Thomas J. Hudson

Q: What Schools Are Affiliated With Thomas J. Hudson

Thomas J. Hudson is affiliated with the following schools: McGill University, Université de Montréal, University of British Columbia, University of Melbourne, Massachusetts Institute of Technology, University of Toronto, Karolinska Institute, University of Helsinki

Thomas J. Hudson's AcademicInfluence.com Rankings

Thomas J. Hudson

Biology

#2243

World Rank

#3592

Historical Rank

Genetics

#262

World Rank

#312

Historical Rank

biology Degrees

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Biology

Why Is Thomas J. Hudson Influential?

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According to Wikipedia, Thomas James Hudson, O.C., 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.

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Thomas J. Hudson's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

A second generation human haplotype map of over 3.1 million SNPs (2007) (4567)
A genome-wide association study identifies novel risk loci for type 2 diabetes (2007) (2994)
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. (1998) (2194)
International network of cancer genome projects (2010) (1839)
High-resolution haplotype structure in the human genome (2001) (1798)
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes (2012) (1752)
A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. (2005) (1647)
Fate tracing reveals the pericyte and not epithelial origin of myofibroblasts in kidney fibrosis. (2010) (1293)
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray (2013) (1223)
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes (2000) (1150)
A Gene Map of the Human Genome (1996) (1080)
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease (2001) (820)
An STS-Based Map of the Human Genome (1995) (818)
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. (2000) (763)
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24 (2007) (757)
Identification of pre-leukemic hematopoietic stem cells in acute leukemia (2014) (701)
A physical map of 30,000 human genes. (1998) (670)
Functional normalization of 450k methylation array data improves replication in large cancer studies (2014) (637)
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 (2008) (629)
Corrigendum: Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia (2014) (620)
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer (2008) (599)
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics (2003) (574)
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci. (2000) (532)
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility (2009) (498)
Characterization of a Common Susceptibility Locus for Asthma-Related Traits (2004) (477)
Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse (2000) (438)
Spatial genomic heterogeneity within localized, multifocal prostate cancer (2015) (401)
A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns (2016) (399)
Macrophage Wnt7b is critical for kidney repair and regeneration (2010) (384)
Susceptibility to leprosy is associated with PARK2 and PACRG (2004) (378)
Patterns of somatic structural variation in human cancer genomes (2020) (377)
Tracing the origins of relapse in acute myeloid leukaemia to stem cells (2017) (374)
Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies. (2002) (373)
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis (2005) (345)
Disease variants alter transcription factor levels and methylation of their binding sites (2015) (341)
Multiancestry association study identifies new asthma risk loci that colocalize with immune cell enhancer marks (2017) (337)
A survey of genes differentially expressed in subcutaneous and visceral adipose tissue in men. (2004) (336)
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome (1998) (330)
Genome-wide analysis of transcript isoform variation in humans (2008) (328)
Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region. (2004) (322)
Genomewide scan of multiple sclerosis in Finnish multiplex families. (1997) (321)
The Genetic Basis for Cancer Treatment Decisions (2012) (310)
Radiation hybrid mapping of the zebrafish genome. (1999) (307)
Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays (2000) (307)
Genetic Mechanisms of Immune Evasion in Colorectal Cancer. (2018) (305)
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. (2013) (300)
An optimized set of human telomere clones for studying telomere integrity and architecture. (2000) (299)
Common Genetic Variation in ABCA1 Is Associated With Altered Lipoprotein Levels and a Modified Risk for Coronary Artery Disease (2001) (292)
Cis-Acting Regulatory Variation in the Human Genome (2004) (283)
A survey of genetic and epigenetic variation affecting human gene expression. (2004) (280)
Discovery of common and rare genetic risk variants for colorectal cancer (2018) (279)
Direct detection of novel expanded trinucleotide repeats in the human genome (1993) (276)
Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases (2016) (266)
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. (1992) (263)
Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy. (2004) (252)
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing (2015) (250)
Differential Allelic Expression in the Human Genome: A Robust Approach To Identify Genetic and Epigenetic Cis-Acting Mechanisms Regulating Gene Expression (2008) (243)
