Abstract is: Thomas James Hudson, O.C., M.D., (born June 12, 1961) is a Canadian genome scientist noted for his leading role in the generation of physical maps of the human and mouse genomes and also his role in the International HapMap Project whose goal is to develop a haplotype map of the human genome. As director of the McGill University and Genome Quebec Innovation Centre, which he established, Hudson and his team have made a number of discoveries in human genetics. These include genes mutated in rare diseases and genes involved in complex diseases such as asthma, type II diabetes and inflammatory bowel disease. In July 2006, he was appointed president and scientific director of the Ontario Institute for Cancer Research. He is also editor-in-chief of the journal Human Genetics. Thomas Hudson is married and has five children.
| human | Q5 |
| P6178 | Dimensions author ID | 01313030250.72 |
| P646 | Freebase ID | /m/0gy_y0 |
| P244 | Library of Congress authority ID | no2011026110 |
| P496 | ORCID iD | 0000-0002-1376-4849 |
| P1153 | Scopus author ID | 7203069638 |
| P10861 | Springer Nature person ID | 01313030250.72 |
| P214 | VIAF ID | 167480906 |
| P10832 | WorldCat Entities ID | E39PBJgd6PT6xQtDV48KdvD8YP |
| P166 | award received | Fellow of the Royal Society of Canada | Q3305342 |
| Officer of the Order of Canada | Q15278116 | ||
| P27 | country of citizenship | Canada | Q16 |
| P69 | educated at | Université de Montréal | Q392189 |
| P108 | employer | McGill University | Q201492 |
| Ontario Institute for Cancer Research | Q1377857 | ||
| P734 | family name | Hudson | Q2720681 |
| Hudson | Q2720681 | ||
| Hudson | Q2720681 | ||
| P735 | given name | James | Q677191 |
| James | Q677191 | ||
| Thomas | Q16428906 | ||
| Thomas | Q16428906 | ||
| P106 | occupation | researcher | Q1650915 |
| geneticist | Q3126128 | ||
| P21 | sex or gender | male | Q6581097 |
| Q57232768 | Q57232768 |
| Q54563363 | 1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes. |
| Q47125349 | 31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016): part two: National Harbor, MD, USA. 9-13 November 2016 |
| Q28818630 | 4th Pediatric Allergy and Asthma Meeting (PAAM) |
| Q43972584 | 5' flanking variants of resistin are associated with obesity |
| Q48134303 | A PCR-based linkage map of human chromosome 1. |
| Q37670967 | A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition |
| Q57232764 | A Second-Generation Association Study of the 5q31 Cytokine Gene Cluster and the Interleukin-4 Receptor in Asthma |
| Q30748699 | A YAC-based physical map of the mouse genome. |
| Q57310420 | A cis-Acting Regulatory Variant in the IL2RA Locus |
| Q28505475 | A combinatorial network of evolutionarily conserved myelin basic protein regulatory sequences confers distinct glial-specific phenotypes |
| Q57310423 | A combined watershed and level set method for segmentation of brightfield cell images |
| Q36906070 | A common RET variant is associated with reduced newborn kidney size and function |
| Q24306420 | A common variant of the PAX2 gene is associated with reduced newborn kidney size |
| Q36379244 | A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. |
| Q43560132 | A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus). |
| Q46294548 | A genome-wide approach to identifying novel-imprinted genes. |
| Q36395306 | A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1. |
| Q28287727 | A genome-wide association study identifies novel risk loci for type 2 diabetes |
| Q24314754 | A map of 75 human ribosomal protein genes |
| Q24615964 | A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis |
| Q57310432 | A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis |
| Q34472139 | A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality |
| Q57310442 | A radiation hybrid map of mouse genes |
| Q30853648 | A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns |
| Q24651939 | A second generation human haplotype map of over 3.1 million SNPs |
| Q32178388 | A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians. |
| Q40621976 | A survey of genetic and epigenetic variation affecting human gene expression |
| Q43952046 | ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels. |
| Q22011182 | ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF |
| Q57310451 | Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16 |
| Q57785668 | Abstract 2190: Fine-mapping of common genetic variants associated with colorectal tumor risk identified potential functional variants |
| Q58047207 | Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk |
| Q92686162 | Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia |
| Q33924952 | Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery |
| Q50475186 | An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. |
| Q25256424 | An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population |
| Q34142087 | An optimized set of human telomere clones for studying telomere integrity and architecture. |
| Q39999220 | Analyses of associations with asthma in four asthma population samples from Canada and Australia |
| Q44523764 | Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases. |
| Q28586902 | Analysis of early C2C12 myogenesis identifies stably and differentially expressed transcriptional regulators whose knock-down inhibits myoblast differentiation |
