Marion Gauthier‐Villars

7.3k total citations · 1 hit paper
67 papers, 2.3k citations indexed

About

Marion Gauthier‐Villars is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Marion Gauthier‐Villars has authored 67 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 23 papers in Genetics and 22 papers in Ophthalmology. Recurrent topics in Marion Gauthier‐Villars's work include Ocular Oncology and Treatments (22 papers), BRCA gene mutations in cancer (15 papers) and Cancer-related Molecular Pathways (14 papers). Marion Gauthier‐Villars is often cited by papers focused on Ocular Oncology and Treatments (22 papers), BRCA gene mutations in cancer (15 papers) and Cancer-related Molecular Pathways (14 papers). Marion Gauthier‐Villars collaborates with scholars based in France, Germany and United Kingdom. Marion Gauthier‐Villars's co-authors include Dominique Stoppa‐Lyonnet, François Doz, Isabelle Aerts, Livia Lumbroso‐Le Rouic, Laurence Desjardins, Claude Houdayer, Catherine Dehainault, Hervé J. Brisse, Laurence Brugières and Virginie Caux‐Moncoutier and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and JNCI Journal of the National Cancer Institute.

In The Last Decade

Marion Gauthier‐Villars

62 papers receiving 2.3k citations

Hit Papers

align trajectories

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.

Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers

2015 467 citations Gaëlle Bougeard, Mariette Renaux‐Petel et al. Journal of Clinical Oncology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marion Gauthier‐Villars France	25	1.0k	838	786	526	413	67	2.3k
Mette Klarskov Andersen Denmark	32	1.6k 1.6×	752 0.9×	329 0.4×	106 0.2×	410 1.0×	92	3.9k
Junne Kamihara United States	14	608 0.6×	296 0.4×	238 0.3×	72 0.1×	310 0.8×	40	1.5k
Harriet Druker Canada	17	553 0.5×	478 0.6×	428 0.5×	37 0.1×	338 0.8×	23	1.6k
K Michalová Czechia	26	844 0.8×	217 0.3×	262 0.3×	227 0.4×	245 0.6×	171	2.1k
Ana Novokmet Canada	11	582 0.6×	472 0.6×	355 0.5×	36 0.1×	444 1.1×	15	1.3k
Rob B. van der Luijt Netherlands	28	802 0.8×	931 1.1×	531 0.7×	40 0.1×	782 1.9×	64	2.7k
Sophie Giraud France	28	889 0.9×	446 0.5×	423 0.5×	70 0.1×	458 1.1×	71	2.4k
Amit Nathwani United Kingdom	24	601 0.6×	302 0.4×	217 0.3×	73 0.1×	142 0.3×	67	1.5k
John C. Krauss United States	31	839 0.8×	1.3k 1.6×	421 0.5×	27 0.1×	292 0.7×	137	3.0k
Henk B. Kal Netherlands	27	732 0.7×	677 0.8×	236 0.3×	55 0.1×	305 0.7×	84	2.6k

Countries citing papers authored by Marion Gauthier‐Villars

Since Specialization

Citations

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

Fields of papers citing papers by Marion Gauthier‐Villars

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marion Gauthier‐Villars. 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 Marion Gauthier‐Villars. The network helps show where Marion Gauthier‐Villars may publish in the future.

Co-authorship network of co-authors of Marion Gauthier‐Villars

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

All Works

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20 of 20 papers shown

Couque, Nathalie, Plamen Bokov, Marion Gauthier‐Villars, et al.. (2025). PHOX2B-associated Congenital Central Hypoventilation Syndrome Revealed Upon Treatment With Dinutuximab-beta. Journal of Pediatric Hematology/Oncology. 47(3). 144–147.

Molina‐Gomes, Denise, Bérénice Herve, Marion Gauthier‐Villars, et al.. (2024). The clinical value of optical genome mapping in the rapid characterization of RB1 duplication and 15q23q24.2 triplication, for more appropriate prenatal genetic counselling. Molecular Genetics & Genomic Medicine. 12(4). e2437–e2437. 2 indexed citations

Moncoutier, Virginie, Mélanie Pagès, Julien Masliah‐Planchon, et al.. (2023). Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh‐frozen breast/ovarian tumor versus blood. Clinical Genetics. 104(1). 107–113. 2 indexed citations