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population (2001) (228)
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk (2014) (218)
Skin barrier function and allergic risk (2006) (211)
Magnitude of Therapeutic STING Activation Determines CD8+ T Cell-Mediated Anti-tumor Immunity. (2018) (206)
CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup. (2009) (202)
Characterization of variability in large-scale gene expression data: implications for study design. (2002) (198)
Meta-analysis of new genome-wide association studies of colorectal cancer risk (2012) (197)
Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. (2001) (191)
Prepublication data sharing (2009) (190)
Molecular scanning of the human PPARa gene: association of the L162v mutation with hyperapobetalipoproteinemia. (2000) (189)
Expression profiling in squamous carcinoma cells reveals pleiotropic effects of vitamin D3 analog EB1089 signaling on cell proliferation, differentiation, and immune system regulation. (2002) (185)
Cancer genomics: technology, discovery, and translation. (2012) (181)
An Epigenome-Wide Association Study of Total Serum Immunoglobulin E Concentration (2014) (179)
A federated ecosystem for sharing genomic, clinical data (2016) (177)
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population (2003) (174)
5' flanking variants of resistin are associated with obesity. (2002) (173)
Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes. (2002) (169)
A Pan-BCL2 inhibitor renders bone-marrow-resident human leukemia stem cells sensitive to tyrosine kinase inhibition. (2013) (166)
A map of 75 human ribosomal protein genes. (1998) (164)
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies (2010) (154)
Mobilized Human Hematopoietic Stem/Progenitor Cells Promote Kidney Repair After Ischemia/Reperfusion Injury (2010) (153)
Characterization of gene-environment interactions for colorectal cancer susceptibility loci. (2012) (149)
Germ-line DNA copy number variation frequencies in a large North American population (2007) (146)
Asthma and genes encoding components of the vitamin D pathway (2009) (146)
Influence of human genome polymorphism on gene expression. (2006) (142)
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria. (2002) (142)
Survey of allelic expression using EST mining. (2005) (138)
Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord (2008) (138)
Genome-wide association study of colorectal cancer identifies six new susceptibility loci (2015) (138)
Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7. (2001) (137)
1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes. (2007) (136)
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus (2007) (136)
Functional classes of bronchial mucosa genes that are differentially expressed in asthma (2004) (134)
Meta-analysis identifies seven susceptibility loci involved in the atopic march (2015) (133)
Microarray analysis of uterine gene expression in mouse and human pregnancy. (2003) (130)
Heritability of alternative splicing in the human genome. (2007) (123)
Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements (2002) (120)
Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study (2015) (119)
Radiation hybrid map of the mouse genome (1999) (119)
Analyses of associations with asthma in four asthma population samples from Canada and Australia (2009) (117)
The melanoma-associated transmembrane glycoprotein Gpnmb controls trafficking of cellular debris for degradation and is essential for tissue repair. (2010) (116)
Genome-wide scan in Portuguese Island families identifies 5q31–5q35 as a susceptibility locus for schizophrenia and psychosis (2004) (116)
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci (2015) (114)
A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. (2002) (109)
Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33. (1998) (108)
Toward Further Mapping of the Association Between the IL2RA Locus and Type 1 Diabetes (2007) (108)
Wanted: regulatory SNPs (2003) (107)
Mapping common regulatory variants to human haplotypes. (2005) (104)
Novel Common Genetic Susceptibility Loci for Colorectal Cancer (2018) (102)
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. (2007) (100)
An Evaluation of the Performance of Tag SNPs Derived from HapMap in a Caucasian Population (2006) (100)
Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L. (2002) (99)
The molecular and cellular heterogeneity of pancreatic ductal adenocarcinoma (2012) (98)
Unraveling the genetics of cancer: genome sequencing and beyond. (2011) (96)
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12. (1999) (95)
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol. (2007) (94)
Toward a comprehensive set of asthma susceptibility genes. (2007) (91)
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants. (2015) (91)
Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. (2005) (89)
A YAC-based physical map of the mouse genome (1999) (88)
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11. (1999) (88)
A Combinatorial Network of Evolutionarily Conserved Myelin Basic Protein Regulatory Sequences Confers Distinct Glial-Specific Phenotypes (2003) (88)
Association of LY9 in UK and Canadian SLE families (2008) (88)
Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies. (2011) (88)
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans (2009) (87)
