Jeroen Schoots

2.1k total citations
14 papers, 854 citations indexed

About

Jeroen Schoots is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jeroen Schoots has authored 14 papers receiving a total of 854 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jeroen Schoots's work include Ion Transport and Channel Regulation (3 papers), Renal Diseases and Glomerulopathies (3 papers) and Tracheal and airway disorders (3 papers). Jeroen Schoots is often cited by papers focused on Ion Transport and Channel Regulation (3 papers), Renal Diseases and Glomerulopathies (3 papers) and Tracheal and airway disorders (3 papers). Jeroen Schoots collaborates with scholars based in Netherlands, United Kingdom and United States. Jeroen Schoots's co-authors include Lies H. Hoefsloot, Ernie M.H.F. Bongers, Nicole Janssen, Conny M.A. van Ravenswaaij‐Arts, Jorieke E. H. Bergman, Lisbeth Tranebjærg, Robert M.W. Hofstra, Hans van Bokhoven, Nine V.A.M. Knoers and Marianne Lodahl and has published in prestigious journals such as Journal of the American Society of Nephrology, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

Jeroen Schoots

14 papers receiving 847 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jeroen Schoots Netherlands	11	451	281	244	210	120	14	854
Sı̇bel Aylı̇n Uğur İşerı̇ Türkiye	13	283 0.6×	218 0.8×	74 0.3×	146 0.7×	40 0.3×	39	690
Christel Thauvin‐Robinet France	21	762 1.7×	532 1.9×	101 0.4×	106 0.5×	166 1.4×	80	1.4k
Raoul Heller Germany	20	1.1k 2.3×	374 1.3×	719 2.9×	84 0.4×	329 2.7×	37	1.5k
Sumita Danda India	16	489 1.1×	269 1.0×	59 0.2×	88 0.4×	70 0.6×	122	1.0k
Naoya Morisada Japan	16	357 0.8×	186 0.7×	86 0.4×	89 0.4×	119 1.0×	62	726
Yuichi Kawagashira Japan	23	665 1.5×	123 0.4×	158 0.6×	149 0.7×	74 0.6×	62	1.7k
Rodger Palmer United Kingdom	13	397 0.9×	494 1.8×	78 0.3×	105 0.5×	76 0.6×	20	915
Vassos Neocleous Cyprus	15	444 1.0×	261 0.9×	60 0.2×	38 0.2×	62 0.5×	61	728
A Seller United Kingdom	15	940 2.1×	797 2.8×	61 0.3×	63 0.3×	100 0.8×	24	1.7k
Nicholas W. Chavkin United States	11	251 0.6×	116 0.4×	60 0.2×	68 0.3×	67 0.6×	29	620

Countries citing papers authored by Jeroen Schoots

Since Specialization

Citations

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

Fields of papers citing papers by Jeroen Schoots

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeroen Schoots

This figure shows the co-authorship network connecting the top 25 collaborators of Jeroen Schoots. A scholar is included among the top collaborators of Jeroen Schoots 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 Jeroen Schoots. Jeroen Schoots is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Rood, Ilse M., Eric Steenbergen, Brigith Willemsen, et al.. (2023). Kidney Disease Associated With Mono-allelic COL4A3 and COL4A4 Variants: A Case Series of 17 Families. Kidney Medicine. 5(4). 100607–100607. 1 indexed citations

Snoeijen‐Schouwenaars, Francesca M., Judith Verhoeven, Petra van Mierlo, et al.. (2018). Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability. Epilepsia. 60(1). 155–164. 60 indexed citations

Bongers, Ernie M.H.F., Luke M. Shelton, Susanne Milatz, et al.. (2017). A Novel Hypokalemic-Alkalotic Salt-Losing Tubulopathy in Patients with CLDN10 Mutations. Journal of the American Society of Nephrology. 28(10). 3118–3128. 44 indexed citations

Hillen, Lisa M., Jeroen Schoots, A.T.M.G. Tiebosch, et al.. (2016). Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome. Fetal and Pediatric Pathology. 35(2). 112–119. 3 indexed citations

Munnik, Sonja A. de, Jolt Roukema, Jeroen Schoots, et al.. (2015). Meier-Gorlin syndrome. Orphanet Journal of Rare Diseases. 10(1). 114–114. 58 indexed citations

Blok, Lot Snijders, Nicole Corsten‐Janssen, David Fitzpatrick, et al.. (2014). Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypes. American Journal of Medical Genetics Part A. 164(11). 2843–2848. 6 indexed citations

Hofstra, Julia M., Sergio Laínez, Jeroen Schoots, et al.. (2013). New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis. Nephrology Dialysis Transplantation. 28(7). 1830–1838. 40 indexed citations

Munnik, Sonja A. de, Sixto García‐Miñáur, Alexander Hoischen, et al.. (2013). A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome. European Journal of Human Genetics. 22(6). 844–846. 36 indexed citations

Bergman, Jorieke E. H., Nicole Janssen, Almer M. van der Sloot, et al.. (2012). A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome. Human Mutation. 33(8). 1251–1260. 50 indexed citations

10.

Janssen, Nicole, Jorieke E. H. Bergman, Morris A. Swertz, et al.. (2012). Mutation update on the CHD7 gene involved in CHARGE syndrome. Human Mutation. 33(8). 1149–1160. 176 indexed citations

11.

Willemsen, Marjolein H., Lisenka E.L.M. Vissers, Michèl A.A.P. Willemsen, et al.. (2012). Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects. Journal of Medical Genetics. 49(3). 179–183. 123 indexed citations

12.

Glaudemans, Bob, Helger G. Yntema, Pedro San‐Cristobal, et al.. (2011). Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome. European Journal of Human Genetics. 20(3). 263–270. 57 indexed citations

13.

Bongers, Ernie M.H.F., F.T.M. Huysmans, Elena Levtchenko, et al.. (2005). Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy. European Journal of Human Genetics. 13(8). 935–946. 87 indexed citations

14.

Bongers, Ernie M.H.F., Pascal H. G. Duijf, Sylvia E. C. van Beersum, et al.. (2004). Mutations in the Human TBX4 Gene Cause Small Patella Syndrome. The American Journal of Human Genetics. 74(6). 1239–1248. 113 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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