Lista de obras -

11q13 is a susceptibility locus for hormone receptor positive breast cancer

artículo científico publicado en 2012

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

artículo científico publicado en 2012

A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations.

artículo científico publicado en 2019

A common coding variant in CASP8 is associated with breast cancer risk

article

Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe

artículo científico publicado en 2016

Apoptosis gene polymorphisms and risk of prostate cancer: a hospital-based study of German patients treated with brachytherapy

artículo científico publicado en 2011

Assessment of a FBXW8 frameshift mutation, c.1312_1313delGT, in breast cancer patients and controls from Central Europe

artículo científico publicado en 2017

Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer

artículo científico publicado en 2017

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association of ESR1 gene tagging SNPs with breast cancer risk

artículo científico publicado en 2009

Association of chromosomal locus 8q24 and risk of prostate cancer: A hospital-based study of German patients treated with brachytherapy

article

Association of genomic variants at the Human Leukocyte Antigen locus with cervical cancer risk, HPV status, and gene expression

artículo científico publicado en 2020

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

artículo científico publicado en 2012

CYP2B6*6 is associated with increased breast cancer risk

artículo científico publicado en 2013

Candidate gene variants of the immune system and sudden infant death syndrome.

artículo científico publicado en 2016

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

artículo científico publicado en 2011

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

artículo científico publicado en 2012

Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

scholarly article published in Nature Genetics

Evidence for an association of interferon gene variants with sudden infant death syndrome

artículo científico publicado en 2019

Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

artículo científico publicado en 2018

Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

scientific article published on 21 November 2019

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

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

artículo científico publicado en 2009

Genetic association study of fatal pulmonary embolism

artículo científico publicado en 2020

Genome-wide association analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

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 identifies novel breast cancer susceptibility loci

artículo científico publicado en 2007

Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome

artículo científico publicado en 2012

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

artículo científico publicado en 2008

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Limited role of interferon-kappa (IFNK) truncating mutations in common variable immunodeficiency

artículo científico publicado en 2017

Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls

artículo científico publicado en 2010

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

artículo científico publicado en 2008

Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer

artículo científico publicado en 2012

Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer

artículo científico publicado en 2014

NBS1 variant I171V and breast cancer risk

scientific article published on 30 November 2007

Neuregulin-1 high-producer genotype is associated with a decreased risk of admission to the neonatal intensive care unit

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Nijmegen Breakage Syndrome mutations and risk of breast cancer

artículo científico publicado en 2008

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

artículo científico publicado en 2019

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

artículo científico publicado en 2015

Rare ATAD5 missense variants in breast and ovarian cancer patients

artículo científico publicado en 2016

Lista de obras de

11q13 is a susceptibility locus for hormone receptor positive breast cancer

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations.

A common coding variant in CASP8 is associated with breast cancer risk

Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe

Apoptosis gene polymorphisms and risk of prostate cancer: a hospital-based study of German patients treated with brachytherapy

Assessment of a FBXW8 frameshift mutation, c.1312_1313delGT, in breast cancer patients and controls from Central Europe

Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer

Association analysis identifies 65 new breast cancer risk loci.

Association of ESR1 gene tagging SNPs with breast cancer risk

Association of chromosomal locus 8q24 and risk of prostate cancer: A hospital-based study of German patients treated with brachytherapy

Association of genomic variants at the Human Leukocyte Antigen locus with cervical cancer risk, HPV status, and gene expression

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

CYP2B6*6 is associated with increased breast cancer risk

Candidate gene variants of the immune system and sudden infant death syndrome.

Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

Evidence for an association of interferon gene variants with sudden infant death syndrome

Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene

Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

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

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

Genetic association study of fatal pulmonary embolism

Genome-wide association analysis identifies three new breast cancer susceptibility loci

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

Genome-wide association study identifies novel breast cancer susceptibility loci

Germline variation in TP53 regulatory network genes associates with breast cancer survival and treatment outcome

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

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

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

Limited role of interferon-kappa (IFNK) truncating mutations in common variable immunodeficiency

Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls

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

Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer

Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer

NBS1 variant I171V and breast cancer risk

Neuregulin-1 high-producer genotype is associated with a decreased risk of admission to the neonatal intensive care unit

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

Nijmegen Breakage Syndrome mutations and risk of breast cancer

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

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

Rare ATAD5 missense variants in breast and ovarian cancer patients