Lista de obras - Laurie Burdett - Dominio Público Uruguay

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

artículo científico publicado en 2015

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

scientific journal article

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

artículo científico publicado en 2010

An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

CYBB, an NADPH-oxidase gene: restricted diversity in humans and evidence for differential long-term purifying selection on transmembrane and cytosolic domains

artículo científico publicado en 2008

Characterization of large structural genetic mosaicism in human autosome

artículo científico publicado en 2015

Combined somatic mutation and copy number analysis in the survival of familial CLL

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

artículo científico publicado en 2013

Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer

artículo científico publicado en 2007

Detectable clonal mosaicism and its relationship to aging and cancer

artículo científico publicado en 2012

Diversity in the glucose transporter-4 gene (SLC2A4) in humans reflects the action of natural selection along the old-world primates evolution

artículo científico publicado en 2010

Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders

artículo científico publicado en 2014

Evolutionary Dynamics of the Human NADPH Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications ⬇️

artículo científico publicado el 2 de julio de 2013

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

artículo científico publicado en 2016

Genetic susceptibility loci, pesticide exposure and prostate cancer risk

artículo científico publicado en 2013

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 susceptibility loci for diffuse large B cell lymphoma

artículo científico publicado en 2014

Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density

artículo científico publicado en 2010

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

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

Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer

artículo científico publicado en 2011

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

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

artículo científico publicado en 2009

Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study

artículo científico publicado en 2016

Sex specific associations in genome wide association analysis of renal cell carcinoma

scientific article published on 23 June 2019

Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas

artículo científico publicado en 2007

The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

artículo científico publicado en 2011

Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

artículo científico publicado en 2019

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

artículo científico publicado en 2016

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Lista de obras de Laurie Burdett

A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

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

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

An unusual suspect: an uncommon human-specific synonymous coding variant within the UGT1A6 gene explains a GWAS signal and protects against bladder cancer

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

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

CYBB, an NADPH-oxidase gene: restricted diversity in humans and evidence for differential long-term purifying selection on transmembrane and cytosolic domains

Characterization of large structural genetic mosaicism in human autosome

Combined somatic mutation and copy number analysis in the survival of familial CLL

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

Common genetic variation in TP53 and its flanking genes, WDR79 and ATP1B2, and susceptibility to breast cancer

Detectable clonal mosaicism and its relationship to aging and cancer

Diversity in the glucose transporter-4 gene (SLC2A4) in humans reflects the action of natural selection along the old-world primates evolution

Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disorders

Evolutionary Dynamics of the Human NADPH Oxidase Genes CYBB, CYBA, NCF2, and NCF4: Functional Implications ⬇️

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

Genetic susceptibility loci, pesticide exposure and prostate cancer risk

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 susceptibility loci for diffuse large B cell lymphoma

Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density

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

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

Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer

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

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

Sex Steroid Hormone Single-Nucleotide Polymorphisms, Pesticide Use, and the Risk of Prostate Cancer: A Nested Case-Control Study within the Agricultural Health Study

Sex specific associations in genome wide association analysis of renal cell carcinoma

Somatic sequence alterations in twenty-one genes selected by expression profile analysis of breast carcinomas

The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene

Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

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