Marga Schepens

1.1k total citations
20 papers, 779 citations indexed

About

Marga Schepens is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marga Schepens has authored 20 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marga Schepens's work include Epigenetics and DNA Methylation (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (4 papers). Marga Schepens is often cited by papers focused on Epigenetics and DNA Methylation (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (4 papers). Marga Schepens collaborates with scholars based in Netherlands, United States and Germany. Marga Schepens's co-authors include Vera M. Kalscheuer, Edwin C.M. Mariman, Helga Rehder, Ad Geurts van Kessel, Eric Schoenmakers, A. Riesewijk, Gerard Merkx, Hans‐Hilger Ropers, Willy M. Nillesen and Helger G. Yntema and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Genomics.

In The Last Decade

Marga Schepens

20 papers receiving 755 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marga Schepens Netherlands 14 539 336 185 120 112 20 779
Yosuke Komoto Japan 10 443 0.8× 260 0.8× 170 0.9× 84 0.7× 94 0.8× 16 726
Jingdong Shan Finland 18 626 1.2× 278 0.8× 80 0.4× 189 1.6× 74 0.7× 30 919
Sevilhan Artan Türkiye 18 308 0.6× 187 0.6× 104 0.6× 75 0.6× 106 0.9× 84 760
Georg Klaus Hinkel Germany 17 498 0.9× 528 1.6× 107 0.6× 82 0.7× 46 0.4× 41 933
Anne Marie Ottesen Denmark 11 371 0.7× 390 1.2× 71 0.4× 79 0.7× 109 1.0× 15 733
Ryuji Fukuzawa Japan 22 870 1.6× 276 0.8× 163 0.9× 295 2.5× 77 0.7× 68 1.2k
Jack L. Spurbeck United States 17 330 0.6× 330 1.0× 112 0.6× 54 0.5× 77 0.7× 25 1.0k
Jonathan P. Park United States 19 462 0.9× 267 0.8× 97 0.5× 49 0.4× 83 0.7× 36 898
Diem Dao United States 9 669 1.2× 356 1.1× 239 1.3× 56 0.5× 67 0.6× 9 871
Leslie A. McNoe New Zealand 9 904 1.7× 530 1.6× 390 2.1× 140 1.2× 90 0.8× 11 1.1k

Countries citing papers authored by Marga Schepens

Since Specialization
Citations

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

Fields of papers citing papers by Marga Schepens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marga Schepens

This figure shows the co-authorship network connecting the top 25 collaborators of Marga Schepens. A scholar is included among the top collaborators of Marga Schepens 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 Marga Schepens. Marga Schepens 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.
Vissers, Lisenka E.L.M., Monica Bonetti, Jeroen Overman, et al.. (2014). Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome. European Journal of Human Genetics. 23(3). 317–324. 51 indexed citations
2.
Nillesen, Willy M., Kyra E. Stuurman, Grétel Oudesluijs, et al.. (2013). Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings. European Journal of Human Genetics. 21(9). 936–942. 93 indexed citations
3.
Schoenmakers, Eric, Jens Bunt, Marga Schepens, et al.. (2012). Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma. Genes Chromosomes and Cancer. 52(1). 11–23. 27 indexed citations
4.
Nillesen, Willy M., Helger G. Yntema, Nienke E. Verbeek, et al.. (2011). Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome. Human Mutation. 32(7). 853–859. 12 indexed citations
5.
Groningen, J.J.M. van, Marga Schepens, Lilian Vreede, et al.. (2007). Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas. Cytogenetic and Genome Research. 118(2-4). 157–165. 33 indexed citations
6.
Bodmer, Daniëlle, Marga Schepens, Marc J. Eleveld, Eric Schoenmakers, & Ad Geurts van Kessel. (2003). Disruption of a novel gene, DIRC3, and expression of DIRC3‐HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21). Genes Chromosomes and Cancer. 38(2). 107–116. 40 indexed citations
7.
Veltman, Imke M., Marga Schepens, Leendert H. J. Looijenga, Louise C. Strong, & Ad Geurts van Kessel. (2003). COMMENTS. Apmis. 111(1). 152–160. 23 indexed citations
8.
Veltman, Imke M., Martien van Asseldonk, Marga Schepens, et al.. (2002). A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat. Cancer Genetics and Cytogenetics. 136(1). 17–22. 12 indexed citations
9.
Bruijn, Diederik R.H. de, Nuno R. dos Santos, Ellen Kater‐Baats, et al.. (2002). The cancer‐related protein SSX2 interacts with the human homologue of a Ras‐like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP. Genes Chromosomes and Cancer. 34(3). 285–298. 50 indexed citations
10.
Hol, Frans A., Marga Schepens, Sylvia E. C. van Beersum, et al.. (2000). Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes. Genomics. 69(2). 174–181. 53 indexed citations
11.
Simons, Annet, Marga Schepens, Judith W. M. Jeuken, et al.. (2000). Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma. Cancer Genetics and Cytogenetics. 118(2). 89–98. 49 indexed citations
12.
Asseldonk, Martien van, Marga Schepens, Diederik de Bruijn, et al.. (2000). Construction of a 350-kb Sequence-Ready 11q13 Cosmid Contig Encompassing the Markers D11S4933 and D11S546: Mapping of 11 Genes and 3 Tumor-Associated Translocation Breakpoints. Genomics. 66(1). 35–42. 25 indexed citations
13.
Braber, Anouk den, Jan Schepens, Marga Schepens, et al.. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of the PTP-SL/PTPBR7 gene (<i>Ptprr</i>/PTPRR) to mouse chromosome region 8A2 by in situ hybridization. Cytogenetic and Genome Research. 84(3-4). 243–244. 6 indexed citations
14.
Simons, Annet, Marga Schepens, Anne Forus, et al.. (1999). A novel chromosomal region of allelic loss, 4q32–q34, in human osteosarcomas revealed by representational difference analysis. Genes Chromosomes and Cancer. 26(2). 115–124. 3 indexed citations
15.
Simons, Annet, Marga Schepens, Anne Forus, et al.. (1999). A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis. Genes Chromosomes and Cancer. 26(2). 115–124. 17 indexed citations
16.
Riesewijk, A., et al.. (1998). Absence of an Obvious Molecular Imprinting Mechanism in a Human Fetus with MonoallelicIGF2RExpression. Biochemical and Biophysical Research Communications. 245(1). 272–277. 12 indexed citations
17.
Maagdenberg, Arn M. J. M. van den, Jan Schepens, Marga Schepens, et al.. (1998). Assignment of <i>Ptprn2</i>, the gene encoding receptor-type protein tyrosine phosphatase IA-2β, a major autoantigen in insulin-dependent diabetes mellitus, to mouse chromosome region 12F. Cytogenetic and Genome Research. 82(3-4). 153–155. 8 indexed citations
18.
Riesewijk, A., et al.. (1996). TheMASProto-Oncogene Is Not Imprinted in Humans. Genomics. 35(2). 380–382. 16 indexed citations
19.
Riesewijk, A., Marga Schepens, Thomas R. Welch, et al.. (1996). Maternal-Specific Methylation of the HumanIGF2RGene Is Not Accompanied by Allele-Specific Transcription. Genomics. 31(2). 158–166. 59 indexed citations
20.
Kalscheuer, Vera M., et al.. (1993). The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans. Nature Genetics. 5(1). 74–78. 190 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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