Dehainault, Catherine, Alexandre Matet, Livia Lumbroso‐Le Rouic, et al.. (2021). Highly Sensitive Detection Method of Retinoblastoma Genetic Predisposition and Biomarkers. Journal of Molecular Diagnostics. 23(12). 1714–1721. 16 indexed citations

Kratz, Christian P., Marjolijn C.J. Jongmans, Hélène Cavé, et al.. (2021). Predisposition to cancer in children and adolescents. The Lancet Child & Adolescent Health. 5(2). 142–154. 63 indexed citations

Réguerre, Yves, Lisa Golmard, Hervé J. Brisse, et al.. (2019). Syndrome associé aux variants pathogènes constitutionnels de DICER1 : Où en sommes-nous en 2019 ?. Bulletin du Cancer. 106(12). 1177–1189. 2 indexed citations

Buecher, Bruno, François Doz, Franck Bourdeaut, et al.. (2018). Syndrome CMMRD (déficience constitutionnelle des gènes MMR) : bases génétiques et aspects cliniques. Bulletin du Cancer. 106(2). 162–172. 4 indexed citations

Eloy, Philippine, Catherine Dehainault, Meriem Sefta, et al.. (2016). A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1. PLoS Genetics. 12(2). e1005888–e1005888. 26 indexed citations

Bougeard, Gaëlle, Mariette Renaux‐Petel, Jean‐Michel Flaman, et al.. (2015). Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers. Journal of Clinical Oncology. 33(21). 2345–2352. 467 indexed citations breakdown →

10.

Jehanne, M, Hervé J. Brisse, Marion Gauthier‐Villars, et al.. (2014). Le rétinoblastome : les avancées récentes. Bulletin du Cancer. 101(4). 380–387. 13 indexed citations

11.

Castéra, Laurent, Catherine Dehainault, Dorothée Michaux, et al.. (2012). Fine mapping of whole RB1 gene deletions in retinoblastoma patients confirms PCDH8 as a candidate gene for psychomotor delay. European Journal of Human Genetics. 21(4). 460–464. 9 indexed citations

12.

Abadie, Caroline, Marion Gauthier‐Villars, Nicolas Sirvent, & Isabelle Coupier. (2012). Mise au pointOncogénétique en oncopédiatrieGenetic predisposition to childhood cancer. Archives de Pédiatrie. 19(8). 1 indexed citations

13.

Foix‐L’Hélias, L., Isabelle Aerts, Laetitia Marchand‐Martin, et al.. (2012). Are children born after infertility treatment at increased risk of retinoblastoma?. Human Reproduction. 27(7). 2186–2192. 32 indexed citations

14.

Bourdeaut, Franck, Sandrine Ferrand, Laurence Brugières, et al.. (2011). ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome. European Journal of Human Genetics. 20(3). 291–297. 32 indexed citations

15.

Gauthier‐Villars, Marion & Dominique Stoppa‐Lyonnet. (2011). Les prédispositions génétiques aux cancers de l’enfant en 2011. Bulletin du Cancer. 98(5). 459–475. 2 indexed citations

16.

Buecher, Bruno, Marion Gauthier‐Villars, Laurence Desjardins, et al.. (2010). Contribution of CDKN2A/P16 INK4A, P14 ARF, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma. Familial Cancer. 9(4). 663–667. 17 indexed citations

17.

Lohmann, Dietmar, Brenda L. Gallie, Charlotte J. Dommering, & Marion Gauthier‐Villars. (2010). Clinical utility gene card for: Retinoblastoma. European Journal of Human Genetics. 19(3). 3–3. 5 indexed citations

18.

Taylor, Mélissa, Catherine Dehainault, Laurence Desjardins, et al.. (2006). Genotype–phenotype correlations in hereditary familial retinoblastoma. Human Mutation. 28(3). 284–293. 62 indexed citations

19.

Mancini, Julien, Catherine Noguès, Claude Adenis, et al.. (2006). Patients’ characteristics and rate of Internet use to obtain cancer information. Journal of Public Health. 28(3). 235–237. 32 indexed citations

20.

Gauthier‐Villars, Marion, Gudrun Schleiermacher, Isabelle Coupier, & Dominique Stoppa‐Lyonnet. (2003). Prédispositions génétiques aux cancers de l‘enfant. Le point en 2003. MTP. Médecine thérapeutique pédiatrie. 6(3). 153–161. 1 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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