Xavier Gérard

783 total citations
17 papers, 404 citations indexed

About

Xavier Gérard is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Xavier Gérard has authored 17 papers receiving a total of 404 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Xavier Gérard's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (4 papers) and Ocular Disorders and Treatments (3 papers). Xavier Gérard is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (4 papers) and Ocular Disorders and Treatments (3 papers). Xavier Gérard collaborates with scholars based in France, United States and Switzerland. Xavier Gérard's co-authors include Jean‐Michel Rozet, Josseline Kaplan, Isabelle Perrault, Arnold Münnich, Marlène Rio, Sylvain Hanein, S. Gerber, Antoine Kichler, Daniel Scherman and Eduardo Silva and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Xavier Gérard

17 papers receiving 401 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xavier Gérard France 10 347 126 69 49 34 17 404
Lucas Fares‐Taie France 8 177 0.5× 86 0.7× 32 0.5× 24 0.5× 20 0.6× 15 238
Jean-Louis Dufier France 7 173 0.5× 61 0.5× 85 1.2× 18 0.4× 25 0.7× 8 288
María González‐del Pozo Spain 13 408 1.2× 123 1.0× 179 2.6× 46 0.9× 11 0.3× 21 461
Rocío Sánchez-Alcudia Spain 14 339 1.0× 72 0.6× 92 1.3× 32 0.7× 118 3.5× 18 418
Neringa Jurkutė United Kingdom 11 362 1.0× 57 0.5× 159 2.3× 34 0.7× 38 1.1× 23 400
Zixi Sun China 11 224 0.6× 67 0.5× 110 1.6× 32 0.7× 5 0.1× 37 304
Luz María González-Huerta Mexico 10 216 0.6× 126 1.0× 46 0.7× 36 0.7× 4 0.1× 39 303
Xavier Zanlonghi France 13 348 1.0× 67 0.5× 274 4.0× 74 1.5× 9 0.3× 44 523
Jan Willem R. Pott Netherlands 11 351 1.0× 35 0.3× 164 2.4× 45 0.9× 29 0.9× 25 460
Ana Fakin Slovenia 12 428 1.2× 54 0.4× 298 4.3× 30 0.6× 7 0.2× 44 543

Countries citing papers authored by Xavier Gérard

Since Specialization
Citations

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

Fields of papers citing papers by Xavier Gérard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xavier Gérard

This figure shows the co-authorship network connecting the top 25 collaborators of Xavier Gérard. A scholar is included among the top collaborators of Xavier Gérard 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 Xavier Gérard. Xavier Gérard 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.
Perrault, Isabelle, Sylvain Hanein, Xavier Gérard, et al.. (2021). Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. Genes. 12(2). 287–287. 4 indexed citations
2.
Mbefo, Martial, Adeline Berger, Xavier Gérard, et al.. (2021). Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy. International Journal of Molecular Sciences. 22(17). 9331–9331. 6 indexed citations
3.
Perrault, Isabelle, Marlène Rio, Hélène Dollfus, et al.. (2019). Description of Two Siblings with Apparently Severe CEP290 Mutations and Unusually Mild Retinal Disease Unrelated to Basal Exon Skipping or Nonsense-Associated Altered Splicing. Advances in experimental medicine and biology. 1185. 189–195. 2 indexed citations
4.
Perrault, Isabelle, Nicolas Goudin, Sabine Defoort‐Dhellemmes, et al.. (2019). AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent CEP290 c.4723A > T Mutation. Fact or Fiction?. Genes. 10(5). 368–368. 18 indexed citations
5.
Perrault, Isabelle, Nicolas Goudin, Marlène Rio, et al.. (2018). Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease. Human Molecular Genetics. 27(15). 2689–2702. 26 indexed citations
6.
Gerber, S., Xavier Gérard, Klaus Zwicker, et al.. (2016). Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy. Journal of Medical Genetics. 54(5). 346–356. 38 indexed citations
7.
Gérard, Xavier, Isabelle Perrault, Arnold Münnich, Josseline Kaplan, & Jean‐Michel Rozet. (2015). Intravitreal Injection of Splice-switching Oligonucleotides to Manipulate Splicing in Retinal Cells. Molecular Therapy — Nucleic Acids. 4. e250–e250. 30 indexed citations
8.
Gérard, Xavier, Alejandro Garanto, Jean‐Michel Rozet, & Rob W.J. Collin. (2015). Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies. Advances in experimental medicine and biology. 854. 517–524. 20 indexed citations
9.
Perrault, Isabelle, Fadi F. Hamdan, Marlène Rio, et al.. (2014). Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness. The American Journal of Human Genetics. 94(6). 891–897. 35 indexed citations
10.
Metodiev, Metodi D., S. Gerber, Laurence Hubert, et al.. (2014). Mutations in the tricarboxylic acid cycle enzyme, aconitase 2, cause either isolated or syndromic optic neuropathy with encephalopathy and cerebellar atrophy. Journal of Medical Genetics. 51(12). 834–838. 70 indexed citations
11.
Gérard, Xavier, Isabelle Perrault, Sylvain Hanein, et al.. (2012). AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring the Common Leber Congenital Amaurosis CEP290 Mutation. Molecular Therapy — Nucleic Acids. 1. e29–e29. 82 indexed citations
12.
Papon, Jean‐François, Isabelle Perrault, A. Coste, et al.. (2010). Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with CEP290 mutations. Journal of Medical Genetics. 47(12). 829–834. 41 indexed citations
13.
Perrault, Isabelle, Sylvain Hanein, Xavier Gérard, et al.. (2010). Spectrum ofSPATA7mutations in Leber congenital amaurosis and delineation of the associated phenotype. Human Mutation. 31(3). E1241–E1250. 19 indexed citations
14.
Perrault, Isabelle, et al.. (2010). Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype.. PubMed. 31(3). E1241–50. 3 indexed citations
15.
Gérard, Xavier, et al.. (2010). [Clinical inertia in geriatrics].. PubMed. 65(5-6). 256–60. 1 indexed citations
16.
Gérard, Xavier, Séverine Charles, Christian Pinset, et al.. (2009). Real-time monitoring of cell transplantation in mouse dystrophic muscles by a secreted alkaline phosphatase reporter gene. Gene Therapy. 16(6). 815–819. 7 indexed citations
17.
Citron, David, Robert Cressy, & Xavier Gérard. (2009). Prospectus forecast publication and forecast errors: the role of venture capitalist certification. Venture Capital. 11(2). 87–105. 2 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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