Ronald Roepman

13.9k total citations · 2 hit papers
92 papers, 5.6k citations indexed

About

Ronald Roepman is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Ronald Roepman has authored 92 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 52 papers in Genetics and 35 papers in Cell Biology. Recurrent topics in Ronald Roepman's work include Genetic and Kidney Cyst Diseases (44 papers), Retinal Development and Disorders (38 papers) and Cellular transport and secretion (20 papers). Ronald Roepman is often cited by papers focused on Genetic and Kidney Cyst Diseases (44 papers), Retinal Development and Disorders (38 papers) and Cellular transport and secretion (20 papers). Ronald Roepman collaborates with scholars based in Netherlands, Germany and United States. Ronald Roepman's co-authors include Anneke I. den Hollander, Frans P.M. Cremers, Robert K. Koenekoop, Uwe Wolfrum, Erwin van Wijk, Hannie Kremer, Rob W.J. Collin, Carel B. Hoyng, Tina Märker and Caroline C. W. Klaver and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Ronald Roepman

91 papers receiving 5.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Non-syndromic retinitis pigmentosa

2018 627 citations Camiel J. F. Boon, Anneke I. den Hollander et al. profile →
Leber congenital amaurosis: Genes, proteins and disease mechanisms

2008 603 citations Anneke I. den Hollander, Ronald Roepman et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Ronald Roepman	4.8k	2.1k	1.3k	1.2k	702	92	5.6k
Tiansen Li	8.1k 1.7×	3.0k 1.5×	1.8k 1.3×	1.9k 1.6×	1.8k 2.5×	108	10.1k
Robert K. Koenekoop	4.5k 0.9×	1.3k 0.6×	2.4k 1.8×	647 0.6×	748 1.1×	119	5.2k
Josseline Kaplan	6.9k 1.5×	1.4k 0.7×	2.6k 1.9×	1.0k 0.9×	911 1.3×	172	9.0k
Charles Searby	3.9k 0.8×	2.8k 1.4×	918 0.7×	934 0.8×	927 1.3×	86	5.8k
Anthony T. Moore	5.9k 1.2×	1.6k 0.8×	2.3k 1.7×	729 0.6×	643 0.9×	107	8.0k
Jean‐Michel Rozet	3.8k 0.8×	1.2k 0.6×	1.8k 1.3×	500 0.4×	654 0.9×	120	4.5k
Philip M. Smallwood	5.4k 1.1×	1.1k 0.5×	576 0.4×	879 0.7×	1.2k 1.8×	52	6.5k
Elise Héon	5.1k 1.1×	1.7k 0.8×	3.9k 2.9×	833 0.7×	775 1.1×	144	7.3k
Rob W.J. Collin	4.5k 0.9×	986 0.5×	1.8k 1.3×	604 0.5×	758 1.1×	138	5.1k
Valeria Marigo	4.3k 0.9×	1.1k 0.5×	658 0.5×	638 0.5×	791 1.1×	88	5.0k

Countries citing papers authored by Ronald Roepman

Since Specialization

Citations

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

Fields of papers citing papers by Ronald Roepman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ronald Roepman. 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 Ronald Roepman. The network helps show where Ronald Roepman may publish in the future.

Co-authorship network of co-authors of Ronald Roepman

This figure shows the co-authorship network connecting the top 25 collaborators of Ronald Roepman. A scholar is included among the top collaborators of Ronald Roepman 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 Ronald Roepman. Ronald Roepman 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

Stecker, Kelly E., et al.. (2025). A network of interacting ciliary tip proteins with opposing activities imparts slow and processive microtubule growth. Nature Structural & Molecular Biology. 32(6). 979–994. 7 indexed citations

Athanasiou, Dimitra, Katarina Jovanović, Karsten Boldt, et al.. (2025). Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoids. Acta Neuropathologica Communications. 13(1). 26–26. 3 indexed citations

Haer‐Wigman, Lonneke, Ralph J. Florijn, Ronald van Beek, et al.. (2024). Utilization of automated cilia analysis to characterize novel INPP5E variants in patients with non-syndromic retinitis pigmentosa. European Journal of Human Genetics. 32(11). 1412–1418. 1 indexed citations

