Erwin van Wijk

5.2k total citations
75 papers, 2.7k citations indexed

About

Erwin van Wijk is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Erwin van Wijk has authored 75 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 28 papers in Sensory Systems and 20 papers in Cell Biology. Recurrent topics in Erwin van Wijk's work include Hearing, Cochlea, Tinnitus, Genetics (28 papers), Retinal Development and Disorders (28 papers) and Cellular transport and secretion (11 papers). Erwin van Wijk is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (28 papers), Retinal Development and Disorders (28 papers) and Cellular transport and secretion (11 papers). Erwin van Wijk collaborates with scholars based in Netherlands, United States and Germany. Erwin van Wijk's co-authors include Hannie Kremer, Ronald Roepman, Uwe Wolfrum, Tina Märker, Frans P.M. Cremers, Cor W. R. J. Cremers, Theo Peters, E. H. J. Wissink, Peter J. M. Rottier and J. J. M. Meulenberg and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Journal of Virology.

In The Last Decade

Erwin van Wijk

72 papers receiving 2.6k 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-authorship network of co-authors of Erwin van Wijk

This figure shows the co-authorship network connecting the top 25 collaborators of Erwin van Wijk. A scholar is included among the top collaborators of Erwin van Wijk 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 Erwin van Wijk. Erwin van Wijk 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	Actigraphy‐based assessment of circadian rhythmicity and sleep in patients with Usher syndrome type 2a: A case–control study 2024 ·Journal of Sleep Research ·(unknown), Juriaan R. Metz, Hildegard Boss, Rob W.J. Collin, Erik de Vrieze, Erwin van Wijk	0
2	RRAGD variants cause cardiac dysfunction in a zebrafish model 2024 ·American Journal of Physiology-Heart and Circulatory Physiology ·(unknown), (unknown), Francisco J. Arjona, Sanne Broekman, Erik de Vrieze, Erwin van Wijk, Joost G.J. Hoenderop, Jeroen H. F. de Baaij	0
3	Generation and Characterization of a Zebrafish Model for ADGRV1-Associated Retinal Dysfunction Using CRISPR/Cas9 Genome Editing Technology 2023 ·Cells ·(unknown), Sanne Broekman, Theo Peters, Hannie Kremer, Erik de Vrieze, Erwin van Wijk	10
4	Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective 2023 ·Journal of Inherited Metabolic Disease ·(unknown), Udo F. H. Engelke, (unknown), (unknown), Jean‐Baptiste Roullet, Sanne Broekman, Erik de Vrieze, Erwin van Wijk, Mirjam M. C. Wamelink, Rafael Artuch, Ivo Barić, Jona Merx, Thomas J. Boltje, (unknown), Michèl A.A.P. Willemsen, Marcel M. Verbeek, Ron A. Wevers, K. Michael Gibson, Karlien L. M. Coene	3
5	A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for USH2A-associated retinitis pigmentosa 2023 ·Molecular Therapy — Nucleic Acids ·(unknown), Sanne Broekman, Theo Peters, (unknown), (unknown), Hanka Venselaar, Hannie Kremer, Erik de Vrieze, Erwin van Wijk	8
6	Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafish 2021 ·Communications Biology ·(unknown), (unknown), Erik de Vrieze, (unknown), Sanne Broekman, Beerend H. J. Winkelman, (unknown), H. Martijn de Gruiter, Erwin van Wijk, Frank Schaeffel, Magda A. Meester‐Smoor, Adam C. Miller, Rob Willemsen, Caroline C. W. Klaver, Adriana I. Iglesias	20
7	Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2 2021 ·Human Genetics ·(unknown), (unknown), (unknown), Gema García‐García, Erwin van Wijk, José M. Millán	28
8	QR-421a, an antisense oligonucleotide, for the treatment of retinitis pigmentosa due to USH2A exon 13 mutations 2019 ·Investigative Ophthalmology & Visual Science ·(unknown), Kalyan Dulla, (unknown), Iris A. Schulkens, Wouter Beumer, (unknown), Cathaline den Besten, Levi C.M. Buil, Janne J. Turunen, (unknown), Sanne Broekman, Erik de Vrieze, Margo Dona, Sílvia Albert, Erwin van Wijk, Peter Adamson	8
