Lista de obras - Amy Hutchinson - Dominio Público Uruguay

A comprehensive candidate gene approach identifies genetic variation associated with osteosarcoma

artículo científico publicado en 2011

A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.

artículo científico publicado en 2009

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

artículo científico publicado en 2011

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

artículo científico publicado en 2007

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

artículo científico publicado en 2010

A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3

scientific journal article

A genome-wide association study of marginal zone lymphoma shows association to the HLA region

artículo científico publicado en 2015

A genome-wide association study of prostate cancer in West African men

artículo científico publicado en 2013

A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance

artículo científico publicado en 1998

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

artículo científico publicado en 2014

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

scientific journal article

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

artículo científico publicado en 2009

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

artículo científico publicado en 1997

A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk

artículo científico publicado en 2013

A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma

artículo científico publicado en 2010

Abstract 2860: Identification of genes associated with osteosarcoma using a genetic pathway approach

article

Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue

Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients

scientific article published on 24 September 2020

Alcohol intake and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (PanScan)

artículo científico publicado en 2010

An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general population

scientific article published on 13 September 2013

Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

artículo científico publicado en 2015

Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).

artículo científico publicado en 2010

Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy

artículo científico publicado en 2001

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

artículo científico publicado en 2016

Blood DNA methylation and breast cancer risk: a meta-analysis of four prospective cohort studies

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

artículo científico publicado en 1996

Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue

scientific article published on 27 February 2014

Clinical Implications of Inter- and Intratumor Heterogeneity of Immune Cell Markers in Lung Cancer

artículo científico publicado en 2022

Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer

artículo científico publicado en 2013

Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancer

artículo científico publicado en 2012

Common genetic variants in the 8q24 region and risk of papillary thyroid cancer

artículo científico publicado en 2012

Common genetic variants in the PSCA gene influence gene expression and bladder cancer risk

artículo científico publicado en 2012

Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer

artículo científico publicado en 2013

Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer

artículo científico publicado en 2009

DNA repair gene polymorphisms and risk of adult meningioma, glioma, and acoustic neuroma

artículo científico publicado en 2009

Detectable clonal mosaicism and its relationship to aging and cancer

artículo científico publicado en 2012

Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium

artículo científico publicado en 2012

Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies

artículo científico publicado en 1999

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

artículo científico publicado en 2016

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

scholarly article

Fine mapping of 14q24.1 breast cancer susceptibility locus

artículo científico publicado en 2011

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

artículo científico publicado en 2011

Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels

artículo científico publicado en 2011

Genetic Admixture and Population Substructure in Guanacaste Costa Rica ⬇️

artículo científico publicado el 13 de octubre de 2010

Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia

artículo científico publicado en 2012

Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia

artículo científico publicado en 2014

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

artículo científico publicado en 2016

Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia

scientific journal article

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region

artículo científico publicado en 2014

Genome-wide association study identifies multiple loci associated with bladder cancer risk

artículo científico publicado en 2014

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

artículo científico publicado en 2013

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

artículo científico publicado en 2014

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

artículo científico publicado en 2009

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

scientific journal article

Genome-wide association study of survival in patients with pancreatic adenocarcinoma

scientific journal article

Genome-wide interaction study of smoking and bladder cancer risk

artículo científico publicado en 2014

Genomic Landscape of Somatic Alterations in Esophageal Squamous Cell Carcinoma and Gastric Cancer

artículo científico publicado en 2016

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease

artículo científico publicado en 1999

Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies

artículo científico publicado en 2012

Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.

artículo científico publicado en 2018

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

artículo científico publicado en 2009

Host Immunogenetics and Control of Human Herpesvirus–8 Infection

scientific article published in 2006

Human and mouse orthologs of a new ATP-binding cassette gene, ABCG4.

artículo científico publicado en 2001

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

artículo científico publicado en 2009

Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

artículo científico publicado en 2016

Immune gene expression profiling reveals heterogeneity in luminal breast tumors

article

Improved imputation of common and uncommon SNPs with a new reference set.

artículo científico publicado en 2011

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

artículo científico publicado en 2014

Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions

artículo científico publicado en 2015

Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

artículo científico publicado en 2014

Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident

artículo científico publicado en 2021

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

artículo científico publicado en 2011

Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background

artículo científico publicado en 2012

Lead exposure, polymorphisms in genes related to oxidative stress, and risk of adult brain tumors

artículo científico publicado en 2009

Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer

artículo científico publicado en 2012

Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia

artículo científico publicado en 2016

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women

artículo científico publicado en 2016

Mosaic loss of chromosome Y is associated with common variation near TCL1A

artículo científico publicado en 2016

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome

artículo científico publicado en 2010

Multiple loci identified in a genome-wide association study of prostate cancer

scientific journal article

Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)

scientific journal article

Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

artículo científico publicado en 1997

New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease

scientific article published on 01 March 2000

Novel breast cancer risk alleles and interaction with ionizing radiation among U.S. radiologic technologists

artículo científico publicado en 2010

On the interplay of telomeres, nevi and the risk of melanoma

artículo científico publicado en 2012

Organization of the ABCR gene: analysis of promoter and splice junction sequences

artículo científico publicado en 1998

Oxidative response gene polymorphisms and risk of adult brain tumors

artículo científico publicado en 2008

Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium

artículo científico publicado en 2010

Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer

artículo científico publicado en 2012

Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4.

