Annick Cabot

540 total citations
5 papers, 240 citations indexed

About

Annick Cabot is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Annick Cabot has authored 5 papers receiving a total of 240 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Surgery. Recurrent topics in Annick Cabot's work include Dermatological and Skeletal Disorders (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Protein Kinase Regulation and GTPase Signaling (1 paper). Annick Cabot is often cited by papers focused on Dermatological and Skeletal Disorders (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Protein Kinase Regulation and GTPase Signaling (1 paper). Annick Cabot collaborates with scholars based in France, Australia and Portugal. Annick Cabot's co-authors include S. Gerber, Jean‐Michel Rozet, Dominique Ducroq, Josseline Kaplan, Isabelle Perrault, Thierry Frébourg, Pascale Saugier-Véber, Eric H. Souied, Asma Smahi and J.L. Dufier and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Muscle & Nerve.

In The Last Decade

Annick Cabot

5 papers receiving 237 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Annick Cabot France 5 167 78 53 52 49 5 240
Lance P. Doucette Canada 9 136 0.8× 141 1.8× 36 0.7× 39 0.8× 21 0.4× 13 283
Caroline Abadie France 8 265 1.6× 20 0.3× 33 0.6× 94 1.8× 15 0.3× 21 358
Zixi Sun China 11 224 1.3× 110 1.4× 19 0.4× 67 1.3× 32 0.7× 37 304
Xinzhang Cai China 10 140 0.8× 13 0.2× 44 0.8× 23 0.4× 37 0.8× 28 235
Luz María González-Huerta Mexico 10 216 1.3× 46 0.6× 10 0.2× 126 2.4× 36 0.7× 39 303
N S Davis Israel 8 221 1.3× 51 0.7× 9 0.2× 38 0.7× 17 0.3× 13 330
Jean-Louis Dufier France 8 236 1.4× 120 1.5× 24 0.5× 19 0.4× 50 1.0× 8 342
Tomokazu Takeuchi Japan 11 265 1.6× 144 1.8× 11 0.2× 35 0.7× 37 0.8× 28 319
Pancy Oi Sin Tam Hong Kong 9 161 1.0× 264 3.4× 30 0.6× 50 1.0× 39 0.8× 11 374
Haixi Miao United States 6 215 1.3× 221 2.8× 66 1.2× 19 0.4× 16 0.3× 10 356

Countries citing papers authored by Annick Cabot

Since Specialization
Citations

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

Fields of papers citing papers by Annick Cabot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annick Cabot

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

All Works

5 of 5 papers shown
1.
Balguérie, X., Alice Goldenberg, Valérie Drouin‐Garraud, et al.. (2012). Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes. European Journal of Human Genetics. 20(5). 584–587. 28 indexed citations
2.
Chastan, Nathalie, Stéphanie Baert‐Desurmont, Pascale Saugier-Véber, et al.. (2005). Cardiac conduction alterations in a French family with amyloidosis of the finnish type with the p.Asp187Tyr mutation in the GSN gene. Muscle & Nerve. 33(1). 113–119. 40 indexed citations
3.
Meur, Nathalie Le, Cosette Martin, Pascale Saugier-Véber, et al.. (2004). Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome. European Journal of Human Genetics. 12(5). 415–418. 32 indexed citations
4.
Cabot, Annick, Jean‐Michel Rozet, S. Gerber, et al.. (1999). A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3. The American Journal of Human Genetics. 64(4). 1141–1146. 66 indexed citations
5.

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