Ruben van ‘t Slot

3.4k total citations
29 papers, 1.5k citations indexed

About

Ruben van ‘t Slot is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Ruben van ‘t Slot has authored 29 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Ruben van ‘t Slot's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Epilepsy research and treatment (4 papers). Ruben van ‘t Slot is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (6 papers) and Epilepsy research and treatment (4 papers). Ruben van ‘t Slot collaborates with scholars based in Netherlands, France and Belgium. Ruben van ‘t Slot's co-authors include Cisca Wijmenga, Ron Hochstenbach, Martin Poot, Isaäc J. Nijman, Christine L. E. Siezen, Barbara Hoebee, Riny Janssen, Tjeerd G. Kimman, Hans C. van Houwelingen and Marieke Ermers and has published in prestigious journals such as PLoS ONE, Stroke and Genome Research.

In The Last Decade

Ruben van ‘t Slot

28 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ruben van ‘t Slot Netherlands	20	580	569	254	220	184	29	1.5k
Rivkah Gonsky United States	22	583 1.0×	837 1.5×	286 1.1×	583 2.6×	84 0.5×	39	2.3k
Theodore B. Moore United States	26	245 0.4×	692 1.2×	320 1.3×	363 1.6×	230 1.3×	99	2.0k
Osama Alsmadi Kuwait	22	462 0.8×	623 1.1×	186 0.7×	204 0.9×	62 0.3×	74	1.6k
Kyuyoung Song South Korea	18	625 1.1×	392 0.7×	310 1.2×	417 1.9×	41 0.2×	55	1.4k
Juan Carlos Jaume United States	29	533 0.9×	745 1.3×	185 0.7×	730 3.3×	111 0.6×	89	3.0k
Luis Benı́tez-Bribiesca Mexico	20	161 0.3×	593 1.0×	195 0.8×	260 1.2×	78 0.4×	65	1.3k
Minyue Dong China	28	248 0.4×	511 0.9×	275 1.1×	537 2.4×	58 0.3×	142	2.1k
Dimitre R. Simeonov United States	15	384 0.7×	922 1.6×	113 0.4×	384 1.7×	115 0.6×	20	1.8k
Ş. Targan United States	19	576 1.0×	316 0.6×	365 1.4×	855 3.9×	73 0.4×	33	1.5k
Nury Steuerwald United States	26	357 0.6×	1.1k 1.9×	219 0.9×	182 0.8×	72 0.4×	86	2.5k

Countries citing papers authored by Ruben van ‘t Slot

Since Specialization

Citations

This map shows the geographic impact of Ruben van ‘t Slot'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 Ruben van ‘t Slot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruben van ‘t Slot more than expected).

Fields of papers citing papers by Ruben van ‘t Slot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ruben van ‘t Slot. 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 Ruben van ‘t Slot. The network helps show where Ruben van ‘t Slot may publish in the future.

Co-authorship network of co-authors of Ruben van ‘t Slot

This figure shows the co-authorship network connecting the top 25 collaborators of Ruben van ‘t Slot. A scholar is included among the top collaborators of Ruben van ‘t Slot 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 Ruben van ‘t Slot. Ruben van ‘t Slot 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

Stevelink, Remi, et al.. (2025). Penetrance of pathogenic epilepsy variants is low and shaped by common genetic background. Epilepsia. 67(3). 1398–1405.

Vriendt, Els De, et al.. (2023). Increased prime edit rates in KCNQ2 and SCN1A via single nicking all-in-one plasmids. BMC Biology. 21(1). 156–156. 7 indexed citations

Lange, Iris, Marco J. Koudijs, Ruben van ‘t Slot, et al.. (2018). Assessment of parental mosaicism in SCN1A-related epilepsy by single-molecule molecular inversion probes and next-generation sequencing. Journal of Medical Genetics. 56(2). 75–80. 18 indexed citations

Jong, Vincent M. de, Arno R. van der Slik, Sandra Laban, et al.. (2016). Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes. Genes and Immunity. 17(6). 342–348. 30 indexed citations

Kovel, Carolien G. F. de, Flip Mulder, Jessica van Setten, et al.. (2016). Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population. PLoS ONE. 11(2). e0146502–e0146502. 5 indexed citations

Hoogstraat, Marlous, Mirjam S. de Pagter, Geert A. Cirkel, et al.. (2013). Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer. Genome Research. 24(2). 200–211. 63 indexed citations

Hochstenbach, Ron, Mariëlle van Gijn, Pieter-Jaap Krijtenburg, et al.. (2012). Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes. Molecular Syndromology. 3(6). 274–283. 7 indexed citations

Daalen, Emma van, Chantal Kemner, Nienke E. Verbeek, et al.. (2011). Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism. Neurogenetics. 12(4). 315–323. 62 indexed citations

Kloosterman, Wigard P., Marlous Hoogstraat, Masoumeh Tavakoli‐Yaraki, et al.. (2011). Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer. Genome biology. 12(10). R103–R103. 161 indexed citations

10.

Manen, Daniëlle van, Olivier Delaneau, Neeltje A. Kootstra, et al.. (2011). Genome-Wide Association Scan in HIV-1-Infected Individuals Identifying Variants Influencing Disease Course. PLoS ONE. 6(7). e22208–e22208. 34 indexed citations

11.

Bol, Sebastiaan, Perry D. Moerland, Sophie Limou, et al.. (2011). Genome-Wide Association Study Identifies Single Nucleotide Polymorphism in DYRK1A Associated with Replication of HIV-1 in Monocyte-Derived Macrophages. PLoS ONE. 6(2). e17190–e17190. 28 indexed citations

12.

Caliebe, Almuth, Hester Y. Kroes, Jasper J. van der Smagt, et al.. (2010). Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene. European Journal of Medical Genetics. 53(4). 179–185. 54 indexed citations

13.

Zwaag, Bert van der, Wouter Staal, Ron Hochstenbach, et al.. (2009). A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(4). 960–966. 80 indexed citations

14.

Poot, Martin, Marc J. Eleveld, Ruben van ‘t Slot, Hans Kristian Ploos van Amstel, & Ron Hochstenbach. (2009). Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex. European Journal of Human Genetics. 18(1). 39–46. 36 indexed citations

15.

Berg, Sophie, Martijn E.T. Dollé, Sandra Imholz, et al.. (2009). Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort study. International Journal of Obesity. 33(10). 1143–1152. 42 indexed citations

16.

Lu, Yingchang, Martijn E.T. Dollé, Sandra Imholz, et al.. (2008). Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations. Journal of Lipid Research. 49(12). 2582–2589. 49 indexed citations

17.

Ruigrok, Ynte M., et al.. (2007). Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms. Stroke. 38(2). 594–594. 13 indexed citations

18.

Janssen, Riny, Louis Bont, Christine L. E. Siezen, et al.. (2007). Genetic Susceptibility to Respiratory Syncytial Virus Bronchiolitis Is Predominantly Associated with Innate Immune Genes. The Journal of Infectious Diseases. 196(6). 826–834. 221 indexed citations

19.

Wapenaar, Martin C., Alienke J. Monsuur, Jos B. Poell, et al.. (2007). The SPINK gene family and celiac disease susceptibility. Immunogenetics. 59(5). 349–57. 42 indexed citations

20.

Smith, Hilde E., et al.. (2000). The cps locus of Streptococcus suis serotype 2: genetic determinant for the synthesis of sialic acid. Microbial Pathogenesis. 29(2). 127–134. 52 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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