Chantal Mérette

9.7k total citations · 2 hit papers
115 papers, 7.0k citations indexed

About

Chantal Mérette is a scholar working on Genetics, Cognitive Neuroscience and Psychiatry and Mental health. According to data from OpenAlex, Chantal Mérette has authored 115 papers receiving a total of 7.0k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Genetics, 34 papers in Cognitive Neuroscience and 33 papers in Psychiatry and Mental health. Recurrent topics in Chantal Mérette's work include Genetic Associations and Epidemiology (26 papers), Schizophrenia research and treatment (24 papers) and Sleep and related disorders (17 papers). Chantal Mérette is often cited by papers focused on Genetic Associations and Epidemiology (26 papers), Schizophrenia research and treatment (24 papers) and Sleep and related disorders (17 papers). Chantal Mérette collaborates with scholars based in Canada, United States and France. Chantal Mérette's co-authors include Charles M. Morin, Mélanie LeBlanc, Hans Ivers, Michel Maziade, Josée Savard, Jean‐Pierre Grégoire, Marc‐André Roy, Lucie Baillargeon, Lynda Bélanger and Annie Vallières and has published in prestigious journals such as JAMA, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Chantal Mérette

112 papers receiving 6.7k citations

Hit Papers

Epidemiology of insomnia:... 2006 2026 2012 2019 2006 2009 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chantal Mérette Canada 43 3.1k 2.7k 1.4k 1.3k 925 115 7.0k
Marcus Ising Germany 53 1.3k 0.4× 1.3k 0.5× 1.3k 0.9× 1.5k 1.2× 898 1.0× 185 10.3k
Thomas W. Uhde United States 47 2.8k 0.9× 2.2k 0.8× 2.1k 1.5× 2.0k 1.6× 576 0.6× 179 8.0k
Masako Okawa Japan 46 3.8k 1.2× 3.0k 1.1× 634 0.4× 647 0.5× 2.6k 2.8× 150 7.7k
Witte J.G. Hoogendijk Netherlands 59 2.1k 0.7× 1.3k 0.5× 1.7k 1.2× 2.1k 1.6× 977 1.1× 208 11.7k
Ruth O’Hara United States 45 1.6k 0.5× 2.6k 0.9× 1.7k 1.2× 927 0.7× 539 0.6× 166 7.1k
Jürgen Deckert Germany 51 1.9k 0.6× 2.0k 0.7× 1.5k 1.0× 1.9k 1.5× 334 0.4× 302 8.5k
Daniel F. Hermens Australia 50 2.4k 0.8× 3.8k 1.4× 3.3k 2.3× 2.1k 1.7× 664 0.7× 284 9.0k
Nils Lindefors Sweden 56 3.1k 1.0× 1.4k 0.5× 2.1k 1.4× 2.5k 1.9× 418 0.5× 179 10.3k
Femke Lamers Netherlands 50 2.9k 0.9× 987 0.4× 1.3k 0.9× 2.1k 1.6× 385 0.4× 171 8.5k
Cristina Colombo Italy 54 2.4k 0.8× 2.5k 0.9× 3.2k 2.3× 1.3k 1.0× 2.0k 2.1× 245 8.8k