GLI2 inhibition abrogates human leukemia stem cell dormancy (2015) (87)
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. (2016) (87)
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers. (1995) (86)
Feasibility of real time next generation sequencing of cancer genes linked to drug response: Results from a clinical trial (2013) (86)
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes. (2004) (83)
Discrimination between serous low malignant potential and invasive epithelial ovarian tumors using molecular profiling (2005) (83)
HMGI(Y) activation by chromosome 6p21 rearrangements in multilineage mesenchymal cells from pulmonary hamartoma. (1997) (82)
Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people. (2005) (82)
Manganese superoxide dismutase induction by iron is impaired in Friedreich ataxia cells (2001) (81)
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11 q 23 and replicates risk loci at 8 q 24 and 18 q 21 (2009) (80)
Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes. (2005) (78)
Microarray analysis of gene expression mirrors the biology of an ovarian cancer model (2001) (78)
Cumulative Burden of Colorectal Cancer-Associated Genetic Variants is More Strongly Associated With Early-onset vs Late-onset Cancer. (2019) (78)
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome). (2006) (77)
Sex-stratified linkage analysis identifies a female-specific locus for IgE to cockroach in Costa Ricans. (2008) (77)
Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French-Canadian Population (2006) (76)
Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study (2005) (76)
A genome-wide approach to identifying novel-imprinted genes (2007) (76)
Effect of apolipoprotein E, peroxisome proliferator-activated receptor alpha and lipoprotein lipase gene mutations on the ability of fenofibrate to improve lipid profiles and reach clinical guideline targets among hypertriglyceridemic patients. (2002) (74)
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk. (2020) (74)
A radiation hybrid map of mouse genes (2001) (74)
Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups: The INTERHEART Genetics Study (2009) (74)
Replication of an association between 17q21 SNPs and asthma in a French-Canadian familial collection (2008) (71)
Correction of Population Stratification in Large Multi-Ethnic Association Studies (2008) (70)
Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16. (1998) (68)
A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13. (2001) (67)
MyD88 and TRIF synergistic interaction is required for TH1‐cell polarization with a synthetic TLR4 agonist adjuvant (2013) (66)
A Dual TLR Agonist Adjuvant Enhances the Immunogenicity and Protective Efficacy of the Tuberculosis Vaccine Antigen ID93 (2014) (66)
Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. (1999) (64)
Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec (2005) (60)
A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus) (2007) (60)
A Distal Upstream Enhancer from the Myelin Basic Protein Gene Regulates Expression in Myelin-Forming Schwann Cells (2001) (60)
Diagnostic misclassification reduces the ability to detect linkage in inflammatory bowel disease genetic studies (2001) (60)
Large-scale recombination rate patterns are conserved among human populations. (2005) (58)
From gene profiling to diagnostic markers: IL‐18 and FGF‐2 complement CA125 as serum‐based markers in epithelial ovarian cancer (2006) (58)
Association of urokinase-type plasminogen activator with asthma and atopy. (2007) (57)
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22. (2001) (57)
The growth factor midkine is modulated by both glucocorticoid and retinoid in fetal lung development. (2003) (57)
Screening for loss of heterozygosity and microsatellite instability in oligodendrogliomas (1998) (57)
A second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma. (2001) (56)
Global analysis of chromosome X gene expression in primary cultures of normal ovarian surface epithelial cells and epithelial ovarian cancer cell lines. (2007) (55)
PRKCA and Multiple Sclerosis: Association in Two Independent Populations (2006) (55)
Genetic Variation in the Familial Mediterranean Fever Gene (MEFV) and Risk for Crohn's Disease and Ulcerative Colitis (2009) (54)
Genotype–Environment Interactions in Microsatellite Stable/Microsatellite Instability-Low Colorectal Cancer: Results from a Genome-Wide Association Study (2011) (54)
Recombinant Listeria promotes tumor rejection by CD8+ T cell-dependent remodeling of the tumor microenvironment (2018) (52)
The molecular basis of glutamate formiminotransferase deficiency (2003) (52)
Immune oncology, immune responsiveness and the theory of everything (2018) (51)
Polymorphisms in the interleukin-22 receptor alpha-1 gene are associated with severe chronic rhinosinusitis (2009) (51)
Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations. (1995) (51)
A PCR-based linkage map of human chromosome 1. (1993) (50)
Gene expression profiling of primary cultures of ovarian epithelial cells identifies novel molecular classifiers of ovarian cancer (2006) (50)
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (50)
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people. (2005) (50)
Genome-Wide Scan for Linkage to Obesity-Associated Hypertension in French Canadians (2005) (50)
Association study between the CX3CR1 gene and asthma (2006) (49)
