Frédéric Laumonnier

4.8k citations

42 papers · 1.9k indexed · 1 hit paper · h-index 19

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

Co-authors: Sylvain Briault Christian Andrés Martine Raynaud Jamel Chelly Claude Moraine Frédérique Bonnet‐Brilhault Nathalie Ronce Catherine Barthélémy
Topics: Genetics and Neurodevelopmental Disorders (27 papers)Autism Spectrum Disorder Research (11 papers)Amyotrophic Lateral Sclerosis Research (6 papers)
Cited by: Genetics Cognitive Neuroscience Developmental Neuroscience
Journals: Nature Genetics American Journal of Psychiatry Biological Psychiatry
Partner nations: France Netherlands Germany

In The Last Decade

Frédéric Laumonnier

40 papers receiving 1.9k 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 Frédéric Laumonnier

Since Specialization

Citations

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

Fields of papers citing papers by Frédéric Laumonnier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frédéric Laumonnier

This figure shows the co-authorship network connecting the top 25 collaborators of Frédéric Laumonnier. A scholar is included among the top collaborators of Frédéric Laumonnier 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 Frédéric Laumonnier. Frédéric Laumonnier 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	Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2 2025 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),(unknown),Marie‐Pierre Moizard,Nathalie Ronce,Paul Guéguen,Frédéric Laumonnier,(unknown),Florent Marguet,A. Laquérrière,(unknown),(unknown),(unknown),Stéphanie Arpin,Médéric Jeanne,Marie‐Laure Vuillaume	0
2	The PTCHD1 protein: A prominent actor in brain function and in neurodevelopmental disorders 2025 ·Neuroscience & Biobehavioral Reviews ·(unknown),Stéphane Martin,Yann Hérault,Frédéric Laumonnier	0
3	Dynamic Expression of Genes Encoding Ubiquitin Conjugating Enzymes (E2s) During Neuronal Differentiation and Maturation: Implications for Neurodevelopmental Disorders and Neurodegenerative Diseases 2024 ·Genes ·(unknown),Sylviane Marouillat,(unknown),Cindy Maurel,(unknown),Hélène Blasco,Philippe Corcia,Frédéric Laumonnier,Christian Andrés,Patrick Vourc’h	1
4	Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders 2023 ·Frontiers in Neuroscience ·(unknown),(unknown),Patrick Vourc’h,Médéric Jeanne,Frédéric Laumonnier	12
5	Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1 2023 ·International Journal of Molecular Sciences ·(unknown),Christian Andrés,Débora Lanznaster,Sylviane Marouillat,Céline Brulard,(unknown),(unknown),Charlotte Veyrat‐Durebex,Frédéric Laumonnier,Hélène Blasco,Philippe Couratier,Philippe Corcia,Patrick Vourc’h	3
6	Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth 2021 ·Human Genetics ·Médéric Jeanne,Marie‐Laure Vuillaume,(unknown),Valerie E. Vancollie,Christel Wagner,Stephan C. Collins,(unknown),Damien Haye,(unknown),Rolph Pfundt,(unknown),Marie‐Pierre Moizard,Sylviane Marouillat,Tjitske Kleefstra,Binnaz Yalcin,Frédéric Laumonnier,Annick Toutain	14
7	Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders 2019 ·Molecular Genetics & Genomic Medicine ·(unknown),Walid Hleihel,Sylviane Marouillat,(unknown),Marie‐Laure Vuillaume,Michel Soufia,Patrick Vourc’h,Frédéric Laumonnier,Christian Andrés	12
8	Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability 2018 ·Clinica Chimica Acta ·Marie‐Laure Vuillaume,Benjamin Cogné,Médéric Jeanne,Anne Boland,(unknown),(unknown),Thomas Besnard,Jean‐François Deleuze,Richard Redon,Stéphane Bezieau,Frédéric Laumonnier,Annick Toutain	10
