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Tumour biological features of BRCA1-induced breast and ovarian cancer

European journal of cancer (1990), 1997-03, Vol.33 (3), p.362-371

1997

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Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations

Cancer research (Chicago, Ill.), 1997-04, Vol.57 (7), p.1222-1227

1997

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The effect of a single BRCA2 mutation on cancer in Iceland

Journal of medical genetics, 2002-07, Vol.39 (7), p.457-462

2002

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Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies

Journal of medical genetics, 2006-11, Vol.43 (11), p.856-862

2006

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High prevalence of the 999del5 mutation in Icelandic breast and ovarian cancer patients

Cancer research (Chicago, Ill.), 1996-08, Vol.56 (16), p.3663-3665

1996

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BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age

Journal of medical genetics, 2001-06, Vol.38 (6), p.361-368

2001

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Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations

British journal of cancer, 1995-09, Vol.72 (3), p.696-701

1995

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Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Icelandic families, and possible relationship to prostatic cancer

American journal of human genetics, 1993-04, Vol.52 (4), p.711-717

1993

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Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer

Journal of medical genetics, 2000-05, Vol.37 (5), p.342-347

2000

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Frequent occurrence of BRCA2 linkage in icelandic breast cancer families and segregation of a common BRCA2 haplotype

American journal of human genetics, 1996-04, Vol.58 (4), p.749-756

1996

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Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas

Cancer research (Chicago, Ill.), 1999-06, Vol.59 (11), p.2682-2689

1999

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Inherited BRCA2 mutation associated with high grade breast cancer

Breast cancer research and treatment, 1998, Vol.47 (2), p.121-127

1998

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

JNCI : Journal of the National Cancer Institute, 1998-08, Vol.90 (15), p.1138-1145

1998

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Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13

Cancer research (Chicago, Ill.), 1995-11, Vol.55 (21), p.4830-4832

1995

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Chromosome imbalance at the 3p14 region in human breast tumours: High frequency in patients with inherited predisposition due to BRCA2

European journal of cancer (1990), 1998-01, Vol.34 (1), p.142-147

1998

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A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland

Journal of medical genetics, 1998-06, Vol.35 (6), p.446-449

1998

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High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers

Oncogene, 1998-01, Vol.16 (1), p.21-26

1998

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Genetic heterogeneity of breast-ovarian cancer revisited

American journal of human genetics, 1995, Vol.57 (4), p.957-958

1995

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Somatic genetic alterations in BRCA2-associated and sporadic male breast cancer

Genes chromosomes & cancer, 1999-01, Vol.24 (1), p.56-61

1999

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High frequency of allelic imbalance at chromosome region 16q22‐23 in human breast cancer: Correlation with high pgr and low s phase

International journal of cancer, 1995-04, Vol.64 (2), p.112-116

1995

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High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4421-4425

1998

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European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables

British Journal of Cancer, 1999-05, Vol.80 (5-6), p.879-882

1999

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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Nature genetics, 2009-02, Vol.41 (2), p.221-227

2009

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Loss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regions

International journal of cancer, 1995-12, Vol.64 (6), p.378-382

1995

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Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

Human genetics, 1995-10, Vol.96 (4), p.437-443

1995

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Tumour biological features of BRCA1-induced breast and ovarian cancer

Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations

The effect of a single BRCA2 mutation on cancer in Iceland

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies

High prevalence of the 999del5 mutation in Icelandic breast and ovarian cancer patients

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age

Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations

Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Icelandic families, and possible relationship to prostatic cancer

Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer

Frequent occurrence of BRCA2 linkage in icelandic breast cancer families and segregation of a common BRCA2 haplotype

Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas

Inherited BRCA2 mutation associated with high grade breast cancer

Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13

Chromosome imbalance at the 3p14 region in human breast tumours: High frequency in patients with inherited predisposition due to BRCA2

A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland

High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers

Genetic heterogeneity of breast-ovarian cancer revisited

Somatic genetic alterations in BRCA2-associated and sporadic male breast cancer

High frequency of allelic imbalance at chromosome region 16q22‐23 in human breast cancer: Correlation with high pgr and low s phase

High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation

European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Loss of heterozygosity on chromosome 9 in human breast cancer: Association with clinical variables and genetic changes at other chromosome regions

Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3

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