Lista de obras - Thomas J. Hudson - Dominio Público Uruguay

1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes.

artículo científico publicado en 2007

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

artículo científico publicado en 2016

4th Pediatric Allergy and Asthma Meeting (PAAM)

artículo científico publicado en 2016

5' flanking variants of resistin are associated with obesity

artículo científico publicado en 2002

A PCR-based linkage map of human chromosome 1.

artículo científico publicado en 1993

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

artículo científico publicado en 2013

A Second-Generation Association Study of the 5q31 Cytokine Gene Cluster and the Interleukin-4 Receptor in Asthma

article

A YAC-based physical map of the mouse genome.

artículo científico publicado en 1999

A cis-Acting Regulatory Variant in the IL2RA Locus

artículo científico publicado en 2009

A combinatorial network of evolutionarily conserved myelin basic protein regulatory sequences confers distinct glial-specific phenotypes

scientific journal article

A combined watershed and level set method for segmentation of brightfield cell images

article

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

artículo científico publicado en 2008

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

artículo científico publicado en 2007

A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

artículo científico publicado en 2015

A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus).

artículo científico publicado en 2007

A genome-wide approach to identifying novel-imprinted genes.

artículo científico publicado en 2007

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.

artículo científico publicado en 2015

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

artículo científico publicado en 2007

A map of 75 human ribosomal protein genes

artículo científico publicado en 1998

A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis

artículo científico publicado en 2002

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

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

artículo científico publicado en 2005

A radiation hybrid map of mouse genes

article

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

artículo científico publicado en 2016

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

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.

artículo científico publicado en 2001

A survey of genetic and epigenetic variation affecting human gene expression

artículo científico publicado en 2004

ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels.

artículo científico publicado en 2002

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

artículo científico publicado en 2000

Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16

artículo científico publicado en 1998

Abstract 2190: Fine-mapping of common genetic variants associated with colorectal tumor risk identified potential functional variants

Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk

article

Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia

artículo científico publicado en 2019

Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery

artículo científico publicado en 2007

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

artículo científico publicado en 2004

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

artículo científico publicado en 2006

An optimized set of human telomere clones for studying telomere integrity and architecture.

artículo científico publicado en 2000

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

artículo científico publicado en 2009

Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.

artículo científico publicado en 2016

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

scientific journal article

Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes

artículo científico publicado en 2005

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

artículo científico publicado en 2015

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

scientific article published on 01 August 2005

Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes

artículo científico publicado en 2004

Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people

artículo científico publicado en 2005

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

artículo científico publicado en 2005

Asthma and genes encoding components of the vitamin D pathway

artículo científico publicado en 2009

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

artículo científico publicado en 1999

Autosomal recessive spastic ataxia of Charlevoix–Saguenay

article published in 1998

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

artículo científico publicado en 2009

CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk

artículo científico publicado en 2016

Characterization of a common susceptibility locus for asthma-related traits

artículo científico publicado en 2004

Characterization of gene-environment interactions for colorectal cancer susceptibility loci

artículo científico publicado en 2012

Common variants in the NLRP3 region contribute to Crohn's disease susceptibility

artículo científico publicado en 2008

Common variants in the obesity-associated genes FTO and MC4R are not associated with risk of colorectal cancer

artículo científico publicado en 2016

Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

scientific article published on 01 July 2019

Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci

artículo científico publicado en 2015

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Discovery of common and rare genetic risk variants for colorectal cancer

artículo científico publicado en 2018

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

artículo científico publicado en 2016

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

artículo científico publicado en 2008

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

artículo científico publicado en 2008

Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants

artículo científico publicado en 2016

Functional classes of bronchial mucosa genes that are differentially expressed in asthma

artículo científico publicado en 2004

G-protein-coupled receptors and asthma endophenotypes: the cysteinyl leukotriene system in perspective

artículo científico publicado en 2006

Genes to diseases (G2D) computational method to identify asthma candidate genes

artículo científico publicado en 2008

Genetic mechanisms of immune evasion in colorectal cancer

artículo científico publicado en 2018

Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer

scientific article published on 27 August 2013

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

article

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

article

Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis

artículo científico publicado en 2009

Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer

artículo científico publicado en 2016

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 of colorectal cancer identifies six new susceptibility loci

