Claudio Plaisant

637 total citations
20 papers, 337 citations indexed

About

Claudio Plaisant is a scholar working on Cell Biology, Molecular Biology and Nutrition and Dietetics. According to data from OpenAlex, Claudio Plaisant has authored 20 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cell Biology, 13 papers in Molecular Biology and 7 papers in Nutrition and Dietetics. Recurrent topics in Claudio Plaisant's work include melanin and skin pigmentation (16 papers), RNA regulation and disease (9 papers) and Biochemical Analysis and Sensing Techniques (7 papers). Claudio Plaisant is often cited by papers focused on melanin and skin pigmentation (16 papers), RNA regulation and disease (9 papers) and Biochemical Analysis and Sensing Techniques (7 papers). Claudio Plaisant collaborates with scholars based in France, United Kingdom and Russia. Claudio Plaisant's co-authors include Benoı̂t Arveiler, Eulalie Lasseaux, Vincent Michaud, Didier Lacombe, Perrine Pennamen, Fanny Morice‐Picard, Aurélien Trimouille, Caroline Rooryck, Angèle Tingaud‐Sequeira and Josseline Kaplan and has published in prestigious journals such as Nature Communications, British Journal of Ophthalmology and Journal of Medical Genetics.

In The Last Decade

Claudio Plaisant

20 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claudio Plaisant France	9	261	192	127	42	42	20	337
Eulalie Lasseaux France	12	330 1.3×	306 1.6×	157 1.2×	59 1.4×	56 1.3×	36	484
Robin Holmes United States	6	246 0.9×	127 0.7×	131 1.0×	168 4.0×	41 1.0×	7	380
Maria Teresa Landi United States	4	161 0.6×	92 0.5×	58 0.5×	91 2.2×	15 0.4×	5	250
Janny E. Lommerts Netherlands	11	272 1.0×	40 0.2×	79 0.6×	93 2.2×	5 0.1×	14	326
Florence Ribiérre France	4	79 0.3×	223 1.2×	13 0.1×	23 0.5×	67 1.6×	5	264
Fabienne Lucchese France	4	227 0.9×	32 0.2×	29 0.2×	88 2.1×	3 0.1×	4	321
Christina Killoran United States	6	24 0.1×	179 0.9×	11 0.1×	20 0.5×	173 4.1×	8	298
Martine Biervliet Belgium	7	76 0.3×	168 0.9×	11 0.1×	4 0.1×	122 2.9×	10	262
David Cruz-García Spain	10	229 0.9×	223 1.2×	5 0.0×	3 0.1×	16 0.4×	14	360
Marisa Encarnação Portugal	9	175 0.7×	105 0.5×	5 0.0×	2 0.0×	7 0.2×	19	318

Countries citing papers authored by Claudio Plaisant

Since Specialization

Citations

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

Fields of papers citing papers by Claudio Plaisant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudio Plaisant

This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Plaisant. A scholar is included among the top collaborators of Claudio Plaisant 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 Claudio Plaisant. Claudio Plaisant 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

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

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

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

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

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

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

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

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

Pennamen, Perrine, Angèle Tingaud‐Sequeira, Vincent Michaud, et al.. (2020). Novel variants in the BLOC1S3 gene in patients presenting a mild form of Hermansky–Pudlak syndrome. Pigment Cell & Melanoma Research. 34(1). 132–135. 7 indexed citations

10.

Pennamen, Perrine, Linh Le, Angèle Tingaud‐Sequeira, et al.. (2020). BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome. Genetics in Medicine. 22(10). 1613–1622. 55 indexed citations

11.

Trimouille, Aurélien, Florent Marguet, Eulalie Lasseaux, et al.. (2020). Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination. Acta Neuropathologica Communications. 8(1). 48–48. 6 indexed citations

12.

Pennamen, Perrine, Angèle Tingaud‐Sequeira, Iveta Gažová, et al.. (2020). Dopachrome tautomerase variants in patients with oculocutaneous albinism. Genetics in Medicine. 23(3). 479–487. 36 indexed citations

13.

Michaud, Vincent, Julien Van‐Gils, Claudio Plaisant, et al.. (2020). Triple diagnosis of Wiedemann‐Steiner, Waardenburg and DLG3‐related intellectual disability association found by WES: A case report. The Journal of Gene Medicine. 22(8). e3197–e3197. 7 indexed citations

14.

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

15.

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

16.

Morice‐Picard, Fanny, Perrine Pennamen, Benoı̂t Arveiler, et al.. (2019). PADDAS syndrome associated with hair dysplasia caused by a de novo missense variant of PUM1. American Journal of Medical Genetics Part A. 179(6). 1030–1033. 5 indexed citations

17.

Lasseaux, Eulalie, Christian Hamel, Sabine Defoort‐Dhellemmes, et al.. (2018). Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene. British Journal of Ophthalmology. 103(9). 1239–1247. 26 indexed citations

18.

Lasseaux, Eulalie, Claudio Plaisant, Vincent Michaud, et al.. (2018). Molecular characterization of a series of 990 index patients with albinism. Pigment Cell & Melanoma Research. 31(4). 466–474. 98 indexed citations

19.

Michaud, Vincent, Eulalie Lasseaux, Claudio Plaisant, et al.. (2017). Clinico‐molecular analysis of eleven patients with Hermansky–Pudlak type 5 syndrome, a mild form of HPS. Pigment Cell & Melanoma Research. 30(6). 563–570. 14 indexed citations

20.

Morice‐Picard, Fanny, Eulalie Lasseaux, Dorothée Cailley, et al.. (2013). High‐resolution array‐CGH in patients with oculocutaneous albinism identifies new deletions of the TYR, OCA2, and SLC45A2 genes and a complex rearrangement of the OCA2 gene. Pigment Cell & Melanoma Research. 27(1). 59–71. 21 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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