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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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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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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 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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Prostate Cancer Progression and Survival in BRCA2 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2007-06, Vol.99 (12), p.929-935

2007

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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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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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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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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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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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Consortium study on 1280 breast carcinomas : Allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters

Cancer research (Chicago, Ill.), 1998-03, Vol.58 (5), p.1004-1012

1998

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Screening for germ line TP53 mutations in breast cancer patients

Cancer research (Chicago, Ill.), 1992-06, Vol.52 (11), p.3234-3236

1992

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Age at Menarche and Menopause and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study

Cancer epidemiology, biomarkers & prevention, 2007-04, Vol.16 (4), p.740-746

2007

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p53 abnormalities and genomic instability in primary human breast carcinomas

Cancer research (Chicago, Ill.), 1995-02, Vol.55 (3), p.646-651

1995

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Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma

The Journal of pathology, 1999-12, Vol.189 (4), p.504-513

1999

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p53 Abnormality and Chromosomal Instability in the Same Breast Tumor Cells

Cancer genetics and cytogenetics, 2000-09, Vol.121 (2), p.150-155

2000

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Male breast cancer in Iceland

International journal of cancer, 1996-02, Vol.65 (4), p.446-449

1996

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TP53 Abnormalities and Genetic Instability in Breast Cancer

Acta oncologica, 1995, Vol.34 (5), p.663-667

1995

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Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization

Cancer genetics and cytogenetics, 1996-05, Vol.88 (1), p.1-7

1996

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Molecular genetics and cytogenetics of breast carcinomas: Comparison of the two methods

Cancer genetics and cytogenetics, 1996-11, Vol.92 (1), p.37-42

1996

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

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

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

Prostate Cancer Progression and Survival in BRCA2 Mutation Carriers

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

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

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

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

Combined effect of low-penetrant SNPs on breast cancer risk

Consortium study on 1280 breast carcinomas : Allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters

Screening for germ line TP53 mutations in breast cancer patients

Age at Menarche and Menopause and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study

p53 abnormalities and genomic instability in primary human breast carcinomas

Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma

p53 Abnormality and Chromosomal Instability in the Same Breast Tumor Cells

Male breast cancer in Iceland

TP53 Abnormalities and Genetic Instability in Breast Cancer

Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization

Molecular genetics and cytogenetics of breast carcinomas: Comparison of the two methods

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