Gaël Manès

1.4k total citations
30 papers, 587 citations indexed

About

Gaël Manès is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Gaël Manès has authored 30 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Ophthalmology. Recurrent topics in Gaël Manès's work include Retinal Development and Disorders (21 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (6 papers). Gaël Manès is often cited by papers focused on Retinal Development and Disorders (21 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (6 papers). Gaël Manès collaborates with scholars based in France, Switzerland and United States. Gaël Manès's co-authors include Isabelle Meunier, Béatrice Bocquet, Christian P. Hamel, Audrey Sénéćhal, Serge Roche, Paul Bello, Vasiliki Kalatzis, Maxime Hebrard, Claire‐Marie Dhaenens and Bernard Puech and has published in prestigious journals such as PLoS ONE, Molecular and Cellular Biology and Biochemical Journal.

In The Last Decade

Gaël Manès

30 papers receiving 585 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gaël Manès France 16 493 202 111 70 65 30 587
Thanh Hoang United States 13 707 1.4× 151 0.7× 113 1.0× 62 0.9× 79 1.2× 20 805
Mingchu Xu United States 19 623 1.3× 184 0.9× 68 0.6× 182 2.6× 92 1.4× 28 760
Mariateresa Pizzo Italy 15 610 1.2× 134 0.7× 51 0.5× 93 1.3× 50 0.8× 20 737
Béatrice Bocquet France 16 527 1.1× 264 1.3× 87 0.8× 80 1.1× 90 1.4× 37 607
Ram Fridlich France 7 419 0.8× 140 0.7× 148 1.3× 46 0.7× 33 0.5× 8 502
Frédéric Blond France 9 408 0.8× 182 0.9× 134 1.2× 29 0.4× 36 0.6× 21 525
Daniela Sanges Italy 12 768 1.6× 218 1.1× 215 1.9× 148 2.1× 124 1.9× 12 861
Birgit Lorenz Germany 7 588 1.2× 383 1.9× 148 1.3× 105 1.5× 65 1.0× 10 720
Roberta Tammaro Italy 11 515 1.0× 87 0.4× 70 0.6× 180 2.6× 91 1.4× 12 615
Carmela Ziviello Italy 11 455 0.9× 238 1.2× 80 0.7× 101 1.4× 45 0.7× 15 545

Countries citing papers authored by Gaël Manès

Since Specialization
Citations

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

Fields of papers citing papers by Gaël Manès

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gaël Manès

This figure shows the co-authorship network connecting the top 25 collaborators of Gaël Manès. A scholar is included among the top collaborators of Gaël Manès 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 Gaël Manès. Gaël Manès 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.
Guéguen, Naïg, Emmanuelle Sarzi, Gaël Manès, et al.. (2021). Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?. Mitochondrion. 59. 169–174. 5 indexed citations
2.
Hamel, Christian, Laëtitia Lagoutte, Gaël Manès, et al.. (2019). Natural models for retinitis pigmentosa: progressive retinal atrophy in dog breeds. Human Genetics. 138(5). 441–453. 33 indexed citations
3.
Erkilic, Nejla, et al.. (2019). Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy. Stem Cell Research. 38. 101478–101478. 5 indexed citations
4.
Erkilic, Nejla, et al.. (2019). Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis. Stem Cell Research. 38. 101476–101476. 5 indexed citations
5.
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Erkilic, Nejla, et al.. (2018). Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2. Stem Cell Research. 33. 247–250. 8 indexed citations
7.
Roubertie, Agathe, Nicolas Leboucq, Marie Picot, et al.. (2015). Neuroradiological findings expand the phenotype of OPA1-related mitochondrial dysfunction. Journal of the Neurological Sciences. 349(1-2). 154–160. 20 indexed citations
8.
Angebault, Claire, Majida Charif, Bénédicte Mousson de Camaret, et al.. (2015). Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability. Human Molecular Genetics. 24(14). 3948–3955. 36 indexed citations
9.
Meunier, Isabelle, Gaël Manès, Béatrice Bocquet, et al.. (2014). Frequency and Clinical Pattern of Vitelliform Macular Dystrophy Caused by Mutations of Interphotoreceptor Matrix IMPG1 and IMPG2 Genes. Ophthalmology. 121(12). 2406–2414. 55 indexed citations
10.
Manès, Gaël, Anurima Majumder, Béatrice Bocquet, et al.. (2014). A Truncated Form of Rod Photoreceptor PDE6 β-Subunit Causes Autosomal Dominant Congenital Stationary Night Blindness by Interfering with the Inhibitory Activity of the γ-Subunit. PLoS ONE. 9(4). e95768–e95768. 21 indexed citations
11.
Benaglio, Paola, Almudena Ávila‐Fernández, Shyana Harper, et al.. (2014). Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosa. PubMed. 20. 843–51. 13 indexed citations
12.
Bocquet, Béatrice, Nour‐Al‐Dain Marzouka, Maxime Hebrard, et al.. (2013). Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations.. PubMed Central. 41 indexed citations
13.
Hebrard, Maxime, et al.. (2011). Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families. European Journal of Human Genetics. 19(12). 1256–1263. 15 indexed citations
14.
Meunier, Isabelle, Audrey Sénéćhal, Claire‐Marie Dhaenens, et al.. (2011). Systematic Screening of BEST1 and PRPH2 in Juvenile and Adult Vitelliform Macular Dystrophies: A Rationale for Molecular Analysis. Ophthalmology. 118(6). 1130–1136. 46 indexed citations
15.
Manès, Gaël, Maxime Hebrard, Béatrice Bocquet, et al.. (2011). A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1. BMC Medical Genetics. 12(1). 54–54. 7 indexed citations
16.
Manès, Gaël, Paul Masendycz, Thao Nguyen, et al.. (2006). A potential role for the Src‐like adapter protein SLAP‐2 in signaling by the colony stimulating factor‐1 receptor. FEBS Journal. 273(8). 1791–1804. 11 indexed citations
17.
Cross, Maddalena, Nicholas J. Wilson, Gaël Manès, et al.. (2004). A novel 110 kDa form of myosin XVIIIA (MysPDZ) is tyrosine-phosphorylated after colony-stimulating factor-1 receptor signalling. Biochemical Journal. 380(1). 243–253. 17 indexed citations
18.
Manès, Gaël, et al.. (2002). Cyclin E and cyclin A are likely targets of Src for PDGF‐induced DNA synthesis in fibroblasts. FEBS Letters. 526(1-3). 82–86. 13 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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