Freddy Cliquet

895 total citations
8 papers, 208 citations indexed

About

Freddy Cliquet is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Freddy Cliquet has authored 8 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Cognitive Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Freddy Cliquet's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers) and Congenital heart defects research (3 papers). Freddy Cliquet is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (5 papers) and Congenital heart defects research (3 papers). Freddy Cliquet collaborates with scholars based in France, United Kingdom and Canada. Freddy Cliquet's co-authors include Thomas Bourgeron, Claire S. Leblond, Richard Delorme, Thomas Rolland, Anne‐Claude Tabet, Alexandre Mathieu, Simon Baron‐Cohen, Anders D. Børglum, Nathalie Lemière and Bhismadev Chakrabarti and has published in prestigious journals such as Annual Review of Genetics, Briefings in Bioinformatics and Molecular and Cellular Neuroscience.

In The Last Decade

Freddy Cliquet

8 papers receiving 206 citations

Peers

Freddy Cliquet

GENET

CN

MB

CP

CMN

Tianyun Wang China

Wei‐Hsien Chien Taiwan

Hyeon Jeong Sim South Korea

Tess Levy United States

Elise Ng‐Cordell United Kingdom

Elizabeth R Hennessy Netherlands

Daniel Moreno‐De‐Luca United States

Lia Boyle United States

Sharon Bade Shrestha United States

Arianne S. Wallace United States

Tianyun Wang China

Freddy Cliquet

97 ×0.9

GENET

89 ×0.8

CN

71 ×1.0

MB

13 ×0.5

CP

12 ×0.6

CMN

Citations per year, relative to Freddy Cliquet Freddy Cliquet (= 1×) peers Tianyun Wang

Countries citing papers authored by Freddy Cliquet

Since Specialization

Citations

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

Fields of papers citing papers by Freddy Cliquet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Freddy Cliquet

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

All Works

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8 of 8 papers shown

1.

Leblond, Claire S., Thomas Rolland, Christine Ecker, et al.. (2024). A Genetic Bridge Between Medicine and Neurodiversity for Autism. Annual Review of Genetics. 58(1). 487–512. 9 indexed citations

2.

Leblond, Claire S., Thomas Rolland, Freddy Cliquet, et al.. (2023). Dissecting the 22q13 region to explore the genetic and phenotypic diversity of patients with Phelan-McDermid syndrome. European Journal of Medical Genetics. 66(5). 104732–104732. 14 indexed citations

3.

Lefebvre, Aline, Julian Tillmann, Freddy Cliquet, et al.. (2022). Tackling hypo and hyper sensory processing heterogeneity in autism: From clinical stratification to genetic pathways. Autism Research. 16(2). 364–378. 5 indexed citations

4.

Pagan, Cécile, Claire S. Leblond, Freddy Cliquet, et al.. (2021). Decreased phenol sulfotransferase activities associated with hyperserotonemia in autism spectrum disorders. Translational Psychiatry. 11(1). 23–23. 18 indexed citations

5.

Leblond, Claire S., Freddy Cliquet, Anne‐Claude Tabet, et al.. (2021). Operative list of genes associated with autism and neurodevelopmental disorders based on database review. Molecular and Cellular Neuroscience. 113. 103623–103623. 54 indexed citations

6.

Warrier, Varun, Roberto Toro, Hyejung Won, et al.. (2019). Social and non-social autism symptoms and trait domains are genetically dissociable. Communications Biology. 2(1). 328–328. 55 indexed citations

7.

Leblond, Claire S., Freddy Cliquet, Guillaume Huguet, et al.. (2019). Both rare and common genetic variants contribute to autism in the Faroe Islands. npj Genomic Medicine. 4(1). 1–1. 52 indexed citations

8.

Loucoubar, Cheikh, Audrey V. Grant, Jean‐François Bureau, et al.. (2016). Detecting multi-way epistasis in family-based association studies. Briefings in Bioinformatics. 18(3). bbw039–bbw039. 1 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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