Martine Raynaud

6.8k citations

57 papers · 3.0k indexed · 1 hit paper · h-index 25

Genetics top 0.5%
Molecular Biology top 5%
Cognitive Neuroscience top 2%
Cellular and Molecular Neuroscience top 5%
Cell Biology top 10%

Co-authors: Claude Moraine Jean‐Pierre Fryns Jamel Chelly Hans‐Hilger Ropers Jozef Gécz Nathalie Ronce Hilde Van Esch Sylvain Briault
Topics: Genetics and Neurodevelopmental Disorders (38 papers)Ubiquitin and proteasome pathways (9 papers)Genomic variations and chromosomal abnormalities (9 papers)
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Nature Genetics Biological Psychiatry Genome Research
Partner nations: France Germany Netherlands

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

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Mutation update for theGPC3gene involved in Simpson-Golabi-Behmel syndrome and review of the literature 2018 ·Human Mutation ·Marie‐Laure Vuillaume,Marie‐Pierre Moizard,(unknown),(unknown),(unknown),Jean‐Luc Alessandri,Tiffany Busa,Estelle Colin,Marion Gérard,Fabienne Giuliano,Laëtitia Lambert,(unknown),(unknown),Sheela Nampoothiri,Irène Netchine,Martine Raynaud,Frédéric Brioude,Annick Toutain	22
2	GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability 2015 ·Molecular Psychiatry ·Frédérique Bonnet‐Brilhault,(unknown),R. Blanc,(unknown),Sylviane Marouillat,(unknown),Christian Andrés,Éric Lemonnier,Catherine Barthélémy,Martine Raynaud,Annick Toutain,Marie Gomot,Frédéric Laumonnier	26
3	Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth 2014 ·The American Journal of Human Genetics ·Claire C. Homan,Raman Kumar,Lam Son Nguyen,Eric Haan,F. Lucy Raymond,Fatima Abidi,Martine Raynaud,Charles E. Schwartz,Stephen A. Wood,Jozef Gécz,Lachlan A. Jolly	100
4	Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation 2013 ·American Journal of Medical Genetics Part A ·Gaëtan Lesca,Marie‐Pierre Moizard,Gérald Bussy,(unknown),Hao Hu,Stefan A. Haas,Hans‐Hilger Ropers,Vera M. Kalscheuer,Vincent des Portes,Audrey Labalme,Damien Sanlaville,Patrick Edery,Martine Raynaud,James Lespinasse	30
5	A functional tetranucleotide (AAAT) polymorphism in an Alu element in the NF1 gene is associated with mental retardation 2011 ·Neuroscience Letters ·(unknown),Patrick Vourc’h,(unknown),Laurence Mignon,(unknown),(unknown),(unknown),(unknown),Claude Moraine,Martine Raynaud,Christian Andrés	10
6	The evolution of infrahissian conduction time in myotonic dystrophy patients: clinical implications 2011 ·Heart ·(unknown),Nicolas Clémenty,(unknown),Bertrand Pierre,Philippe Corcia,Laurent Fauchier,Martine Raynaud,(unknown),Dominique Babuty	19
7	Twenty-five novel mutations including duplications in the ATP7A gene 2010 ·Clinical Genetics ·(unknown),Nathalie Ronce,(unknown),Éric Bieth,Lydie Bürglen,Cyril Mignot,Isabelle Mortemousque,(unknown),(unknown),Cesare Danesino,(unknown),Pierre Castelnau,Annick Toutain,Claude Moraine,Martine Raynaud	15
8	A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C 2010 ·PubMed ·Lars Riff Jensen,H. Bartenschlager,Sinitdhorn Rujirabanjerd,Andreas Tzschach,Astrid Nümann,Andreas Janecke,Ralf Spörle,Sigmar Stricker,Martine Raynaud,John W. Nelson,Anna Hackett,Jean‐Pierre Fryns,Jamel Chelly,Arjan PM de Brouwer,Ben C.J. Hamel,Jozef Gécz,Hans‐Hilger Ropers,Andreas W. Kuß	32
9	Novel missense mutations in the ubiquitination‐related gene UBE2A cause a recognizable X‐linked mental retardation syndrome 2010 ·Clinical Genetics ·Bartłomiej Budny,Magdalena Badura‐Stronka,Anna Materna‐Kiryluk,Andreas Tzschach,Martine Raynaud,Anna Latos‐Bieleńska,HH Ropers	40
10	Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism 2009 ·Molecular Psychiatry ·Frédéric Laumonnier,Cheryl Shoubridge,Catherine Antar,Lam Son Nguyen,Hilde Van Esch,Tjitske Kleefstra,Sylvain Briault,J. P. Fryns,B Hamel,Jamel Chelly,Hans‐Hilger Ropers,Nathalie Ronce,(unknown),Claude Moraine,Jozef Gécz,Martine Raynaud	89
