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C. Meloche · SciRah

Researcher profile · Semantic Scholar

C. Meloche

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C. Meloche — researcher profile on SciRah

h-index: 14
Works: 34
Citations: 1,623

Most-cited papers

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
F. Hamdan, Candace T. Myers, P. Cossette, P. Lemay +102 more
2017American Journal of Human Genetics417 citations Open access
Semantic Scholar
SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
A. Fassio, L. Patry, Sonia Congia, F. Onofri +17 more
2011Human Molecular Genetics231 citations
Semantic Scholar
Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
A. Montpetit, S. Côté, E. Brustein, C. Drouin +7 more
2008PLoS Genetics161 citations Open access
Semantic Scholar
Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.
Maxime Cadieux-Dion, Maude Turcotte-Gauthier, A. Noreau, C. Martin +6 more
2014JAMA Neurology116 citations
Semantic Scholar
Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy
P. Lachance-Touchette, P. Brown, C. Meloche, P. Kinirons +7 more
2011European Journal of Neuroscience112 citations
Semantic Scholar
Prostate cancer susceptibility genes: lessons learned and challenges posed.
Jacques Simard, M. Dumont, D. Labuda, Daniel Sinnett +6 more
2003Endocrine-Related Cancer109 citations Open access
Semantic Scholar
Whole-transcriptome analysis in acute lymphoblastic leukemia: a report from the DFCI ALL Consortium Protocol 16-001
T. Tran, S. Langlois, C. Meloche, M. Caron +22 more
2021Blood Advances73 citations Open access
Semantic Scholar
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
P. May, S. Girard, Merle Harrer, D. Bobbili +121 more
2018Lancet Neurology72 citations Open access
Semantic Scholar
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease
M. Cadieux-Dion, E. Andermann, P. Lachance-Touchette, O. Ansorge +10 more
2013Clinical Genetics72 citations
Semantic Scholar
A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French‐Canadian population
C. Martin, C. Meloche, M. Rioux, D. Nguyen +4 more
2014Clinical Genetics46 citations
Semantic Scholar
Genome-wide characterization of copy number variants in epilepsy patients
Jean Monlong, S. Girard, C. Meloche, Maxime Cadieux-Dion +12 more
2017bioRxiv44 citations Open access
Semantic Scholar
Human copy number variants are enriched in regions of low mappability
Jean Monlong, P. Cossette, C. Meloche, G. Rouleau +2 more
2015bioRxiv43 citations Open access
Semantic Scholar
Early Nutritional Intervention to Promote Healthy Eating Habits in Pediatric Oncology: A Feasibility Study
Véronique Bélanger, Josianne Delorme, Mélanie Napartuk, I. Bouchard +6 more
2022Nutrients27 citations Open access
Semantic Scholar
The VIE study: feasibility of a physical activity intervention in a multidisciplinary program in children with cancer
M. Caru, Gabrielle E. Duhamel, V. Marcil, Serge Sultan +7 more
2019Supportive Care in Cancer17 citations
Semantic Scholar
Nutrition education and cooking workshops for families of children with cancer: a feasibility study
S. Beaulieu-Gagnon, Véronique Bélanger, C. Meloche, D. Curnier +4 more
2019BMC Nutrition13 citations Open access
Semantic Scholar
Improvement of Diet after an Early Nutritional Intervention in Pediatric Oncology
Mélanie Napartuk, Véronique Bélanger, I. Bouchard, C. Meloche +5 more
2023Children12 citations Open access
Semantic Scholar
Impact of Early Nutritional Intervention During Cancer Treatment on Dietary Intakes and Cardiometabolic Health in Children and Adolescents
Josianne Delorme, Andra Dima, Véronique Bélanger, Mélanie Napartuk +7 more
2025Cancers9 citations
Semantic Scholar
TREX-1-Related Disease Associated with the Presence of Cryofibrinogenemia
C. Paradis, M. Cadieux-Dion, C. Meloche, Micheline Gravel +5 more
2019Journal of Clinical Immunology9 citations
