Jeroen Schoots

2.1k citations

14 papers · 854 indexed · h-index 11

Molecular Biology
Genetics top 10%
Genetics top 5%
Pulmonary and Respiratory Medicine top 10%
Surgery

Co-authors: Lies H. Hoefsloot Ernie M.H.F. Bongers Nicole Janssen Jorieke E. H. Bergman Conny M.A. van Ravenswaaij‐Arts Lisbeth Tranebjærg Robert M.W. Hofstra Hans van Bokhoven
Topics: Ion Transport and Channel Regulation (3 papers)Renal Diseases and Glomerulopathies (3 papers)Tracheal and airway disorders (3 papers)
Cited by: Genetics Nephrology
Journals: Journal of the American Society of Nephrology The American Journal of Human Genetics Epilepsia
Partner nations: Netherlands United Kingdom Denmark

In The Last Decade

Jeroen Schoots

14 papers receiving 847 citations

Peers

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

#	Work	Indexed citations
1	Kidney Disease Associated With Mono-allelic COL4A3 and COL4A4 Variants: A Case Series of 17 Families 2023 ·Kidney Medicine ·(unknown),Ilse M. Rood,Eric Steenbergen,Brigith Willemsen,Henry Dijkman,Michel van Geel,Jeroen Schoots,Jack F.M. Wetzels,Dorien Lugtenberg,Jeroen K. Deegens,Ernie M.H.F. Bongers	1
2	Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability 2018 ·Epilepsia ·Francesca M. Snoeijen‐Schouwenaars,(unknown),Judith Verhoeven,Petra van Mierlo,Hilde M. H. Braakman,Eric Smeets,Joost Nicolai,Jeroen Schoots,(unknown),Rob P.W. Rouhl,Francis Tan,Helger G. Yntema,Han G. Brunner,Rolph Pfundt,Alexander P.A. Stegmann,Erik‐Jan Kamsteeg,Helenius J. Schelhaas,Marjolein H. Willemsen	60
3	A Novel Hypokalemic-Alkalotic Salt-Losing Tubulopathy in Patients with CLDN10 Mutations 2017 ·Journal of the American Society of Nephrology ·Ernie M.H.F. Bongers,Luke M. Shelton,Susanne Milatz,Sjoerd Verkaart,Anneke Bech,Jeroen Schoots,Elisabeth A. M. Cornelissen,Markus Bleich,Joost G.J. Hoenderop,Jack F.M. Wetzels,Dorien Lugtenberg,Tom Nijenhuis	44
4	Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome 2016 ·Fetal and Pediatric Pathology ·Lisa M. Hillen,(unknown),Jeroen Schoots,A.T.M.G. Tiebosch,Ernst‐Jan M. Speel,Guido M.J.M. Roemen,(unknown),Constance T. R. M. Stumpel	3
5	Meier-Gorlin syndrome 2015 ·Orphanet Journal of Rare Diseases ·Sonja A. de Munnik,(unknown),Jolt Roukema,Jeroen Schoots,Nine Knoers,Han G. Brunner,Andrew P. Jackson,Ernie M.H.F. Bongers	58
6	Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypes 2014 ·American Journal of Medical Genetics Part A ·Lot Snijders Blok,Nicole Corsten‐Janssen,David Fitzpatrick,Corrado Romano,Marco Fichera,Girolamo Aurelio Vitello,Marjolein H. Willemsen,Jeroen Schoots,Rolph Pfundt,Conny M.A. van Ravenswaaij‐Arts,Lies H. Hoefsloot,Tjitske Kleefstra	6
7	New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis 2013 ·Nephrology Dialysis Transplantation ·Julia M. Hofstra,Sergio Laínez,(unknown),Jeroen Schoots,Marijke Baltissen,Lies H. Hoefsloot,Nine V.A.M. Knoers,Jo H. M. Berden,René J.M. Bindels,Johan van der Vlag,Joost G.J. Hoenderop,Jack F.M. Wetzels,Tom Nijenhuis	40
