Catherine Burési

3.5k total citations · 1 hit paper
43 papers, 2.6k citations indexed

About

Catherine Burési is a scholar working on Psychiatry and Mental health, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Catherine Burési has authored 43 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Psychiatry and Mental health, 16 papers in Molecular Biology and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Catherine Burési's work include Neurotransmitter Receptor Influence on Behavior (10 papers), Bipolar Disorder and Treatment (8 papers) and Suicide and Self-Harm Studies (7 papers). Catherine Burési is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (10 papers), Bipolar Disorder and Treatment (8 papers) and Suicide and Self-Harm Studies (7 papers). Catherine Burési collaborates with scholars based in France, Switzerland and Tunisia. Catherine Burési's co-authors include Alain Malafosse, Bruno Moulard, Denys Chaigne, Alexis Brice, Stéphanie Baulac, Bryan T. MacDonald, Eric Leguern, Miriam H. Meisler, Gilles Huberfeld and Isabelle An-Gourfinkel and has published in prestigious journals such as Nature, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Catherine Burési

42 papers receiving 2.5k 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.

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
Catherine Burési France	23	1.1k	1.0k	1.0k	789	411	43	2.6k
Virginia L. Willour United States	24	408 0.4×	608 0.6×	665 0.7×	788 1.0×	346 0.8×	45	2.3k
Gillian Spurlock United Kingdom	25	938 0.9×	561 0.5×	1.2k 1.2×	913 1.2×	158 0.4×	60	2.8k
Gary A. Heiman United States	33	868 0.8×	381 0.4×	303 0.3×	430 0.5×	434 1.1×	62	2.4k
Aleksandra Szczepankiewicz Poland	25	352 0.3×	607 0.6×	417 0.4×	352 0.4×	246 0.6×	130	1.9k
Andrew McQuillin United Kingdom	31	387 0.4×	772 0.7×	1000 1.0×	1.2k 1.5×	146 0.4×	106	2.7k
Mónica Bayés Spain	29	464 0.4×	430 0.4×	1.1k 1.1×	555 0.7×	234 0.6×	55	2.6k
Maria Skibińska Poland	26	585 0.6×	835 0.8×	383 0.4×	426 0.5×	313 0.8×	107	2.1k
Miki Bundo Japan	29	471 0.4×	639 0.6×	2.3k 2.3×	1.3k 1.6×	143 0.3×	70	3.6k
Lourdes Martorell Spain	22	255 0.2×	436 0.4×	594 0.6×	410 0.5×	146 0.4×	82	1.8k
Ronnen H. Segman Israel	27	527 0.5×	757 0.7×	569 0.6×	721 0.9×	281 0.7×	40	2.1k

Countries citing papers authored by Catherine Burési

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Burési

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Burési

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Burési. A scholar is included among the top collaborators of Catherine Burési 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 Catherine Burési. Catherine Burési 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, Michel Guipponi, Peter J. Lyons, et al.. (2011). Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Human Mutation. 33(1). 124–135. 33 indexed citations

Etter, Jean‐François, Jean‐Charles Hoda, Nader Perroud, et al.. (2009). Association of genes coding for the α-4, α-5, β-2 and β-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence. Addictive Behaviors. 34(9). 772–775. 34 indexed citations

Perroud, Nader, P. Courtet, Isabelle Jaussent, et al.. (2007). Interaction between BDNF Val66Met and childhood trauma on adult’s violent suicide attempt. Genes Brain & Behavior. 7(3). 314–322. 84 indexed citations

Jollant, Fabrice, Catherine Burési, Sébastien Guillaume, et al.. (2007). The influence of four serotonin‐related genes on decision‐making in suicide attempters. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(5). 615–624. 70 indexed citations

Baud, Patrick, Philippe Courtet, Nader Perroud, et al.. (2007). Catechol‐O‐methyltransferase polymorphism (COMT) in suicide attempters: A possible gender effect on anger traits. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(8). 1042–1047. 34 indexed citations

Delorme, Richard, Christelle M. Durand, Catalina Betancur, et al.. (2006). No Human Tryptophan Hydroxylase-2 Gene R441H Mutation in a Large Cohort of Psychiatric Patients and Control Subjects. Biological Psychiatry. 60(2). 202–203. 43 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

Courtet, Philippe, Marie‐Christine Picot, Frank Bellivier, et al.. (2003). Serotonin transporter gene may be involved in short-term risk of subsequent suicide attempts. Biological Psychiatry. 55(1). 46–51. 72 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

10.

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 →

11.

Karege, Félicien, Catherine Burési, Jean Golaz, Michèle Schwald, & Alain Malafosse. (2000). Decreased expression of G?s mRNA and protein levels in lithium-treated bipolar affective disorder. Human Psychopharmacology Clinical and Experimental. 15(3). 191–197. 1 indexed citations

12.

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

13.

Lalioti, Maria D., Hamish S. Scott, Pierre Genton, et al.. (1998). A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset. The American Journal of Human Genetics. 62(4). 842–847. 52 indexed citations

14.

Bellivier, Frank, Marion Leboyer, Catherine Burési, et al.. (1998). Association Between the Tryptophan Hydroxylase Gene and Manic-depressive Illness. Archives of General Psychiatry. 55(1). 33–33. 161 indexed citations

15.

Lalioti, Maria D., Hamish S. Scott, Catherine Burési, et al.. (1997). Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy. Nature. 386(6627). 847–851. 257 indexed citations

16.

Labauge, Pierre, Réda Ouazzani, A. Mrabet, et al.. (1997). Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene. Annals of Neurology. 41(5). 686–689. 3 indexed citations

17.

Burési, Catherine, Érick Desmarais, Suzanne Vigneron, et al.. (1996). Structural Analysis of the Minisatellite Present at the 3' end of the Human Apolipoprotein B Gene: New Definition of the Alleles and Evolutionary Implications. Human Molecular Genetics. 5(1). 61–68. 19 indexed citations

18.

Burési, Catherine, et al.. (1995). Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups. Genetic Epidemiology. 12(4). 381–389. 9 indexed citations

19.

Bernard, Frédéric, et al.. (1991). HindIII/Eco RI RFLP of the human immunoglobulin IGHE gene detected with a C? probe in the French and Tunisian populations. Human Genetics. 87(1). 101–101. 2 indexed citations

20.

Ghanem, N., Catherine Burési, M. Abbal, et al.. (1990). Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia. Human Genetics. 86(2). 117–25. 5 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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