Chantal Esculpavit

932 total citations
4 papers, 66 citations indexed

About

Chantal Esculpavit is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chantal Esculpavit has authored 4 papers receiving a total of 66 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chantal Esculpavit's work include Craniofacial Disorders and Treatments (2 papers), Prenatal Screening and Diagnostics (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Chantal Esculpavit is often cited by papers focused on Craniofacial Disorders and Treatments (2 papers), Prenatal Screening and Diagnostics (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Chantal Esculpavit collaborates with scholars based in France, Belgium and Japan. Chantal Esculpavit's co-authors include Férechté Encha‐Razavi, Michel Vekemans, Maryse Bonnière, Nicole Morichon, Tania Attié‐Bitach, Alexandra Benachi, Françis Brunelle, Arnold Münnich, Géraldine Viot and Rémi Salomon and has published in prestigious journals such as Pathology and American Journal of Medical Genetics Part A.

In The Last Decade

Chantal Esculpavit

4 papers receiving 65 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chantal Esculpavit France 4 40 30 21 8 8 4 66
Mathilde Pacault France 6 23 0.6× 41 1.4× 28 1.3× 6 0.8× 4 0.5× 9 82
Futoshi Sekiguchi Japan 7 59 1.5× 16 0.5× 27 1.3× 4 0.5× 2 0.3× 12 94
Stacey Curry United States 4 60 1.5× 41 1.4× 56 2.7× 21 2.6× 6 0.8× 4 150
María Eugenia Rocha Germany 5 32 0.8× 11 0.4× 34 1.6× 5 0.6× 8 1.0× 8 70
Carol Gardiner United Kingdom 4 29 0.7× 12 0.4× 18 0.9× 4 0.5× 3 0.4× 7 59
Melissa Crenshaw United States 6 27 0.7× 13 0.4× 36 1.7× 8 1.0× 6 0.8× 13 83
H. Melanie Bedford Canada 5 26 0.7× 22 0.7× 18 0.9× 18 2.3× 9 1.1× 5 76
Lucia L. Ferraro Spain 8 41 1.0× 12 0.4× 18 0.9× 3 0.4× 7 0.9× 10 166
X. Hernandoréna France 6 110 2.8× 36 1.2× 10 0.5× 6 0.8× 8 1.0× 17 166
Timothy Morgan New Zealand 3 23 0.6× 16 0.5× 33 1.6× 24 3.0× 7 0.9× 3 71

Countries citing papers authored by Chantal Esculpavit

Since Specialization
Citations

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

Fields of papers citing papers by Chantal Esculpavit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chantal Esculpavit

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

All Works

4 of 4 papers shown
1.
Benachi, Alexandra, Maryse Bonnière, Chantal Esculpavit, et al.. (2010). PAX2 mutations in fetal renal hypodysplasia. American Journal of Medical Genetics Part A. 152A(4). 830–835. 28 indexed citations
2.
Encha‐Razavi, Férechté, Marie Gonzalès, Annie Laquerrière, et al.. (2008). A practical approach to the examination of the malformed fetal brain: impact on genetic counselling. Pathology. 40(2). 180–187. 3 indexed citations
3.
Golzio, Christelle, Valérie Malan, Maryse Bonnière, et al.. (2007). Matthew‐Wood syndrome: Report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2. American Journal of Medical Genetics Part A. 143A(3). 219–228. 12 indexed citations
4.
Viot, Géraldine, Pascale Sonigo, Isabelle Simon, et al.. (2003). Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different. American Journal of Medical Genetics Part A. 126A(2). 123–128. 23 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Mathilde Pacault Breakdown of academic impact, for papers by Futoshi Sekiguchi Breakdown of academic impact, for papers by Stacey Curry Breakdown of academic impact, for papers by María Eugenia Rocha Breakdown of academic impact, for papers by Carol Gardiner Breakdown of academic impact, for papers by Melissa Crenshaw Breakdown of academic impact, for papers by H. Melanie Bedford Breakdown of academic impact, for papers by Lucia L. Ferraro Breakdown of academic impact, for papers by X. Hernandoréna Breakdown of academic impact, for papers by Timothy Morgan
Rankless by CCL
2026