| Q28304750 | Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes |
| Q35246178 | Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants |
| Q80939817 | Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes |
| Q81052868 | Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes |
| Q46513306 | Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people |
| Q81448175 | Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people |
| Q21284419 | Asthma and genes encoding components of the vitamin D pathway |
| Q30828962 | Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11. |
| Q58850960 | Autosomal recessive spastic ataxia of Charlevoix–Saguenay |
| Q24644358 | CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup |
| Q36750746 | CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk |
| Q28255640 | Characterization of a common susceptibility locus for asthma-related traits |
| Q36030354 | Characterization of gene-environment interactions for colorectal cancer susceptibility loci |
| Q37310504 | Common variants in the NLRP3 region contribute to Crohn's disease susceptibility |
| Q51622312 | Common variants in the obesity-associated genes FTO and MC4R are not associated with risk of colorectal cancer. |
| Q93118070 | Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer |
| Q50240714 | Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci |
| Q28388475 | Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations |
| Q37409157 | Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals |
| Q60472142 | Discovery of common and rare genetic risk variants for colorectal cancer |
| Q39130364 | Disease variants alter transcription factor levels and methylation of their binding sites |
| Q21092468 | Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord |
| Q24300035 | FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A |
| Q36068167 | Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants |
| Q24795231 | Functional classes of bronchial mucosa genes that are differentially expressed in asthma |
| Q28212087 | G-protein-coupled receptors and asthma endophenotypes: the cysteinyl leukotriene system in perspective |
| Q21092184 | Genes to diseases (G2D) computational method to identify asthma candidate genes |
| Q50420634 | Genetic mechanisms of immune evasion in colorectal cancer |
| Q37281843 | Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer |
| Q63976721 | Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer |
| Q57606857 | Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease |
| Q33507084 | Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis |
| Q36159275 | Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer |
| Q37422744 | Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. |
| Q37140021 | Genome-wide association study of colorectal cancer identifies six new susceptibility loci |
| Q23000444 | Genome-wide detection and characterization of positive selection in human populations |
| Q36317729 | Genome-wide meta-analysis of common variant differences between men and women |
| Q34321689 | Genome-wide search for gene-gene interactions in colorectal cancer |
| Q34020351 | Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height |
| Q44865544 | Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region |
| Q24632653 | Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L |
| Q29416993 | Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis |
| Q36069872 | Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer |
| Q24541342 | Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics |
| Q24338843 | Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants |
| Q24539565 | Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements |
| Q24611474 | International network of cancer genome projects |
| Q97595643 | Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival |
| Q34389112 | Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. |
| Q35153463 | Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci |
| Q36341386 | Meta-analysis identifies seven susceptibility loci involved in the atopic march |
| Q29417081 | Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer |
| Q35670184 | Meta-analysis of new genome-wide association studies of colorectal cancer risk |
| Q24672287 | Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome) |
| Q34642008 | No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk |
| Q56359054 | Novel Common Genetic Susceptibility Loci for Colorectal Cancer |
| Q24595981 | Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes |
| Q37570238 | Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia |
| Q26283296 | Prepublication data sharing |
| Q38871309 | Spatial genomic heterogeneity within localized, multifocal prostate cancer |
| Q27662106 | The K5 Lyase KflA Combines a Viral Tail Spike Structure with a Bacterial Polysaccharide Lyase Mechanism |
| Q24800302 | The acute neurotoxicity of mefloquine may be mediated through a disruption of calcium homeostasis and ER function in vitro |
| Q24290189 | The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes |
| Q26849200 | The genetic basis for cancer treatment decisions |
| Q28118593 | The molecular basis of glutamate formiminotransferase deficiency |
| Thomas J. Hudson | wikipedia | |
| Thomas J. Hudson | wikipedia |
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