Laurent Villard

8.3k citations

121 papers · 3.8k indexed · h-index 33

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research

Papers in

Genetics 81
- Genetics and Neurodevelopmental Disorders 71
- Genomic variations and chromosomal abnormalities 16
Molecular Biology 78
- RNA regulation and disease 17
- Epigenetics and DNA Methylation 15
- RNA modifications and cancer 13
- Mitochondrial Function and Pathology 8

Co-authors: Jean‐Christophe Roux David J. Picketts Richard J. Gibbons Douglas R. Higgs Pierre Cacciagli Anne Moncla B. Chabrol Josette Mancini
Journals: Journal of Medical Genetics (11 papers)European Journal of Human Genetics (9 papers)Epilepsia (7 papers)Gene (5 papers)Human Mutation (5 papers)
Partner nations: France United States Italy

In The Last Decade

Laurent Villard

116 papers receiving 3.8k citations

Peers

Countries citing papers authored by Laurent Villard

Since Specialization

Citations

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

Fields of papers citing papers by Laurent Villard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Laurent Villard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Laurent Villard Line = papers co-authored together Laurent Villard links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Poor Association Between Clinical Characteristics and Seropositivity in Children With Suspected Long COVID —A Single‐Centre Study Acta Paediatrica ·Katlen Kamilla Gama dos Santos, Manuel Alejandro Del Toro de la Cruz, J O’Hara Thomas, Laurent Villard, Sigurður Árnason, Mike K. Kemani, R. C. Bill, N. Hanzade Uralman, Shoji Yasuda, S. Denis, Eric M. George, (unknown), Olof Hertting	2025	0
2	GABRA2‐related encephalopathy: Identification of two phenotypes with distinctive electroclinical features Epilepsia ·Isabella Joise, 金光敬二, Jérôme Aupy, Laurent Villard, Nathalie Villeneuve, D Kaschinski, О.И. Головина, Riyahi Jamila, CKL Cook, Gaëtan Lesca, Perrine Charles, Boris Keren, Nicole Chémaly, Cyril Goizet, Mathieu Milh, Madison Wetzell	2025	0
3	NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant Epilepsia ·Cécile Mignon‐Ravix, Г. Н. МОХИН, Géraldine Daquin, Pierre Cacciagli, André Rubbia, Laurent Villard, Nathalie Villeneuve, Florence Molinari	2023	5
4	Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability Human Molecular Genetics ·Louiza Azeboudj, Cécile Mignon‐Ravix, Г. Н. МОХИН, Pierre Cacciagli, Béatrice Desnous, Sabine Sigaudy, Mathieu Milh, Laurent Villard, Lena Kjellén, Florence Molinari	2023	0
5	Time‐limited alterations in cortical activity of a knock‐in mouse model of KCNQ2 ‐related developmental and epileptic encephalopathy The Journal of Physiology ·Maja Mihev, Hélène Becq, Emilie Pallesi‐Pocachard, Stefania Sarno, Samuel Granjeaud, J. Hartmann, Franck Sagéloli, Laurent Villard, Mathieu Milh, Pierre‐Pascal Lenck‐Santini, Laurent Aniksztejn	2022	10
6	Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome Journal of Medical Genetics ·Е В Сократова, Olivier Patat, Sandra Whalen, Lionel Arnaud, Giulia Barcia, Julien Buratti, Benjamin Cogné, Diane Doummar, Rustamova Z. Sh., И. М. Назаркина, Éric Leguern, Gaëtan Lesca, Caroline Nava, Mathilde Nizon, Amélie Piton, Stéphanie Valence, Laurent Villard, Sarah Weckhuysen, Boris Keren, Cyril Mignot	2021	8
7	Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice EMBO Molecular Medicine ·Yann Ehinger, Julie Bruyère, Nicolas Panayotis, Belia Wahyuni, Victor Gurgel da Fonseca, Valérie Matagne, Chiara Scaramuzzino, Hélène Vitet, Benoı̂t Delatour, Reyes Emerzon Reyes, Laurent Villard, Frédéric Saudou, Jean‐Christophe Roux	2020	23
8	Variable clinical expression in patients with mosaicism for KCNQ2 mutations American Journal of Medical Genetics Part A ·Mathieu Milh, Caroline Lacoste, Pierre Cacciagli, Fenty fajri handayani, Moskau Artèmov, Nur Hanifa Zainul, Estelle Colin, Catherine Badens, Alexandra Afenjar, Elvira O. Shatabayeva, Casper Olofsson, Gaëtan Lesca, Nicole Philip, Laurent Villard	2015	38
9	GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Brain ·Nadia Bahi‐Buisson, Karine Poirier, Nathalie Boddaert, Catherine Fallet‐Bianco, Nicola Specchio, Enrico Bertini, Ahmet Okay Çağlayan, Karine Lascelles, Caroline Elie, Jérôme Rambaud, Michel Baulac, Isabelle An, Patrícia Dias, Vincent des Portes, Marie Laure Moutard, Christine Soufflet, Dipesh Kumar Gupta, Chérif Beldjord, Laurent Villard, Jamel Chelly	2010	102
