Jean Mathieu

7.9k citations

142 papers · 4.9k indexed · 1 hit paper · h-index 38

Impact in

Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 0.5%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders

Papers in ⓘ

Cellular and Molecular Neuroscience 99
- Genetic Neurodegenerative Diseases 96
- Hereditary Neurological Disorders 13
Neurology 64
- Parkinson's Disease Mechanisms and Treatments 42
- Botulinum Toxin and Related Neurological Disorders 17
- Neurological diseases and metabolism 9
- Neurological disorders and treatments 8

Co-authors: Paul Bégin (7 shared papers)Claude Prévost (17 shared papers)Cynthia Gagnon (52 shared papers)Jean‐Pierre Bouchard (20 shared papers)Bernard Brais (33 shared papers)Luc Laberge (18 shared papers)Marc De Braekeleer (9 shared papers)Hélène Boivin (2 shared papers)
Journals: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (17 papers)Neuromuscular Disorders (15 papers)Neurology (11 papers)Journal of the Neurological Sciences (7 papers)Muscle & Nerve (5 papers)
Partner nations: Canada United States France

In The Last Decade

Jean Mathieu

135 papers receiving 4.8k citations

Hit Papers

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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy 1998 · 583 citations

Peers

Countries citing papers authored by Jean Mathieu

Since Specialization

Citations

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

Fields of papers citing papers by Jean Mathieu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jean Mathieu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jean Mathieu Line = papers co-authored together Jean Mathieu links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 142 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy Nature Genetics ·Bernard Brais, Jean‐Pierre Bouchard, Ya‐Gang Xie, Daniel Rochefort, Nathalie Chrétien, F.M.S. Tomé, Ronald G. Lafrentére, Johanna M. Rommens, Eichiro Uyama, O. Nohira, Segiu Blumen, Amos D. Korcyn, Peter Heutink, Jean Mathieu, André Duranceau, François Codère, Michel Fardeau, Guy A. Rouleau Hit paper breakdown →	1998	583
2	Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy Neurology ·Jean Mathieu, Hélène Boivin, Danièle Meunier, M. Gaudreault, Paul Bégin	2001	318
3	ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF Nature Genetics ·James C. Engert, Pierre Bérubé, Jocelyne Mercier, Carole Doré, Patricia Lepage, Bing Ge, Jean‐Pierre Bouchard, Jean Mathieu, Serge B. Melançon, Martin Schalling, Eric S. Lander, Kenneth Morgan, Thomas J. Hudson, Andréa Richter	2000	295
4	A 10-year study of mortality in a cohort of patients with myotonic dystrophy Neurology ·Jean Mathieu, Per Allard, Lynne A. Potvin, Claude Prévost, Paul Bégin	1999	276
5	Specific Pathological Tau Protein Variants Characterize Pickʼs Disease Journal of Neuropathology & Experimental Neurology ·André Delacourte, Yves Robitaille, Nicolas Sergeant, Luc Buée, Patrick R. Hof, A. Wattez, A. Laroche-Cholette, Jean Mathieu, Pierre Chagnon, D. Gauvreau	1996	181
6	Measuring participation in children with disabilities using the Assessment of Life Habits Developmental Medicine & Child Neurology ·Luc Noreau, Céline Lepage, Lucie Boissière, Roger Picard, Patrick Fougeyrollas, Jean Mathieu, Gilbert Desmarais, Line Nadeau	2007	140
7	Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans PLoS Biology ·Vafa Bayat, Isabelle Thiffault, Manish Jaiswal, Martine Tétreault, Taraka Donti, Florin Sasarman, Geneviève Bernard, Julie Demers-Lamarche, Marie‐Josée Dicaire, Jean Mathieu, Michel Vanasse, Jean‐Pierre Bouchard, Marie‐France Rioux, Charles Marques Lourenço, Zhihong Li, Claire Haueter, Eric A. Shoubridge, Brett H. Graham, Bernard Brais, Hugo J. Bellen	2012	121
8	Autosomal recessive spastic ataxia of Charlevoix–Saguenay Neuromuscular Disorders ·Jean‐Pierre Bouchard, Andréa Richter, Jean Mathieu, Denis Brunet, Thomas J. Hudson, Kenneth Morgan, Serge B. Melançon	1998	104
