Marie-Pierre Dube, Ph.D.

Affiliations: 
2000 McGill University, Montreal, QC, Canada 
Area:
Neurogenetics
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"Marie-Pierre Dube"
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Parents

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Guy A. Rouleau grad student 2000 McGill
 (New approaches in human genetic analysis.)
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Publications

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Pellerin D, Danzi MC, Wilke C, et al. (2022) Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine
Peretz I, Ross J, Bourassa CV, et al. (2022) Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia? Annals of the New York Academy of Sciences
Girard SL, Bourassa CV, Lemieux Perreault LP, et al. (2016) Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals. Plos One. 11: e0164212
Lessard S, Manning AK, Low-Kam C, et al. (2016) Testing the Role of Predicted Gene Knockouts in Human Anthropometric Trait Variation. Human Molecular Genetics
Girard SL, Dion PA, Bourassa CV, et al. (2015) Mutation burden of rare variants in schizophrenia candidate genes. Plos One. 10: e0128988
Legault MA, Girard S, Lemieux Perreault LP, et al. (2015) Comparison of sequencing based CNV discovery methods using monozygotic twin quartets. Plos One. 10: e0122287
Preuss C, Capredon M, Asselin G, et al. (2013) Linkage Mapping and Whole-Exome Sequencing in a Family With Left Ventricular Outflow Tract Obstruction Canadian Journal of Cardiology. 29: S88
Guernsey DL, Dubé MP, Jiang H, et al. (2010) Novel mutations in the sacsin gene in ataxia patients from Maritime Canada. Journal of the Neurological Sciences. 288: 79-87
Guernsey DL, Jiang H, Evans SC, et al. (2009) Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2. American Journal of Human Genetics. 85: 120-9
Jiang H, Orr A, Guernsey DL, et al. (2009) Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data. Plos One. 4: e5280
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