Jeroen van Reeuwijk

5.0k citations

20 papers · 1.1k indexed · h-index 14

Genetics top 5%
- Genetic and Kidney Cyst Diseases 7
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 2
Endocrinology top 5%
Cell Biology top 10%
Molecular Biology top 10%
- Protist diversity and phylogeny 3
- Renal and related cancers 3
- Epigenetics and DNA Methylation 2
- Congenital heart defects research 2
Food Science top 10%

Co-authors: Ronald Roepman Brian M. M. Ahmer Fred Heffron T. S. Wallis Patricia R. Watson Heleen H. Arts Dorus A. Mans Hans van Bokhoven
Cited by: Genetics Endocrinology Cell Biology
Journals: Human Molecular Genetics (3 papers)Nature Genetics (2 papers)European Journal of Human Genetics (2 papers)
Partner nations: Netherlands Germany United States

In The Last Decade

Jeroen van Reeuwijk

20 papers receiving 1.1k citations

Peers

Countries citing papers authored by Jeroen van Reeuwijk

Since Specialization

Citations

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

Fields of papers citing papers by Jeroen van Reeuwijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals Nature Medicine ·Alexander J.M. Dingemans,Sandra Jansen,Jeroen van Reeuwijk,Nicole de Leeuw,Rolph Pfundt,Janneke Schuurs-Hoeijmakers,Bregje W.M. van Bon,Carlo Marcelis,Charlotte W. Ockeloen,Marjolein H. Willemsen,Pleuntje J. van der Sluijs,Gijs W.E. Santen,R. Frank Kooy,Anneke T. Vulto‐van Silfhout,Tjitske Kleefstra,David A. Koolen,Lisenka E.L.M. Vissers,Bert B.A. de Vries	2024	4
2	Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants European Journal of Human Genetics ·寛之片桐,Maartje Pennings,T. David Waite,Michael Kwint,Jeroen van Reeuwijk,Jordi Corominas Galbany,Ronald van Beek,Eveline J. Kamping,Moacir Marchiori Filho,Erik‐Jan Kamsteeg,Lonneke Haer‐Wigman,Yaginuma Hideyuki,Susanne Roosing,Christian Gilissen,Hannie Kremer,Han G. Brunner,Helger G. Yntema,Lisenka E.L.M. Vissers	2024	1
3	A complex structural variant near SOX3 causes X-linked split-hand/foot malformation Human Genetics and Genomics Advances ·Elke de Boer,Carlo Marcelis,Kornelia Neveling,Ellen van Beusekom,Alexander Hoischen,Willemijn M. Klein,Nicole de Leeuw,Tuomo Mantere,Uirá Souto Melo,Jeroen van Reeuwijk,Dominique Smeets,Malte Spielmann,Tjitske Kleefstra,Hans van Bokhoven,Lisenka E.L.M. Vissers	2023	1
4	Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disorders Genetics in Medicine ·Alexander J.M. Dingemans,Max Hinne,Sandra Jansen,Jeroen van Reeuwijk,Nicole de Leeuw,Rolph Pfundt,Bregje W.M. van Bon,Anneke T. Vulto‐van Silfhout,Tjitske Kleefstra,David A. Koolen,Marcel van Gerven,Lisenka E.L.M. Vissers,Bert B.A. de Vries	2021	7
5	Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy Pediatric Nephrology ·Marijn F. Stokman,Bert van der Zwaag,Nicole C. A. J. van de Kar,Mieke M. van Haelst,Albertien M. van Eerde,Joost W van der Heijden,Hester Y. Kroes,Elly F. Ippel,Roghyyeh Zakizadeh,Koen L.I. van Gassen,Iris A.L.M. van Rooij,Rachel H. Giles,Philip L. Beales,Ronald Roepman,Heleen H. Arts,Ernie M.H.F. Bongers,Kirsten Y. Renkema,Nine Knoers,Jeroen van Reeuwijk,Marc R. Liliën	2018	17
6	Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signaling Human Molecular Genetics ·Miloš Vojinović,René H. M. te Morsche,Jeroen van Reeuwijk,Nicola Horn,达奇,嬌一小林,Dorus A. Mans,Marius Ueffing,Karsten Boldt,Joost P.H. Drenth,Ronald Roepman	2017	10
7	Elution Profile Analysis of SDS-induced Subcomplexes by Quantitative Mass Spectrometry Molecular & Cellular Proteomics ·Yves Texier,Grischa Toedt,Matteo Gorza,Dorus A. Mans,Jeroen van Reeuwijk,Nicola Horn,Jason R. Willer,Nicholas Katsanis,Ronald Roepman,Toby J. Gibson,Marius Ueffing,Karsten Boldt	2014	24
8	Regulation of E2F1 by the von Hippel–Lindau tumour suppressor protein predicts survival in renal cell cancer patients The Journal of Pathology ·Dorus A. Mans,Joost S.P. Vermaat,Bart Weijts,Ellen van Rooijen,Jeroen van Reeuwijk,Karsten Boldt,Laura G.M. Daenen,Petra van der Groep,Benjamin D. Rowland,Judith Jans,Ronald Roepman,Emile E. Voest,P. J. van Diest,Marianne C. Verhaar,Alain de Bruin,Rachel H. Giles	2013	15
9	The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia SHILAP Revista de lepidopterología ·М.М. Янгляева,Karlien L. M. Coene,Karsten Boldt,C. Christensen,Jeroen van Reeuwijk,Melania del Riego Casado,Emine Bolat,Lude Franke,Lisette Hetterschijt,Sonia Guadalupe Contreras Medina,Adriana Almeira,Heymut Omran,Fpm Cremers,Marius Ueffing,Ronald Roepman	2012	1
