Jacqueline Vigneron

2.4k total citations · 1 hit paper
18 papers, 826 citations indexed

About

Jacqueline Vigneron is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jacqueline Vigneron has authored 18 papers receiving a total of 826 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Jacqueline Vigneron's work include Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (5 papers) and Head and Neck Anomalies (3 papers). Jacqueline Vigneron is often cited by papers focused on Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (5 papers) and Head and Neck Anomalies (3 papers). Jacqueline Vigneron collaborates with scholars based in France, United States and Belgium. Jacqueline Vigneron's co-authors include Didier Lacombe, Delphine Samson, Katia Boven, Nicole Van Regemorter, Iman Sahly, C. Vincent, Corinne Cruaud, P Bedbeder, Maria Bitner‐Glindzicz and Jean Weissenbach and has published in prestigious journals such as Nature Genetics, Neurology and The Journal of Pediatrics.

In The Last Decade

Jacqueline Vigneron

18 papers receiving 813 citations

Hit Papers

A human homologue of the Drosophila eyes absent gene unde... 1997 2026 2006 2016 1997 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
    1997 467 citations Sonia Abdelhak, Vasiliki Kalatzis et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacqueline Vigneron France 11 486 336 191 117 85 18 826
Sylvie Compain France 5 395 0.8× 128 0.4× 250 1.3× 80 0.7× 111 1.3× 6 675
Tuula Rinne Netherlands 15 601 1.2× 253 0.8× 101 0.5× 48 0.4× 60 0.7× 32 997
Susanne Morlot Germany 17 631 1.3× 399 1.2× 105 0.5× 82 0.7× 34 0.4× 35 960
Derek Silvius United States 11 981 2.0× 252 0.8× 203 1.1× 82 0.7× 206 2.4× 18 1.3k
James Lespinasse France 15 702 1.4× 619 1.8× 82 0.4× 77 0.7× 54 0.6× 35 1.4k
Dan Zou United States 7 466 1.0× 127 0.4× 144 0.8× 40 0.3× 146 1.7× 9 677
P Bedbeder France 4 301 0.6× 90 0.3× 172 0.9× 68 0.6× 87 1.0× 11 556
Patricia Blanchet France 16 501 1.0× 245 0.7× 65 0.3× 100 0.9× 268 3.2× 47 828
Ralf Spörle Germany 14 967 2.0× 292 0.9× 53 0.3× 92 0.8× 39 0.5× 18 1.2k
Florence Dastot‐Le Moal France 14 720 1.5× 454 1.4× 378 2.0× 82 0.7× 132 1.6× 17 1.4k

Countries citing papers authored by Jacqueline Vigneron

Since Specialization
Citations

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

Fields of papers citing papers by Jacqueline Vigneron

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Vigneron

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

All Works

18 of 18 papers shown
1.
Vincent, Marie, Corinne Collet, Alain Verloès, et al.. (2013). Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability. European Journal of Human Genetics. 22(1). 52–56. 15 indexed citations
2.
Giannandrea, Maila, Nathalie Fieremans, Jelle Verbeeck, et al.. (2013). Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains. Human Mutation. 35(3). 377–383. 47 indexed citations
3.
Béri‐Dexheimer, Mylène, Céline Bonnet, Myriam Bronner, et al.. (2012). RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability. American Journal of Medical Genetics Part A. 158A(7). 1782–1784. 5 indexed citations
4.
Aliferis, Konstantinos A., Corinne Stoetzel, Valérie Pelletier, et al.. (2011). A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype. Ophthalmic Genetics. 32(4). 250–255. 14 indexed citations
5.
Bénéteau, Claire, Emilie Landais, C. Philippe, et al.. (2011). Microtriplication of 11q24.1: a highly recognisable phenotype with short stature, distinctive facial features, keratoconus, overweight, and intellectual disability. Journal of Medical Genetics. 48(9). 635–639. 9 indexed citations
6.
Becdelièvre, Alix de, Marie Legendre, Jacqueline Vigneron, et al.. (2010). Notable contribution of large CFTR gene rearrangements to the diagnosis of cystic fibrosis in fetuses with bowel anomalies. European Journal of Human Genetics. 18(10). 1166–1169. 3 indexed citations
7.
Stoetzel, Corinne, S. Riehm, Jacqueline Vigneron, et al.. (2009). Confirmation of TFAP2A gene involvement in branchio‐oculo‐facial syndrome (BOFS) and report of temporal bone anomalies. American Journal of Medical Genetics Part A. 149A(10). 2141–2146. 26 indexed citations
8.
Maldergem, Lionel Van, Memnune Yüksel‐Apak, Hülya Kayserili, et al.. (2008). Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type. Neurology. 71(20). 1602–1608. 27 indexed citations
9.
Dubourg, Christèle, Jocelyne Attia‐Sobol, Jacqueline Vigneron, et al.. (2003). Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations. Human Genetics. 112(2). 131–134. 40 indexed citations
10.
Perrin, Aurore, et al.. (2001). Evolution des dispensations d'antirétroviraux, conseil pharmaceutique et satisfaction des patients dans un centre hospitalier universitaire. Journal de Pharmacie Clinique. 19(4). 303–314. 1 indexed citations
11.
David, A., Pierre Bitoun, Didier Lacombe, et al.. (1999). Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes. Journal of Medical Genetics. 36(8). 599–603. 72 indexed citations
12.
Marec, B. Le, et al.. (1998). Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: A review. American Journal of Medical Genetics. 75(4). 389–394. 40 indexed citations
13.
Odent, Sylvie, B. Le Marec, Annick Toutain, et al.. (1998). Central nervous system malformations and early end‐stage renal disease in oro‐facio‐digital syndrome type I: A review. American Journal of Medical Genetics. 75(4). 389–394. 2 indexed citations
14.
Gérard, H, et al.. (1997). [Unusual facial clefts].. PubMed. 42(5). 401–41. 1 indexed citations
15.
Abdelhak, Sonia, Vasiliki Kalatzis, Roland Heilig, et al.. (1997). A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family. Nature Genetics. 15(2). 157–164. 467 indexed citations breakdown →
16.
Bonaventure, Jacky, C. Philippe, Ghislaine Plessis, et al.. (1992). Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene. Human Genetics. 90(1-2). 164–8. 25 indexed citations
17.
Vigneron, Jacqueline, et al.. (1991). Postaxial acrofacial dysostosis (Miller) syndrome: a new case.. Journal of Medical Genetics. 28(9). 636–638. 8 indexed citations
18.
André, Márcia, Jacqueline Vigneron, & F Didier. (1981). Abnormal facies, cleft palate, and generalized dysostosis: A lethal X-linked syndrome. The Journal of Pediatrics. 98(5). 747–752. 24 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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