Lista de obras -

A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

artículo científico publicado en 2015

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

artículo científico publicado en 2005

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

artículo científico publicado en 2014

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 transposon-based genetic screen in mice identifies genes altered in colorectal cancer

artículo científico publicado en 2009

AA9int: SNP interaction pattern search using non-hierarchical additive model set

Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers

artículo científico publicado en 2016

Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study

artículo científico publicado en 2016

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families

artículo científico publicado en 2012

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome

artículo científico publicado en 2015

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

artículo científico publicado en 2016

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

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

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

scholarly article published in Nature Genetics

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

scientific article published in Nature Communications

Blood lipids and prostate cancer: a Mendelian randomization analysis

artículo científico publicado en 2016

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers

artículo científico publicado en 2011

Cancer risks for MLH1 and MSH2 mutation carriers

artículo científico publicado en 2013

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

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study

artículo científico publicado en 2012

Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2007

Determining the frequency of de novo germline mutations in DNA mismatch repair genes

artículo científico publicado en 2011

Efficient recovery of proteins from multiple source samples after TRIzol(®) or TRIzol(®)LS RNA extraction and long-term storage.

artículo científico publicado en 2013

Evaluation of a new high-dimensional miRNA profiling platform

artículo científico publicado en 2009

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

artículo científico publicado en 2013

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.

artículo científico publicado en 2013

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

artículo científico publicado en 2018

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

artículo científico publicado en 2014

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

artículo científico publicado en 2016

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

artículo científico publicado en 2018

Gene networks and microRNAs implicated in aggressive prostate cancer

artículo científico publicado en 2009

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 of prostate cancer-specific survival

artículo científico publicado en 2015

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

artículo científico publicado en 2010

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

artículo científico publicado en 2009

Germline variation at 8q24 and prostate cancer risk in men of European ancestry

artículo científico publicado en 2018

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

artículo científico publicado en 2012

Human colon cancer profiles show differential microRNA expression depending on mismatch repair status and are characteristic of undifferentiated proliferative states

artículo científico publicado en 2009

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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

Investigating the possible causal role of coffee consumption with prostate cancer risk and progression using Mendelian randomization analysis

artículo científico publicado en 2016

Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium

artículo científico publicado en 2008

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

artículo científico publicado en 2015

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

artículo científico publicado en 2016

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

artículo científico publicado en 2007

Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium

artículo científico publicado en 2016

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

artículo científico publicado en 2006

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

artículo científico publicado en 2016

Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort

artículo científico publicado en 2016

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

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

Risks of Lynch syndrome cancers for MSH6 mutation carriers

artículo científico publicado en 2009

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives

artículo científico publicado en 2014

SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns

artículo científico publicado en 2017

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

artículo científico publicado en 2011

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

artículo científico publicado en 2015

Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

artículo científico publicado en 2021

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts

artículo científico publicado en 2016

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

gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels

artículo científico publicado en 2017

miRNA expression in colon polyps provides evidence for a multihit model of colon cancer

artículo científico publicado en 2011

Lista de obras de

A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

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

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

A transposon-based genetic screen in mice identifies genes altered in colorectal cancer

AA9int: SNP interaction pattern search using non-hierarchical additive model set

Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers

Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families

Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

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

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

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

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

Blood lipids and prostate cancer: a Mendelian randomization analysis

Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers

Cancer risks for MLH1 and MSH2 mutation carriers

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

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study

Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

Determining the frequency of de novo germline mutations in DNA mismatch repair genes

Efficient recovery of proteins from multiple source samples after TRIzol(®) or TRIzol(®)LS RNA extraction and long-term storage.

Evaluation of a new high-dimensional miRNA profiling platform

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.

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

Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

Gene networks and microRNAs implicated in aggressive prostate cancer

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 of prostate cancer-specific survival

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

Genome-wide transcriptional profiling reveals microRNA-correlated genes and biological processes in human lymphoblastoid cell lines

Germline variation at 8q24 and prostate cancer risk in men of European ancestry

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

Human colon cancer profiles show differential microRNA expression depending on mismatch repair status and are characteristic of undifferentiated proliferative states

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

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

Investigating the possible causal role of coffee consumption with prostate cancer risk and progression using Mendelian randomization analysis

Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium

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

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium

Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics

Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies

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

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer

Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants

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

Risks of Lynch syndrome cancers for MSH6 mutation carriers

Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives

SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns

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

Shared heritability and functional enrichment across six solid cancers

Shared heritability and functional enrichment across six solid cancers

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts

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)

gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels

miRNA expression in colon polyps provides evidence for a multihit model of colon cancer