Marga Schepens

1.1k citations

20 papers · 779 indexed · h-index 14

Impact in

Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics

Papers in ⓘ

Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 4
Cancer Research 4
- Cancer Genomics and Diagnostics 4

Co-authors: Vera M. Kalscheuer (4 shared papers)Edwin C.M. Mariman (2 shared papers)Helga Rehder (1 shared paper)Ad Geurts van Kessel (9 shared papers)Eric Schoenmakers (3 shared papers)A. Riesewijk (3 shared papers)Hans‐Hilger Ropers (2 shared papers)Gerard Merkx (3 shared papers)
Journals: Genes Chromosomes and Cancer (5 papers)Genomics (4 papers)Cytogenetic and Genome Research (3 papers)European Journal of Human Genetics (2 papers)Nature Genetics (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

Marga Schepens

20 papers receiving 755 citations

Peers

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-authors

The 25 scholars most cited alongside Marga Schepens, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marga Schepens Line = papers co-authored together Marga Schepens links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans Nature Genetics ·Vera M. Kalscheuer, Edwin C.M. Mariman, Marga Schepens, Helga Rehder, Hans-Hilger Ropers	1993	190
2	Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings European Journal of Human Genetics ·Ellen A. Croonen, Willy M. Nillesen, Kyra E. Stuurman, Grétel Oudesluijs, Ingrid M B M van de Laar, Liesbeth Martens, Charlotte W. Ockeloen, Inge B. Mathijssen, Marga Schepens, Martina Ruiterkamp‐Versteeg, Hans Scheffer, Brigitte H. W. Faas, Ineke van der Burgt, Helger G. Yntema	2013	93
3	Maternal-Specific Methylation of the HumanIGF2RGene Is Not Accompanied by Allele-Specific Transcription Genomics ·A. Riesewijk, Marga Schepens, Thomas R. Welch, Ella M. van den Berg‐Loonen, Edwin M. Mariman, Hans‐Hilger Ropers, Vera M. Kalscheuer	1996	59
4	Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes Genomics ·Frans A. Hol, Marga Schepens, Sylvia E. C. van Beersum, Elena Redolfi, Maurizio Affer, Paolo Vezzoni, Ben C.J. Hamel, Pamela S. Karnes, Edwin C.M. Mariman, Ileana Zucchi	2000	53
5	Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome European Journal of Human Genetics ·Lisenka E.L.M. Vissers, Monica Bonetti, Jeroen Overman, Willy M. Nillesen, Suzanna G.M. Frints, Joep de Ligt, Giuseppe Zampino, Ana Justino, José Carlos Machado, Marga Schepens, Han G. Brunner, Joris A. Veltman, Hans Scheffer, Piet Gros, José Luís Costa, Marco Tartaglia, Ineke van der Burgt, Helger G. Yntema, Jeroen den Hertog	2014	51
6	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 ·Diederik R.H. de Bruijn, Nuno R. dos Santos, Ellen Kater‐Baats, José Thijssen, Lieke van den Berk, Jiska Stap, M. Balemans, Marga Schepens, Gerard Merkx, Ad Geurts van Kessel	2002	50
7	Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma Cancer Genetics and Cytogenetics ·Annet Simons, Marga Schepens, Judith W. M. Jeuken, Sandra H. E. Sprenger, Guillaume van de Zande, Bodil Bjerkehagen, Anne Forus, Vines Weibolt, Ineke Molenaar, Eva van den Berg, Ola Myklebost, Julia A. Bridge, Ad Geurts van Kessel, Ron F. Suijkerbuijk	2000	49
8	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 ·Daniëlle Bodmer, Marga Schepens, Marc J. Eleveld, Eric Schoenmakers, Ad Geurts van Kessel	2003	40
9	Molecular mechanisms underlying the MiT translocation subgroup of renal cell carcinomas Cytogenetic and Genome Research ·Klaas Medendorp, J.J.M. van Groningen, Marga Schepens, Lilian Vreede, Jessica A G M Thijssen, Eric Schoenmakers, Helma van den Hurk, Ad Geurts van Kessel, Roland P. Kuiper	2007	33
10	Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma Genes Chromosomes and Cancer ·Eric Schoenmakers, Jens Bunt, Lianne Hermers, Marga Schepens, Gerard Merkx, Bert Janssen, M. Kersten, Erik Huys, Patrick Pauwels, Maria Dêbiec‐Rychter, Ad Geurts van Kessel	2012	27
