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Telomere Length Is Predictive of Breast Cancer Risk in BRCA2 Mutation Carriers

Cancer epidemiology, biomarkers & prevention, 2017-08, Vol.26 (8), p.1248-1254

2017

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Linkage of DNA Methylation Quantitative Trait Loci to Human Cancer Risk

Cell reports (Cambridge), 2014-04, Vol.7 (2), p.331-338

2014

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Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

Breast cancer research and treatment, 2011-12, Vol.130 (3), p.905-916

2011

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Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Nature (London), 2016-06, Vol.534 (7605), p.47-54

2016

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The topography of mutational processes in breast cancer genomes

Nature communications, 2016-05, Vol.7 (1), p.11383-11, Article 11383

2016

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Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

Cancer research (Chicago, Ill.), 2017-09, Vol.77 (18), p.4755-4762

2017

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DLC-1 gene inhibits human breast cancer cell growth and in vivo tumorigenicity

Oncogene, 2003-01, Vol.22 (3), p.445-450

2003

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Cytogenetic polyclonality of breast carcinomas: Association with Clinico-Pathological Characteristics and Outcome

Genes chromosomes & cancer, 2011-11, Vol.50 (11), p.930-939

2011

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DNA methylation profiling in breast cancer discordant identical twins identifies DOK7 as novel epigenetic biomarker

Carcinogenesis (New York), 2013-01, Vol.34 (1), p.102-108

2013

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Germline Brca2 heterozygosity promotes Kras(G12D) -driven carcinogenesis in a murine model of familial pancreatic cancer

Cancer cell, 2010-11, Vol.18 (5), p.499

2010

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Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers

British journal of cancer, 2016-09, Vol.115 (7), p.776-783

2016

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Epigenetic silencing and deletion of the BRCA1 gene in sporadic breast cancer

Breast cancer research : BCR, 2006-01, Vol.8 (4), p.R38-R38

2006

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A comprehensive DNA methylation profile of epithelial-to-mesenchymal transition

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19), p.5608-5619

2014

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The Icelandic founder mutation BRCA2 999del5: analysis of expression

Breast cancer research : BCR, 2004-01, Vol.6 (4), p.R284-R290, Article R284

2004

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Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome

PloS one, 2014-06, Vol.9 (6), p.e98229-e98229

2014

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BRCA1 Promoter Methylation Status in 1031 Primary Breast Cancers Predicts Favorable Outcomes Following Chemotherapy

JNCI cancer spectrum, 2020-04, Vol.4 (2), p.pkz100-pkz100

2020

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Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Nature (London), 2019-02, Vol.566 (7742), p.E1-E1

2019

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Population-Based Study of Changing Breast Cancer Risk in Icelandic BRCA2 Mutation Carriers, 1920–2000

JNCI : Journal of the National Cancer Institute, 2006-01, Vol.98 (2), p.116-122

2006

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Tumour diploidy and survival in breast cancer patients with BRCA2 mutations

Breast cancer research and treatment, 2013-07, Vol.140 (2), p.375-384

2013

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Genomic and phenotypic analysis of BRCA2 mutated breast cancers reveals co-occurring changes linked to progression

Breast cancer research : BCR, 2011-09, Vol.13 (5), p.R95-R95

2011

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Inbreeding and homozygosity in breast cancer survival

Scientific reports, 2015-11, Vol.5 (1), p.16467-16467, Article 16467

2015

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Aurora A is a prognostic marker for breast cancer arising in BRCA2 mutation carriers

The journal of pathology. Clinical research, 2015-01, Vol.1 (1), p.33-40

2015

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GSTM1, GSTT1, and GSTP1 Genotypes in Relation to Breast Cancer Risk and Frequency of Mutations in the p53 Gene

Cancer epidemiology, biomarkers & prevention, 2001-11, Vol.10 (11), p.1169-1173

2001

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BRCA2mutation carriers, reproductive factors and breast cancer risk

Breast cancer research : BCR, 2003-10, Vol.5 (5), Article R121

2003

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Telomere Length Is Predictive of Breast Cancer Risk in BRCA2 Mutation Carriers

Linkage of DNA Methylation Quantitative Trait Loci to Human Cancer Risk

Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

Landscape of somatic mutations in 560 breast cancer whole-genome sequences

HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures

The topography of mutational processes in breast cancer genomes

Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

DLC-1 gene inhibits human breast cancer cell growth and in vivo tumorigenicity

Cytogenetic polyclonality of breast carcinomas: Association with Clinico-Pathological Characteristics and Outcome

DNA methylation profiling in breast cancer discordant identical twins identifies DOK7 as novel epigenetic biomarker

Germline Brca2 heterozygosity promotes Kras(G12D) -driven carcinogenesis in a murine model of familial pancreatic cancer

Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers

Epigenetic silencing and deletion of the BRCA1 gene in sporadic breast cancer

A comprehensive DNA methylation profile of epithelial-to-mesenchymal transition

The Icelandic founder mutation BRCA2 999del5: analysis of expression

Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome

BRCA1 Promoter Methylation Status in 1031 Primary Breast Cancers Predicts Favorable Outcomes Following Chemotherapy

Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Population-Based Study of Changing Breast Cancer Risk in Icelandic BRCA2 Mutation Carriers, 1920–2000

Tumour diploidy and survival in breast cancer patients with BRCA2 mutations

Genomic and phenotypic analysis of BRCA2 mutated breast cancers reveals co-occurring changes linked to progression

Inbreeding and homozygosity in breast cancer survival

Aurora A is a prognostic marker for breast cancer arising in BRCA2 mutation carriers

GSTM1, GSTT1, and GSTP1 Genotypes in Relation to Breast Cancer Risk and Frequency of Mutations in the p53 Gene

BRCA2mutation carriers, reproductive factors and breast cancer risk

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