Sébastien Moutton

3.3k citations

17 papers · 367 indexed · h-index 12

Co-authors: Laurence Colleaux Didier Lacombe Frédéric Tran Mau‐Them Antonio Vitobello Christophe Philippe Marlène Rio Laurence Faivre Karine Siquier-Pernet
Topics: Genetics and Neurodevelopmental Disorders (8 papers)Genomics and Rare Diseases (7 papers)Genomic variations and chromosomal abnormalities (7 papers)
Cited by: Genetics Developmental Neuroscience Cellular and Molecular Neuroscience
Journals: The American Journal of Human Genetics Human Molecular Genetics Human Mutation
Partner nations: France United States Netherlands

In The Last Decade

Sébastien Moutton

17 papers receiving 353 citations

Peers

Countries citing papers authored by Sébastien Moutton

Since Specialization

Citations

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

Fields of papers citing papers by Sébastien Moutton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sébastien Moutton

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Microdeletions at 19p13.11p12 in five individuals with neurodevelopmental delay 2022 ·European Journal of Medical Genetics ·(unknown),Sébastien Moutton,(unknown),Katharina Steindl,Bernt Popp,Bruno Leheup,Céline Bonnet,Beatrice Oneda,Anita Rauch,André Reis,Mandy Krumbiegel,Ulrike Hüffmeier	1
2	Interest of exome sequencing trio‐like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases 2021 ·Molecular Genetics & Genomic Medicine ·Frédéric Tran Mau‐Them,Yannis Duffourd,Antonio Vitobello,Ange‐Line Bruel,Anne‐Sophie Denommé‐Pichon,Sophie Nambot,Julian Delanne,Sébastien Moutton,Arthur Sorlin,(unknown),(unknown),(unknown),Martin Chevarin,Charlotte Pöe,Anne‐Laure Mosca‐Boidron,Patrick Callier,(unknown),Laurence Faivre,Christophe Philippe,Christel Thauvin‐Robinet	4
3	Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother 2021 ·Stem Cell Research* ·Elena Longobardi,Francesco Miceli,Agnese Secondo,Rita Cicatiello,Antonella Izzo,Nadia Tinto,Sébastien Moutton,Frédéric Tran Mau‐Them,Antonio Vitobello,Maurizio Taglialatela	4
4	Next‐generation sequencing approaches and challenges in the diagnosis of developmental anomalies and intellectual disability 2020 ·Clinical Genetics ·Ange‐Line Bruel,Antonio Vitobello,Frédéric Tran Mau‐Them,Sophie Nambot,Arthur Sorlin,Anne‐Sophie Denommé‐Pichon,Julian Delanne,Sébastien Moutton,Patrick Callier,Yannis Duffourd,Christophe Philippe,Laurence Faivre,Christel Thauvin‐Robinet	11
5	Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing 2019 ·European Journal of Human Genetics ·Ange‐Line Bruel,Sophie Nambot,(unknown),Antonio Vitobello,Julien Thévenon,Mirna Assoum,Sébastien Moutton,Nada Houcinat,Daphné Lehalle,Nolwenn Jean‐Marçais,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Martin Chevarin,Thibaud Jouan,Charlotte Pöe,Patrick Callier,(unknown),Christophe Philippe,Frédéric Tran Mau‐Them,Yannis Duffourd,Laurence Faivre,Christel Thauvin‐Robinet	39
6	Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants 2019 ·Genetics in Medicine ·François Lecoquierre,Yannis Duffourd,Antonio Vitobello,Ange‐Line Bruel,(unknown),Christine Coubes,(unknown),Sophie Nambot,Martin Chevarin,Thibaud Jouan,Sébastien Moutton,Frédéric Tran Mau‐Them,Christophe Philippe,Arthur Sorlin,Laurence Faivre,Christel Thauvin‐Robinet	20
7	HNRNPR Variants that Impair Homeobox Gene Expression Drive Developmental Disorders in Humans 2019 ·The American Journal of Human Genetics ·Floor A.M. Duijkers,Andrew McDonald,Georges E. Janssens,Marco Lezzerini,Aldo Jongejan,Silvana van Koningsbruggen,(unknown),Marcin W. Włodarski,Sébastien Moutton,Frédéric Tran Mau‐Them,Christel Thauvin‐Robinet,Laurence Faivre,Kristin G. Monaghan,Thomas Smol,Odile Boute‐Bénéjean,Roger L. Ladda,Susan L. Sell,Ange‐Line Bruel,Riekelt H. Houtkooper,Alyson W. MacInnes	23