8	A de novo non-sense mutation in ZBTB18 in a patient with features of the 1q43q44 microdeletion syndrome 2013 ·European Journal of Human Genetics ·Sonja A. de Munnik,Sixto García‐Miñáur,Alexander Hoischen,Bregje W.M. van Bon,Kym M. Boycott,Jeroen Schoots,Lies H. Hoefsloot,Nine Knoers,Ernie M.H.F. Bongers,Han G. Brunner	36
9	A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome 2012 ·Human Mutation ·Jorieke E. H. Bergman,Nicole Janssen,Almer M. van der Sloot,Hermien E. K. de Walle,Jeroen Schoots,Nanna Dahl Rendtorff,Lisbeth Tranebjærg,Lies H. Hoefsloot,Conny M.A. van Ravenswaaij‐Arts,Robert M.W. Hofstra	50
10	Mutation update on the CHD7 gene involved in CHARGE syndrome 2012 ·Human Mutation ·Nicole Janssen,Jorieke E. H. Bergman,Morris A. Swertz,Lisbeth Tranebjærg,Marianne Lodahl,Jeroen Schoots,Robert M.W. Hofstra,Conny M.A. van Ravenswaaij‐Arts,Lies H. Hoefsloot	176
11	Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects 2012 ·Journal of Medical Genetics ·Marjolein H. Willemsen,Lisenka E.L.M. Vissers,Michèl A.A.P. Willemsen,Bregje W.M. van Bon,Thessa Kroes,Joep de Ligt,(unknown),Jeroen Schoots,Dorien Lugtenberg,Ben C.J. Hamel,Hans van Bokhoven,Han G. Brunner,Joris A. Veltman,Tjitske Kleefstra	123
12	Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome 2011 ·European Journal of Human Genetics ·Bob Glaudemans,Helger G. Yntema,Pedro San‐Cristobal,Jeroen Schoots,Rolph Pfundt,(unknown),René J.M. Bindels,Nine V.A.M. Knoers,Joost G.J. Hoenderop,Lies H. Hoefsloot	57
13	Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy 2005 ·European Journal of Human Genetics ·Ernie M.H.F. Bongers,F.T.M. Huysmans,Elena Levtchenko,(unknown),Johan G. Blickman,R.J.C. Admiraal,P.L.M. Huygen,J.R.M. Cruysberg,(unknown),Judith B. Prins,Paul F. M. Krabbe,George F. Borm,Jeroen Schoots,Hans van Bokhoven,(unknown),Lies H. Hoefsloot,Albert van Kampen,Nine V.A.M. Knoers	87
14	Mutations in the Human TBX4 Gene Cause Small Patella Syndrome 2004 ·The American Journal of Human Genetics ·Ernie M.H.F. Bongers,Pascal H. G. Duijf,Sylvia E. C. van Beersum,Jeroen Schoots,Albert van Kampen,(unknown),Ben C.J. Hamel,(unknown),Lies H. Hoefsloot,Helger G. Yntema,Nine V.A.M. Knoers,Hans van Bokhoven	113

About Jeroen Schoots

Jeroen Schoots is a scholar working on Genetics, Nephrology and Developmental Biology, having authored 14 papers that have together received 854 indexed citations. Recurring topics across this work include Ion Transport and Channel Regulation (3 papers), Renal Diseases and Glomerulopathies (3 papers) and Tracheal and airway disorders (3 papers). The work is most often cited by research in Genetics (244 citations), Nephrology (95 citations) and Genetics (281 citations). Jeroen Schoots has collaborated with scholars based in Netherlands, United Kingdom and Denmark. Frequent co-authors include Lies H. Hoefsloot, Ernie M.H.F. Bongers, Nicole Janssen, Jorieke E. H. Bergman, Conny M.A. van Ravenswaaij‐Arts, Lisbeth Tranebjærg, Robert M.W. Hofstra, Hans van Bokhoven, Nine V.A.M. Knoers and Marianne Lodahl. Their work appears in journals such as Journal of the American Society of Nephrology, The American Journal of Human Genetics and Epilepsia.

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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