Semantic Scholar
Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes
Géraldine Mathonnet, D. Labuda, C. Meloche, T. Wambach +2 more
2003Journal of Human Genetics9 citations
Semantic Scholar
Abnormal HDL lipid and protein composition following pediatric cancer treatment: an associative study
Véronique Bélanger, Sophia Morel, Mélanie Napartuk, I. Bouchard +6 more
2023Lipids in Health and Disease7 citations Open access
Semantic Scholar
Global characterization of copy number variants in epilepsy patients from whole genome sequencing
Jean Monlong, Simon L. Girard, C. Meloche, M. Cadieux-Dion +12 more
2018PLoS Genetics7 citations Open access
Semantic Scholar
Needs, Barriers and Facilitators of Adolescents Participating in a Lifestyle Promotion Program in Oncology: Stakeholders, Adolescents and Parents’ Perspective
Johanne Kerba, C. Demers, Véronique Bélanger, Mélanie Napartuk +11 more
2022Children5 citations Open access
Semantic Scholar
Cardiometabolic Health After Pediatric Cancer Treatment: Adolescents Are More Affected than Children
Véronique Bélanger, Mélanie Napartuk, I. Bouchard, C. Meloche +5 more
2022Nutrition and Cancer4 citations
Semantic Scholar
Exploration of the impact of participation in a multidisciplinary family lifestyle intervention on exercise and diet quality during treatment for childhood cancer: the VIE program
Ariane Levesque, D. Curnier, Valérie Marcil, Véronique Bélanger +11 more
2025BMC Pediatrics3 citations Open access
Semantic Scholar
Implementing health promotion interventions in a pediatric oncology setting: A qualitative study among families impacted by cancer and healthcare professionals
Catherine Demers, Isabelle Gélinas, Johanne Kerba, Keven Lee +10 more
2025Journal of Child Health Care2 citations Open access
Semantic Scholar
Acceptability and functional benefits of a health promotion program in pediatric oncology: a mixed-methods study
Catherine Demers, Johanne Higgins, Johanne Kerba, I. Bouchard +7 more
2026Frontiers in Pediatrics1 citations Open access
Semantic Scholar
A new locus for pure Spinocerebellar Ataxia associated with Erythrokeratodermia maps to chromosome 6p12.3-q16.1
M. Gauthier, D. Nguyen, C. Meloche, John Poirier +14 more
20091 citations
Semantic Scholar
Explaining adherence to contrasted physical activity and nutrition scenarios in post-treatment childhood cancer patients: A cross-sectional study using variables from the Theory of Planned Behavior
Ariane Levesque, D. Curnier, Valérie Marcil, M. Caru +7 more
2025Health Psychology Open0 citations Open access
Semantic Scholar
Abstract A57: Feasibility of physical activity in children with cancer: A multidisciplinary program in the context of the VIE study
M. Caru, Gabrielle E. Duhamel, V. Marcil, Serge Sultan +7 more
20200 citations
Semantic Scholar
Abstract B59: Cardiometabolic complications after pediatric cancer: Associations with chemotherapeutic agents and body-mass-index fluctuations
Véronique Bélanger, Alexandre Warin, Elitsa Tonova, I. Bouchard +6 more
20200 citations
Semantic Scholar
High rate of recurrent de novo mutations in developmental and epileptic encephalopathies
F. Hamdan, Candace Myers, Patrick Cossette, P. Lemay +25 more
20200 citations
Semantic Scholar
Author’s response to reviews Title: Nutrition education and cooking workshops for families of children with cancer: a feasibility study Authors:
S. Beaulieu-Gagnon, Véronique Bélanger, C. Meloche, M. Reicks +1 more
20190 citations
Semantic Scholar
Rare coding variants in GABAA receptor encoding genes in genetic generalized epilepsies: an exome-based case-control study
P. May, S. Girard, Merle Harrer, D. Bobbili +104 more
20180 citations
Semantic Scholar
Variabilité génétique au niveau des gènes de réparation de l'ADN
C. Meloche
20030 citations Open access
Semantic Scholar

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