List of works - Alexandre Montpetit

A genome-wide association study identifies novel risk loci for type 2 diabetes

scientific article

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

A second generation human haplotype map of over 3.1 million SNPs

scientific article

An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.

scientific article published on 25 November 2004

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population

scientific article

Analyses of associations with asthma in four asthma population samples from Canada and Australia

scientific article

Analysis of the conservation of synteny between Fugu and human chromosome 12

scientific article

CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup

scientific article

Corrigendum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

scientific article published in Nature

Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord

scientific article published in December 2008

Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

scientific article (publication date: 29 January 2012)

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

scientific article

Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study

scientific article

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

scientific article published on 30 March 2008

Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

scientific article

Genome-wide detection and characterization of positive selection in human populations

scientific article

Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations

scientific article (publication date: May 2014)

Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

scientific article

K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

scientific article

Lung cancer susceptibility locus at 5p15.33

scientific article

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

scientific article

Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.

scientific article published on 10 September 2015

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

scientific article published on 05 August 2015

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study

scientific article

List of works by Alexandre Montpetit

A genome-wide association study identifies novel risk loci for type 2 diabetes

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

A second generation human haplotype map of over 3.1 million SNPs

An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population

Analyses of associations with asthma in four asthma population samples from Canada and Australia

Analysis of the conservation of synteny between Fugu and human chromosome 12

CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup

Corrigendum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord

Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

Genome-wide detection and characterization of positive selection in human populations

Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations

Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

Lung cancer susceptibility locus at 5p15.33

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age.

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study