J. M. Cobben

1.4k total citations
16 papers, 936 citations indexed

About

J. M. Cobben is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, J. M. Cobben has authored 16 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Genetics. Recurrent topics in J. M. Cobben's work include Prenatal Screening and Diagnostics (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (3 papers). J. M. Cobben is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and RNA modifications and cancer (3 papers). J. M. Cobben collaborates with scholars based in Netherlands, United Kingdom and United States. J. M. Cobben's co-authors include Hans Scheffer, C.H.C.M. Buys, P.M. Grootscholten, Gerrit van der Steege, Marianne de Visser, Gerard Pals, Fleur S. van Dijk, Rick R. van Rijn, Peter G. J. Nikkels and Ariana Kariminejad and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

J. M. Cobben

14 papers receiving 889 citations

Peers

J. M. Cobben

GENET

SURGE

PPCH

Ann Haskins Olney United States

Louise C. Wilson United Kingdom

Yves Lacassie United States

Annalaura Torella Italy

B. Le Marec France

Brad Angle United States

Rossella Capolino Italy

Sylvie Manouvrier‐Hanu France

Martine Blayau France

Carol A. Crowe United States

Ann Haskins Olney United States

J. M. Cobben

842 ×1.4

716 ×1.8

GENET

93 ×0.3

GENET

169 ×0.9

SURGE

214 ×1.4

PPCH

Citations per year, relative to J. M. Cobben J. M. Cobben (= 1×) peers Ann Haskins Olney

Countries citing papers authored by J. M. Cobben

Since Specialization

Citations

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

Fields of papers citing papers by J. M. Cobben

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. M. 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 J. M. Cobben. The network helps show where J. M. Cobben may publish in the future.

Co-authorship network of co-authors of J. M. Cobben

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

All Works

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16 of 16 papers shown

Cheng, Edward Y., et al.. (2022). A Novel PPP2CA Gene Variant Presenting with Dystonia and Progressive Brain Atrophy. 6(1).

Teeuw, Marieke, Zoltán Bochdanovits, Sander Ouburg, et al.. (2015). Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome. BMC Medical Genetics. 16(1). 50–50. 1 indexed citations

Jansen, F. A. R., Yair J. Blumenfeld, Andmorgan Fisher, et al.. (2014). Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta‐analysis. Ultrasound in Obstetrics and Gynecology. 45(1). 27–35. 91 indexed citations

Dijk, Fleur S. van, J. M. Cobben, Ariana Kariminejad, et al.. (2011). Osteogenesis Imperfecta: A Review with Clinical Examples. Molecular Syndromology. 2(1). 1–20. 142 indexed citations

Wakeling, Emma, Mariëlle Alders, Jet Bliek, et al.. (2010). Epigenotype–phenotype correlations in Silver–Russell syndrome. Journal of Medical Genetics. 47(11). 760–768. 120 indexed citations

Dijk, Fleur S. van, Ben C.J. Hamel, Yvonne Hilhorst‐Hofstee, et al.. (2008). Compound-heterozygous Marfan syndrome. European Journal of Medical Genetics. 52(1). 1–5. 21 indexed citations

Cobben, J. M., A Bröcker-Vriends, & N. J. Leschot. (2002). [Prenatal diagnosis for hereditary predisposition to mammary and ovarian carcinoma--defining a position].. PubMed. 146(31). 1461–5. 2 indexed citations

Veldink, Jan H., Leonard H. van den Berg, J. M. Cobben, et al.. (2001). Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 56(6). 749–752. 80 indexed citations

Jongbloed, R. J. E., Arthur A.M. Wilde, J. L. M. C. Geelen, et al.. (1999). Novel KCNQ1 and HERG missense mutations in Dutch long-QT families. Human Mutation. 13(4). 301–310. 51 indexed citations

10.

Moog, Ute, et al.. (1997). Oculocerebrocutaneous syndrome: report of three additional cases and aetiological considerations. Clinical Genetics. 52(4). 219–225. 28 indexed citations

11.

Cobben, J. M., et al.. (1996). The EEC syndrome: a literature study. Clinical Dysmorphology. 5(2). 115–127. 101 indexed citations

12.

Grootscholten, P.M., J. M. Cobben, Stefania Zappata, et al.. (1996). Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5.. PubMed. 59(4). 834–8. 86 indexed citations

13.

Cobben, J. M., Gerrit van der Steege, P.M. Grootscholten, et al.. (1995). Deletions of the survival motor neuron gene in unaffected siblings of patients with spinal muscular atrophy.. PubMed. 57(4). 805–8. 174 indexed citations

14.

Cobben, J. M., et al.. (1994). Fluorescence in situ hybridisation on formalin fixed fetal tissue in the diagnosis of chromosomal syndromes.. PubMed. 5(2). 141–5. 5 indexed citations

15.

Cobben, J. M., et al.. (1992). A boy with Poland anomaly and facio‐auriculo‐vertebral dysplasia. Clinical Genetics. 41(2). 105–107. 12 indexed citations

16.

Scheffer, Hans, et al.. (1991). LINKAGE ANALYSIS IN FAMILIES WITH PROXIMAL SPINAL MUSCULAR-ATROPHY FROM THE NETHERLANDS. The American Journal of Human Genetics. 49(4). 203–203. 22 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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