Nigro, Elisa Agnese, Laura Cassina, Christine Podrini, et al.. (2023). Primary cilia sense glutamine availability and respond via asparagine synthetase. Nature Metabolism. 5(3). 385–397. 20 indexed citations

Schoenmaker, Chantal, et al.. (2023). Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9. Stem Cell Research. 68. 103053–103053. 2 indexed citations

Mercey, Olivier, Katrin Junger, Alejandro Garanto, et al.. (2023). Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme. JCI Insight. 8(10). 13 indexed citations

Letteboer, Stef J.F., Katrin Junger, Rossano Butcher, et al.. (2023). PDE6D Mediates Trafficking of Prenylated Proteins NIM1K and UBL3 to Primary Cilia. Cells. 12(2). 312–312. 8 indexed citations

Aslanyan, Mariam G., Gaurav D. Diwan, Zeinab Anvarian, et al.. (2023). A targeted multi-proteomics approach generates a blueprint of the ciliary ubiquitinome. Frontiers in Cell and Developmental Biology. 11. 1113656–1113656. 13 indexed citations

Corral-Serrano, Julio C., et al.. (2021). A look into retinal organoids: methods, analytical techniques, and applications. Cellular and Molecular Life Sciences. 78(19-20). 6505–6532. 63 indexed citations

10.

Frikstad, Kari‐Anne M., Elisa Molinari, Marianne Thoresen, et al.. (2019). A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling. Cell Reports. 28(7). 1907–1922.e6. 31 indexed citations

11.

Vriend, Jelle, Janny G.P. Peters, Tom T.G. Nieskens, et al.. (2019). Flow stimulates drug transport in a human kidney proximal tubule-on-a-chip independent of primary cilia. Biochimica et Biophysica Acta (BBA) - General Subjects. 1864(1). 129433–129433. 58 indexed citations

12.

Falk, Nathalie, Kristin Kessler, Karsten Boldt, et al.. (2018). Functional analyses of Pericentrin and Syne-2 interaction in ciliogenesis. Journal of Cell Science. 131(16). 8 indexed citations

13.

Letteboer, Stef J.F., et al.. (2015). Investigating the role of C2orf71 in the pathogenesis of retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 56(7). 4643–4643. 1 indexed citations

14.

Wolfrum, Uwe, et al.. (2014). Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis. Investigative Ophthalmology & Visual Science. 55(13). 6016–6016. 1 indexed citations

15.

Roosing, Susanne, Klaus Rohrschneider, Avigail Beryozkin, et al.. (2013). Mutations in RAB28, Encoding a Farnesylated Small GTPase, Are Associated with Autosomal-Recessive Cone-Rod Dystrophy. The American Journal of Human Genetics. 93(1). 110–117. 67 indexed citations

16.

Boldt, Karsten, Dorus A. Mans, Jungyeon Won, et al.. (2011). Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. Journal of Clinical Investigation. 121(6). 2169–2180. 81 indexed citations

17.

Boldt, Karsten, Jeroen van Reeuwijk, Christian Johannes Gloeckner, Marius Ueffing, & Ronald Roepman. (2009). Tandem Affinity Purification of Ciliopathy-Associated Protein Complexes. Methods in cell biology. 91. 143–160. 14 indexed citations

18.

Wijk, Erwin van, Ferry F.J. Kersten, Elmar Krieger, et al.. (2007). MPP1 links the Usher protein network and the Crumbs protein complex in the retina. Human Molecular Genetics. 16(16). 1993–2003. 34 indexed citations

19.

Wolfrum, Uwe, Nora Overlack, Erwin van Wijk, et al.. (2007). The Molecular Arrangement of on Usher Syndrome Protein Network at the Photoreceptor Cilium and Its Role in the Intersegmental Transport in Photoreceptors. Investigative Ophthalmology & Visual Science. 48(13). 3066–3066. 1 indexed citations

20.

Wolfrum, Uwe, Erwin van Wijk, Karin Jürgens, et al.. (2005). Molecular Linkage Between Usher Syndrome 1 and 2 by Interacting Within Supramolecular Usher Protein Complexes. Investigative Ophthalmology & Visual Science. 46(13). 5173–5173. 1 indexed citations

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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