Autosomal recessive spastic ataxia of Charlevoix–Saguenay (1998) (49)
Caring About Women and Cancer (CAWAC): a European survey of the perspectives and experiences of women with female cancers. (1999) (48)
Type 1 diabetes and the OAS gene cluster: association with splicing polymorphism or haplotype? (2005) (48)
The K5 Lyase KflA Combines a Viral Tail Spike Structure with a Bacterial Polysaccharide Lyase Mechanism* (2010) (48)
Functional Organization of a Schwann Cell Enhancer (2005) (47)
The utility and predictive value of combinations of low penetrance genes for screening and risk prediction of colorectal cancer (2010) (47)
Mucosal delivery switches the response to an adjuvanted tuberculosis vaccine from systemic TH1 to tissue-resident TH17 responses without impacting the protective efficacy. (2015) (46)
A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16. (2001) (46)
Common Genetic Variation in ABCA 1 Is Associated With Altered Lipoprotein Levels and a Modified Risk for Coronary Artery Disease (2001) (45)
Genome maps 7. The human transcript map. Wall chart. (1996) (45)
Association between Allergies and Risk of Pancreatic Cancer (2014) (45)
A combined watershed and level set method for segmentation of brightfield cell images (2009) (44)
Reduced proportions of natural killer T cells are present in the relatives of lupus patients and are associated with autoimmunity (2008) (43)
Cooperative intracellular interactions between MyD88 and TRIF are required for CD4 T cell T H 1 polarization with a synthetic TLR4 agonist adjuvant (2013) (43)
Development of a screening set for new (CAG/CTG)n dynamic mutations. (1996) (42)
Analysis of early C2C12 myogenesis identifies stably and differentially expressed transcriptional regulators whose knock-down inhibits myoblast differentiation. (2012) (41)
Sex differences in oncogenic mutational processes (2019) (41)
The TLR4 Agonist Vaccine Adjuvant, GLA-SE, Requires Canonical and Atypical Mechanisms of Action for TH1 Induction (2016) (41)
Polymorphisms in interleukin‐1 receptor‐associated kinase 4 are associated with total serum IgE (2009) (40)
Specific Variants in the MLH1 Gene Region May Drive DNA Methylation, Loss of Protein Expression, and MSI-H Colorectal Cancer (2010) (40)
Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants (2013) (40)
Genes to Diseases (G2D) Computational Method to Identify Asthma Candidate Genes (2008) (40)
The Gene for Schnyder's Crystalline Corneal Dystrophy Maps to Human Chromosome 1p34.1–p36 (1996) (39)
Characterization of short tandem repeats from thirty-one human telomeres. (1997) (39)
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype. (2000) (39)
Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival (2020) (38)
Distinct pattern of lung gene expression in the Cftr-KO mice developing spontaneous lung disease compared with their littermate controls. (2006) (38)
Genome-Wide Search for Gene-Gene Interactions in Colorectal Cancer (2012) (38)
Somatic variation and cancer: therapies lost in the mix (2011) (37)
To the editor [3] (2005) (37)
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22 (2005) (36)
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia (2013) (36)
Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer. (1996) (36)
Genetic Variants and Susceptibility to Neurological Complications Following West Nile Virus Infection (2011) (35)
Functional promoter SNPs in cell cycle checkpoint genes. (2005) (34)
Influence of leukotriene gene polymorphisms on chronic rhinosinusitis (2008) (34)
The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. (1997) (34)
Haplotype mapping indicates two independent origins for the Cmv1s susceptibility allele to cytomegalovirus infection and refines its localization within the Ly49 cluster (2001) (33)
Constitutive activation of extracellular signal-regulated kinase predisposes diffuse large B-cell lymphoma cell lines to CD40-mediated cell death. (2006) (33)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) (1979) (32)
A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 (2015) (32)
Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on Chromosome region 2q35 (2000) (32)
Elucidating cis- and trans-regulatory variation using genetical genomics. (2006) (32)
Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk (2015) (31)
Genetic and epigenetic profiling of CLL disease progression reveals limited somatic evolution and suggests a relationship to memory-cell development (2015) (31)
Genome-wide meta-analysis of common variant differences between men and women (2012) (31)
Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica. (2007) (31)
Introduction to SNPs: discovery of markers for disease. (2002) (31)
Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes. (2006) (31)
Genetic Predictors of Circulating 25-Hydroxyvitamin D and Risk of Colorectal Cancer (2013) (30)
Translating genomics to the clinic: implications of cancer heterogeneity. (2013) (29)
Polymorphisms in the tumour necrosis factor alpha-induced protein 3 (TNFAIP3) gene are associated with chronic rhinosinusitis. (2009) (29)
Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in TP53-Associated Cancer Susceptibility. (2016) (28)
Patterns of expression of chromosome 17 genes in primary cultures of normal ovarian surface epithelia and epithelial ovarian cancer cell lines (2003) (28)
Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (28)
Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer. (2015) (28)
GeneExpression in HL60 Granulocytoids and Human PolymorphonuclearLeukocytes Exposed to Candidaalbicans† (2004) (28)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11. (1999) (27)
Large-Scale Uniform Analysis of Cancer Whole Genomes in Multiple Computing Environments (2017) (26)
Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica (2006) (26)
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer (2016) (24)
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population (2008) (24)
Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors (2005) (23)
Gene expression microarray analysis and genome databases facilitate the characterization of a chromosome 22 derived homogenously staining region (2004) (23)
Finding genetic modifiers of cystic fibrosis. (2005) (23)
A cis-Acting Regulatory Variant in the IL2RA Locus1 (2009) (22)
Modulation of the allergic asthma transcriptome following resiquimod treatment. (2009) (22)
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8 (2004) (22)
Mapping cis-acting regulatory variation in recombinant congenic strains. (2006) (21)
Genetic architectures of proximal and distal colorectal cancer are partly distinct (2020) (21)
Germline EPHB2 Receptor Variants in Familial Colorectal Cancer (2008) (21)
Microarray analysis of brain RNA in mice with methylenetetrahydrofolate reductase deficiency and hyperhomocysteinemia. (2002) (20)
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects (2010) (20)
Vaccination Produces CD4 T Cells with a Novel CD154–CD40-Dependent Cytolytic Mechanism (2015) (19)
Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3. (2004) (19)
Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica (2006) (19)
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk (2016) (19)
Resources for genetic variation studies. (2006) (18)
MLH1 Region Polymorphisms Show a Significant Association with CpG Island Shore Methylation in a Large Cohort of Healthy Individuals (2012) (18)
Genetic variation in immune signaling genes differentially expressed in asthmatic lung tissues. (2008) (18)
Expression profiles of 290 ESTs mapped to chromosome 3 in human epithelial ovarian cancer cell lines using DNA expression oligonucleotide microarrays. (2002) (18)
Long-range mapping and construction of a YAC contig within the cat eye syndrome critical region. (1994) (17)
Caring about women and cancer (CAWAC): a European survey of the perspectives and experiences of women with female cancers (1999) (16)
Navigating the perfect [data] storm (2012) (16)
The art and science of biobanking (2011) (15)
The living microarray: a high-throughput platform for measuring transcription dynamics in single cells (2011) (15)
Assessment of Toll-like receptor 2 gene polymorphisms in severe chronic rhinosinusitis. (2008) (15)
Functional characterization of GATA 3 mutations causing the hypoparathyroidism-deafness-renal ( HDR ) dysplasia syndrome : insight into mechanisms of DNA binding by the GATA 3 transcription factor (2007) (14)
Personalized medicine: a transformative approach is needed. (2009) (14)
G-protein-coupled receptors and asthma endophenotypes: the cysteinyl leukotriene system in perspective. (2006) (14)
Clinical genomics information management software linking cancer genome sequence and clinical decisions. (2013) (13)
Assessing DNA sequence variations in human ESTs in a phylogenetic context using high-density oligonucleotide arrays. (2002) (13)
Adverse reaction to the recombinant hepatitis B vaccine. (1991) (12)
Common variants in the obesity-associated genes FTO and MC4R are not associated with risk of colorectal cancer. (2016) (12)
Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia. (2019) (12)
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. (2001) (12)
Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjects (2007) (11)
31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016): part two (2016) (11)
Cycling Toward Leukemia Stem Cell Elimination Wtih a Selective Sonic Hedgehog Antagonist (2011) (11)
From genomic databases to translation: a call to action (2011) (11)
Genomics: Comparisons across cancers (2013) (11)
Genome-wide search for exonic variants affecting translational efficiency (2013) (11)
A haplotype map of the human genome The International HapMap Consortium (2005) (10)
The Escherichia coli K5 Capsule Is Not Synthesized in a Protected Compartment within the Cytoplasm (2008) (10)
Transcriptome-wide characterization of the endogenous miR-34A-p53 tumor suppressor network (2016) (10)
Molecular and Pathology Features of Colorectal Tumors and Patient Outcomes Are Associated with Fusobacterium nucleatum and Its Subspecies animalis (2021) (9)
Magnitude of Therapeutic STING Activation Determines CD8+ T Cell-Mediated Anti-tumor Immunity. (2019) (9)
A balance score between immune stimulatory and suppressive microenvironments identifies mediators of tumour immunity and predicts pan-cancer survival (2020) (9)
G-Protein-Coupled Receptors and Asthma Endophenotypes (2012) (9)
Multilevel Space-Time Aggregation for Bright Field Cell Microscopy Segmentation and Tracking (2010) (9)
No Evidence of Gene–Calcium Interactions from Genome-Wide Analysis of Colorectal Cancer Risk (2014) (9)
Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels (2010) (9)
Bacterial Polysaccharide Capsules (2010) (8)
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2022) (8)
