François Muratet

428 total citations
3 papers, 213 citations indexed

About

François Muratet is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, François Muratet has authored 3 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Genetics. Recurrent topics in François Muratet's work include Genomics and Rare Diseases (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Diabetes and associated disorders (1 paper). François Muratet is often cited by papers focused on Genomics and Rare Diseases (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Diabetes and associated disorders (1 paper). François Muratet collaborates with scholars based in France, United States and Switzerland. François Muratet's co-authors include Paige M. Siper, Silvia De Rubeis, Joseph D. Buxbaum, Alexander Kolevzon, Allison Durkin, Yitzchak Frank, Reymundo Lozano, Jordana Weissman, Catalina Betancur and A. Ting Wang and has published in prestigious journals such as Molecular Autism and Neurology Genetics.

In The Last Decade

François Muratet

3 papers receiving 212 citations

Peers

Countries citing papers authored by François Muratet

Since Specialization

Citations

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

Fields of papers citing papers by François Muratet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of François Muratet

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

All Works

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3 of 3 papers shown

#	Work	Indexed citations
1	Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS 2019 ·Neurology Genetics ·Maria del Mar Amador, François Muratet, Elisa Teyssou, Guillaume Banneau, Véronique Danel-Brunaud, E. Allart, Jean‐Christophe Antoine, Jean‐Philippe Camdessanché, Mathieu Anheim, Gabrielle Rudolf, Christine Tranchant, Marie‐Céline Fleury, E Bernard, Giovanni Stévanin, Stéphanie Millecamps	15
2	Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations 2018 ·Molecular Autism ·Silvia De Rubeis, Paige M. Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, M. Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A. Ting Wang, J. Lloyd Holder, Catalina Betancur, Joseph D. Buxbaum, Alexander Kolevzon	138
3	Prospective investigation of FOXP1 syndrome 2017 ·Molecular Autism ·Paige M. Siper, Silvia De Rubeis, Maria del Pilar Trelles, Allison Durkin, Daniele Di Marino, François Muratet, Yitzchak Frank, Reymundo Lozano, Evan E. Eichler, (unknown), Jennifer S. Beighley, Jennifer Gerdts, Arianne S. Wallace, Heather C. Mefford, Raphael Bernier, Alexander Kolevzon, Joseph D. Buxbaum	60

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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