Frédéric Laumonnier

4.8k total citations · 1 hit paper
42 papers, 1.9k citations indexed

About

Frédéric Laumonnier is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Frédéric Laumonnier has authored 42 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 23 papers in Molecular Biology and 11 papers in Cognitive Neuroscience. Recurrent topics in Frédéric Laumonnier's work include Genetics and Neurodevelopmental Disorders (27 papers), Autism Spectrum Disorder Research (11 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Frédéric Laumonnier is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Autism Spectrum Disorder Research (11 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Frédéric Laumonnier collaborates with scholars based in France, Netherlands and Germany. Frédéric Laumonnier's co-authors include Sylvain Briault, Christian Andrés, Martine Raynaud, Jamel Chelly, Claude Moraine, Nathalie Ronce, Frédérique Bonnet‐Brilhault, Catherine Barthélémy, Ben C.J. Hamel and Patrick Vourc’h and has published in prestigious journals such as Nature Genetics, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Frédéric Laumonnier

40 papers receiving 1.9k citations

Hit Papers

align trajectories sort by overperformance

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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Frédéric Laumonnier France	19	1.1k	1.0k	653	343	165	42	1.9k
Patrice L. Whitehead United States	21	798 0.7×	842 0.8×	722 1.1×	281 0.8×	147 0.9×	41	1.8k
Yuji Kajiwara United States	22	997 0.9×	747 0.7×	636 1.0×	367 1.1×	172 1.0×	46	2.2k
Paolo Moretti United States	15	1.6k 1.4×	1.0k 1.0×	665 1.0×	293 0.9×	72 0.4×	35	2.5k
Cindy Skinner United States	25	1.4k 1.3×	1.6k 1.6×	907 1.4×	257 0.7×	134 0.8×	64	2.5k
Hsien‐Sung Huang United States	18	1.8k 1.6×	1.1k 1.0×	387 0.6×	518 1.5×	55 0.3×	34	2.5k
J. Lloyd Holder United States	20	530 0.5×	715 0.7×	532 0.8×	246 0.7×	141 0.9×	40	1.5k
Hanoch Kaphzan Israel	20	1.1k 1.0×	735 0.7×	473 0.7×	560 1.6×	265 1.6×	50	1.9k
Federico Bolognani United States	27	1.2k 1.1×	543 0.5×	417 0.6×	317 0.9×	57 0.3×	61	2.2k
Tomoko Toyota Japan	31	1.5k 1.3×	850 0.8×	398 0.6×	818 2.4×	192 1.2×	87	2.8k
Patrizia D’Adamo Italy	28	1.8k 1.6×	837 0.8×	369 0.6×	693 2.0×	443 2.7×	46	2.9k

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

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20 of 20 papers shown

Moizard, Marie‐Pierre, Nathalie Ronce, Paul Guéguen, et al.. (2025). Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2. American Journal of Medical Genetics Part A. 200(3). 744–748.

Marouillat, Sylviane, Cindy Maurel, Hélène Blasco, et al.. (2024). Dynamic Expression of Genes Encoding Ubiquitin Conjugating Enzymes (E2s) During Neuronal Differentiation and Maturation: Implications for Neurodevelopmental Disorders and Neurodegenerative Diseases. Genes. 15(11). 1381–1381. 1 indexed citations

Vourc’h, Patrick, et al.. (2023). Contribution of the dihydropyrimidinase-like proteins family in synaptic physiology and in neurodevelopmental disorders. Frontiers in Neuroscience. 17. 1154446–1154446. 12 indexed citations

Andrés, Christian, Débora Lanznaster, Sylviane Marouillat, et al.. (2023). Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1. International Journal of Molecular Sciences. 24(2). 1268–1268. 3 indexed citations

Jeanne, Médéric, Marie‐Laure Vuillaume, Valerie E. Vancollie, et al.. (2021). Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. Human Genetics. 140(6). 885–896. 14 indexed citations

Marouillat, Sylviane, Céline Brulard, Frédéric Laumonnier, et al.. (2021). Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation. International Journal of Molecular Sciences. 22(4). 1796–1796. 11 indexed citations

Hleihel, Walid, Sylviane Marouillat, Marie‐Laure Vuillaume, et al.. (2019). Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders. Molecular Genetics & Genomic Medicine. 7(8). e786–e786. 12 indexed citations

Marouillat, Sylviane, Joëlle Malvy, Annick Toutain, et al.. (2015). Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism. Psychiatric Genetics. 25(6). 263–267. 18 indexed citations

Veyrat‐Durebex, Charlotte, Philippe Corcia, Éric Piver, et al.. (2015). Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis. Molecular Neurobiology. 53(10). 6910–6924. 38 indexed citations

10.

Charon, Céline, Audrey Guilmatre, Patrick Vourc’h, et al.. (2013). Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families. Behavior Genetics. 43(2). 132–140. 7 indexed citations

11.

Mavel, Sylvie, Lydie Nadal‐Desbarats, Hélène Blasco, et al.. (2013). 1H–13C NMR-based urine metabolic profiling in autism spectrum disorders. Talanta. 114. 95–102. 68 indexed citations

12.

Veyrat‐Durebex, Charlotte, Philippe Corcia, Frédéric Laumonnier, et al.. (2013). Advances in Cellular Models to Explore the Pathophysiology of Amyotrophic Lateral Sclerosis. Molecular Neurobiology. 49(2). 966–983. 16 indexed citations

13.

Perche, Olivier, Béatrice Laudier, Arnaud Menuet, et al.. (2012). FG syndrome: The FGS2 locus revisited. American Journal of Medical Genetics Part A. 158A(6). 1489–1492. 3 indexed citations

14.

Vourc’h, Patrick, Frédéric Laumonnier, Béatrice Vallée, et al.. (2012). LIMK2d, a truncated isoform of Lim kinase 2 regulates neurite growth in absence of the LIM kinase domain. Biochemical and Biophysical Research Communications. 420(2). 247–252. 5 indexed citations

15.

Zanni, Ginevra, Hilde Van Esch, Yoann Saillour, et al.. (2009). A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation. Neurogenetics. 11(2). 251–255. 43 indexed citations

16.

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

17.

Laumonnier, Frédéric, et al.. (2007). The Role of Neuronal Complexes in Human X-Linked Brain Diseases. The American Journal of Human Genetics. 80(2). 205–220. 80 indexed citations

18.

Laumonnier, Frédéric, Sébastien Roger, Pascaline Guérin, et al.. (2006). Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation. American Journal of Psychiatry. 163(9). 1622–1629. 135 indexed citations

19.

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 →

20.

Laumonnier, Frédéric, Nathalie Ronce, Ben C.J. Hamel, et al.. (2002). Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency. The American Journal of Human Genetics. 71(6). 1450–1455. 232 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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