Lista de obras - Liesel FitzGerald - Dominio Público Uruguay

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

artículo científico publicado en 2012

A three-protein biomarker panel assessed in diagnostic tissue predicts death from prostate cancer for men with localized disease

artículo científico publicado en 2014

Analysis of recently identified prostate cancer susceptibility loci in a population-based study: associations with family history and clinical features

artículo científico publicado en 2009

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

artículo científico publicado en 2018

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

artículo científico publicado en 2013

Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis.

artículo científico publicado en 2008

Association of TMPRSS2-ERG gene fusion with clinical characteristics and outcomes: results from a population-based study of prostate cancer

artículo científico publicado en 2008

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases

artículo científico publicado en 2015

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

artículo científico publicado en 2016

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene

artículo científico publicado en 2002

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

artículo científico publicado en 2011

Clinical utility of five genetic variants for predicting prostate cancer risk and mortality

artículo científico publicado en 2009

Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage

artículo científico publicado en 2009

Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype?

artículo científico publicado en 2004

Effect of MELANOTAN, [Nle(4), D-Phe(7)]-alpha-MSH, on melanin synthesis in humans with MC1R variant alleles

artículo científico publicado en 2005

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus ⬇️

artículo científico publicado en 2010

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

artículo científico publicado en 2018

Genetic variants in the LEPR, CRY1, RNASEL, IL4, and ARVCF genes are prognostic markers of prostate cancer-specific mortality

artículo científico publicado en 2011

Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study

artículo científico publicado en 2017

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

artículo científico publicado en 2016

Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer

artículo científico publicado en 2011

Genome-wide association study of prostate cancer-specific survival

artículo científico publicado en 2015

Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

artículo científico publicado en 2010

Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study

artículo científico publicado en 2016

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia

artículo científico publicado en 2005

Germline missense variants in the BTNL2 gene are associated with prostate cancer susceptibility

artículo científico publicado en 2013

Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases

artículo científico publicado en 2018

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

article by Artitaya Lophatananon et al published 20 March 2018 in British Journal of Cancer

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

artículo científico publicado en 2013

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

artículo científico publicado en 2008

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

artículo científico publicado en 2009

Identifying Genetic Risk Factors for Diabetic Macular Edema and the Response to Treatment

scientific article published on 12 November 2020

Interest in genetic testing among affected men from hereditary prostate cancer families and their unaffected male relatives

artículo científico publicado en 2009

Investigation of the relationship between prostate cancer and MSMB and NCOA4 genetic variants and protein expression

artículo científico publicado en 2012

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

artículo científico publicado en 2015

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

artículo científico publicado en 2003

Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity

artículo científico publicado en 2006

National Cancer Institute Prostate Cancer Genetics Workshop

artículo científico publicado en 2011

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

artículo científico publicado en 2019

Novel associations between blood DNA methylation and body mass index in middle-aged and older adults

artículo científico publicado en 2017

Pharmacogenomic Biomarkers in Docetaxel Treatment of Prostate Cancer: From Discovery to Implementation

artículo científico publicado en 2019

Prediction of individual genetic risk to prostate cancer using a polygenic score

artículo científico publicado en 2015

Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status

artículo científico publicado en 2016

Reliability of DNA methylation measures from dried blood spots and mononuclear cells using the HumanMethylation450k BeadArray

artículo científico publicado en 2016

Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

artículo científico publicado en 2015

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk: a replication study in an ethnically homogeneous population

artículo científico publicado en 2008

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

artículo científico publicado en 2011

Testing the circadian gene hypothesis in prostate cancer: a population-based case-control study

artículo científico publicado en 2009

The advantages of dense marker sets for linkage analysis with very large families.

artículo científico publicado en 2007

Tools for translational epigenetic studies involving formalin-fixed paraffin-embedded human tissue: applying the Infinium HumanMethyation450 Beadchip assay to large population-based studies

artículo científico publicado en 2015

Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk

artículo científico publicado en 2016

Use of aspirin and other nonsteroidal antiinflammatory medications in relation to prostate cancer risk

artículo científico publicado en 2010

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

artículo científico publicado en 2011

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

Lista de obras de Liesel FitzGerald

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

A three-protein biomarker panel assessed in diagnostic tissue predicts death from prostate cancer for men with localized disease

Analysis of recently identified prostate cancer susceptibility loci in a population-based study: associations with family history and clinical features

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis.

Association of TMPRSS2-ERG gene fusion with clinical characteristics and outcomes: results from a population-based study of prostate cancer

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

Clinical utility of five genetic variants for predicting prostate cancer risk and mortality

Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage

Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype?

Effect of MELANOTAN, [Nle(4), D-Phe(7)]-alpha-MSH, on melanin synthesis in humans with MC1R variant alleles

Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus ⬇️

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

Genetic variants in the LEPR, CRY1, RNASEL, IL4, and ARVCF genes are prognostic markers of prostate cancer-specific mortality

Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.

Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer

Genome-wide association study of prostate cancer-specific survival

Genome-wide linkage analyses of hereditary prostate cancer families with colon cancer provide further evidence for a susceptibility locus on 15q11-q14.

Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia

Germline missense variants in the BTNL2 gene are associated with prostate cancer susceptibility

Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases

Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

Identifying Genetic Risk Factors for Diabetic Macular Edema and the Response to Treatment

Interest in genetic testing among affected men from hereditary prostate cancer families and their unaffected male relatives

Investigation of the relationship between prostate cancer and MSMB and NCOA4 genetic variants and protein expression

Multiple novel prostate cancer susceptibility signals identified by fine-mapping of known risk loci among Europeans

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

Mutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity

National Cancer Institute Prostate Cancer Genetics Workshop

Novel Common Genetic Susceptibility Loci for Colorectal Cancer

Novel associations between blood DNA methylation and body mass index in middle-aged and older adults

Pharmacogenomic Biomarkers in Docetaxel Treatment of Prostate Cancer: From Discovery to Implementation

Prediction of individual genetic risk to prostate cancer using a polygenic score

Prostate cancer risk regions at 8q24 and 17q24 are differentially associated with somatic TMPRSS2:ERG fusion status

Reliability of DNA methylation measures from dried blood spots and mononuclear cells using the HumanMethylation450k BeadArray

Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk: a replication study in an ethnically homogeneous population

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

Testing the circadian gene hypothesis in prostate cancer: a population-based case-control study

The advantages of dense marker sets for linkage analysis with very large families.

Tools for translational epigenetic studies involving formalin-fixed paraffin-embedded human tissue: applying the Infinium HumanMethyation450 Beadchip assay to large population-based studies

Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk

Use of aspirin and other nonsteroidal antiinflammatory medications in relation to prostate cancer risk

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

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