Butler enables rapid cloud-based analysis of thousands of human genomes (2020) (8)
Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants (2014) (8)
Correction: Corrigendum: Genome-wide association study of colorectal cancer identifies six new susceptibility loci (2015) (7)
A Comprehensive Assessment of Somatic Mutation Calling in Cancer Genomes (2014) (7)
Isolation and regional mapping of 110 chromosome 22 STSs. (1994) (7)
Cancer genomes. (2010) (7)
Reflections on the founding of the International Cancer Genome Consortium. (2013) (6)
ARSACS Possibly a lysosomal storage disease (1996) (6)
Discovery of common and rare genetic risk variants for colorectal cancer (2018) (6)
STREGA: a ‘How-To’ guide for reporting genetic associations (2009) (6)
Assessment of TP53 Polymorphisms and MDM2 SNP309 in Premenopausal Breast Cancer Risk (2017) (6)
Abstract 3935: International Cancer Genome Consortium (ICGC) (2010) (6)
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population (2008) (5)
Patterns of variation in DNA segments upstream of transcription start sites (2007) (5)
Cancer genome variation in children, adolescents, and young adults (2011) (5)
Dinucleotide repeat polymorphism at the D9S126 locus (9p21). (1993) (5)
Erratum: A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns (2016) (5)
DNMT3a Mutations Define a Pre-Leukemic Stem Cell Reservoir In Human Acute Myeloid Leukemia (2013) (4)
Integrated Genomic, Transcriptomic, and RNA-Interference Analysis of Genes in Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma (2013) (4)
The effect of 5-fluorouracil/leucovorin chemotherapy on CpG methylation, or the confounding role of leukocyte heterogeneity: An illustration. (2015) (4)
NRAMP1 is not associated with asthma, atopy, and serum immunoglobulin E levels in the French Canadian population (2005) (4)
Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures (2022) (4)
From Community Genetics to Community Genomics: The Quebec Experience (2001) (4)
Application of expression microarrays to the investigation of fetal lung development in a glucocorticoid receptor knockout mouse model. (2002) (4)
4th Pediatric Allergy and Asthma Meeting (PAAM) (2016) (4)
Functional organization of an Mbp enhancer exposes striking transcriptional regulatory diversity within myelinating glia (2016) (4)
Contribution of HLA class II genes to susceptibility to ulcerative colitis (UC) in a Canadian inflammatory bowel disease (IBD) population (1998) (3)
Construction of small-insert libraries from genomic DNA. (2001) (3)
Abstract B48: Feasibility study of molecular profiling (MP) in patients (Pts) with advanced solid cancers using targeted mutation analysis and targeted exome sequencing. (2011) (3)
BCL2 Splice Isoform Switching Promotes Leukemia Stem Cell Survival and Sensitivity to a Novel Pan BCL2 Inhibitor (2011) (3)
Abstract 5287: Heterogeneity of mutation calling and annotation: a survey of cancer next-generation sequencing initiatives by the Global Alliance for Genomics and Health (GA4GH): (2016) (2)
Response to Li and Hopper. (2021) (2)
Novel Associations of Genetic Polymorphisms in the Interleukin-1 receptor/Toll-like Receptor Signaling Pathways with Atopy and Atopic Asthma (2009) (2)
Genomic variation in a global village: Report of the 10th annual Human Genome Variation Meeting 2008 (2009) (2)
Abstract 631: Intratumoral activation of STING with a synthetic cyclic dinucleotide elicits antitumor CD8 T-cell immunity that effectively combines with checkpoint inhibitors (2018) (2)
The melanoma‐associated transmembrane glycoprotein Gpnmb controls trafficking of cellular debris for degradation and is essential for tissue repair (2010) (2)
Abstract 2988: International cancer genome consortium (ICGC) (2015) (1)
Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (1)
Polymorphisms in TLR9 Gene Influence Response to Corticosteroids in Severe Chronic Rhinosinusitis (2008) (1)
Hydrocortisone Upregulates Th2-type Cytokine and Chemokine Receptor mRNA on Human B-lymphocytes. (2006) (1)
Mutations in TMEM76* Cause Mucopolysaccharidosis IIIC (2006) (1)
Genetic regulation of DNA methylation yields novel discoveries in GWAS of colorectal cancer. (2022) (1)
Fishing for Allergens: Bloodworm-Induced Asthma (2005) (1)
Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (1)
104 Tumor Microenvironment and Genetic Association With Colorectal Cancer Risk (2012) (1)
Colony Hybridization to Screen for Microsatellites (1997) (1)
Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
Personalized medicine: A transformative approach is needed (2009) (1)
Abstract 5230: Large scale whole genome sequencing with imputation into GWAS improves our understanding of the genetic architecture of colorectal cancer (2016) (1)
Europa Uomo: the European Prostate Cancer Coalition. (2007) (1)
4P-1177 HDL-cholesterol and other covariables associated with CAD-free survival among familial hypercholesterolemic heterozygotes or homozygotes over 70 years of age (2003) (1)
A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1 (2015) (1)
Abstract 5221: Linking the molecular profile of colorectal tumors to germline genetic and environmental risk factors (2016) (1)
11:10: TLR Signalling Gene Polymorphisms in Chronic Rhinosinusitis (2007) (1)
On the Origins of AML Relapse (2015) (1)
Functional normalization of 450k methylation array data improves replication in large cancer studies (2014) (1)
