Lista de obras -

A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus

artículo científico publicado en 2017

A common 8q24 variant in prostate and breast cancer from a large nested case-control study

artículo científico publicado en 2007

A comprehensive analysis of the androgen receptor gene and risk of breast cancer: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2006

A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer

artículo científico publicado en 2014

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

artículo científico publicado en 2012

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

artículo científico publicado en 2007

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 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 new era for treatment development in HER2-positive breast cancer

artículo científico publicado en 2018

A polymorphism in the 3' untranslated region of the gene encoding prostaglandin endoperoxide synthase 2 is not associated with an increase in breast cancer risk: a nested case-control study

artículo científico publicado en 2007

AACR Special Conference: SNPs, haplotypes, and cancer - applications in molecular epidemiology, Key Biscayne, Florida, USA, 13-17 September 2003

artículo científico publicado en 2004

ATM haplotypes and cellular response to DNA damage: association with breast cancer risk and clinical radiosensitivity

artículo científico publicado en 2003

Abstract LB-272: Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma

Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques

artículo científico publicado en 2005

Active and passive cigarette smoking and breast cancer risk: Results from the EPIC cohort

artículo científico publicado en 2014

Adiposity, hormone replacement therapy use and breast cancer risk by age and hormone receptor status: a large prospective cohort study

artículo científico publicado en 2012

Age at cancer onset in germline TP53 mutation carriers: association with polymorphisms in predicted G-quadruplex structures

artículo científico publicado en 2013

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

artículo científico publicado en 2015

Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes

artículo científico publicado en 2017

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

artículo científico publicado en 2017

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association between TP53 R249S mutation and polymorphisms in TP53 intron 1 in hepatocellular carcinoma

artículo científico publicado en 2013

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States

artículo científico publicado en 2016

Breast cancer susceptibility loci and mammographic density

artículo científico publicado en 2008

CYP17 genetic variation and risk of breast and prostate cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2007

Common genetic variants in prostate cancer risk prediction--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)

artículo científico publicado en 2012

Common genetic variation in IGF1, IGFBP-1, and IGFBP-3 in relation to mammographic density: a cross-sectional study

artículo científico publicado en 2007

Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma

artículo científico publicado en 2012

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

artículo científico publicado en 2011

Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium

artículo científico publicado en 2010

Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort

artículo científico publicado en 2017

Determinants of folate and vitamin B12 plasma levels in the French E3N-EPIC cohort

artículo científico publicado en 2016

Dietary fat intake and development of specific breast cancer subtypes

artículo científico publicado en 2014

Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

artículo científico publicado en 2009

GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients

artículo científico publicado en 2016

Gene x Gene interaction between MnSOD and GPX-1 and breast cancer risk: a nested case-control study

artículo científico publicado en 2006

Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2009

Genetic variability of the mTOR pathway and prostate cancer risk in the European Prospective Investigation on Cancer (EPIC).

artículo científico publicado en 2011

Genetic variation at the CYP19A1 locus predicts circulating estrogen levels but not breast cancer risk in postmenopausal women

artículo científico publicado en 2007

Genetic variation in DNA repair pathway genes and premenopausal breast cancer risk

artículo científico publicado en 2008

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

artículo científico publicado en 2016

Genome-Wide Association Study of Event-Free Survival in Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy

artículo científico publicado en 2015

Genome-wide association studies and the clinic: a focus on breast cancer

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Genome-wide association study identifies novel breast cancer susceptibility loci

artículo científico publicado en 2007

Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women

artículo científico publicado en 2012

Genome-wide association study of prostate cancer-specific survival

artículo científico publicado en 2015

HLA class I and II diversity contributes to the etiologic heterogeneity of non-Hodgkin lymphoma subtypes.

artículo científico publicado en 2018

Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer

artículo científico publicado en 2005

Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies

artículo científico publicado en 2006

Haplotypes of the estrogen receptor beta gene and breast cancer risk

artículo científico publicado en 2008

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

artículo científico publicado en 2008

IGF-1, IGFBP-1, and IGFBP-3 polymorphisms predict circulating IGF levels but not breast cancer risk: findings from the Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2008

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Impact of Body Mass Index, Age, Prostate Volume, and Genetic Polymorphisms on Prostate-specific Antigen Levels in a Control Population.