Countries citing papers authored by Chantal Mérette

Since Specialization
Citations

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

Fields of papers citing papers by Chantal Mérette

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chantal Mérette

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

All Works

20 of 20 papers shown
1.
Hébert, Marc, et al.. (2022). Developing a clinical decision tool based on electroretinogram to monitor the risk of severe mental illness. BMC Psychiatry. 22(1). 718–718. 5 indexed citations
2.
Sirois, Caroline, Louis Rochette, Simon Patry, et al.. (2022). The 5-year longitudinal diagnostic profile and health services utilization of patients treated with electroconvulsive therapy in Quebec: a population-based study. Social Psychiatry and Psychiatric Epidemiology. 58(4). 629–639. 6 indexed citations
4.
Hébert, Marc, Chantal Mérette, Anne-Marie Gagné, et al.. (2019). The Electroretinogram May Differentiate Schizophrenia From Bipolar Disorder. Biological Psychiatry. 87(3). 263–270. 68 indexed citations
5.
Jomphe, Valérie, et al.. (2018). Cluster analysis identifies two cognitive profiles among offspring of patients with a major psychiatric disorder: The healthy and impaired profiles. 2(2). 3 indexed citations
6.
Hébert, Marc, Chantal Mérette, Thomas Paccalet, Anne-Marie Gagné, & Michel Maziade. (2016). Electroretinographic anomalies in medicated and drug free patients with major depression: Tagging the developmental roots of major psychiatric disorders. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 75. 10–15. 44 indexed citations
7.
Gross, Jeffrey, Alexandre Bureau, Jordie Croteau, et al.. (2015). A Genome-Wide Copy Number Variant Study of Suicidal Behavior. PLoS ONE. 10(5). e0128369–e0128369. 22 indexed citations
8.
Mamdani, Firoza, et al.. (2011). Gene expression biomarkers of response to citalopram treatment in major depressive disorder. Translational Psychiatry. 1(6). e13–e13. 49 indexed citations
9.
Maziade, Michel, Nancie Rouleau, Caroline Cellard, et al.. (2011). Young Offspring at Genetic Risk of Adult Psychoses: The Form of the Trajectory of IQ or Memory May Orient to the Right Dysfunction at the Right Time. PLoS ONE. 6(4). e19153–e19153. 18 indexed citations
10.
Fiori, Laura M., Alexandre Bureau, Aurélie Labbe, et al.. (2011). Global gene expression profiling of the polyamine system in suicide completers. The International Journal of Neuropsychopharmacology. 14(5). 595–605. 40 indexed citations
12.
Labbe, Aurélie, Alexandre Bureau, & Chantal Mérette. (2009). Integration of Genetic Familial Dependence Structure in Latent Class Models. The International Journal of Biostatistics. 5(1). 6 indexed citations
13.
Achim, Amélie M., et al.. (2009). How Prevalent Are Anxiety Disorders in Schizophrenia? A Meta-Analysis and Critical Review on a Significant Association. Schizophrenia Bulletin. 37(4). 811–821. 397 indexed citations
14.
Morin, Charles M., Lynda Bélanger, Mélanie LeBlanc, et al.. (2009). The Natural History of Insomnia. Archives of Internal Medicine. 169(5). 447–447. 368 indexed citations
15.
Maziade, Michel, Marie‐Christine Chagnon, Denis Cliche, et al.. (2004). Shared and specific susceptibility loci for schizophrenia and bipolar disorder: a dense genome scan in Eastern Quebec families. Molecular Psychiatry. 10(5). 486–499. 131 indexed citations
16.
Szatmári, Péter, Chantal Mérette, Claudia Émond, et al.. (2003). Disentangling the autism phenotype; a sib-pair analysis. The American Journal of Human Genetics. 73(5). 391. 1 indexed citations
17.
Thivierge, Jacques, Chantal Mérette, & Michel Maziade. (2002). Prolonged Brainstem Auditory Evoked Potentials: An Autism-Specific or Autism-Nonspecific Marker. Archives of General Psychiatry. 59(3). 289–289.
18.
Bouchard, Roch-Hugo, Emmanuelle Pourcher, Chantal Mérette, et al.. (1998). One-year follow-up of schizophrenic patients treated with Risperidone or classical neuroleptics: a prospective, randomized, multicentered open-study. European Neuropsychopharmacology. 8. S253–S253. 4 indexed citations
19.
Mérette, Chantal, et al.. (1994). Update on a linkage trend between schizophrenia (SZ) and the 11q21-22 region in pedigrees of Eastern Quebec. The American Journal of Human Genetics. 55. 1 indexed citations
20.
Brzustowicz, Linda M., et al.. (1993). Molecular and statistical approaches to the detection and correction of errors in genotype databases.. PubMed. 53(5). 1137–45. 69 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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