Michel Vanasse

5.0k citations

84 papers · 3.1k indexed · h-index 29

Impact in

Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Psychiatry and Mental health top 2%
- Epilepsy research and treatment

Papers in

Cellular and Molecular Neuroscience 23
- Hereditary Neurological Disorders 13
- Genetic Neurodegenerative Diseases 12
Genetics 13
- Neurogenetic and Muscular Disorders Research 12

Co-authors: Guy A. Rouleau Anne Lortie Lionel Carmant Patrick Cossette Jean‐Marc Saint‐Hilaire Haiheng Dong Yu Tian Wang Katéri Brisebois
Journals: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (14 papers)Pediatric Neurology (6 papers)Neurology (4 papers)Journal of Child Neurology (4 papers)The Journal of Pediatrics (3 papers)
Partner nations: Canada United States France

In The Last Decade

Michel Vanasse

80 papers receiving 3.0k citations

Peers

Countries citing papers authored by Michel Vanasse

Since Specialization

Citations

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

Fields of papers citing papers by Michel Vanasse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Michel Vanasse, 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 Michel Vanasse Line = papers co-authored together Michel Vanasse links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Gross Motor Function Measure Evolution Ratio: Use as a Control for Natural Progression in Cerebral Palsy Archives of Physical Medicine and Rehabilitation ·Pierre Marois, Zhongqiang Huang, 新見正喜, Michel Vanasse, Jean Lambert, Laurent Ballaz	2015	18
2	LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy SHILAP Revista de lepidopterología ·Inge A. Meijer, Florin Sasarman, Jelena Srebric, Elsa Rossignol, Michel Vanasse, 姚恒璐, Grant A. Mitchell, Catherine Brunel‐Guitton	2015	19
3	Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 Gene Journal of Child Neurology ·Roberta La Piana, Michel Vanasse, Bernard Brais, Geneviève Bernard	2014	20
4	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, Lu Zhang, 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
5	Lemierre Syndrome: Two Preschool Children with Cerebral Infarcts SHILAP Revista de lepidopterología ·Miriam Santschi, Michéle David, Laurent Garel, Michel Vanasse, France Gauvin	2008	1
6	Acute Combined Central and Peripheral Nervous System Demyelination in Children Pediatric Neurology ·A. F. B. Isabel, Émilie Riou, Geneviève Bernard, Michel Vanasse, Jean‐Claude Décarie, Chantal Poulin, France Gauvin	2008	17
7	Long‐term outcome of Leigh syndrome caused by the NARP‐T8993C mtDNA mutation American Journal of Medical Genetics Part A ·François‐Guillaume Debray, Marie Lambert, Anne Lortie, Michel Vanasse, Grant A. Mitchell	2007	38
8	Evolution and Treatment of Childhood Chronic Inflammatory Polyneuropathy Pediatric Neurology ·Elsa Rossignol, Guy D’Anjou, Normand Lapointe, Élie Haddad, Michel Vanasse	2007	31
9	Autosomal dominant juvenile myoclonic epilepsy and GABRA1. PubMed ·Patrick Cossette, Anne Lortie, Michel Vanasse, Jean‐Marc Saint‐Hilaire, Guy A. Rouleau	2005	6
10	Les maladies neuromusculaires chez l'enfant et l'adolescent Michel Vanasse	2004	1
11	Hyperbaric oxygen for children with cerebral palsy: a randomised multicentre trial The Lancet ·Jean‐Paul Collet, Michel Vanasse, Pierre Marois, Yi He, Joanne Goldberg, Jean Lambert, Maryse Lassonde, aDResearch, J. André Fortin, S I Lipkin, David Montgomery, HaiBin Chen, Ann Robinson, Annette Majnemer	2001	93
12	Novel 3678delA mutation in exon 26 of the dystrophin gene causing duchenne muscular dystrophy Human Mutation ·Alka Agarwal-Mawal, Michel Vanasse, Louise R. Simard	1998	1
13	SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): Genotype/phenotype correlations with disease severity American Journal of Medical Genetics ·Louise R. Simard, Camille Rochette, Alexandre Semionov, Kenneth Morgan, Michel Vanasse	1997	37
14	Clinical and genetic study of chronic (types II and III) childhood onset spinal muscular atrophy Neuromuscular Disorders ·Homer J. Moore, Louise R. Simard, ML Millenson, Camille Rochette, Jean Lambert, Michel Vanasse	1996	19
15	Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French — Canadian population Human Molecular Genetics ·Louise R. Simard, L Ocheretná, Camille Rochette, Kenneth Morgan, H. Kleinau, Christina E. Pentlow, Serge B. Melançon, Michel Vanasse	1994	24
16	Myoblast transfer in duchenne muscular dystrophy Annals of Neurology ·George Karpati, عبدالحمید نظمی بسیونی, Douglas L. Arnold, Robert B. Gledhill, Ronald D. Guttmann, Paul C. Holland, P. Koch, Eric A. Shoubridge, 桓友山崎, Michel Vanasse, Gordon V. Watters, Michał Abrahamowicz, Catherine Duff, Ronald G. Worton	1993	235
17	Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: Neurologic, ophthalmologic, and neuropsychologic examination of six patients The Journal of Pediatrics ·Jacinthe Lemay, Marie Lambert, Grant A. Mitchell, Michel Vanasse, David Valle, S Reed, Johanne Dubé, fei yang, Marie Laberge, L Lafleur, Nijmegen Heineman, Insaf Ahmed Qureshi, Raynald Déry	1992	25
18	Maturation of Short Latency Somatosensory Evoked Potentials by Median Nerve Stimulation: a Cross-Sectional Study in a Large Group of Children Elsevier eBooks ·M Zemlin, Dyah Nawang Palupi, Michel Vanasse, Und Der, Maurice Ptito	1990	9
19	Somatosensory evoked potentials and auditory brain-stem responses in congenital hypothyroidism. II. A cross-sectional study in childhood. Correlations with hormonal levels and developmental quotients Electroencephalography and Clinical Neurophysiology ·Dyah Nawang Palupi, 铭心, Michel Vanasse, Jacques Letarte, Jacqueline Glorieux, Michèle Desjardins, Jean H. Dussault	1987	19
20	Oral Lecithin and Linoleic Acid in Friedreich’s Ataxia: I. Design of the Study, Material and Methods Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·S. Melançon, Louis Dallaire, (unknown), Michel Vanasse, P. Marois, G. Geoffroy, A. Barbeau	1982	1

About Michel Vanasse

Michel Vanasse is a scholar working on Cellular and Molecular Neuroscience, Genetics, Clinical Biochemistry, Neurology and Psychiatry and Mental health, having authored 84 papers that have together received 3.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (12 papers), Neurogenetic and Muscular Disorders Research (12 papers), Mitochondrial Function and Pathology (10 papers), Muscle Physiology and Disorders (10 papers), Metabolism and Genetic Disorders (8 papers), RNA modifications and cancer (7 papers) and Peripheral Neuropathies and Disorders (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (795 citations), Psychiatry and Mental health (591 citations), Genetics (385 citations), Clinical Biochemistry (245 citations) and Molecular Biology (1.7k citations). Michel Vanasse has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Guy A. Rouleau, Anne Lortie, Lionel Carmant, Patrick Cossette, Jean‐Marc Saint‐Hilaire, Haiheng Dong, Yu Tian Wang, Katéri Brisebois, Andrei Verner and Lidong Liu. Their work appears in journals such as Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Pediatric Neurology, Neurology, Journal of Child Neurology and The Journal of Pediatrics.

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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