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List of works by Thomas J. Hudson

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A second generation human haplotype map of over 3.1 million SNPs

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

scientific article
International network of cancer genome projects

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

scientific article
A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality

scientific article
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

scientific article
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

scientific article
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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

scientific article
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

scientific article
A survey of genetic and epigenetic variation affecting human gene expression

scientific article published on 15 January 2004
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility

scientific article published on 21 December 2008
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis

scientific article published on 22 December 2012
Characterization of a common susceptibility locus for asthma-related traits

scientific article
Spatial genomic heterogeneity within localized, multifocal prostate cancer

scientific article published on 25 May 2015
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

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

A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns

scientific article
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region

scientific article published in May 2004
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.

scientific article published on 11 April 2016
Prepublication data sharing

scientific article
The genetic basis for cancer treatment decisions

scientific article
Meta-analysis of new genome-wide association studies of colorectal cancer risk

scientific article published on 15 July 2011
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

scientific article
Disease variants alter transcription factor levels and methylation of their binding sites

scientific article published on 5 December 2016
An optimized set of human telomere clones for studying telomere integrity and architecture.

scientific article
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

scientific article
Characterization of gene-environment interactions for colorectal cancer susceptibility loci

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

scientific article
A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition

scientific article published on 17 January 2013
A Map of 75 Human Ribosomal Protein Genes

scientific article published on May 1, 1998
Genetic mechanisms of immune evasion in colorectal cancer

scientific article published on 6 March 2018
5' flanking variants of resistin are associated with obesity

scientific article published in May 2002
Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

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

scientific article published in December 2008
Asthma and genes encoding components of the vitamin D pathway

scientific article
Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals

scientific article published on 05 April 2012
1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes

scientific article published on 9 January 2007
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci

scientific article
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants

scientific article
Analysis of early C2C12 myogenesis identifies stably and differentially expressed transcriptional regulators whose knock-down inhibits myoblast differentiation

scientific journal article
A common RET variant is associated with reduced newborn kidney size and function

scientific article published on October 2008
Functional classes of bronchial mucosa genes that are differentially expressed in asthma

scientific article
Genome-wide association study of colorectal cancer identifies six new susceptibility loci

scientific article published on 07 July 2015
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population

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

scientific article
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

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

scientific article
A common variant of the PAX2 gene is associated with reduced newborn kidney size

scientific article

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