Isabelle Perthus

1.1k total citations
20 papers, 409 citations indexed

About

Isabelle Perthus is a scholar working on Pediatrics, Perinatology and Child Health, Surgery and Molecular Biology. According to data from OpenAlex, Isabelle Perthus has authored 20 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pediatrics, Perinatology and Child Health, 5 papers in Surgery and 5 papers in Molecular Biology. Recurrent topics in Isabelle Perthus's work include Prenatal Screening and Diagnostics (7 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Isabelle Perthus is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Isabelle Perthus collaborates with scholars based in France, United Kingdom and Réunion. Isabelle Perthus's co-authors include D. Lémery, Christine Francannet, Denis Gallot, Jacques Jani, Karen Coste, Vincent Sapin, Antoine Labbé, Jan Deprest, Elisabeth Robert‐Gnansia and Caroline Boda and has published in prestigious journals such as Neurology, Clinica Chimica Acta and Journal of Medical Genetics.

In The Last Decade

Isabelle Perthus

17 papers receiving 393 citations

Peers

Isabelle Perthus
Zafer Kozacıoğlu Türkiye
Eva Landmann Germany
Sergei Roumiantsev United States
Elaine Utomo Netherlands
Erol Özdi̇ler Türkiye
Kye Shik Shim South Korea
Johanne Dubé Canada
Maria Angela Ziveri Italy
Ekaterina Pigarova Russia
J. Simon Germany
Zafer Kozacıoğlu Türkiye
Isabelle Perthus
Citations per year, relative to Isabelle Perthus Isabelle Perthus (= 1×) peers Zafer Kozacıoğlu

Countries citing papers authored by Isabelle Perthus

Since Specialization
Citations

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

Fields of papers citing papers by Isabelle Perthus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Perthus

This figure shows the co-authorship network connecting the top 25 collaborators of Isabelle Perthus. A scholar is included among the top collaborators of Isabelle Perthus 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 Isabelle Perthus. Isabelle Perthus 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.
Bouvagnet, Patrice, Anne‐Claire Bréhin, Alexis Hermida, et al.. (2025). MYH6 in Congenital Heart Defects: A Genotype–Phenotype Characterization in a French Cohort. Pediatric Cardiology.
2.
Goumy, Carole, Gwendoline Soler, Éléonore Eymard-Pierre, et al.. (2023). Optical genome mapping for prenatal diagnosis: A prospective study. Clinica Chimica Acta. 551. 117594–117594. 12 indexed citations
3.
Goumy, Carole, Éléonore Eymard-Pierre, Gwendoline Soler, et al.. (2023). Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination. Diagnostics. 13(23). 3576–3576. 1 indexed citations
4.
Plaisancié, Julie, Jelena Martinović, Sandra Whalen, et al.. (2023). Clinical, genetic and biochemical signatures of RBP4-related ocular malformations. Journal of Medical Genetics. 61(1). 84–92. 2 indexed citations
5.
Vaché, Christel, Julie Bianchi, Isabelle Perthus, et al.. (2022). Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss. Diagnostics. 12(1). 207–207. 6 indexed citations
6.
Khoshnood, Babak, Ferdinand Dhombres, Hanitra Randrianaivo, et al.. (2020). Cost and outcomes of the ultrasound screening program for birth defects over time: a population-based study in France. BMJ Open. 10(7). e036566–e036566. 3 indexed citations
7.
Dhombres, Ferdinand, Babak Khoshnood, Hanitra Randrianaivo, et al.. (2019). Trends in resource use and effectiveness of ultrasound detection of fetal structural anomalies in France: a multiple registry-based study. BMJ Open. 9(2). e025482–e025482. 9 indexed citations
8.
Blotière, Pierre‐Olivier, F. Raguideau, Alain Weill, et al.. (2019). Risks of 23 specific malformations associated with prenatal exposure to 10 antiepileptic drugs. Neurology. 93(2). e167–e180. 73 indexed citations
9.
Kwiatkowski, Fabrice, Isabelle Perthus, Nancy Uhrhammer, et al.. (2019). Association between hereditary predisposition to common cancers and congenital multimalformations. Congenital Anomalies. 60(1). 22–31. 3 indexed citations
10.
Marie, Cécile, Stéphanie Leger, Olivier Rivière, et al.. (2018). In utero exposure to arsenic in tap water and congenital anomalies: A French semi-ecological study. International Journal of Hygiene and Environmental Health. 221(8). 1116–1123. 14 indexed citations
11.
Debost‐Legrand, Anne, Isabelle Perthus, Olivier Rivière, et al.. (2017). Are there risk factors for false-positive malformation diagnoses on obstetric ultrasound? A nested case-control study. Journal of Gynecology Obstetrics and Human Reproduction. 47(3). 107–111. 2 indexed citations
12.
Köhler, M., Bérénice Doray, D. Lémery, et al.. (2017). Congenital unilateral renal agenesis: Prevalence, prenatal diagnosis, associated anomalies. Data from two birth‐defect registries. Birth Defects Research. 109(15). 1204–1211. 31 indexed citations
13.
Debost‐Legrand, Anne, Carole Goumy, H. Laurichesse‐Delmas, et al.. (2015). Prenatal diagnosis of the VACTERL association using routine ultrasound examination. Birth Defects Research Part A Clinical and Molecular Teratology. 103(10). 880–886. 7 indexed citations
14.
Debost‐Legrand, Anne, Lemlih Ouchchane, Christine Francannet, et al.. (2015). Impact of prenatal diagnosis on the outcome of patients with a transposition of great arteries: A 24‐year population‐based study. Birth Defects Research Part A Clinical and Molecular Teratology. 106(3). 178–184. 4 indexed citations
15.
Debost‐Legrand, Anne, H. Laurichesse‐Delmas, Christine Francannet, et al.. (2014). False positive morphologic diagnoses at the anomaly scan: marginal or real problem, a population-based cohort study. BMC Pregnancy and Childbirth. 14(1). 112–112. 10 indexed citations
16.
Ouchchane, Lemlih, Xinran Li, Isabelle Perthus, et al.. (2013). Performance map of a cluster detection test using extended power. International Journal of Health Geographics. 12(1). 47–47. 9 indexed citations
17.
Ruivard, M., et al.. (2008). Prevalence of Iron Deficiency and Health-related Quality of Life among Female Students. Journal of the American College of Nutrition. 27(2). 337–341. 37 indexed citations
18.
Bloch, Juliette, Christine Cans, C. De Vigan, et al.. (2008). Faisabilité de la surveillance du syndrome d’alcoolisation fœtale (SAF). Archives de Pédiatrie. 15(5). 507–509. 4 indexed citations
19.
Gallot, Denis, Caroline Boda, Sylvie Ughetto, et al.. (2006). Prenatal detection and outcome of congenital diaphragmatic hernia: a French registry‐based study. Ultrasound in Obstetrics and Gynecology. 29(3). 276–283. 182 indexed citations
20.
Gallot, D., et al.. (2005). 8 Évaluation du devenir obstétrical et néonatal immédiat en cas de liquide amniotique méconial dès la rupture de la poche des eaux : étude rétrospective de 82 cas. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 34(3). 283–283.

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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