Céline Dupont

2.0k total citations
38 papers, 645 citations indexed

About

Céline Dupont is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Céline Dupont has authored 38 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 18 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Céline Dupont's work include Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (11 papers) and Prenatal Screening and Diagnostics (10 papers). Céline Dupont is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (11 papers) and Prenatal Screening and Diagnostics (10 papers). Céline Dupont collaborates with scholars based in France, Italy and Australia. Céline Dupont's co-authors include Alain Verloès, Brigitte Benzacken, Anne‐Claude Tabet, Eva Pipiras, Azzedine Aboura, Séverine Drunat, Clarisse Baumann, M.‐P. Audrézet, L. Le Bodic and J.-P. Bernard and has published in prestigious journals such as Journal of Medical Genetics, Ultrasound in Obstetrics and Gynecology and European Journal of Human Genetics.

In The Last Decade

Céline Dupont

37 papers receiving 558 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Céline Dupont France 15 328 213 184 123 118 38 645
Chantal Missirian France 16 418 1.3× 404 1.9× 57 0.3× 100 0.8× 35 0.3× 39 720
Nicholas J. Neill United States 11 265 0.8× 257 1.2× 42 0.2× 146 1.2× 37 0.3× 16 565
Pietro Palumbo Italy 15 325 1.0× 314 1.5× 67 0.4× 61 0.5× 32 0.3× 64 620
Vanna Pecile Italy 17 499 1.5× 443 2.1× 70 0.4× 175 1.4× 30 0.3× 54 825
Marsha Speevak Canada 17 420 1.3× 302 1.4× 41 0.2× 141 1.1× 34 0.3× 37 636
Dunja Niedrist Switzerland 8 279 0.9× 263 1.2× 110 0.6× 119 1.0× 17 0.1× 11 571
Mark V. Sauer United States 17 212 0.6× 990 4.6× 117 0.6× 147 1.2× 40 0.3× 28 1.3k
Sophia Kitsiou‐Tzeli Greece 16 407 1.2× 422 2.0× 49 0.3× 77 0.6× 40 0.3× 39 656
Brian P. Perry United States 12 233 0.7× 137 0.6× 61 0.3× 79 0.6× 34 0.3× 27 509
Isabel Filges Switzerland 18 435 1.3× 338 1.6× 64 0.3× 278 2.3× 31 0.3× 44 773

Countries citing papers authored by Céline Dupont

Since Specialization
Citations

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

Fields of papers citing papers by Céline Dupont

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Dupont

This figure shows the co-authorship network connecting the top 25 collaborators of Céline Dupont. A scholar is included among the top collaborators of Céline Dupont 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 Céline Dupont. Céline Dupont 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.
Capri, Yline, Céline Dupont, Fabien Guimiot, et al.. (2023). DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy. Clinical Genetics. 104(5). 587–592. 2 indexed citations
2.
Lévy, Jonathan, Anna Maruani, Céline Dupont, et al.. (2021). Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder. Clinical Genetics. 101(3). 364–370. 8 indexed citations
3.
Lévy, Jonathan, Yline Capri, Céline Dupont, et al.. (2020). LEF1 haploinsufficiency causes ectodermal dysplasia. Clinical Genetics. 97(4). 595–600. 12 indexed citations
4.
Lévy, Jonathan, Damien Haye, Nicola Marziliano, et al.. (2018). EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder. Clinical Genetics. 93(6). 1141–1147. 19 indexed citations
5.
Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations
6.
Guimiot, Fabien, et al.. (2018). Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses. American Journal of Medical Genetics Part A. 176(11). 2325–2330. 1 indexed citations
7.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
8.
Tabet, Anne‐Claude, Céline Dupont, Nathalie Pouvreau, et al.. (2014). De novo deletion of TBL1XR1 in a child with non‐specific developmental delay supports its implication in intellectual disability. American Journal of Medical Genetics Part A. 164(9). 2335–2337. 24 indexed citations
9.
Ageeli, Essam Al, Séverine Drunat, Catherine Delanöe, et al.. (2013). Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases. European Journal of Medical Genetics. 57(1). 5–14. 67 indexed citations
10.
Spaggiari, Emmanuel, Clarisse Baumann, Marianne Alison, et al.. (2013). Mowat–Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: Advocacy for standard autopsy. European Journal of Medical Genetics. 56(6). 297–300. 13 indexed citations
11.
Rambaud, Jérôme, Isabelle Marey, Céline Dupont, et al.. (2012). Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication. American Journal of Medical Genetics Part A. 158A(9). 2277–2282. 2 indexed citations
12.
Grati, Francesca Romana, D. Molina Gomes, Devika Ganesamoorthy, et al.. (2012). Application of a new molecular technique for the genetic evaluation of products of conception. Prenatal Diagnosis. 33(1). 32–41. 15 indexed citations
13.
Spaggiari, Emmanuel, Azzedine Aboura, Martine Sinico, et al.. (2012). Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre–Chotzen syndrome. European Journal of Medical Genetics. 55(8-9). 498–501. 4 indexed citations
14.
Auger, Jacques, Céline Dupont, Dominique Le Tessier, et al.. (2010). Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management. European Journal of Medical Genetics. 53(3). 127–132. 6 indexed citations
15.
Dupont, Céline, R. Allemand, & Jean‐Marie Delpuech. (2010). Induction by Chlorpyrifos, of the Confusion of Males in Discriminating Female Sexual Pheromones Used for Mate Finding by Two SympatricTrichogrammaSpecies (Hymenoptera: Trichogrammatidae). Environmental Entomology. 39(2). 535–544. 14 indexed citations
16.
Toutain, Annick, Céline Dupont, Anne Claude Tabet, et al.. (2009). Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3. European Journal of Medical Genetics. 52(5). 328–332. 41 indexed citations
17.
Gérard‐Blanluet, Marion, Stéphane Serero, Clarisse Baumann, et al.. (2008). Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome. American Journal of Medical Genetics Part A. 146A(14). 1871–1874. 9 indexed citations
18.
Vidailhet, M, Arnaud Bocquet, J.-L. Bresson, et al.. (2008). Prévention par l’acide folique des défauts de fermeture du tube neural : la question n’est toujours pas réglée. Archives de Pédiatrie. 15(7). 1223–1231. 7 indexed citations
19.
Dupont, Céline, Aziza Lebbar, Cécile Teinturier, et al.. (2007). First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation. American Journal of Medical Genetics Part A. 143A(11). 1236–1243. 11 indexed citations
20.
Pipiras, Eva, Céline Dupont, Sandra Chantot‐Bastaraud, et al.. (2004). Structural chromosomal mosaicism and prenatal diagnosis. Prenatal Diagnosis. 24(2). 101–103. 15 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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