P. Vabres

16.3k total citations
135 papers, 2.8k citations indexed

About

P. Vabres is a scholar working on Molecular Biology, Genetics and Dermatology. According to data from OpenAlex, P. Vabres has authored 135 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 41 papers in Genetics and 39 papers in Dermatology. Recurrent topics in P. Vabres's work include Genetic and rare skin diseases. (23 papers), Vascular Malformations and Hemangiomas (23 papers) and Cancer and Skin Lesions (16 papers). P. Vabres is often cited by papers focused on Genetic and rare skin diseases. (23 papers), Vascular Malformations and Hemangiomas (23 papers) and Cancer and Skin Lesions (16 papers). P. Vabres collaborates with scholars based in France, United States and United Kingdom. P. Vabres's co-authors include J. Mazereeuw‐Hautier, S. Hadj‐Rabia, Christine Bodemer, S. Barbarot, Y. De Prost, Dominique Hamel‐Teillac, Stanislas Lyonnet, Arnold Münnich, Emmanuel Jacquemin and Lekbir Baala and has published in prestigious journals such as Nature Communications, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

P. Vabres

124 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P. Vabres France	29	917	620	560	497	483	135	2.8k
Mi Ryung Roh South Korea	29	562 0.6×	1.1k 1.7×	210 0.4×	423 0.9×	286 0.6×	134	2.3k
John C. Maize United States	33	751 0.8×	1.2k 2.0×	787 1.4×	340 0.7×	449 0.9×	135	3.8k
Brian J. Nickoloff United States	33	1.1k 1.2×	1.1k 1.7×	503 0.9×	544 1.1×	342 0.7×	49	4.3k
April Deng United States	24	444 0.5×	487 0.8×	249 0.4×	189 0.4×	418 0.9×	84	1.9k
Nobuo Kanazawa Japan	27	1.1k 1.2×	322 0.5×	319 0.6×	256 0.5×	220 0.5×	131	3.5k
Hjalmar Kurzen Germany	25	629 0.7×	1.1k 1.8×	186 0.3×	582 1.2×	246 0.5×	59	2.3k
John T. Seykora United States	35	2.2k 2.4×	1.1k 1.8×	320 0.6×	230 0.5×	908 1.9×	108	4.8k
Ralph J. Tuthill United States	29	745 0.8×	429 0.7×	441 0.8×	236 0.5×	129 0.3×	84	2.7k
Carlo Cota Italy	26	351 0.4×	1.1k 1.7×	341 0.6×	155 0.3×	473 1.0×	115	2.1k
J.P.W. van der Veen Netherlands	25	425 0.5×	774 1.2×	159 0.3×	233 0.5×	1.0k 2.2×	67	2.4k

Countries citing papers authored by P. Vabres

Since Specialization

Citations

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

Fields of papers citing papers by P. Vabres

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Vabres

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bonniaud, B., Maxime Luu, Catherine Cormier, et al.. (2025). Lack of behavioural improvement with sirolimus in a patient with MTOR-related macrocephaly with pigmentary mosaicism: A new case report. European Journal of Medical Genetics. 75. 105012–105012.

Kuentz, Paul, Rachida Tacine, Marie Vincent, et al.. (2025). A postzygotic GNA13 variant upregulates the RHOA/ROCK pathway and alters melanocyte function in a mosaic skin hypopigmentation syndrome. Nature Communications. 16(1). 1751–1751. 2 indexed citations

Chevarin, Martin, Juliette Piard, Quentin Thomas, et al.. (2024). Allelic heterogeneity in a patient with postzygotic MTOR ‐related hypomelanosis of Ito with neurodevelopmental abnormalities. Clinical Genetics. 105(5). 581–583. 2 indexed citations

Chevarin, Martin, Antonio Vitobello, Cyril Fournier, et al.. (2022). A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European Journal of Human Genetics. 31(7). 761–768. 6 indexed citations

Vabres, P., et al.. (2022). Muscle hemihypertrophy syndrome with PIK3CA gene mutation associated with Tourette syndrome. JAAD Case Reports. 30. 128–130. 1 indexed citations

Theiler, Martin, Lisa Weibel, Stéphanie Christen‐Zaech, et al.. (2021). Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations. Journal of the European Academy of Dermatology and Venereology. 35(10). 2085–2090. 4 indexed citations

Park, Hyun‐Sook, Daniel Bachmann, Markus Plomann, et al.. (2021). ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies. Communications Biology. 4(1). 544–544. 6 indexed citations

Carmignac, Virginie, Arthur Sorlin, Yannis Duffourd, et al.. (2021). Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway. Ultrasound in Obstetrics and Gynecology. 59(4). 532–542. 7 indexed citations

Douzgou, Sofia, Eulàlia Baselga, Moise Danielpour, et al.. (2021). A standard of care for individuals with PIK3CA ‐related disorders: An international expert consensus statement. Clinical Genetics. 101(1). 32–47. 20 indexed citations

10.

Kinsler, Veronica A., O. Boccara, Sylvie Fraïtag, et al.. (2019). Mosaic abnormalities of the skin: review and guidelines from the European Reference Network for rare skin diseases. British Journal of Dermatology. 182(3). 552–563. 32 indexed citations

11.

Bris, Céline, Vincent Procaccio, Patrizia Amati‐Bonneau, et al.. (2019). Deciphering exome sequencing data: Bringing mitochondrial DNA variants to light. Human Mutation. 40(12). 2430–2443. 7 indexed citations

12.

Lefebvre, Mathilde, Christine Francannet, Hélène Laurichesse, et al.. (2018). Extending the ALDH18A1 clinical spectrum to severe autosomal recessive fetal cutis laxa with corpus callosum agenesis. American Journal of Medical Genetics Part A. 176(11). 2509–2512. 6 indexed citations

13.

Castela, E., Meri K. Tulić, Aurore Rozières, et al.. (2018). Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment. British Journal of Dermatology. 180(2). 357–364. 38 indexed citations

14.

Bal, Élodie, Emmanuel Laplantine, Yamina Hamel, et al.. (2017). Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti. Journal of Allergy and Clinical Immunology. 140(6). 1671–1682.e2. 13 indexed citations

15.

Dreyfus, I., E. Bourrat, A. Maruani, et al.. (2014). Factors Associated with Impaired Quality of Life in Adult Patients Suffering from Ichthyosis. Acta Dermato Venereologica. 94(3). 344–346. 24 indexed citations

16.

Vabres, P., et al.. (2008). Macules mélanotiques congénitales de la langue. Annales de Dermatologie et de Vénéréologie. 135(8-9). 567–570. 6 indexed citations

17.

Dighiero, P., et al.. (2004). Corneal recurrent erosions and mutations in the gene COL7A1. Investigative Ophthalmology & Visual Science. 45(13). 1510–1510. 1 indexed citations

18.

Mégarbané, André, et al.. (2002). Linear and whorled nevoid hypermelanosis with bilateral giant cerebral aneurysms. American Journal of Medical Genetics. 112(1). 95–98. 8 indexed citations

19.

Mcheik, Jiad N., P. Vabres, Dominique Bonneau, Michel Longy, & G. Levard. (2002). Maladie de Cowden chez un adolescent. Annales de Chirurgie. 127(2). 138–141. 1 indexed citations

20.

Larrègue, M, et al.. (1997). Toxidermies fébriles de l'enfant.. La Revue du praticien. 47(13). 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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