Catherine Fourneau

600 total citations
12 papers, 405 citations indexed

About

Catherine Fourneau is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Catherine Fourneau has authored 12 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Catherine Fourneau's work include Congenital Anomalies and Fetal Surgery (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Catherine Fourneau is often cited by papers focused on Congenital Anomalies and Fetal Surgery (3 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Catherine Fourneau collaborates with scholars based in Belgium, France and Netherlands. Catherine Fourneau's co-authors include Y. Gillerot, Lionel Van Maldergem, Alain Verloès, Marjo Kestilä, LL Wang, Eric Jauniaux, Maximilian Muenke, Juanliang Cai, Sharon E. Plon and H. Annika Siitonen and has published in prestigious journals such as PEDIATRICS, Cancer and Radiology.

In The Last Decade

Catherine Fourneau

12 papers receiving 383 citations

Peers

Catherine Fourneau
Ilaria Laface Italy
Manuela Tumino Italy
P. L. T. Ilbery Australia
Vijaya Kumar Pidugu Taiwan
Ingermarie Reintoft Denmark
Kimiko Kasahara Japan
Irene Boll Germany
V A McKusick United States
Shida Zhu China
Jin Han China
Ilaria Laface Italy
Catherine Fourneau
Citations per year, relative to Catherine Fourneau Catherine Fourneau (= 1×) peers Ilaria Laface

Countries citing papers authored by Catherine Fourneau

Since Specialization
Citations

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

Fields of papers citing papers by Catherine Fourneau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Fourneau

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

All Works

12 of 12 papers shown
1.
Kang, Xin, Mieke Cannie, Owen J. Arthurs, et al.. (2017). Post-mortem whole-body magnetic resonance imaging of human fetuses: a comparison of 3-T vs. 1.5-T MR imaging with classical autopsy. European Radiology. 27(8). 3542–3553. 38 indexed citations
2.
Cannie, Mieke, Frederik De Keyzer, Johan De Mey, et al.. (2015). Potential Heating Effect in the Gravid Uterus by Using 3-T MR Imaging Protocols: Experimental Study in Miniature Pigs. Radiology. 279(3). 754–761. 24 indexed citations
3.
Destrèe, Anne, et al.. (2005). Prenatal diagnosis of trisomy 6 mosaicism. Prenatal Diagnosis. 25(5). 354–357. 22 indexed citations
4.
Maldergem, Lionel Van, H. Annika Siitonen, Nadine Jalkh, et al.. (2005). Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. Journal of Medical Genetics. 43(2). 148–152. 162 indexed citations
5.
Maldergem, Lionel Van, David Tuerlinckx, Ronald J. A. Wanders, et al.. (2000). Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings. European Journal of Pediatrics. 159(1-2). 108–112. 5 indexed citations
6.
Gillerot, Y., Catherine Fourneau, Tineke P. Willems, & Lionel Van Maldergem. (1997). Lethal femoral-facial syndrome: a case with unusual manifestations.. Journal of Medical Genetics. 34(6). 518–519. 13 indexed citations
7.
Gillerot, Y., Marianne Heimann, Catherine Fourneau, Christine Verellen‐Dumoulin, & Lionel Van Maldergem. (1993). Oral‐facial‐digital syndrome type I in a newborn male. American Journal of Medical Genetics. 46(3). 335–338. 22 indexed citations
8.
Catte, Luc De, et al.. (1993). Prenatal diagnosis of pentalogy of Cantrell. Journal of Obstetrics and Gynaecology. 13(1). 36–37. 1 indexed citations
9.
Maldergem, Lionel Van, et al.. (1992). Mental retardation with blepharo‐naso‐facial abnormalities and hand malformations: a new syndrome?. Clinical Genetics. 41(1). 22–24. 19 indexed citations
10.
Maldergem, Lionel Van, Eric Jauniaux, Catherine Fourneau, & Y. Gillerot. (1992). Genetic Causes of Hydrops Fetalis. PEDIATRICS. 89(1). 81–86. 40 indexed citations
11.
Pierquin, Geneviève, Nicole Van Regemorter, Catherine Fourneau, et al.. (1991). Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome. Human Genetics. 87(5). 587–591. 29 indexed citations
12.
Verhest, Alain, Róbert Kiss, Denis Larsimont, et al.. (1990). Characterization of human colorectal mucosa, polyps, and cancers by means of computerized morphonuclear image analyses. Cancer. 65(9). 2047–2054. 30 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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2026