artículo científico publicado en 2016

Influence of multiple APOE genetic variants on cognitive function in a cohort of older men - results from the Normative Aging Study

artículo científico publicado en 2014

Interactions between genome-wide significant genetic variants and circulating concentrations of insulin-like growth factor 1, sex hormones, and binding proteins in relation to prostate cancer risk in the National Cancer Institute Breast and Prostate

artículo científico publicado en 2012

Large-scale evaluation of genetic variants in candidate genes for colorectal cancer risk in the Nurses' Health Study and the Health Professionals' Follow-up Study.

artículo científico publicado en 2008

Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma

artículo científico publicado en 2017

Mannose-binding lectin 2 gene and risk of adult glioma

artículo científico publicado en 2013

Mitochondrial haplogroups modify the effect of black carbon on age-related cognitive impairment

artículo científico publicado en 2014

N-Acetyltransferase 2 Polymorphisms, Tobacco Smoking, and Breast Cancer Risk in the Breast and Prostate Cancer Cohort Consortium ⬇️

artículo científico publicado el 10 de noviembre de 2011

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

artículo científico publicado en 2009

No association between BRCA2 N372H and breast cancer risk

artículo científico publicado en 2005

No association between GPX1 Pro198Leu and breast cancer risk

artículo científico publicado en 2004

PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).

artículo científico publicado en 2009

Performance of common genetic variants in breast-cancer risk models

artículo científico publicado en 2010

Polymorphisms in the ICAM gene locus are not associated with breast cancer Risk

artículo científico publicado en 2006

Polymorphisms in xenobiotic metabolizing genes, intakes of heterocyclic amines and red meat, and postmenopausal breast cancer

artículo científico publicado en 2013

Polymorphisms of the AURKA (STK15/Aurora Kinase) Gene and Breast Cancer Risk (United States).

artículo científico publicado en 2006

Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women

artículo científico publicado en 2014

Prediagnostic plasma IgE levels and risk of adult glioma in four prospective cohort studies

artículo científico publicado en 2011

Renin-angiotensin system polymorphisms and risk of hypertension: influence of environmental factors

artículo científico publicado en 2008

Single-nucleotide polymorphisms of allergy-related genes and risk of adult glioma

artículo científico publicado en 2013

Study designs for genome-wide association studies

artículo científico publicado en 2008

T.I.M.S: TaqMan Information Management System, tools to organize data flow in a genotyping laboratory

artículo científico publicado en 2005

TGFB1 and TGFBR1 polymorphisms and breast cancer risk in the Nurses' Health Study

artículo científico publicado en 2007

Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2

artículo científico publicado en 2015

The XRCC1 -77T->C variant: haplotypes, breast cancer risk, response to radiotherapy and the cellular response to DNA damage.

artículo científico publicado en 2006

The erbB2/HER2/neu receptor polymorphism Ile655Val and breast cancer risk

artículo científico publicado en 2005

The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk

artículo científico publicado en 2009

The p53 Arg72Pro and MDM2 -309 polymorphisms and risk of breast cancer in the nurses' health studies.

artículo científico publicado en 2007

The p53 codon 72 polymorphism, sunburns, and risk of skin cancer in US Caucasian women

artículo científico publicado en 2006

The role of microRNA-binding site polymorphisms in DNA repair genes as risk factors for bladder cancer and breast cancer and their impact on radiotherapy outcomes ⬇️

artículo científico publicado en 2011

The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

artículo científico publicado en 2011

Therogenetics: transferring GWAS technology to the clinic

artículo científico publicado en 2015

Vitamin D receptor polymorphisms and breast cancer risk: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium

artículo científico publicado en 2009

Lista de obras de

A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus

A common 8q24 variant in prostate and breast cancer from a large nested case-control study

A comprehensive analysis of the androgen receptor gene and risk of breast cancer: results from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer

A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation

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

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

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

A new era for treatment development in HER2-positive breast cancer

A polymorphism in the 3' untranslated region of the gene encoding prostaglandin endoperoxide synthase 2 is not associated with an increase in breast cancer risk: a nested case-control study

AACR Special Conference: SNPs, haplotypes, and cancer - applications in molecular epidemiology, Key Biscayne, Florida, USA, 13-17 September 2003

ATM haplotypes and cellular response to DNA damage: association with breast cancer risk and clinical radiosensitivity

Abstract LB-272: Genome-wide association study identifies multiple susceptibility loci for diffuse large B-cell lymphoma

Accounting for haplotype uncertainty in matched association studies: a comparison of simple and flexible techniques

Active and passive cigarette smoking and breast cancer risk: Results from the EPIC cohort

Adiposity, hormone replacement therapy use and breast cancer risk by age and hormone receptor status: a large prospective cohort study

Age at cancer onset in germline TP53 mutation carriers: association with polymorphisms in predicted G-quadruplex structures

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

Association analysis identifies 65 new breast cancer risk loci.

