Virginie G. Peter

616 total citations
17 papers, 325 citations indexed

About

Virginie G. Peter is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Virginie G. Peter has authored 17 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Virginie G. Peter's work include Retinal Development and Disorders (6 papers), RNA regulation and disease (4 papers) and Genomics and Rare Diseases (2 papers). Virginie G. Peter is often cited by papers focused on Retinal Development and Disorders (6 papers), RNA regulation and disease (4 papers) and Genomics and Rare Diseases (2 papers). Virginie G. Peter collaborates with scholars based in Switzerland, United Kingdom and Portugal. Virginie G. Peter's co-authors include Carlo Rivolta, Mathieu Quinodoz, Andrea Superti‐Furga, Katarina Cisarova, Luísa Coutinho Santos, Ana Berta Sousa, Sheila Unger, Raquel Rodrigues, Nicola Bedoni and Béryl Royer‐Bertrand and has published in prestigious journals such as Nature Communications, The EMBO Journal and Scientific Reports.

In The Last Decade

Virginie G. Peter

17 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Virginie G. Peter Switzerland 10 198 121 65 41 25 17 325
Kelly E. Jackson United States 8 204 1.0× 211 1.7× 30 0.5× 26 0.6× 24 1.0× 15 375
Zixi Sun China 11 224 1.1× 67 0.6× 110 1.7× 32 0.8× 15 0.6× 37 304
Mohammed E. El‐Asrag United Kingdom 10 153 0.8× 58 0.5× 51 0.8× 32 0.8× 17 0.7× 17 211
Kristin McDonald Gibson United States 8 272 1.4× 118 1.0× 20 0.3× 43 1.0× 19 0.8× 9 424
Sara Barbato Italy 8 248 1.3× 53 0.4× 35 0.5× 14 0.3× 34 1.4× 10 329
Davood Zare‐Abdollahi Iran 10 224 1.1× 61 0.5× 17 0.3× 30 0.7× 29 1.2× 26 308
Luz María González-Huerta Mexico 10 216 1.1× 126 1.0× 46 0.7× 36 0.9× 18 0.7× 39 303
Åsa Blixt Sweden 7 372 1.9× 164 1.4× 95 1.5× 42 1.0× 13 0.5× 9 463
Han Zhong Pei China 12 412 2.1× 55 0.5× 123 1.9× 67 1.6× 42 1.7× 19 509
Ana Arteche‐López Spain 9 172 0.9× 95 0.8× 58 0.9× 22 0.5× 24 1.0× 23 262

Countries citing papers authored by Virginie G. Peter

Since Specialization
Citations

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

Fields of papers citing papers by Virginie G. Peter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Virginie G. Peter. 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 Virginie G. Peter. The network helps show where Virginie G. Peter may publish in the future.

Co-authorship network of co-authors of Virginie G. Peter

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

All Works

17 of 17 papers shown
1.
Vaz-Pereira, Sara, Lilianne Duarte, Ana Berta Sousa, et al.. (2024). Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe s Archive for Clinical and Experimental Ophthalmology. 262(6). 1883–1897. 5 indexed citations
2.
Quinodoz, Mathieu, Virginie G. Peter, Livia Garavelli, et al.. (2024). De novo variants in LRRC8C resulting in constitutive channel activation cause a human multisystem disorder. The EMBO Journal. 44(2). 413–436. 5 indexed citations
3.
Peter, Virginie G., Mathieu Quinodoz, Katarina Cisarova, et al.. (2023). The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesis. PNAS Nexus. 2(3). pgad043–pgad043. 19 indexed citations
4.
Peter, Virginie G., et al.. (2023). Investigating the Ocular Surface Microbiome: What Can It Tell Us?. Clinical ophthalmology. Volume 17. 259–271. 17 indexed citations
5.
Quinodoz, Mathieu, Virginie G. Peter, Katarina Cisarova, et al.. (2022). Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity. The American Journal of Human Genetics. 109(3). 457–470. 49 indexed citations
6.
Peter, Virginie G., et al.. (2022). A novel phenotype associated with the R162W variant in the KCNJ13 gene. Ophthalmic Genetics. 43(4). 500–507. 1 indexed citations
7.
Quinodoz, Mathieu, Virginie G. Peter, Nicola Bedoni, et al.. (2021). AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data. Nature Communications. 12(1). 518–518. 85 indexed citations
8.
Bedoni, Nicola, Arash Salmaninejad, Virginie G. Peter, et al.. (2021). Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies. Scientific Reports. 11(1). 19332–19332. 5 indexed citations
9.
Lebon, Sébastien, Mathieu Quinodoz, Virginie G. Peter, et al.. (2021). Agenesis of the Corpus Callosum with Facial Dysmorphism and Intellectual Disability in Sibs Associated with Compound Heterozygous KDM5B Variants. Genes. 12(9). 1397–1397. 2 indexed citations
10.
Peter, Virginie G., et al.. (2020). Exploring the genetic landscape of inherited retinal diseases in North-Western Pakistan reveals a high degree of autozygosity and prevalent founder mutations. Investigative Ophthalmology & Visual Science. 61(7). 2385–2385. 1 indexed citations
11.
Cisarova, Katarina, Marc Folcher, Ikram El Zaoui, et al.. (2020). Genomic and transcriptomic landscape of conjunctival melanoma. PLoS Genetics. 16(12). e1009201–e1009201. 28 indexed citations
12.
Peter, Virginie G., Mathieu Quinodoz, Marta Soares, et al.. (2020). New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV. Human Mutation. 42(3). 261–271. 25 indexed citations
13.
Bedoni, Nicola, J Cunningham, Eric S. Tucker, et al.. (2019). Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. PLoS Genetics. 15(8). e1008315–e1008315. 20 indexed citations
14.
Peter, Virginie G., Konstantinos Nikopoulos, Mathieu Quinodoz, et al.. (2019). A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa. Ophthalmic Genetics. 40(2). 177–181. 12 indexed citations
15.
Peter, Virginie G., Mathieu Quinodoz, Jorge Pinto‐Basto, et al.. (2019). The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene. Genetics in Medicine. 21(12). 2734–2743. 35 indexed citations
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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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2026