10	Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice Journal of Clinical Investigation ·Karsten Boldt,Dorus A. Mans,Jungyeon Won,Jeroen van Reeuwijk,Andreas Vogt,Norbert Kinkl,Stef J.F. Letteboer,Wanda L. Hicks,R.E. Hurd,Jürgen Κ. Naggert,Yves Texier,Anneke I. den Hollander,Robert K. Koenekoop,Serrano Ríos M,Frans P.M. Cremers,Christian Johannes Gloeckner,Patsy M. Nishina,Ronald Roepman,Marius Ueffing	2011	81
11	Scrutinizing ciliopathies by unraveling ciliary interaction networks Human Molecular Genetics ·Jeroen van Reeuwijk,Heleen H. Arts,Ronald Roepman	2011	43
12	The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase Human Molecular Genetics ·Karlien L. M. Coene,Dorus A. Mans,Karsten Boldt,Christian Johannes Gloeckner,Jeroen van Reeuwijk,Emine Bolat,Susanne Roosing,Stef J.F. Letteboer,Theo Peters,Frans P.M. Cremers,Marius Ueffing,Ronald Roepman	2011	52
13	Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome The American Journal of Human Genetics ·Christian Gilissen,Heleen H. Arts,Alexander Hoischen,Liesbeth Spruijt,Dorus A. Mans,Peer Arts,Bart van Lier,Marloes Steehouwer,Jeroen van Reeuwijk,Sarina G. Kant,Ronald Roepman,Nine V.A.M. Knoers,Joris A. Veltman,Han G. Brunner	2010	197
14	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
15	Tandem Affinity Purification of Ciliopathy-Associated Protein Complexes Methods in cell biology ·Karsten Boldt,Jeroen van Reeuwijk,Christian Johannes Gloeckner,Marius Ueffing,Ronald Roepman	2009	14
16	Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 Nature Genetics ·(unknown),Uwe Kornak,Ellen Reynders,Aikaterini Dimopoulou,Jeroen van Reeuwijk,Bjoern Fischer,Anna Rajab,Birgit Budde,Peter Nürnberg,François Foulquier,Dirk J. Lefeber,Zsolt Urbán,海外建設防災協会,Wim Annaert,Han G. Brunner,Hans van Bokhoven,Ron A. Wevers,Éva Morava,Gert Matthijs,Lionel Van Maldergem,Stefan Mundlos	2007	259
17	Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation European Journal of Human Genetics ·Éva Morava,Dirk J. Lefeber,Zsolt Urbán,Linda De Meırleır,Peter Meinecke,H.-R. Chen,Jolanta Sykut‐Cegielska,Michael S. Adamowicz,Ira S. Salafsky,Judith D. Ranells,Emmanuelle Lemyre,Jeroen van Reeuwijk,Han G. Brunner,Ron A. Wevers	2007	47
18	ZNF674: A New Krüppel-Associated Box–Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation The American Journal of Human Genetics ·Dorien Lugtenberg,Helger G. Yntema,Xinru Shen,Astrid Oudakker,Helen V. Firth,Lionel Willatt,Martine Raynaud,Tjitske Kleefstra,Jean‐Pierre Fryns,Hans‐Hilger Ropers,Jamel Chelly,Claude Moraine,Jozef Gécz,Jeroen van Reeuwijk,Sander B. Nabuurs,Bert B.A. de Vries,Ben C.J. Hamel,Arjan P.M. de Brouwer,Hans van Bokhoven	2006	60
19	MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome Nature Genetics ·Hans van Bokhoven,Jacopo Celli,Jeroen van Reeuwijk,Tuula Rinne,Bob Glaudemans,Ellen van Beusekom,Paul N.M.A. Rieu,Ruth Newbury‐Ecob,Chin Chiang,Han G. Brunner	2005	110
20	Salmonella SirA is a global regulator of genes mediating enteropathogenesis Molecular Microbiology ·Brian M. M. Ahmer,Jeroen van Reeuwijk,Patricia R. Watson,T. S. Wallis,Fred Heffron	1999	158

About Jeroen van Reeuwijk

Jeroen van Reeuwijk is a scholar working on Genetics, Developmental Biology, Sensory Systems, Molecular Biology and Endocrinology, having authored 20 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Protist diversity and phylogeny (3 papers), Renal and related cancers (3 papers), Genetic Syndromes and Imprinting (2 papers), Epigenetics and DNA Methylation (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (556 citations), Endocrinology (101 citations), Cell Biology (196 citations), Molecular Biology (739 citations) and Food Science (119 citations). Jeroen van Reeuwijk has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Ronald Roepman, Brian M. M. Ahmer, Fred Heffron, T. S. Wallis, Patricia R. Watson, Heleen H. Arts, Dorus A. Mans, Hans van Bokhoven, Han G. Brunner and Dirk J. Lefeber. Their work appears in journals such as Human Molecular Genetics, Nature Genetics, European Journal of Human Genetics, The American Journal of Human Genetics and Molecular Microbiology.

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