Luijendijk, Erwin van Wijk, Anne M.L.C. Bischoff, Elmar Krieger, P.L.M. Huygen, Ronald J. E. Pennings, Han G. Brunner, Cor W. R. J. Cremers, Frans P.M. Cremers, Hannie Kremer	2004	41
19	A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa Hearing Research ·Bas P. Hartel, Maria Löfgren, P.L.M. Huygen, Iris Guchelaar, Nicole Lo-A-Njoe Kort, Mehdi Sadeghi, Erwin van Wijk, Lisbeth Tranebjærg, Hannie Kremer, William J. Kimberling, Cor W. R. J. Cremers, Claes Möller, Ronald J. E. Pennings	2016	38
20	Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein Human Molecular Genetics ·Erwin van Wijk, Ferry F.J. Kersten, Aileen Kartono, Dorus A. Mans, Kim Brandwijk, Stef J.F. Letteboer, Theo Peters, Tina Märker, Xiumin Yan, Cor W. R. J. Cremers, Frans P.M. Cremers, Uwe Wolfrum, Ronald Roepman, Hannie Kremer	2008	37

About Erwin van Wijk

Erwin van Wijk is a scholar working on Molecular Biology, Sensory Systems, Cell Biology, Genetics and Cellular and Molecular Neuroscience, having authored 76 papers that have together received 2.7k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (27 papers), Retinal Development and Disorders (24 papers), Cellular transport and secretion (9 papers), RNA regulation and disease (9 papers), RNA Research and Splicing (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Connexins and lens biology (7 papers) and Advanced biosensing and bioanalysis techniques (7 papers). The work is most often cited by research in Sensory Systems (815 citations), Neurology (239 citations), Animal Science and Zoology (291 citations), Molecular Biology (1.6k citations) and Genetics (648 citations). Erwin van Wijk has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Hannie Kremer, Ronald Roepman, Uwe Wolfrum, Tina Märker, Frans P.M. Cremers, Cor W. R. J. Cremers, Theo Peters, J. J. M. Meulenberg, Peter J. M. Rottier and E. H. J. Wissink. Their work appears in journals such as Human Molecular Genetics, Investigative Ophthalmology & Visual Science, Molecular Therapy — Nucleic Acids, International Journal of Molecular Sciences and The American Journal of Human Genetics.

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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