Lista de obras -

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

artículo científico publicado en 2014

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2011

A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis

artículo científico publicado en 2014

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

artículo científico publicado en 2010

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

artículo científico publicado en 2012

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

artículo científico publicado en 2020

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

Analysis of the Chemotherapy-Free Interval following Image-Guided Ablation in Sarcoma Patients

artículo científico publicado en 2020

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

artículo científico publicado en 2015

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

artículo científico publicado en 2021

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

artículo científico publicado en 2010

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

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

artículo científico publicado en 2011

Composite likelihood-based meta-analysis of breast cancer association studies.

artículo científico publicado en 2011

Exome sequence read depth methods for identifying copy number changes

artículo científico publicado en 2014

Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.

artículo científico publicado en 2012

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

artículo científico publicado en 2014

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

artículo científico publicado en 2013

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

Genome-wide association study of germline variants and breast cancer-specific mortality

artículo científico publicado en 2019

Genomic Landscape of Uterine Sarcomas Defined through Prospective Clinical Sequencing

scientific article published on 16 April 2020

Genomic Profiling Identifies Association of IDH1/IDH2 Mutation with Longer Relapse-Free and Metastasis-Free Survival in High-Grade Chondrosarcoma

scientific article published on 15 October 2019

Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women

artículo científico publicado en 2017

HLA Genotyping in Synovial Sarcoma: Identifying HLA-A*02 and its Association with Clinical Outcome

artículo científico publicado en 2020

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

artículo científico publicado en 2016

Identification of inherited genetic variations influencing prognosis in early-onset breast cancer

scientific journal article

Long-term Follow-up and Patterns of Response, Progression, and Hyperprogression in Patients after PD-1 Blockade in Advanced Sarcoma

artículo científico publicado en 2022

Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations

artículo científico publicado en 2014

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

artículo científico publicado en 2021

Meta-analysis of three genome-wide association studies identifies two loci that predict survival and treatment outcome in breast cancer

artículo científico publicado en 2017

Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis

scientific article published on 26 November 2008

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

artículo científico publicado en 2016

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

artículo científico publicado en 2019

Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy

artículo científico publicado en 2015

Prediction and clinical utility of a contralateral breast cancer risk model

scientific article published on 17 December 2019

Prediction of breast cancer risk based on profiling with common genetic variants

artículo científico publicado en 2015

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

artículo científico publicado en 2014

Safety and Efficacy of Hepatic Artery Embolization in Treating Solitary Fibrous Tumor Metastatic to the Liver

artículo científico publicado en 2019

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients

artículo científico publicado en 2015

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Two truncating variants in FANCC and breast cancer risk

artículo científico publicado en 2019

Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations

artículo científico publicado en 2015

Lista de obras de

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

Analysis of the Chemotherapy-Free Interval following Image-Guided Ablation in Sarcoma Patients

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

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

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

Composite likelihood-based meta-analysis of breast cancer association studies.

Exome sequence read depth methods for identifying copy number changes

Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Genome-wide association study of germline variants and breast cancer-specific mortality

Genomic Landscape of Uterine Sarcomas Defined through Prospective Clinical Sequencing

Genomic Profiling Identifies Association of IDH1/IDH2 Mutation with Longer Relapse-Free and Metastasis-Free Survival in High-Grade Chondrosarcoma

Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women

HLA Genotyping in Synovial Sarcoma: Identifying HLA-A*02 and its Association with Clinical Outcome

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

Identification of inherited genetic variations influencing prognosis in early-onset breast cancer

Long-term Follow-up and Patterns of Response, Progression, and Hyperprogression in Patients after PD-1 Blockade in Advanced Sarcoma

Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

Meta-analysis of three genome-wide association studies identifies two loci that predict survival and treatment outcome in breast cancer

Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis

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

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy

Prediction and clinical utility of a contralateral breast cancer risk model

Prediction of breast cancer risk based on profiling with common genetic variants

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

Safety and Efficacy of Hepatic Artery Embolization in Treating Solitary Fibrous Tumor Metastatic to the Liver

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

Two truncating variants in FANCC and breast cancer risk

Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populations