Bruno Moulard

1.7k total citations · 1 hit paper
20 papers, 1.3k citations indexed

About

Bruno Moulard is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bruno Moulard has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Psychiatry and Mental health and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bruno Moulard's work include Epilepsy research and treatment (7 papers), Ion channel regulation and function (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Bruno Moulard is often cited by papers focused on Epilepsy research and treatment (7 papers), Ion channel regulation and function (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Bruno Moulard collaborates with scholars based in Switzerland, France and Canada. Bruno Moulard's co-authors include Alain Malafosse, Catherine Burési, Denys Chaigne, Eric Leguern, Isabelle An-Gourfinkel, Gilles Huberfeld, Miriam H. Meisler, Alexis Brice, Andrew Escayg and Bryan T. MacDonald and has published in prestigious journals such as Nature Genetics, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Bruno Moulard

19 papers receiving 1.2k 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.

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

2000 739 citations Andrew Escayg, Bryan T. MacDonald et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bruno Moulard Switzerland	11	663	644	523	358	263	20	1.3k
Ann Löfgren Belgium	13	722 1.1×	227 0.4×	502 1.0×	189 0.5×	126 0.5×	16	1.1k
Jacy L. Wagnon United States	20	607 0.9×	516 0.8×	466 0.9×	418 1.2×	68 0.3×	26	1.1k
John A. Damiano Australia	18	398 0.6×	389 0.6×	141 0.3×	444 1.2×	262 1.0×	32	1.3k
Zaid Afawi Israel	17	442 0.7×	449 0.7×	266 0.5×	441 1.2×	65 0.2×	27	1.1k
Inge A. Meijer Canada	14	369 0.6×	79 0.1×	362 0.7×	150 0.4×	129 0.5×	22	811
Tracy Dixon‐Salazar United States	12	556 0.8×	279 0.4×	178 0.3×	525 1.5×	35 0.1×	26	1.1k
Giovanni Vazza Italy	17	360 0.5×	79 0.1×	227 0.4×	99 0.3×	98 0.4×	33	752
Emmanuelle Buhler France	14	367 0.6×	61 0.1×	298 0.6×	117 0.3×	126 0.5×	28	755
Lena E. Hjermind Denmark	18	405 0.6×	69 0.1×	403 0.8×	98 0.3×	388 1.5×	47	904
Claude Mignard France	5	690 1.0×	51 0.1×	688 1.3×	49 0.1×	238 0.9×	7	865

Countries citing papers authored by Bruno Moulard

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Moulard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Moulard

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno Moulard. A scholar is included among the top collaborators of Bruno Moulard 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 Bruno Moulard. Bruno Moulard 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

Salzmann, Annick, Bruno Moulard, Arielle Crespel, et al.. (2005). GABA_B Receptor 1 Polymorphism (G1465A) and Temporal Lobe Epilepsy. Epilepsia. 46(6). 931–933. 13 indexed citations

Moulard, Bruno, Françoise Darcel, Marc Jeanpierre, et al.. (2003). Founder Effect in Patients with Unverricht‐Lundborg Disease on Reunion Island. Epilepsia. 44(10). 1357–1360. 8 indexed citations

Moulard, Bruno, Françoise Darcel, Marc Jeanpierre, et al.. (2002). L'épilepsie myoclonique progressive de type Unverricht-Lundborg sur l'île de la Réunion. 14(2). 99–106. 1 indexed citations

Malafosse, Alain & Bruno Moulard. (2002). [Genetic aspects of epilepsy: current knowledge and perspectives].. PubMed. 158(3). 283–91. 1 indexed citations

Moulard, Bruno & Daniel Bertrand. (2002). Epilepsy and sodium channel blockers. Expert Opinion on Therapeutic Patents. 12(1). 85–91. 1 indexed citations

Malafosse, Alain, et al.. (2001). Aspects génétiques de l’épilepsie myoclonique juvénile. 13(2). 97–102. 3 indexed citations

Moore, Tom, Dorothée Ville, Djamel Grid, et al.. (2001). Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME. Epilepsy Research. 46(2). 157–167. 30 indexed citations

Moulard, Bruno, Fabienne Picard, Stéphanie Le Hellard, et al.. (2001). Ion channel variation causes epilepsies. Brain Research Reviews. 36(2-3). 275–284. 64 indexed citations

Escayg, Andrew, Bryan T. MacDonald, Miriam H. Meisler, et al.. (2000). Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2. Nature Genetics. 24(4). 343–345. 739 indexed citations breakdown →

10.

Moulard, Bruno, Catherine Burési, & Alain Malafosse. (2000). Study of the voltage-gated sodium channel ?1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC). Human Mutation. 16(2). 139–142. 9 indexed citations

11.

Moulard, Bruno, Denys Chaigne, & Alain Malafosse. (2000). Clinical heterogeneity in pedigrees with 2q-linked febrile seizures. Annals of Neurology. 47(6). 839–840. 1 indexed citations

12.

Moulard, Bruno, Arielle Crespel, Alain Malafosse, & M Baldy-Moulinier. (2000). [Recent insights about genetics of human idiopathic epilepsies and febrile seizures].. PubMed. 156(10). 819–28. 3 indexed citations

13.

Khoris, Jawad, Bruno Moulard, Michaela Hayer, et al.. (2000). Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country. European Journal of Neurology. 7(2). 207–211. 29 indexed citations

14.

Moulard, Bruno, Denys Chaigne, Dominique Mouthon, et al.. (1999). Identification of a New Locus for Generalized Epilepsy with Febrile Seizures Plus (GEFS+) on Chromosome 2q24-q33. The American Journal of Human Genetics. 65(5). 1396–1400. 107 indexed citations

15.

Camu, William, Jawad Khoris, Bruno Moulard, et al.. (1999). Genetics of familial ALS and consequences for diagnosis. Journal of the Neurological Sciences. 165. S21–S26. 65 indexed citations

16.

Khoris, Jawad, Bruno Moulard, François Salachas, et al.. (1998). Identification of Six Novel SOD1 Gene Mutations in Familial Amyotrophic Lateral Sclerosis. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 25(3). 192–196. 59 indexed citations

17.

Moulard, Bruno, François Salachas, B. Chassande, et al.. (1998). Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron disease. Annals of Neurology. 43(5). 640–644. 55 indexed citations

18.

Moulard, Bruno, et al.. (1997). [Clinical study of familial forms of amyotrophic lateral sclerosis. Review of the literature].. PubMed. 153(5). 314–24. 5 indexed citations

19.

Moulard, Bruno, et al.. (1996). Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis. Journal of the Neurological Sciences. 139. 34–37. 71 indexed citations

20.

Beck, Christian, Bruno Moulard, Ortrud K. Steinlein, et al.. (1994). A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI). Neurobiology of Disease. 1(1-2). 95–99. 32 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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