Association between TP53 R249S mutation and polymorphisms in TP53 intron 1 in hepatocellular carcinoma

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

Breast Cancer Risk From Modifiable and Nonmodifiable Risk Factors Among White Women in the United States

Breast cancer susceptibility loci and mammographic density

CYP17 genetic variation and risk of breast and prostate cancer from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

Common genetic variants in prostate cancer risk prediction--results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)

Common genetic variation in IGF1, IGFBP-1, and IGFBP-3 in relation to mammographic density: a cross-sectional study

Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium

Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort

Determinants of folate and vitamin B12 plasma levels in the French E3N-EPIC cohort

Dietary fat intake and development of specific breast cancer subtypes

Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients

Gene x Gene interaction between MnSOD and GPX-1 and breast cancer risk: a nested case-control study

Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3).

Genetic variability of the mTOR pathway and prostate cancer risk in the European Prospective Investigation on Cancer (EPIC).

Genetic variation at the CYP19A1 locus predicts circulating estrogen levels but not breast cancer risk in postmenopausal women

Genetic variation in DNA repair pathway genes and premenopausal breast cancer risk

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

Genome-Wide Association Study of Event-Free Survival in Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy

Genome-wide association studies and the clinic: a focus on breast cancer

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

Genome-wide association study identifies novel breast cancer susceptibility loci

Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women

Genome-wide association study of prostate cancer-specific survival

HLA class I and II diversity contributes to the etiologic heterogeneity of non-Hodgkin lymphoma subtypes.

Haplotype analysis of common variants in the BRCA1 gene and risk of sporadic breast cancer

Haplotype analysis of the HSD17B1 gene and risk of breast cancer: a comprehensive approach to multicenter analyses of prospective cohort studies

Haplotypes of the estrogen receptor beta gene and breast cancer risk

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

IGF-1, IGFBP-1, and IGFBP-3 polymorphisms predict circulating IGF levels but not breast cancer risk: findings from the Breast and Prostate Cancer Cohort Consortium (BPC3).

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Impact of Body Mass Index, Age, Prostate Volume, and Genetic Polymorphisms on Prostate-specific Antigen Levels in a Control Population.

Influence of multiple APOE genetic variants on cognitive function in a cohort of older men - results from the Normative Aging Study

Interactions between genome-wide significant genetic variants and circulating concentrations of insulin-like growth factor 1, sex hormones, and binding proteins in relation to prostate cancer risk in the National Cancer Institute Breast and Prostate

Large-scale evaluation of genetic variants in candidate genes for colorectal cancer risk in the Nurses' Health Study and the Health Professionals' Follow-up Study.

Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma

Mannose-binding lectin 2 gene and risk of adult glioma

Mitochondrial haplogroups modify the effect of black carbon on age-related cognitive impairment

N-Acetyltransferase 2 Polymorphisms, Tobacco Smoking, and Breast Cancer Risk in the Breast and Prostate Cancer Cohort Consortium ⬇️

Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

No association between BRCA2 N372H and breast cancer risk

No association between GPX1 Pro198Leu and breast cancer risk

PTGS2 and IL6 genetic variation and risk of breast and prostate cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3).

Performance of common genetic variants in breast-cancer risk models

Polymorphisms in the ICAM gene locus are not associated with breast cancer Risk

Polymorphisms in xenobiotic metabolizing genes, intakes of heterocyclic amines and red meat, and postmenopausal breast cancer

Polymorphisms of the AURKA (STK15/Aurora Kinase) Gene and Breast Cancer Risk (United States).

Post-GWAS gene-environment interplay in breast cancer: results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79,000 women

Prediagnostic plasma IgE levels and risk of adult glioma in four prospective cohort studies

Renin-angiotensin system polymorphisms and risk of hypertension: influence of environmental factors

Single-nucleotide polymorphisms of allergy-related genes and risk of adult glioma

Study designs for genome-wide association studies

T.I.M.S: TaqMan Information Management System, tools to organize data flow in a genotyping laboratory

TGFB1 and TGFBR1 polymorphisms and breast cancer risk in the Nurses' Health Study

Targeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2