8	A novel homozygous KCNQ3 loss‐of‐function variant causes non‐syndromic intellectual disability and neonatal‐onset pharmacodependent epilepsy 2019 ·Epilepsia Open ·Anna Lauritano,Sébastien Moutton,Elena Longobardi,Frédéric Tran Mau‐Them,Giusy Laudati,(unknown),Maria Virginia Soldovieri,Paolo Ambrosino,Mauro Cataldi,Thibaud Jouan,Daphné Lehalle,Hélène Maurey,Christophe Philippe,Francesco Miceli,Antonio Vitobello,Maurizio Taglialatela	33
9	Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features 2018 ·Clinical Genetics ·Sébastien Moutton,Ange‐Line Bruel,Mirna Assoum,Martin Chevarin,Elisabeth Sarrazin,Cyril Goizet,(unknown),Aude Charollais,Perrine Charles,D. Héron,Anne Faudet,Nada Houcinat,Antonio Vitobello,(unknown),Christophe Philippe,Yannis Duffourd,(unknown),Laurence Faivre	17
10	Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variant 2018 ·European Journal of Medical Genetics ·(unknown),Julien Van‐Gils,Antoine Bigourdan,Pierre‐Simon Jouk,Didier Lacombe,Patrice Ménégon,Sébastien Moutton,Florence Riant,Guilhem Solé,Elisabeth Tournier‐Lasserve,Aurélien Trimouille,Marie Vincent,Cyril Goizet	30
11	Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype 2016 ·European Journal of Human Genetics ·Fanny Morice‐Picard,Giovanni Bénard,Hamid Rezvani,Eulalie Lasseaux,Delphine Simon,Sébastien Moutton,Caroline Rooryck,Didier Lacombe,Clarisse Baumann,Benoı̂t Arveiler	27
12	Recurrent KIF2A mutations are responsible for classic lissencephaly 2016 ·Neurogenetics ·Mara Cavallin,Emilia K. Bijlsma,(unknown),Sébastien Moutton,E Peeters,(unknown),Jean Michel Pedespan,Anne‐Marie Guerrot,(unknown),Christine Coubes,David Geneviève,Christine Bôle‐Feysot,Cécile Fourrage,Julie Steffann,Nadia Bahi‐Buisson	21
13	A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy 2015 ·European Journal of Human Genetics ·Lam Son Nguyen,Taiane Schneider,Marlène Rio,Sébastien Moutton,Karine Siquier-Pernet,(unknown),Nathalie Boddaert,Isabelle Desguerre,(unknown),José Luís Rosa,Valérie Cormier‐Daire,Laurence Colleaux	39
14	Homozygous 16p13.11 duplication associated with mild intellectual disability and urinary tract malformations in two siblings born from consanguineous parents 2015 ·American Journal of Medical Genetics Part A ·Nada Houcinat,Brigitte Llanas,Sébastien Moutton,Jérôme Toutain,Dorothée Cailley,Benoı̂t Arveiler,Christian Combe,Didier Lacombe,Caroline Rooryck	21
15	Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth 2013 ·Human Molecular Genetics ·Lionel Van Maldergem,Qingming Hou,Vera M. Kalscheuer,Marlène Rio,Martine Doco‐Fenzy,Ana Medeira,Arjan P.M. de Brouwer,Christelle Cabrol,Stefan A. Haas,Pierre Cacciagli,Sébastien Moutton,Emilie Landais,Jacques Motté,Laurence Colleaux,Céline Bonnet,Laurent Villard,Juliette Dupont,Heng‐Ye Man	55
16	Mutation in TTI2 Reveals a Role for Triple T Complex in Human Brain Development 2013 ·Human Mutation ·Maéva Langouët,(unknown),Guillaume Rieunier,Sébastien Moutton,Karine Siquier-Pernet,Marie Fernet,Patrick Nitschké,Arnold Münnich,Marc‐Henri Stern,Malika Chaouch,Laurence Colleaux	18
17	Dysmorphic features in subtelomeric 20p13 deletion excluding JAG1: A recognizable microdeletion phenotype? 2012 ·European Journal of Medical Genetics ·Sébastien Moutton,Caroline Rooryck,Jérôme Toutain,Dorothée Cailley,Julie Bouron,Frédéric Villega,(unknown),Didier Lacombe,Benoı̂t Arveiler,Cyril Goizet	4

About Sébastien Moutton

Sébastien Moutton is a scholar working on Genetics, Molecular Biology and Cell Biology, having authored 17 papers that have together received 367 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (211 citations), Developmental Neuroscience (16 citations) and Cellular and Molecular Neuroscience (64 citations). Sébastien Moutton has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Laurence Colleaux, Didier Lacombe, Frédéric Tran Mau‐Them, Antonio Vitobello, Christophe Philippe, Marlène Rio, Laurence Faivre, Karine Siquier-Pernet, Ange‐Line Bruel and Benoı̂t Arveiler. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics 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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