Marie-Pierre Dube, Ph.D.
Affiliations: | 2000 | McGill University, Montreal, QC, Canada |
Area:
NeurogeneticsGoogle:
"Marie-Pierre Dube"Mean distance: 19.61 (cluster 28)
Parents
Sign in to add mentorGuy 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 |