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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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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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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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Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes

Breast cancer research : BCR, 2009-01, Vol.11 (4), p.R47-R47

2009

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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 DNA methylation-based definition of biologically distinct breast cancer subtypes

Molecular oncology, 2015-03, Vol.9 (3), p.555-568

2015

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Breast cancer risk factors and age at diagnosis: An Icelandic cohort study

International journal of cancer, 2002-04, Vol.98 (4), p.604-608

2002

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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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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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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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The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

Clinical cancer research, 2006-02, Vol.12 (4), p.1157-1167

2006

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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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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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A candidate CpG SNP approach identifies a breast cancer associated ESR1‐SNP

International journal of cancer, 2011-10, Vol.129 (7), p.1689-1698

2011

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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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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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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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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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Tetraploidy in BRCA2 breast tumours

European journal of cancer (1990), 2012-02, Vol.48 (3), p.305-310

2012

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Breast cancer risk associated with AURKA 91T → A polymorphism in relation to BRCA mutations

Cancer letters, 2007-06, Vol.250 (2), p.206-212

2007

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Aurora-A amplification associated with BRCA2 mutation in breast tumours

Cancer letters, 2007-04, Vol.248 (1), p.96-102

2007

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AURKA and breast cancer in BRCA1/2 mutation carriers

Cancer epidemiology, biomarkers & prevention, 2007-11, Vol.16 (11), p.2517-2517

2007

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BRCA2 and p53 mutations in primary breast cancer in relation to genetic instability

Cancer research (Chicago, Ill.), 1998-03, Vol.58 (5), p.859-862

1998

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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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BRCA2 mutation carriers, reproductive factors and breast cancer risk

Breast cancer research : BCR, 2003, Vol.5 (5), p.R121-R128

2003

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

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

Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes

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

A DNA methylation-based definition of biologically distinct breast cancer subtypes

Breast cancer risk factors and age at diagnosis: An Icelandic cohort study

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

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

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

The clinical value of somatic TP53 gene mutations in 1,794 patients with breast cancer

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

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

A candidate CpG SNP approach identifies a breast cancer associated ESR1‐SNP

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

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

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

Tumour diploidy and survival in breast cancer patients with BRCA2 mutations

Tetraploidy in BRCA2 breast tumours

Breast cancer risk associated with AURKA 91T → A polymorphism in relation to BRCA mutations

Aurora-A amplification associated with BRCA2 mutation in breast tumours

AURKA and breast cancer in BRCA1/2 mutation carriers

BRCA2 and p53 mutations in primary breast cancer in relation to genetic instability

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

BRCA2 mutation carriers, reproductive factors and breast cancer risk

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