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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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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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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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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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Germline Brca2 Heterozygosity Promotes KrasG12D -Driven Carcinogenesis in a Murine Model of Familial Pancreatic Cancer

Cancer cell, 2010-11, Vol.18 (5), p.499-509

2010

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Breastfeeding and Reduced Risk of Breast Cancer in an Icelandic Cohort Study

American journal of epidemiology, 2001-07, Vol.154 (1), p.37-42

2001

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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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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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Positive association between DNA strand breaks in peripheral blood mononuclear cells and polyunsaturated fatty acids in red blood cells from women

Nutrition and cancer, 2007-01, Vol.59 (1), p.21-28

2007

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Population-based study of risk of breast cancer in carriers of BRCA2 mutation

The Lancet (British edition), 1998-10, Vol.352 (9137), p.1337-1339

1998

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Somatic p53 mutations in human breast carcinomas in an Icelandic population : a prognostic factor

Cancer research (Chicago, Ill.), 1993-04, Vol.53 (7), p.1637-1641

1993

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BRCA2 Haploinsufficiency in Telomere Maintenance

Genes, 2021-12, Vol.13 (1), p.83

2021

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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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Abstract 3307: BRCA1 promoter methylation analyzed in 1032 primary breast cancers predicts favorable response to chemotherapy independently of p53 mutations

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.3307-3307

2018

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A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

Nature genetics, 1996-05, Vol.13 (1), p.117-119

1996

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Dysfunctional telomeres in human BRCA2 mutated breast tumors and cell lines

Mutation research, 2012-01, Vol.729 (1-2), p.90-99

2012

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Combined effect of low-penetrant SNPs on breast cancer risk

British journal of cancer, 2012-01, Vol.106 (2), p.389-396

2012

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MYC amplification and TERT expression in breast tumor progression

Cancer genetics and cytogenetics, 2007-07, Vol.176 (2), p.93-99

2007

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

Breast cancer research : BCR, 2009-01, Vol.11 (5), p.404-404

2009

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Linkage of DNA methylation quantitative trait loci to human cancer risk

Cell reports (Cambridge), 2014-04

2014

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Linkage of DNA methylation quantitative trait loci to human cancer risk

Cell reports (Cambridge), 2014-04

2014

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Genomic and phenotypic analysis of BRCA2mutated breast cancers reveals co-occurring changes linked to progression

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

2011

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Centriole movements in mammalian epithelial cells during cytokinesis

BMC cell biology, 2010-05, Vol.11 (1), p.34, Article 34

2010

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Abstract 3371: Analysis of telomere length and dysfunction in normal breast tissue from BRCA2 mutation carriers

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.3371-3371

2018

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

Aurora-A amplification associated with BRCA2 mutation in breast tumours

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

AURKA and breast cancer in BRCA1/2 mutation carriers

Germline Brca2 Heterozygosity Promotes KrasG12D -Driven Carcinogenesis in a Murine Model of Familial Pancreatic Cancer

Breastfeeding and Reduced Risk of Breast Cancer in an Icelandic Cohort Study

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

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

Positive association between DNA strand breaks in peripheral blood mononuclear cells and polyunsaturated fatty acids in red blood cells from women

Population-based study of risk of breast cancer in carriers of BRCA2 mutation

Somatic p53 mutations in human breast carcinomas in an Icelandic population : a prognostic factor

BRCA2 Haploinsufficiency in Telomere Maintenance

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

Abstract 3307: BRCA1 promoter methylation analyzed in 1032 primary breast cancers predicts favorable response to chemotherapy independently of p53 mutations

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes

Dysfunctional telomeres in human BRCA2 mutated breast tumors and cell lines

Combined effect of low-penetrant SNPs on breast cancer risk

MYC amplification and TERT expression in breast tumor progression

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

Linkage of DNA methylation quantitative trait loci to human cancer risk

Linkage of DNA methylation quantitative trait loci to human cancer risk

Genomic and phenotypic analysis of BRCA2mutated breast cancers reveals co-occurring changes linked to progression

Centriole movements in mammalian epithelial cells during cytokinesis

Abstract 3371: Analysis of telomere length and dysfunction in normal breast tissue from BRCA2 mutation carriers

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