Mathieu Quinodoz

4.6k total citations
40 papers, 622 citations indexed

About

Mathieu Quinodoz is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Mathieu Quinodoz has authored 40 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 16 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Mathieu Quinodoz's work include Retinal Development and Disorders (17 papers), Genomics and Rare Diseases (8 papers) and RNA regulation and disease (6 papers). Mathieu Quinodoz is often cited by papers focused on Retinal Development and Disorders (17 papers), Genomics and Rare Diseases (8 papers) and RNA regulation and disease (6 papers). Mathieu Quinodoz collaborates with scholars based in Switzerland, United Kingdom and United States. Mathieu Quinodoz's co-authors include Carlo Rivolta, Andrea Superti‐Furga, Virginie G. Peter, Katarina Cisarova, Béryl Royer‐Bertrand, Silvio Alessandro Di Gioia, Luísa Coutinho Santos, Ana Berta Sousa, Sheila Unger and Nicola Bedoni and has published in prestigious journals such as Nature Communications, The EMBO Journal and Nature Biotechnology.

In The Last Decade

Mathieu Quinodoz

36 papers receiving 614 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mathieu Quinodoz Switzerland 15 419 220 75 62 51 40 622
Ingvild Aukrust Norway 16 464 1.1× 275 1.3× 61 0.8× 77 1.2× 31 0.6× 41 709
Salma Ben‐Salem United Arab Emirates 13 256 0.6× 209 0.9× 41 0.5× 37 0.6× 64 1.3× 26 470
Janneke Schuurs-Hoeijmakers Netherlands 14 463 1.1× 398 1.8× 37 0.5× 66 1.1× 14 0.3× 29 773
Cristina Méndez‐Vidal Spain 16 595 1.4× 122 0.6× 182 2.4× 52 0.8× 110 2.2× 28 725
Qing‐Shuo Zhang United States 11 656 1.6× 76 0.3× 96 1.3× 40 0.6× 33 0.6× 20 804
Maartje van de Vorst Netherlands 9 360 0.9× 186 0.8× 111 1.5× 27 0.4× 37 0.7× 13 593
Béryl Royer‐Bertrand Switzerland 12 268 0.6× 160 0.7× 56 0.7× 54 0.9× 166 3.3× 17 515
Hatice Duzkale United States 7 325 0.8× 105 0.5× 40 0.5× 44 0.7× 88 1.7× 12 423
Corinne Bareil France 16 527 1.3× 102 0.5× 79 1.1× 51 0.8× 90 1.8× 26 823
Pinghu Liu United States 9 375 0.9× 90 0.4× 72 1.0× 67 1.1× 32 0.6× 12 558

Countries citing papers authored by Mathieu Quinodoz

Since Specialization
Citations

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

Fields of papers citing papers by Mathieu Quinodoz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathieu Quinodoz

This figure shows the co-authorship network connecting the top 25 collaborators of Mathieu Quinodoz. A scholar is included among the top collaborators of Mathieu Quinodoz 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 Mathieu Quinodoz. Mathieu Quinodoz 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.
Pfau, Kristina, Stephan Michels, Chantal Dysli, et al.. (2025). Topography of Slowed Dark Adaptation in Pseudoxanthoma Elasticum: PROPXE Study Report 1. Investigative Ophthalmology & Visual Science. 66(2). 17–17.
2.
Ullah, Mukhtar, Mathieu Quinodoz, Abdur Rashid, et al.. (2025). A comprehensive genetic landscape of inherited retinal diseases in a large Pakistani cohort. npj Genomic Medicine. 10(1). 31–31. 2 indexed citations
3.
Mata, Nathan L., Shi-Jun Weng, Peter Charbel Issa, et al.. (2025). Bisretinoids as a Source of Early Photoreceptor Pathology in Stargardt Disease. Ophthalmic Research. 68(1). 555–572. 1 indexed citations
4.
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
5.
Quinodoz, Mathieu, Marc Folcher, Siying Lin, et al.. (2024). Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa. The American Journal of Human Genetics. 111(10). 2299–2306. 1 indexed citations
6.
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
7.
Hahaut, Vincent, Dinko Pavlinić, Walter Carbone, et al.. (2022). Fast and highly sensitive full-length single-cell RNA sequencing using FLASH-seq. Nature Biotechnology. 40(10). 1447–1451. 53 indexed citations
8.
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
9.
Patzke, Sebastian, Pernille Martens, Mathieu Quinodoz, et al.. (2021). CEP78 functions downstream of CEP350 to control biogenesis of primary cilia by negatively regulating CP110 levels. eLife. 10. 23 indexed citations
10.
Perea‐Romero, Irene, Fiona Blanco‐Kelly, Iker Sánchez‐Navarro, et al.. (2021). NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases. Human Genetics. 140(12). 1665–1678. 12 indexed citations
11.
Guy, Alyson, Lu Liu, Mathieu Quinodoz, et al.. (2021). Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder. Human Molecular Genetics. 31(12). 1970–1978. 2 indexed citations
12.
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
13.
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
14.
Salmaninejad, Arash, Nicola Bedoni, Mathieu Quinodoz, et al.. (2020). Whole exome sequencing and homozygosity mapping reveals genetic defects in consanguineous Iranian families with inherited retinal dystrophies. Scientific Reports. 10(1). 19413–19413. 7 indexed citations
15.
Quinodoz, Mathieu, Marie‐Claude Addor, Béryl Royer‐Bertrand, et al.. (2020). Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literature. BMC Neurology. 20(1). 17–17. 13 indexed citations
16.
Bibert, Stéphanie, Jocelyne Piret, Mathieu Quinodoz, et al.. (2019). Herpes simplex encephalitis in adult patients with MASP-2 deficiency. PLoS Pathogens. 15(12). e1008168–e1008168. 19 indexed citations
17.
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
18.
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
19.
Fregni, Giulia, Mathieu Quinodoz, Emely Möller, et al.. (2018). Reciprocal modulation of mesenchymal stem cells and tumor cells promotes lung cancer metastasis. EBioMedicine. 29. 128–145. 61 indexed citations
20.
Quinodoz, Mathieu, Béryl Royer‐Bertrand, Katarina Cisarova, et al.. (2017). DOMINO: Using Machine Learning to Predict Genes Associated with Dominant Disorders. The American Journal of Human Genetics. 101(4). 623–629. 66 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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