Human Genetics’ 50th Anniversary Issue (2014) (1)
whose knock-down inhibits myoblast differentiation and differentially expressed transcriptional regulators Analysis of early C2C12 myogenesis identifies stably (2015) (0)
Abstract 5185: Redefining the somatic landscape of pancreatic adenocarcinoma (2014) (0)
Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival (2023) (0)
Costa Rica function in families of children with asthma in Genome-wide linkage analysis of pulmonary Freimer (2007) (0)
Polymorphisms in the IRAK-4 Gene are Associated with Total Serum IgE in Chronic Rhinosinusitis Patients (2008) (0)
Identification of two novel susceptibility loci in a Canadian inflammatory bowel disease population (2000) (0)
Identification of FOXC1 targets genes utilizing a novel caged FOXC1 molecule and microarray analysis. (2004) (0)
Towards an STS-content map of the human genome (1994) (0)
P3G Observatory: A Tool for Population Research Projects In Genomics (2006) (0)
Association Study Between Interleukin 1 Receptor Type 2 (IL1R2) Pathway Genes And Asthma Related Phenotypes In Two Independent Familial Studies (2011) (0)
Abstract A9: The pancreatic ductal adenocarcinoma project at the Ontario Institute for Cancer Research. (2012) (0)
Patent Number : ( 45 ) Date of Patent : 5 , 102 , 659 Apr . 7 , 1992 (2017) (0)
An Integrated BAC/PAC Resource for identifying chromosomal abnormalities in solid tumors (2000) (0)
Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk. (2013) (0)
COLIPHAGE K5A LYASE (2010) (0)
Abstract 1304: The contribution of rare and low-frequency variants to colorectal cancer heritability (2017) (0)
Identification of Novel Chromosomal Regions Associated with Airway Hyperresponsiveness (AHR) in Recombinant Congenic Strains of Mice (2006) (0)
Explorer COGENT ( COlorectal cancer GENeTics ) : an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2017) (0)
Edinburgh Research Explorer COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer role (2009) (0)
Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer (2019) (0)
Gene-environment interactions in CRC risk loci 1 Title: Characterization of gene-environment interactions for colorectal cancer susceptibility loci Authors and Affiliations: (2012) (0)
Erratum: COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (British Journal of Cancer 102 (447-454) DOI: 10.1038/sj.bjc.6605338)) (2010) (0)
Abstract 1598: Deep targeted sequencing of colorectal cancer cases to study associations of molecular subtypes with clinical, genetic, and lifestyle risk factors (2019) (0)
Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries (2023) (0)
Title COGENT ( COlorectal cancer GENeTics ) : An international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2009) (0)
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer (2010) (0)
Mechanism CD40-Dependent Cytolytic - Novel CD154 Vaccination Produces CD4 T Cells with a (2015) (0)
COGENT cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. (2009) (0)
Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
Association between germline variants and somatic mutations in colorectal cancer (2022) (0)
Joe Doupe Young Investigators Award. The Human Genome Project: tools for the identification of disease genes. (1998) (0)
Chromosomal deletions rather than microsatellite instability are important in the pathogenesis of human oligodendrogliomas (1998) (0)
Cross-cancer genome-wide association analysis of lung, ovary, breast, prostate and colon cancer identifies a novel cancer locus at 1q22 (2015) (0)
The molecular basis of glutamate formiminotransferase deficiency (2003) (0)
Abstract 4664: Impact of TP53 mutations, single nucleotide variants and global methylation patterns on pre-menopausal breast cancer risk (2015) (0)
Cumulative impact of 10 common genetic variants on colorectal cancer risk in 42,333 individuals from eight populations (2013) (0)
Meta-analysis of new genome-wide association studies of colorectal cancer risk (2011) (0)
Abstract 136: Refining the molecular profile of colorectal tumors to expand prevention and treatment opportunities (2016) (0)
751 Identification of a Common Variant With Potential Pleiotropic Effect on Risk of Inflammatory Bowel Disease and Colorectal Cancer (2013) (0)
A haplotype association analysis in UK families indicates that variation at the 3 ' end of PDCD1 increases risk of SLE (2005) (0)
Null Results in Brief No Evidence of Gene – Calcium Interactions from Genome-Wide Analysis of Colorectal Cancer Risk (2014) (0)
Wang , the Human Genome Genotyping of Single-Nucleotide Polymorphisms in Large-Scale Identification , Mapping (2007) (0)
Abstract 1286: Targeted deep sequencing of colorectal tumor tissues to study associations of tumor subtypes with germline genetic, lifestyle, and environmental risk factors (2017) (0)
Mo-P6:391 Identification of a chromosome 8P locus for coronary heart disease in the French Canadian founder population (2006) (0)
Abstract 3184: Whole genome sequencing of low-input fresh frozen prostate cancer biopsies (2012) (0)
Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
HHRR Association Results for the Dense Set of 211SNPs in Finnish and Canadian MS Families (2006) (0)
2P-0353 Prevalence and geographic distribution of a frequent genotypic combination of hyperapo B in the Quebec population (2003) (0)
Effect of diagnostic misclassification on the ability to detect linkage in inflammatory bowel disease (IBD) (2000) (0)