9	Usherin defects lead to early-onset retinal dysfunction in zebrafish 2018 ·Experimental Eye Research ·Margo Dona, Ralph Slijkerman, (unknown), Sanne Broekman, Jeremy Wegner, (unknown), Theo Peters, Lisette Hetterschijt, (unknown), 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	51
10	Poor Splice-Site Recognition in a Humanized Zebrafish Knockin Model for the Recurrent Deep-Intronic c.7595-2144A>G Mutation in USH2A 2018 ·Zebrafish ·Ralph Slijkerman, (unknown), Sanne Broekman, Erik de Vrieze, Lisette Hetterschijt, Theo Peters, (unknown), Hannie Kremer, Erwin van Wijk	20
11	Antisense Oligonucleotide-induced Skipping of USH2A exon13 Restores Visual Function in Zebrafish 2017 ·Investigative Ophthalmology & Visual Science ·Erwin van Wijk, Margo Dona, Ralph Slijkerman, Peter Adamson, Janne J. Turunen, Maarten Kamermans, Stephan C. F. Neuhauss, (unknown)	2
12	Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum 2016 ·Scientific Reports ·(unknown), Ideke J.C. Lamers, Miriam Schmidts, Muhammad Ajmal, (unknown), Ehsan Ullah, (unknown), (unknown), (unknown), Bethan E. Hoskins, Erwin van Wijk, Linda Koster‐Kamphuis, Muhammad Imran Khan, Phil Beales, Frans P.M. Cremers, Ronald Roepman, Maleeha Azam, Heleen H. Arts, Raheel Qamar	31
13	Visual Prognosis in USH2A-Associated Retinitis Pigmentosa Is Worse for Patients with Usher Syndrome Type IIa Than for Those with Nonsyndromic Retinitis Pigmentosa 2016 ·Ophthalmology ·(unknown), Bas P. Hartel, Erwin van Wijk, Magda A. Meester‐Smoor, Frans P.M. Cremers, Elfride De Baere, 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	67
14	Nonsyndromic Hearing Loss Caused by USH1G Mutations 2014 ·Ear and Hearing ·(unknown), Ramon A. C. van Huet, (unknown), Jaap Oostrik, Hanka Venselaar, Erwin van Wijk, Andy J. Beynon, Henricus P. M. Kunst, Carel B. Hoyng, Hannie Kremer, Margit Schraders, Ronald J. E. Pennings	20
15	CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia 2014 ·PLoS Genetics ·Francisco J. Arjona, Jeroen H. F. de Baaij, Karl P. Schlingmann, Anke L. Lameris, Erwin van Wijk, Gert Flik, (unknown), Georg Christoph Korenke, Birgit Neophytou, Stephan Rust, (unknown), Martin Konrad, René J.M. Bindels, Joost G.J. Hoenderop	92
16	Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Nora Overlack, (unknown), (unknown), Tina Märker, Hannie Kremer, Erwin van Wijk, Uwe Wolfrum	29
17	MPP1 links the Usher protein network and the Crumbs protein complex in the retina 2007 ·Human Molecular Genetics ·(unknown), Erwin van Wijk, Ferry F.J. Kersten, Elmar Krieger, B. van der Zwaag, Tina Märker, Stef J.F. Letteboer, Simone Dusseljee, Theo Peters, Henk A. Spierenburg, (unknown), Uwe Wolfrum, Frans P.M. Cremers, Hannie Kremer, Ronald Roepman	34
18	The Molecular Arrangement of on Usher Syndrome Protein Network at the Photoreceptor Cilium and Its Role in the Intersegmental Transport in Photoreceptors 2007 ·Investigative Ophthalmology & Visual Science ·Uwe Wolfrum, Nora Overlack, Erwin van Wijk, Boris Reidel, Tobias Goldmann, Ronald Roepman, Hannie Kremer, Tina Märker	1
19	Molecular Linkage Between Usher Syndrome 1 and 2 by Interacting Within Supramolecular Usher Protein Complexes 2005 ·Investigative Ophthalmology & Visual Science ·Uwe Wolfrum, (unknown), Erwin van Wijk, Karin Jürgens, Ronald Roepman, Hannie Kremer, Jan Reiners	1
20	Identification of porcine alveolar macrophage glycoproteins involved in infection of porcine respiratory and reproductive syndrome virus 2003 ·Archives of Virology ·E. H. J. Wissink, Erwin van Wijk, J. M. A. Pol, Gert-Jan Godeke, Piet A. van Rijn, Peter J. M. Rottier, J. J. M. Meulenberg	15

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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