9	LIMK2-1 is a Hominidae-Specific Isoform of LIMK2 Expressed in Central Nervous System and Associated with Intellectual Disability 2018 ·Neuroscience ·(unknown),(unknown),Béatrice Vallée,Annick Toutain,Martine Raynaud,Sylviane Marouillat,(unknown),Frédéric Laumonnier,Frédérique Bonnet‐Brilhault,Patrick Vourc’h,Christian Andrés,Hélène Bénédetti	6
10	Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism 2015 ·Psychiatric Genetics ·(unknown),(unknown),Sylviane Marouillat,Joëlle Malvy,(unknown),Annick Toutain,(unknown),(unknown),Hélène Bénédetti,Frédéric Laumonnier,Catherine Barthélémy,Frédérique Bonnet‐Brilhault,Christian Andrés,Patrick Vourc’h	18
11	Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis 2015 ·Molecular Neurobiology ·Charlotte Veyrat‐Durebex,Philippe Corcia,Éric Piver,David Devos,(unknown),Flore Gouel,Patrick Vourc’h,Patrick Emond,Frédéric Laumonnier,Lydie Nadal‐Desbarats,Gordon Gilbert,Christian Andrés,Hélène Blasco	38
12	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
13	Advances in Cellular Models to Explore the Pathophysiology of Amyotrophic Lateral Sclerosis 2013 ·Molecular Neurobiology ·Charlotte Veyrat‐Durebex,Philippe Corcia,(unknown),Frédéric Laumonnier,Éric Piver,Gordon Gilbert,Christian Andrés,Patrick Vourc’h,Hélène Blasco	16
14	1H–13C NMR-based urine metabolic profiling in autism spectrum disorders 2013 ·Talanta ·Sylvie Mavel,Lydie Nadal‐Desbarats,Hélène Blasco,Frédérique Bonnet‐Brilhault,Catherine Barthélémy,Frédéric Montigny,Pierre Sarda,Frédéric Laumonnier,Patrick Vourc’h,Christian Andrés,Patrick Emond	68
15	FG syndrome: The FGS2 locus revisited 2012 ·American Journal of Medical Genetics Part A ·Olivier Perche,Béatrice Laudier,Arnaud Menuet,Sylvie Odent,Frédéric Laumonnier,Sylvain Briault	3
16	LIMK2d, a truncated isoform of Lim kinase 2 regulates neurite growth in absence of the LIM kinase domain 2012 ·Biochemical and Biophysical Research Communications ·(unknown),Patrick Vourc’h,Frédéric Laumonnier,Béatrice Vallée,Caroline Michelle,Anne Duittoz,(unknown),Christian Andrés	5
17	Autisme, génétique et anomalies de la fonction synaptique 2010 ·Pathologie Biologie ·Olivier Perche,Frédéric Laumonnier,Lekbir Baala,Maryvonne Ardourel,Arnaud Menuet,(unknown),Stéphane Mortaud,(unknown),(unknown),Jacques Pichon,Sylvain Briault	6
18	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
19	Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation 2006 ·American Journal of Psychiatry ·Frédéric Laumonnier,Sébastien Roger,Pascaline Guérin,Florence Molinari,Ridha Mrad,Dominique Cahard,A. Belhadj,(unknown),Antonio M. Persico,Maurizio Elia,Valentino Romano,Sébastien Holbert,Christian Andrés,Habiba Chaâbouni,Laurence Colleaux,Jacques Constant,Jean-Yves Le Guennec,Sylvain Briault	135
20	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

About Frédéric Laumonnier

Frédéric Laumonnier is a scholar working on Genetics, Cognitive Neuroscience and Genetics, having authored 42 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (27 papers), Autism Spectrum Disorder Research (11 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). The work is most often cited by research in Genetics (1.0k citations), Cognitive Neuroscience (653 citations) and Developmental Neuroscience (110 citations). Frédéric Laumonnier has collaborated with scholars based in France, Netherlands and Germany. Frequent co-authors include Sylvain Briault, Christian Andrés, Martine Raynaud, Jamel Chelly, Claude Moraine, Frédérique Bonnet‐Brilhault, Nathalie Ronce, Catherine Barthélémy, Ben C.J. Hamel and Patrick Vourc’h. Their work appears in journals such as Nature Genetics, American Journal of Psychiatry and Biological Psychiatry.

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