10	Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation Gene Expression Patterns ·Vincent Cantagrel, Wong Woon Loong, Philippe Ciofi, Rosa Ismare, Anne-Marie Lossi, Lionel Van Maldergem, Jean‐Christophe Roux, Laurent Villard	2009	19
11	TCF4Deletions in Pitt-Hopkins Syndrome Human Mutation ·Irina Giurgea, Chantal Missirian, Pierre Cacciagli, Sandra Whalen, Tessa Fredriksen, Edmond Lebée, Julia Rankin, Michèle Mathieu‐Dramard, G Morin, Dominique Martin‐Coignard, Christèle Dubourg, B. Chabrol, E Torroella-Menendez-Fortun, Fabienne Giuliano, Mark Matsunagaa, Nicole Philip, Pierre Sarda, Laurent Villard, Michel Goossens, Anne Moncla	2008	45
12	Identification of coagulase negative Staphylo- cocci isolated from dairy products using mole- cular methods Revue Méd Vét ·Nicoletta Murru, Angéli Kodjo, Laurent Villard, Xianchang Liu, 秀明三宅, Maria Grazia Tozzi, Maria Luisa Cortesi	2005	2
13	Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update European Journal of Medical Genetics ·Christophe Philippe, Laurent Villard, Nicolás de Roux, Martine Raynaud, 芳人斉藤, Laurent Pasquier, Gaëtan Lesca, Julien Mancini, Philippe Jonveaux, A. Moncla, Jamel Chelly, Thierry Bienvenu	2005	57
14	Performance of Random Amplified Polymorphic DNA (RADP) analysis and Pulsed Field Gel Electrophoresis (PFGE) for the characterisation of Staphylococcus xylosus strains Revue Méd Vét ·Laurent Villard, Rebecca Boddy, Victoria Izquierdo Cubillos, S. G. Prolongo, Yolande Richard, Angéli Kodjo	2003	3
15	Spectrum of MECP2 Mutations in Rett Syndrome Genetic Testing ·Thierry Bienvenu, Laurent Villard, Nicolás de Roux, Violaine Bourdon, Michel Fontés, Chérif Beldjord, Marc Tardieu, Philippe Jonveaux, Jamel Chelly	2002	14
16	A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28 The American Journal of Human Genetics ·Laurent Villard, Karine Nguyen, Carlos Cardoso, Christa Lese Martin, Vasil Tchaban, Fatine Drhimer, Arthur W. Grix, John M. Graham, Robin M. Winter, Richard J. Leventer, William B. Dobyns	2002	79
17	Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation Journal of Medical Genetics ·Anne-Marie Lossi, Yaset Abdi یاسر عبدی, D. Depétris, Jozef Gécz, Ági K. Gedeon, R. Frank Kooy, CE Schwartz, Marie‐Geneviève Mattéi, M. F. Croquette, Laurent Villard	2002	23
18	Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome withoutMECP2 mutation: implications for the disease Journal of Medical Genetics ·Laurent Villard, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	2001	47
19	Molecular characterization of a new human T-box gene (TBX22) located in Xq21.1 encoding a protein containing a truncated T-domain Gene ·Yaset Abdi یاسر عبدی, Laurent Villard	2000	18
20	Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome) Cell ·Richard J. Gibbons, David J. Picketts, Laurent Villard, Douglas R. Higgs	1995	458

About Laurent Villard

Laurent Villard is a scholar working on Genetics, Molecular Biology, Developmental Biology, Cognitive Neuroscience and Cell Biology, having authored 121 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (71 papers), RNA regulation and disease (17 papers), Autism Spectrum Disorder Research (16 papers), Genomic variations and chromosomal abnormalities (16 papers), Epigenetics and DNA Methylation (15 papers), RNA modifications and cancer (13 papers), Epilepsy research and treatment (10 papers) and Mitochondrial Function and Pathology (8 papers). The work is most often cited by research in Genetics (2.4k citations), Cognitive Neuroscience (926 citations), Molecular Biology (2.2k citations), Developmental Neuroscience (132 citations) and Endocrine and Autonomic Systems (206 citations). Laurent Villard has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Jean‐Christophe Roux, David J. Picketts, Richard J. Gibbons, Douglas R. Higgs, Pierre Cacciagli, Anne Moncla, B. Chabrol, Josette Mancini, Nicolas Panayotis and Carlos Cardoso. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Epilepsia, Gene and Human Mutation.

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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