Correction: A balance score between immune stimulatory and suppressive microenvironments identifies mediators of tumour immunity and predicts pan-cancer survival (2020) (0)
Target Directed Drug Discovery: A Technology Driven Approach to Combating Malaria (2004) (0)
Stage I: SNP Results of the Association Analysis in the Primary Study (2006) (0)
Cancer Genomics in the Clinic: Methods and Lessons (2013) (0)
From Genomes to Populations: Relevance to Human Genetic Diseases (2000) (0)
GLI2 inhibition abrogates human leukemia stem cell dormancy (2015) (0)
Genome-wide scan for linkage to obesity-associated hypertension in French canadians. Commentary (2005) (0)
Analyses of Genotype-Phenotype Associations in Asthma and Atopy in Four Population Samples (2012) (0)
Abstract B50: Synergistic antitumor efficacy in mice with immunotherapy regimens combining recombinant live-attenuated Listeria with immune checkpoint inhibitors (2017) (0)
Abstract 1300: Genetic predictors of gene expression associated with risk of colorectal cancer (2017) (0)
Lines to CD 40-Mediated Cell Death Kinase Predisposes Diffuse Large B-Cell Lymphoma Cell Constitutive Activation of Extracellular Signal-Regulated (2006) (0)
The MHC and multiple sclerosis susceptibility - several levels of complexity (2004) (0)
Long CAG/CTG repeats in mice (1998) (0)
Genetic variation and cancer (2008) (0)
Abstract B13: Whole-genome mutation landscape in pancreatic ductal adenocarcinoma. (2012) (0)
Cancer Genome Researchers Band Together (2011) (0)
Does the likelihood of malignancy in thyroid nodules with RAS mutations increase in direct proportion with the allele frequency percentage? (2023) (0)
SNP Haplotypes and the Corresponding p-Values (Haploview) Tested in Finnish MS Families (2006) (0)
Abstract B129: Clinical implications of inter- and intra- prostatic heterogeneity. (2013) (0)
Locus IL 2 RA-Acting Regulatory Variant in the cis A (2009) (0)
Abstract 1853: Identification and characterization of genes in regions of recurrent genomic gain as putative therapeutic targets in pancreatic ductal adenocarcinoma (2012) (0)
Abstract LB-230: A prospective clinical trial to evaluate DNA sequencing as a diagnostic tool to guide cancer therapy: results from the initial 50 patients (2012) (0)
Abstract 1058: Novel insights into the genetic and epigenetic regulation of the MLH1 CpG island and shore in colorectal cancer (2015) (0)
Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes (2005) (0)
Abstract 16: Impact of germline TP53 mutations and polymorphisms in women with premenopausal breast cancer (2014) (0)
Abstract NG05: TP53-mediated human cancer susceptibility is defined by epigenetic dysregulation of microRNA-34A (2017) (0)
A method for diagnosis of ovarian cancer (2006) (0)
Abstract A013: Favorable changes in tumor microenvironment following intravenous dosing with live attenuatedListeria monocytogenes-based immunotherapy (2016) (0)
An integrated BAC/PAC molecular cytogenetic resource for human genetics: Applications to disease (1996) (0)
Abstract B18: Genomic analysis of pancreatic ductal adenocarcinoma. (2012) (0)
PTPN 22 with type 1 diabetes in a family based study polymorphism in the protein tyrosine phosphatase Confirmation of the association of the R 620 W (2005) (0)
Congress Committee (1963) (0)
Toward Identification of Chronic Rhinosinusitis Susceptibility Genes by Use of Pooling-Based Genomewide Association Scan (2008) (0)
42 HAPLOTYPE STRUCTURE AND ASSOCIATION OF COMMON VARIANTS IN THE GENE ENCODING THE ISLET ATP-SENSITIVE POTASSIUM CHANNEL WITH TYPE 2 DIABETES. (2004) (0)
F.31. Lost Inhibitions? T Cell Activation Pathways in SLE (2009) (0)
Abstract 2966: The mutational landscape of localized gleason 6 and 7 prostate cancer (2015) (0)
Obituary of Leena Peltonen-Palotie (2010) (0)
Abstract 1224: Deep targeted tumor sequencing of colorectal cancer cases to study associations of molecular subtypes with clinical, genetic, and lifestyle risk factors (2018) (0)
Abstract 2003: A molecular portrait of potentially curable prostate cancer. (2013) (0)
PTPN22 with type 1 diabetes in a family based study polymorphism in the protein tyrosine phosphatase Confirmation of the association of the R620W (2005) (0)
O-12-180 Chromosomal deletions rather than microsatellite instability are important in the pathogenesis of oligodendrogliomas (1997) (0)
Polymorphisms in the IL22RA1 Gene and Chronic Rhinosinusitis (2008) (0)
Correction regarding an adverse reaction to the recombinant hepatitis B vaccine. (1993) (0)
Abstract 5063: International Cancer Genome Consortium (ICGC) (2012) (0)
Genetic susceptibility in a Canadian inflammatory bowel disease (IBD) population (1998) (0)
A genome-wide scan in a canadian inflammatory bowel disease (IBD) population reveals two novel susceptibility loci (2000) (0)
Common functional polymorphisms in toll-like receptor 4 (TLR4) are not associated with asthma or atopy-related phenotypes. (2002) (0)
2HT01-3 Glycerolemia and glucose intolerance prediction: Illustration of the application of genomic research to medical practice (2003) (0)
Population-Based Association Study Of TLR Gene Polymorphisms In Chronic Rhinosinusitis (2007) (0)
Abstract 3561: Genetic Variants Associated with Acute Myocardial Infarction Risk in Five Ethnic Groups: The INTERHEART genetics study (2007) (0)

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