11	Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair 2008 ·Genome Research ·Marijke Bauters,Hilde Van Esch,Michael J. Friez,Odile Boespflug‐Tanguy,Martin Zenker,Angela Maria Vianna‐Morgante,Carla Rosenberg,Jaakko Ignatius,Martine Raynaud,Karen Hollanders,Karen Govaerts,(unknown),Florence Niel,Pierre Blanc,Roger E. Stevenson,Jean‐Pierre Fryns,Peter Marynen,Charles E. Schwartz,Guy Froyen	92
12	Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males 2006 ·Hilde Van Esch,Marijke Bauters,Jaakko Ignatius,Martine Raynaud,Karen Hollanders,Dorien Lugtenberg,T. Bienvenu,(unknown),(unknown),Peter Marynen,(unknown),Jean‐Pierre Fryns	1
13	A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome 2006 ·Human Genetics ·Bartłomiej Budny,Wei Chen,Heymut Omran,Manfred Fliegauf,Andreas Tzschach,Marzena Wiśniewska,Lars Riff Jensen,Martine Raynaud,Sarah A. Shoichet,(unknown),Steffen Lenzner,Anna Latos‐Bieleńska,Hans‐Hilger Ropers	122
14	Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update 2005 ·European Journal of Medical Genetics ·Christophe Philippe,Laurent Villard,Nicolás de Roux,Martine Raynaud,(unknown),Laurent Pasquier,Gaëtan Lesca,Julien Mancini,Philippe Jonveaux,A. Moncla,Jamel Chelly,Thierry Bienvenu	57
15	Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis 2005 ·Neurogenetics ·Karine Poirier,Didier Lacombe,Brigitte Gilbert‐Dussardier,Martine Raynaud,Vincent Desportes,Arjan P.M. de Brouwer,Claude Moraine,J P Fryns,Hans‐Hilger Ropers,C. Beldjord,Jamel Chelly,Thierry Bienvenu	32
16	X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Familybreakdown → 2004 ·The American Journal of Human Genetics ·Frédéric Laumonnier,Frédérique Bonnet‐Brilhault,Marie Gomot,Romuald Blanc,Albert David,Marie‐Pierre Moizard,Martine Raynaud,Nathalie Ronce,Éric Lemonnier,Patrick Calvas,Béatrice Laudier,Jamel Chelly,Jean‐Pierre Fryns,Hans‐Hilger Ropers,Ben C.J. Hamel,Christian Andrés,Catherine Barthélémy,Claude Moraine,Sylvain Briault	553
17	Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5 (CDKL5/STK9) Gene Are Associated with Severe Neurodevelopmental Retardation 2004 ·The American Journal of Human Genetics ·Jiong Tao,Hilde Van Esch,(unknown),Kirsten Hoffmann,Bettina A. Moser,Martine Raynaud,Jürgen Sperner,Jean‐Pierre Fryns,E. Schwinger,Jozef Gécz,Hans‐Hilger Ropers,Vera M. Kalscheuer	236
18	Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome 2003 ·European Journal of Human Genetics ·Martine Raynaud,(unknown),Nathalie Ronce,John M. Opitz,Marcus Pembrey,Corrado Romano,Claude Moraine,Sylvain Briault	2
19	X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1 1996 ·American Journal of Medical Genetics ·Martine Raynaud,Chantal Gendrot,(unknown),Anne Moncla,(unknown),Marie‐Pierre Moizard,Annick Toutain,Sylvain Briault,Laurent Villard,Nathalie Ronce,Claude Moraine	12
20	X chromosome and infantile autism 1996 ·Biological Psychiatry ·Élisabeth Petit,Jósiane Hérault,Martine Raynaud,(unknown),Anne Perrot,Catherine Barthélémy,G Lelord,Jean‐Pierre Müh	25

About Martine Raynaud

Martine Raynaud is a scholar working on Genetics, Molecular Biology and Developmental Biology, having authored 57 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (38 papers), Ubiquitin and proteasome pathways (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). The work is most often cited by research in Genetics (2.1k citations), Cognitive Neuroscience (757 citations) and Molecular Biology (1.9k citations). Martine Raynaud has collaborated with scholars based in France, Germany and Netherlands. Frequent 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. Their work appears in journals such as Nature Genetics, Biological Psychiatry and Genome Research.

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.

Explore authors with similar magnitude of impact