Audrey Sénéćhal

839 total citations
15 papers, 297 citations indexed

About

Audrey Sénéćhal is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Audrey Sénéćhal has authored 15 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Ophthalmology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Audrey Sénéćhal's work include Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (3 papers). Audrey Sénéćhal is often cited by papers focused on Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Photoreceptor and optogenetics research (3 papers). Audrey Sénéćhal collaborates with scholars based in France, Tunisia and Morocco. Audrey Sénéćhal's co-authors include Christian P. Hamel, Béatrice Bocquet, Gaël Manès, Isabelle Meunier, Florence Apparailly, Christian Jørgensen, Yves‐Marie Pers, Isabelle Duroux-Richard, Rosanna Ferreira and Carl Arndt and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Ophthalmology.

In The Last Decade

Audrey Sénéćhal

15 papers receiving 296 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Audrey Sénéćhal France	9	246	149	50	39	37	15	297
Jason S. Salvo United States	5	280 1.1×	62 0.4×	27 0.5×	43 1.1×	49 1.3×	5	330
Yue Xie China	11	255 1.0×	115 0.8×	29 0.6×	54 1.4×	48 1.3×	35	339
Hatice Duzkale United States	7	325 1.3×	88 0.6×	65 1.3×	40 1.0×	105 2.8×	12	423
C. Zhi United States	4	369 1.5×	170 1.1×	57 1.1×	118 3.0×	27 0.7×	5	464
Monica Aronsson Sweden	9	240 1.0×	142 1.0×	47 0.9×	45 1.2×	13 0.4×	20	309
Nagasamy Soumittra India	14	336 1.4×	236 1.6×	27 0.5×	38 1.0×	113 3.1×	27	490
Meghan J. Marino United States	11	223 0.9×	203 1.4×	46 0.9×	30 0.8×	25 0.7×	18	341
Leen Abu‐Safieh Saudi Arabia	9	544 2.2×	168 1.1×	59 1.2×	24 0.6×	117 3.2×	16	621
Alex Jones United States	9	175 0.7×	143 1.0×	29 0.6×	62 1.6×	10 0.3×	11	316
Fanny Depasse Belgium	8	199 0.8×	119 0.8×	24 0.5×	19 0.5×	104 2.8×	8	282

Countries citing papers authored by Audrey Sénéćhal

Since Specialization

Citations

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

Fields of papers citing papers by Audrey Sénéćhal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Audrey Sénéćhal

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

All Works

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15 of 15 papers shown

Balandraud, Nathalie, Nathalie Lambert, Isabelle Auger, et al.. (2017). TMEM187-IRAK1Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin. Journal of Immunology Research. 2017. 1–12. 9 indexed citations

Manès, Gaël, Anne‐Claire Richard, Audrey Sénéćhal, et al.. (2017). Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.. PubMed. 23. 198–209. 21 indexed citations

Pers, Yves‐Marie, et al.. (2017). 02.10 X-linked mirnas associated with gender differences in rheumatoid arthritis. Annals of the Rheumatic Diseases. 76. A12–A12. 1 indexed citations

Pers, Yves‐Marie, Rosanna Ferreira, Audrey Sénéćhal, et al.. (2016). X-Linked miRNAs Associated with Gender Differences in Rheumatoid Arthritis. International Journal of Molecular Sciences. 17(11). 1852–1852. 55 indexed citations

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

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

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

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

Abidi, Omar, Majida Charif, Audrey Sénéćhal, et al.. (2011). Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.. PubMed. 17. 3541–7. 17 indexed citations

10.

Sénéćhal, Audrey, et al.. (2010). Screening genes of the visual cycleRGR,RBP1andRBP3identifies rare sequence variations. Ophthalmic Genetics. 31(4). 200–204. 4 indexed citations

11.

Sénéćhal, Audrey, et al.. (2010). Screening for a Canine Model of Choroideremia Exclusively Identifies Nonpathogenic <i>CHM</i> Variants. Ophthalmic Research. 45(3). 155–163. 4 indexed citations

12.

Sénéćhal, Audrey, et al.. (2008). Novel KCNV2 Mutations in Cone Dystrophy with Supernormal Rod Electroretinogram. American Journal of Ophthalmology. 145(6). 1099–1106. 32 indexed citations

13.

Sénéćhal, Audrey, et al.. (2007). RRH, Encoding the RPE-Expressed Opsin-Like Peropsin, Is Not Mutated in Retinitis Pigmentosa and Allied Diseases. Ophthalmic Genetics. 28(1). 31–37. 2 indexed citations

14.

Sénéćhal, Audrey, et al.. (2007). Kcnv2 Mutations in Cone Dystrophy With Supernormal Rod Electroretinogram. 48(13). 1658–1658. 1 indexed citations

15.

Sénéćhal, Audrey, Bernard Arnaud, Carl Arndt, et al.. (2006). Screening Genes of the Retinoid Metabolism: Novel LRAT Mutation in Leber Congenital Amaurosis. American Journal of Ophthalmology. 142(4). 702–704. 36 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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