Fabrice Riet

1.1k total citations
9 papers, 314 citations indexed

About

Fabrice Riet is a scholar working on Molecular Biology, Genetics and Social Psychology. According to data from OpenAlex, Fabrice Riet has authored 9 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Social Psychology. Recurrent topics in Fabrice Riet's work include Genetics and Neurodevelopmental Disorders (5 papers), Neuroendocrine regulation and behavior (2 papers) and Epigenetics and DNA Methylation (2 papers). Fabrice Riet is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Neuroendocrine regulation and behavior (2 papers) and Epigenetics and DNA Methylation (2 papers). Fabrice Riet collaborates with scholars based in France, Netherlands and Italy. Fabrice Riet's co-authors include Hamid Méziane, Valéry Matarazzo, Š. Bauer, Gilles Guillon, Fabienne Schaller, Michel G. Desarménien, Claude Villard, M. Tauber, Françoise Muscatelli and Daniel Lafitte and has published in prestigious journals such as Nucleic Acids Research, Neuron and Scientific Reports.

In The Last Decade

Fabrice Riet

9 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabrice Riet France 7 161 127 90 82 41 9 314
Ozlem Bozdagi-Gunal United States 7 142 0.9× 120 0.9× 71 0.8× 56 0.7× 96 2.3× 11 355
Gina Kang United States 8 152 0.9× 114 0.9× 45 0.5× 30 0.4× 83 2.0× 14 281
Hanna Hörnberg Germany 7 262 1.6× 178 1.4× 100 1.1× 122 1.5× 107 2.6× 11 561
Masako Taniike Japan 6 94 0.6× 43 0.3× 102 1.1× 16 0.2× 36 0.9× 13 295
Brian L. Teng United States 6 99 0.6× 128 1.0× 135 1.5× 59 0.7× 138 3.4× 6 335
Rhinda Goedken United States 10 144 0.9× 272 2.1× 134 1.5× 34 0.4× 170 4.1× 15 536
Yohan Yee Canada 10 127 0.8× 85 0.7× 53 0.6× 50 0.6× 129 3.1× 17 415
Nycole A. Copping United States 11 219 1.4× 298 2.3× 47 0.5× 85 1.0× 142 3.5× 13 454
Terri M. Driessen United States 14 120 0.7× 56 0.4× 157 1.7× 79 1.0× 47 1.1× 23 400
Satoko Ise Japan 7 284 1.8× 242 1.9× 85 0.9× 138 1.7× 211 5.1× 8 531

Countries citing papers authored by Fabrice Riet

Since Specialization
Citations

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

Fields of papers citing papers by Fabrice Riet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabrice Riet

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

All Works

9 of 9 papers shown
1.
Kharouf, Naji, Yvan de Féraudy, Gergő Gógl, et al.. (2024). The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome. Scientific Reports. 14(1). 445–445. 2 indexed citations
2.
Tabet, Ricardos, Fabrice Riet, Doulaye Dembélé, et al.. (2022). AAV‐delivered diacylglycerol kinase DGKk achieves long‐term rescue of fragile X syndrome mouse model. EMBO Molecular Medicine. 14(5). e14649–e14649. 12 indexed citations
3.
Riet, Fabrice, et al.. (2022). Behavioral Testing Design for Evaluation of Cognitive Disabilities. Current Protocols. 2(2). e382–e382. 2 indexed citations
4.
Deng, Jianwen, Véronique Pfister, Mustapha Oulad‐Abdelghani, et al.. (2021). Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases. Neuron. 109(11). 1825–1835.e5. 79 indexed citations
5.
Dubos, Aline, Hamid Méziane, Giovanni Iacono, et al.. (2018). A new mouse model of ARX dup24 recapitulates the patients’ behavioral and fine motor alterations. Human Molecular Genetics. 27(12). 2138–2153. 14 indexed citations
6.
Iacono, Giovanni, Aline Dubos, Hamid Méziane, et al.. (2018). Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome. Nucleic Acids Research. 46(10). 4950–4965. 31 indexed citations
7.
Méziane, Hamid, Malik Khelfaoui, Noemi Morello, et al.. (2016). Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability. Human Molecular Genetics. 25(11). 2314–2323. 29 indexed citations
8.
Méziane, Hamid, Fabienne Schaller, Š. Bauer, et al.. (2014). An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism. Biological Psychiatry. 78(2). 85–94. 139 indexed citations
9.
Méziane, Hamid, Valérie Fraulob, Fabrice Riet, et al.. (2013). The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord. PeerJ. 1. e142–e142. 6 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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