Alexandre Montpetit
occupation: researcher
Articles 18
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Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.
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Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations
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K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas
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Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
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Corrigendum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study
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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height
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Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
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Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord
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Lung cancer susceptibility locus at 5p15.33
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Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study
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Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
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Genome-wide detection and characterization of positive selection in human populations
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A second generation human haplotype map of over 3.1 million SNPs
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A genome-wide association study identifies novel risk loci for type 2 diabetes
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An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population
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Analysis of the conservation of synteny between Fugu and human chromosome 12
Human - wd:Q30004450