Jan-Maarten Cobben

1.4k total citations
24 papers, 439 citations indexed

About

Jan-Maarten Cobben is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jan-Maarten Cobben has authored 24 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Genetics. Recurrent topics in Jan-Maarten Cobben's work include Neurogenetic and Muscular Disorders Research (8 papers), RNA modifications and cancer (6 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Jan-Maarten Cobben is often cited by papers focused on Neurogenetic and Muscular Disorders Research (8 papers), RNA modifications and cancer (6 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Jan-Maarten Cobben collaborates with scholars based in Netherlands, United States and Canada. Jan-Maarten Cobben's co-authors include Michiel M. Winter, M. G. J. Duffels, Michel E. Weijerman, Sylvia Huisman, Barbara J.M. Mulder, Bwee Tien Poll‐The, Matthan W.A. Caan, Linda Smit, Frank Baas and Mårten Kyllerman and has published in prestigious journals such as Brain, The American Journal of Human Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Jan-Maarten Cobben

22 papers receiving 410 citations

Peers

Jan-Maarten Cobben
Vinciane Dideberg Belgium
Gemma García‐Fructuoso Spain
T. Voit Germany
Yingjun Xie China
Renata Gaillyová Czechia
Lailá Bastaki Kuwait
Mary O’Driscoll United Kingdom
Jean‐Michel Pedespan France
Tomoko Tanaka United States
Marta Jones Argentina
Vinciane Dideberg Belgium
Jan-Maarten Cobben
Citations per year, relative to Jan-Maarten Cobben Jan-Maarten Cobben (= 1×) peers Vinciane Dideberg

Countries citing papers authored by Jan-Maarten Cobben

Since Specialization
Citations

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

Fields of papers citing papers by Jan-Maarten Cobben

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan-Maarten Cobben. 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 Jan-Maarten Cobben. The network helps show where Jan-Maarten Cobben may publish in the future.

Co-authorship network of co-authors of Jan-Maarten Cobben

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

All Works

20 of 20 papers shown
1.
Bosch, Annet M., Erik‐Jan Kamsteeg, Richard J. Rodenburg, et al.. (2018). Coenzyme Q10 deficiency due to a COQ4 gene defect causes childhood-onset spinocerebellar ataxia and stroke-like episodes. Molecular Genetics and Metabolism Reports. 17. 19–21. 24 indexed citations
2.
Veenendaal, Nicole R. van, Cynthia Kusters, Roelof‐Jan Oostra, Jorieke E. H. Bergman, & Jan-Maarten Cobben. (2016). When the right (Drug) should be left: Prenatal drug exposure and heterotaxy syndrome. Birth Defects Research Part A Clinical and Molecular Teratology. 106(7). 573–579. 5 indexed citations
3.
Stray‐Pedersen, Asbjørg, Jan-Maarten Cobben, Trine Prescott, et al.. (2015). Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. The American Journal of Human Genetics. 98(1). 202–209. 35 indexed citations
4.
Rudnik‐Schöneborn, Sabine, Thomas Eggermann, Wolfram Kreß, et al.. (2015). Clinical utility gene card for: Proximal spinal muscular atrophy (SMA) – update 2015. European Journal of Human Genetics. 23(11). 1–3. 16 indexed citations
5.
Hammond, Peter, Shane McKee, Michael Suttie, et al.. (2014). Opposite effects on facial morphology due to gene dosage sensitivity. Human Genetics. 133(9). 1117–1125. 11 indexed citations
6.
Cobben, Jan-Maarten, Marjan M. Weiss, Fleur S. van Dijk, et al.. (2014). A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability. European Journal of Medical Genetics. 57(11-12). 636–638. 31 indexed citations
7.
Verrips, Aad, Bwee Tien Poll‐The, Jan-Maarten Cobben, et al.. (2013). Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in the Netherlands. Neuromuscular Disorders. 23(6). 461–468. 10 indexed citations
8.
Dijk, Fleur S van, Jan-Maarten Cobben, Alessandra Maugeri, et al.. (2012). Osteogenesis imperfecta: klinische en genetische heterogeniteit. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 156(21). 1 indexed citations
9.
Rudnik‐Schöneborn, Sabine, Thomas Eggermann, Wolfram Kreß, et al.. (2012). Clinical utility gene card for: proximal spinal muscular atrophy. European Journal of Human Genetics. 20(6). 713–713. 3 indexed citations
10.
Piepers, Sanne, Jan-Maarten Cobben, Peter Sodaar, et al.. (2010). Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid. Journal of Neurology Neurosurgery & Psychiatry. 82(8). 850–852. 35 indexed citations
11.
Duffels, M. G. J., Michiel M. Winter, Michel E. Weijerman, et al.. (2009). Down syndrome: a cardiovascular perspective. Journal of Intellectual Disability Research. 53(5). 419–425. 129 indexed citations
12.
Barth, P. G., Charles B.L.M. Majoie, Matthan W.A. Caan, et al.. (2007). Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance. Brain. 130(9). 2258–2266. 78 indexed citations
13.
Deurloo, K. L., et al.. (2004). Prenatal diagnosis of tetrasomy 9p in a 19‐week‐old fetus with Dandy–Walker malformation: a case report. Prenatal Diagnosis. 24(10). 796–798. 15 indexed citations
14.
Cobben, Jan-Maarten, M. de Visser, & Hans Scheffer. (2001). [From gene to disease; 'survival' motor neuron protein and hereditary proximal spinal muscle atrophy].. PubMed. 145(52). 2525–7. 8 indexed citations
15.
Leegte, Beike, et al.. (2001). Two unbalanced segregation products due to a maternal t(7;16)inv(16). Prenatal Diagnosis. 21(7). 550–552.
16.
Wong, S.C., et al.. (1998). Karsch-Neugebauer syndrome in two sibs with unaffected parents. American Journal of Medical Genetics. 75(2). 207–210. 5 indexed citations
17.
Oostra, Roelof‐Jan, et al.. (1997). On the many faces of Leber hereditary optic neuropathy. Clinical Genetics. 51(6). 388–393. 9 indexed citations
18.
Steege, Gerrit van der, Jan-Maarten Cobben, Jan Osinga, et al.. (1995). A sublocus of the multicopy microsatellite marker CMS1 maps proximal to spinal muscular atrophy (SMA) as shown by recombinant analysis. Human Genetics. 96(5). 589–591. 2 indexed citations
19.
Cobben, Jan-Maarten, et al.. (1994). Genetic counseling in limb reduction defects.. PubMed. 5(3). 243–8. 5 indexed citations
20.
Steege, Gerrit van der, Jan-Maarten Cobben, Christina Brahe, et al.. (1994). Identification of Key Recombinants in Multiplex SMA Families. Genomics. 22(1). 219–222. 4 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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