Martine Raynaud

6.8k total citations · 1 hit paper
57 papers, 3.0k citations indexed

About

Martine Raynaud is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Martine Raynaud has authored 57 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 34 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Martine Raynaud's work include Genetics and Neurodevelopmental Disorders (38 papers), Ubiquitin and proteasome pathways (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Martine Raynaud is often cited by papers focused on Genetics and Neurodevelopmental Disorders (38 papers), Ubiquitin and proteasome pathways (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Martine Raynaud collaborates with scholars based in France, Germany and Netherlands. Martine Raynaud's co-authors include Claude Moraine, Jean‐Pierre Fryns, Jamel Chelly, Hans‐Hilger Ropers, Jozef Gécz, Nathalie Ronce, Hilde Van Esch, Sylvain Briault, Frédéric Laumonnier and Ben C.J. Hamel and has published in prestigious journals such as Nature Genetics, Biological Psychiatry and Genome Research.

In The Last Decade

Martine Raynaud

56 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault et al. The American Journal of Human Genetics profile →

Peers

Martine Raynaud

GENET

CMN

Sylvain Briault France

Montserrat Milà Spain

Dag H. Yasui United States

Claude Moraine France

Ági K. Gedeon Australia

Luis de la Torre-Ubieta United States

Peter Huppke Germany

Melissa B. Ramocki United States

Richard J. Schroer United States

Stephen T. Warren United States

Sylvain Briault France

Martine Raynaud

1.6k ×0.8

GENET

1.8k ×1.0

610 ×0.8

426 ×1.4

CMN

334 ×1.8

Citations per year, relative to Martine Raynaud Martine Raynaud (= 1×) peers Sylvain Briault

Countries citing papers authored by Martine Raynaud

Since Specialization

Citations

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

Fields of papers citing papers by Martine Raynaud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Raynaud

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

All Works

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20 of 20 papers shown

Vuillaume, Marie‐Laure, Marie‐Pierre Moizard, Jean‐Luc Alessandri, et al.. (2018). Mutation update for theGPC3gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. Human Mutation. 39(6). 790–805. 22 indexed citations

Bonnet‐Brilhault, Frédérique, R. Blanc, Sylviane Marouillat, et al.. (2015). GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability. Molecular Psychiatry. 21(3). 411–418. 26 indexed citations

Homan, Claire C., Raman Kumar, Lam Son Nguyen, et al.. (2014). Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth. The American Journal of Human Genetics. 94(3). 470–478. 100 indexed citations

Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations

Vourc’h, Patrick, et al.. (2011). A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardation. Neuroscience Letters. 491(2). 118–121. 10 indexed citations

Clémenty, Nicolas, Bertrand Pierre, Philippe Corcia, et al.. (2011). The evolution of infrahissian conduction time in myotonic dystrophy patients: clinical implications. Heart. 98(4). 291–296. 19 indexed citations

Ronce, Nathalie, Éric Bieth, Lydie Bürglen, et al.. (2010). Twenty-five novel mutations including duplications in the ATP7A gene. Clinical Genetics. 79(3). 243–253. 15 indexed citations

Jensen, Lars Riff, H. Bartenschlager, Sinitdhorn Rujirabanjerd, et al.. (2010). A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. PubMed. 3(1). 2–2. 32 indexed citations

Budny, Bartłomiej, Magdalena Badura‐Stronka, Anna Materna‐Kiryluk, et al.. (2010). Novel missense mutations in the ubiquitination‐related gene UBE2A cause a recognizable X‐linked mental retardation syndrome. Clinical Genetics. 77(6). 541–551. 40 indexed citations

10.

Laumonnier, Frédéric, Cheryl Shoubridge, Catherine Antar, et al.. (2009). Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. Molecular Psychiatry. 15(7). 767–776. 89 indexed citations

11.

Bauters, Marijke, Hilde Van Esch, Michael J. Friez, et al.. (2008). Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Research. 18(6). 847–858. 92 indexed citations

12.

Esch, Hilde Van, Marijke Bauters, Jaakko Ignatius, et al.. (2006). Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males. 17(1). 119–119. 1 indexed citations

13.

Budny, Bartłomiej, Wei Chen, Heymut Omran, et al.. (2006). A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome. Human Genetics. 120(2). 171–178. 122 indexed citations

14.

Philippe, Christophe, Laurent Villard, Nicolás de Roux, et al.. (2005). Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update. European Journal of Medical Genetics. 49(1). 9–18. 57 indexed citations

15.

Poirier, Karine, Didier Lacombe, Brigitte Gilbert‐Dussardier, et al.. (2005). Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis. Neurogenetics. 7(1). 39–46. 32 indexed citations

16.

Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

17.

Tao, Jiong, Hilde Van Esch, Kirsten Hoffmann, et al.. (2004). Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation. The American Journal of Human Genetics. 75(6). 1149–1154. 236 indexed citations

18.

Raynaud, Martine, Nathalie Ronce, John M. Opitz, et al.. (2003). Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome. European Journal of Human Genetics. 11(4). 352–356. 2 indexed citations

19.

Raynaud, Martine, Chantal Gendrot, Anne Moncla, et al.. (1996). X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1. American Journal of Medical Genetics. 64(1). 97–106. 12 indexed citations

20.

Petit, Élisabeth, Jósiane Hérault, Martine Raynaud, et al.. (1996). X chromosome and infantile autism. Biological Psychiatry. 40(6). 457–464. 25 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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