11	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 ·Martien van Asseldonk, Marga Schepens, Diederik de Bruijn, Bert Janssen, Gerard Merkx, Ad Geurts van Kessel	2000	25
12	COMMENTS Apmis ·Imke M. Veltman, Marga Schepens, Leendert H. J. Looijenga, Louise C. Strong, Ad Geurts van Kessel	2003	23
13	A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis Genes Chromosomes and Cancer ·Annet Simons, Marga Schepens, Anne Forus, Linda H. Godager, Martien van Asseldonk, Ola Myklebost, Ad Geurts van Kessel	1999	17
14	TheMASProto-Oncogene Is Not Imprinted in Humans Genomics ·A. Riesewijk, Marga Schepens, Edwin M. Mariman, Hans‐Hilger Ropers, Vera M. Kalscheuer	1996	16
15	Absence of an Obvious Molecular Imprinting Mechanism in a Human Fetus with MonoallelicIGF2RExpression Biochemical and Biophysical Research Communications ·A. Riesewijk, XU Yong-qin, Marga Schepens, Edwin M. Mariman, Constantin Polychronakos, Hans-Hilger Ropers, Vera M. Kalscheuer	1998	12
16	A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat Cancer Genetics and Cytogenetics ·Imke M. Veltman, Martien van Asseldonk, Marga Schepens, Hans Stoop, Leendert H. J. Looijenga, Carine Wouters, Lutgarde Govaerts, Ron F. Suijkerbuijk, Ad Geurts van Kessel	2002	12
17	Characterization of a novel transcript of the EHMT1 gene reveals important diagnostic implications for Kleefstra syndrome Human Mutation ·Willy M. Nillesen, Helger G. Yntema, Marco Moscarda, Nienke E. Verbeek, Louise C. Wilson, Frances M. Cowan, Marga Schepens, Annick Raas‐Rothschild, Orly Gafni-Weinstein, Marcella Zollino, Raymon Vijzelaar, Giovanni Neri, Marcel Nelen, Hans van Bokhoven, Jacques C. Giltay, Tjitske Kleefstra	2011	12
18	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 ·Arn M. J. M. van den Maagdenberg, Jan Schepens, Marga Schepens, Barry A. Pepers, Bé Wieringa, A.Geurts Geurts van Kessel, Wiljan Hendriks	1998	8
19	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 ·Anouk den Braber, Jan Schepens, Marga Schepens, G.F. Merkx, F. Darroudi, B. Wieringa, Ad Geurts van Kessel, Wiljan Hendriks	1999	6
20	A novel chromosomal region of allelic loss, 4q32–q34, in human osteosarcomas revealed by representational difference analysis Genes Chromosomes and Cancer ·Annet Simons, Marga Schepens, Anne Forus, Linda H. Godager, Martien van Asseldonk, Ola Myklebost, Ad Geurts van Kessel	1999	3

About Marga Schepens

Marga Schepens is a scholar working on Genetics, Cancer Research, Molecular Biology, Pediatrics, Perinatology and Child Health and Urology, having authored 20 papers that have together received 779 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Protein Tyrosine Phosphatases (4 papers), Prenatal Screening and Diagnostics (4 papers), Genetic Syndromes and Imprinting (4 papers), Cancer Genomics and Diagnostics (4 papers), Galectins and Cancer Biology (3 papers) and Renal and related cancers (3 papers). The work is most often cited by research in Genetics (336 citations), Pediatrics, Perinatology and Child Health (185 citations), Molecular Biology (539 citations), Cancer Research (112 citations) and Immunology (83 citations). Marga Schepens has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Vera M. Kalscheuer, Edwin C.M. Mariman, Helga Rehder, Ad Geurts van Kessel, Eric Schoenmakers, A. Riesewijk, Hans‐Hilger Ropers, Gerard Merkx, Helger G. Yntema and Willy M. Nillesen. Their work appears in journals such as Genes Chromosomes and Cancer, Genomics, Cytogenetic and Genome Research, European Journal of Human Genetics and Nature Genetics.

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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