artículo científico publicado en 2015

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

artículo científico publicado en 2007

Genome-wide meta-analysis of common variant differences between men and women

artículo científico publicado en 2012

Genome-wide search for gene-gene interactions in colorectal cancer

artículo científico publicado en 2012

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

artículo científico publicado en 2001

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

artículo científico publicado en 2004

Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L

artículo científico publicado en 2002

Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis

artículo científico publicado en 2012

Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer

artículo científico publicado en 2015

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

artículo científico publicado en 2003

Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants

artículo científico publicado en 2014

Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

artículo científico publicado en 2002

International network of cancer genome projects

artículo científico publicado en 2010

Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival

artículo científico publicado en 2020

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

artículo científico publicado en 1999

Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci

artículo científico publicado en 2015

Meta-analysis identifies seven susceptibility loci involved in the atopic march

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome)

artículo científico publicado en 2006

No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk

artículo científico publicado en 2014

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

artículo científico publicado en 2019

Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

artículo científico publicado en 2012

Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia

artículo científico publicado en 2013

Prepublication data sharing

artículo científico publicado en 2009

Spatial genomic heterogeneity within localized, multifocal prostate cancer

artículo científico publicado en 2015

The K5 Lyase KflA Combines a Viral Tail Spike Structure with a Bacterial Polysaccharide Lyase Mechanism

artículo científico publicado en 2010

The acute neurotoxicity of mefloquine may be mediated through a disruption of calcium homeostasis and ER function in vitro

artículo científico publicado en 2003

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

artículo científico publicado en 2000

The genetic basis for cancer treatment decisions

artículo científico publicado en 2012

The molecular basis of glutamate formiminotransferase deficiency

scientific journal article

Lista de obras de Thomas J. Hudson

1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processes.

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

4th Pediatric Allergy and Asthma Meeting (PAAM)

5' flanking variants of resistin are associated with obesity

A PCR-based linkage map of human chromosome 1.

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

A Second-Generation Association Study of the 5q31 Cytokine Gene Cluster and the Interleukin-4 Receptor in Asthma

A YAC-based physical map of the mouse genome.

A cis-Acting Regulatory Variant in the IL2RA Locus

A combinatorial network of evolutionarily conserved myelin basic protein regulatory sequences confers distinct glial-specific phenotypes

A combined watershed and level set method for segmentation of brightfield cell images

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

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

A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.

A genetic linkage map of the vervet monkey (Chlorocebus aethiops sabaeus).

A genome-wide approach to identifying novel-imprinted genes.

A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1.

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

A map of 75 human ribosomal protein genes

A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis

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

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

A radiation hybrid map of mouse genes

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

A second generation human haplotype map of over 3.1 million SNPs

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.

A survey of genetic and epigenetic variation affecting human gene expression

ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels.

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF

Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16

Abstract 2190: Fine-mapping of common genetic variants associated with colorectal tumor risk identified potential functional variants

Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk

Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia

Allele-specific expression in the germline of patients with familial pancreatic cancer: an unbiased approach to cancer gene discovery

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

An optimized set of human telomere clones for studying telomere integrity and architecture.

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

Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases.

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

Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes

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

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes

Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

Asthma and genes encoding components of the vitamin D pathway

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.

Autosomal recessive spastic ataxia of Charlevoix–Saguenay

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

CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk

Characterization of a common susceptibility locus for asthma-related traits

Characterization of gene-environment interactions for colorectal cancer susceptibility loci

Common variants in the NLRP3 region contribute to Crohn's disease susceptibility

Common variants in the obesity-associated genes FTO and MC4R are not associated with risk of colorectal cancer

Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci

Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

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

Discovery of common and rare genetic risk variants for colorectal cancer

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

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

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

Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants

Functional classes of bronchial mucosa genes that are differentially expressed in asthma

G-protein-coupled receptors and asthma endophenotypes: the cysteinyl leukotriene system in perspective

Genes to diseases (G2D) computational method to identify asthma candidate genes

Genetic mechanisms of immune evasion in colorectal cancer

Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

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

Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis

Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer

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

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

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

Genome-wide meta-analysis of common variant differences between men and women

Genome-wide search for gene-gene interactions in colorectal cancer

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