Benoı̂t Arveiler

6.4k total citations
137 papers, 3.1k citations indexed

About

Benoı̂t Arveiler is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Benoı̂t Arveiler has authored 137 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Molecular Biology, 51 papers in Genetics and 39 papers in Cell Biology. Recurrent topics in Benoı̂t Arveiler's work include melanin and skin pigmentation (35 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA regulation and disease (20 papers). Benoı̂t Arveiler is often cited by papers focused on melanin and skin pigmentation (35 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA regulation and disease (20 papers). Benoı̂t Arveiler collaborates with scholars based in France, United Kingdom and United States. Benoı̂t Arveiler's co-authors include Didier Lacombe, Caroline Rooryck, Jean‐Louis Mandel, Fanny Morice‐Picard, Cyril Goizet, Eulalie Lasseaux, David J. Porteous, Dorothée Cailley, Marie‐Ange Delrue and I. Oberlé and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Benoı̂t Arveiler

135 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benoı̂t Arveiler France 33 1.7k 1.2k 693 311 301 137 3.1k
Andreas Janecke Austria 37 2.2k 1.3× 1.3k 1.1× 694 1.0× 319 1.0× 333 1.1× 132 4.4k
Yoshinori Tsurusaki Japan 37 2.6k 1.5× 1.6k 1.3× 392 0.6× 224 0.7× 90 0.3× 146 3.9k
Stéphane Schurmans Belgium 32 2.3k 1.4× 912 0.8× 632 0.9× 509 1.6× 421 1.4× 94 4.1k
Shanthini Sockanathan United States 29 2.9k 1.7× 1.1k 0.9× 557 0.8× 259 0.8× 106 0.4× 45 3.9k
Anna‐Elina Lehesjoki Finland 39 2.1k 1.2× 1.6k 1.3× 943 1.4× 441 1.4× 69 0.2× 126 4.9k
Atsushi Watanabe Japan 29 1.1k 0.7× 438 0.4× 414 0.6× 186 0.6× 195 0.6× 137 3.0k
Annick Raas‐Rothschild Israel 34 1.7k 1.0× 898 0.7× 781 1.1× 134 0.4× 50 0.2× 108 3.8k
Yoshiro Toyama Japan 33 1.8k 1.1× 716 0.6× 761 1.1× 257 0.8× 52 0.2× 112 3.7k
Maurizio D’Esposito Italy 34 2.9k 1.7× 1.2k 1.0× 470 0.7× 196 0.6× 64 0.2× 67 3.8k
Andreas W. Kuß Germany 33 1.8k 1.1× 1.0k 0.9× 275 0.4× 372 1.2× 64 0.2× 87 3.2k

Countries citing papers authored by Benoı̂t Arveiler

Since Specialization
Citations

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

Fields of papers citing papers by Benoı̂t Arveiler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benoı̂t Arveiler