artículo científico publicado en 2013

Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China

artículo científico publicado en 2009

Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2.

artículo científico publicado en 2010

Sources of pre-analytical variations in yield of DNA extracted from blood samples: analysis of 50,000 DNA samples in EPIC.

artículo científico publicado en 2012

Successful genome-wide scan in paired blood and buccal samples

artículo científico publicado en 2007

The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease

artículo científico publicado en 2014

The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia

artículo científico publicado en 2010

The ABCR Gene in Recessive and Dominant Stargardt Diseases: A Genetic Pathway in Macular Degeneration

article

Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia

artículo científico publicado en 2018

Two susceptibility loci identified for prostate cancer aggressiveness

artículo científico publicado en 2015

Variant ABO blood group alleles, secretor status, and risk of pancreatic cancer: results from the pancreatic cancer cohort consortium

artículo científico publicado en 2010

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma

artículo científico publicado en 2010

Whole exome sequencing in 75 high-risk families with validation and replication in independent case-control studies identifies TANGO2, OR5H14, and CHAD as new prostate cancer susceptibility genes

artículo científico publicado en 2016

Worldwide genetic structure in 37 genes important in telomere biology

artículo científico publicado en 2011

Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry

artículo científico publicado en 2012

Lista de obras de Amy Hutchinson

A comprehensive candidate gene approach identifies genetic variation associated with osteosarcoma

A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3

A genome-wide association study of marginal zone lymphoma shows association to the HLA region

A genome-wide association study of prostate cancer in West African men

A human placenta-specific ATP-binding cassette gene (ABCP) on chromosome 4q22 that is involved in multidrug resistance

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

A resequence analysis of genomic loci on chromosomes 1q32.1, 5p15.33, and 13q22.1 associated with pancreatic cancer risk

A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma

Abstract 2860: Identification of genes associated with osteosarcoma using a genetic pathway approach

Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue

Age-related DNA methylation in paired normal and tumour breast tissue in Chinese breast cancer patients

Alcohol intake and pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium (PanScan)

An absolute risk model to identify individuals at elevated risk for pancreatic cancer in the general population

Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

Anthropometric measures, body mass index, and pancreatic cancer: a pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan).

Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

Blood DNA methylation and breast cancer risk: a meta-analysis of four prospective cohort studies

Characterization of large structural genetic mosaicism in human autosome

Characterization of the human ABC superfamily: isolation and mapping of 21 new genes using the expressed sequence tags database

Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue

Clinical Implications of Inter- and Intratumor Heterogeneity of Immune Cell Markers in Lung Cancer

Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer

Common genetic variants in metabolism and detoxification pathways and the risk of papillary thyroid cancer

Common genetic variants in the 8q24 region and risk of papillary thyroid cancer

Common genetic variants in the PSCA gene influence gene expression and bladder cancer risk

Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer

Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer

DNA repair gene polymorphisms and risk of adult meningioma, glioma, and acoustic neuroma

Detectable clonal mosaicism and its relationship to aging and cancer

Diabetes and risk of pancreatic cancer: a pooled analysis from the pancreatic cancer cohort consortium

Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

Fine mapping of 14q24.1 breast cancer susceptibility locus

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels

Genetic Admixture and Population Substructure in Guanacaste Costa Rica ⬇️

Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia

Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia

Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region

Genome-wide association study identifies multiple loci associated with bladder cancer risk

Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

Genome-wide association study of survival in patients with pancreatic adenocarcinoma

Genome-wide interaction study of smoking and bladder cancer risk

Genomic Landscape of Somatic Alterations in Esophageal Squamous Cell Carcinoma and Gastric Cancer

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease

Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies

Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

Host Immunogenetics and Control of Human Herpesvirus–8 Infection

Human and mouse orthologs of a new ATP-binding cassette gene, ABCG4.

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

Immune gene expression profiling reveals heterogeneity in luminal breast tumors

Improved imputation of common and uncommon SNPs with a new reference set.

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

Integration of multiethnic fine-mapping and genomic annotation to prioritize candidate functional SNPs at prostate cancer susceptibility regions

Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident

Large-scale fine mapping of the HNF1B locus and prostate cancer risk

Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background

Lead exposure, polymorphisms in genes related to oxidative stress, and risk of adult brain tumors

Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer

Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia

Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women

Mosaic loss of chromosome Y is associated with common variation near TCL1A