9	Genealogical reconstruction of myotonic dystrophy in the Saguenay‐Lac‐Saint‐ Jean area (Quebec, Canada) Neurology ·Jean Mathieu, Marc De Braekeleer, Claude Prévost	1990	99
10	Myotonic dystrophy Neurology ·Jean Mathieu, Marc De Braekeleer, Claude Prévost, Camil Boily	1992	97
11	Relationship Between Chronic Hypercapnia and Inspiratory-Muscle Weakness in Myotonic Dystrophy American Journal of Respiratory and Critical Care Medicine ·Paul Bégin, Jean Mathieu, José Almirall, A. Grassino	1997	92
12	Sleep complaints in patients with myotonic dystrophy Journal of Sleep Research ·Luc Laberge, Paul Bégin, Jacques Montplaisir, Jean Mathieu	2004	83
13	Predictors of Disrupted Social Participation in Myotonic Dystrophy Type 1 Archives of Physical Medicine and Rehabilitation ·Cynthia Gagnon, Jean Mathieu, Stéphane Jean, Luc Laberge, Michel Perron, Suzanne Veillette, Louis Richer, Luc Noreau	2008	81
14	Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy Annals of Neurology ·Antoine Duquette, Katel Roddier, Julia McNabb‐Baltar, Isabelle Gosselin, Anik St‐Denis, Marie‐Josée Dicaire, Lina Loisel, Damian Labuda, Luc Marchand, Jean Mathieu, Jean‐Pierre Bouchard, Bernard Brais	2005	78
15	A polysomnographic study of daytime sleepiness in myotonic dystrophy type 1 Journal of Neurology Neurosurgery & Psychiatry ·Luc Laberge, Paul Bégin, Yves Dauvilliers, Michel Beaudry, Mario Laforte, Sossa Jean, Jean Mathieu	2009	72
16	Hereditary motor and sensory neuropathy with agenesis of the corpus callosum Annals of Neurology ·Nicolas Dupré, Heidi Howard, Jean Mathieu, George Karpati, Michel Vanasse, Jean‐Pierre Bouchard, Stirling Carpenter, Guy A. Rouleau	2003	64
17	Cognitive decline over time in adults with myotonic dystrophy type 1: A 9-year longitudinal study Neuromuscular Disorders ·Benjamin Gallais, Cynthia Gagnon, Jean Mathieu, Louis Richer	2016	63
18	Location Score and Haplotype Analyses of the Locus for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay, in Chromosome Region 13q11 The American Journal of Human Genetics ·Andréa Richter, John D. Rioux, Jean‐Pierre Bouchard, Jocelyne Mercier, Jean Mathieu, Bing Ge, Josée Poirier, Dominique Julien, Gàbor Gyapay, Jean Weissenbach, Thomas J. Hudson, Serge B. Melançon, Kenneth Morgan	1999	61
19	Health supervision and anticipatory guidance in adult myotonic dystrophy type 1 Neuromuscular Disorders ·Cynthia Gagnon, Maud‐Christine Chouinard, Luc Laberge, S. Veillette, Paul Bégin, Robert Breton, Sossa Jean, Diane Brisson, Daniel Gaudet, Jean Mathieu	2010	61
20	A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac‐Saint‐Jean region (Quebec, Canada) Annals of Human Genetics ·Marc De Braekeleer, Louis Përusse, Mario Cantín, Jean-Marie Bouchard, Jean Mathieu	1996	61

About Jean Mathieu

Jean Mathieu is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Psychiatry and Mental health and Molecular Biology, having authored 142 papers that have together received 4.9k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (96 papers), Parkinson's Disease Mechanisms and Treatments (42 papers), Mitochondrial Function and Pathology (30 papers), Muscle Physiology and Disorders (21 papers), Botulinum Toxin and Related Neurological Disorders (17 papers), Hereditary Neurological Disorders (13 papers), Neurological diseases and metabolism (9 papers) and Neurological disorders and treatments (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.2k citations), Neurology (1.8k citations), Neurology (505 citations), Molecular Biology (2.8k citations) and Psychiatry and Mental health (431 citations). Jean Mathieu has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Paul Bégin, Claude Prévost, Cynthia Gagnon, Jean‐Pierre Bouchard, Bernard Brais, Luc Laberge, Marc De Braekeleer, Hélène Boivin, M. Gaudreault and Luc Noreau. Their work appears in journals such as Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Neuromuscular Disorders, Neurology, Journal of the Neurological Sciences and Muscle & Nerve.

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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