This figure shows the co-authorship network connecting the top 25 collaborators of Benoı̂t Arveiler. A scholar is included among the top collaborators of Benoı̂t Arveiler 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 Benoı̂t Arveiler. Benoı̂t Arveiler 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.
Michaud, Vincent, et al.. (2025). A patient with TPCN2-related hypopigmentation and ocular phenotype. European Journal of Human Genetics. 33(3). 383–386. 1 indexed citations
2.
Green, David J., Vincent Michaud, Eulalie Lasseaux, et al.. (2024). The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism. Nature Communications. 15(1). 8436–8436. 3 indexed citations
3.
Plaisant, Claudio, Angèle Tingaud‐Sequeira, Sophie Javerzat, et al.. (2024). Genotypic spectrum of albinism in Mali. Pigment Cell & Melanoma Research. 37(6). 752–761. 3 indexed citations
4.
Lasseaux, Eulalie, et al.. (2024). Crossed VEP asymmetry in a patient with AHR-linked infantile nystagmus and foveal hypoplasia. Documenta Ophthalmologica. 149(1). 47–52. 1 indexed citations
5.
Michaud, Vincent, Angèle Tingaud‐Sequeira, Eulalie Lasseaux, et al.. (2023). Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism. Pigment Cell & Melanoma Research. 37(5). 534–545. 4 indexed citations
6.
Sergouniotis, Panagiotis I., Vincent Michaud, Eulalie Lasseaux, et al.. (2023). A multilayered approach to the analysis of genetic data from individuals with suspected albinism. Journal of Medical Genetics. 60(12). 1245–1249. 1 indexed citations
7.
Michaud, Vincent, Eulalie Lasseaux, Vivien Vasseur, et al.. (2022). Foveal hypoplasia in parents of patients with albinism. Ophthalmic Genetics. 43(6). 817–823. 2 indexed citations
8.
Tingaud‐Sequeira, Angèle, Vincent Michaud, Benoı̂t Pinson, et al.. (2022). The Dct−/− Mouse Model to Unravel Retinogenesis Misregulation in Patients with Albinism. Genes. 13(7). 1164–1164. 4 indexed citations
9.
Morice‐Picard, Fanny, Eulalie Lasseaux, Matthieu P. Robert, et al.. (2022). Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation. Genes. 13(12). 2198–2198. 6 indexed citations
10.
Michaud, Vincent, Eulalie Lasseaux, David Green, et al.. (2022). The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism. Nature Communications. 13(1). 3939–3939. 24 indexed citations
11.
Elalaoui, Siham Chafai, Julien Van‐Gils, Patricia Fergelot, et al.. (2021). Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome. African Health Sciences. 21(2). 960–967. 1 indexed citations
12.
Morice‐Picard, Fanny, Dominique Brémond‐Gignac, Stéphanie Leclerc‐Mercier, et al.. (2021). Management of albinism: French guidelines for diagnosis and care. Journal of the European Academy of Dermatology and Venereology. 35(7). 1449–1459. 11 indexed citations
13.
Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Rachel Stapleton, et al.. (2021). A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum. Human Genetics. 140(6). 933–944. 16 indexed citations
14.
Michaud, Vincent, Mathieu Fiore, Jean‐Claude Bordet, et al.. (2020). A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies. Platelets. 32(3). 420–423. 8 indexed citations
15.
Van‐Gils, Julien, Sophie Naudion, Jérôme Toutain, et al.. (2019). Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations. Clinical Genetics. 95(3). 420–426. 8 indexed citations
16.
Michaud, Vincent, Sabine Defoort‐Dhellemmes, Isabelle Drumare, et al.. (2019). Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinism. Ophthalmic Genetics. 40(2). 161–164. 1 indexed citations
17.
Lasseaux, Eulalie, et al.. (2019). A Novel Non-Sense Mutation in a Senegalese Patient with Hermansky-Pudlak Type 1 Syndrome. Journal of Molecular and Genetic Medicine. 13(1). 1–4. 1 indexed citations
18.
Lasseaux, Eulalie, Khaled Ezzedine, C. Léauté‐Labrèze, et al.. (2017). Lessons of a day hospital: Comprehensive assessment of patients with albinism in a European setting. Pigment Cell & Melanoma Research. 31(2). 318–329. 26 indexed citations
19.
Mignot, Cyril, Marie‐Laure Moutard, Oriane Trouillard, et al.. (2011). STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Epilepsia. 52(10). 1820–1827. 76 indexed citations
20.
Rooryck, Caroline, et al.. (2009). Genetic basis of oculocutaneous albinism. Expert Review of Dermatology. 4(6). 611–622. 14 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 Andreas Janecke Breakdown of academic impact, for papers by Yoshinori Tsurusaki Breakdown of academic impact, for papers by Stéphane Schurmans Breakdown of academic impact, for papers by Shanthini Sockanathan Breakdown of academic impact, for papers by Anna‐Elina Lehesjoki Breakdown of academic impact, for papers by Atsushi Watanabe Breakdown of academic impact, for papers by Annick Raas‐Rothschild Breakdown of academic impact, for papers by Yoshiro Toyama Breakdown of academic impact, for papers by Maurizio D’Esposito Breakdown of academic impact, for papers by Andreas W. Kuß
Rankless by CCL
2026