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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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Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

British journal of cancer, 2004-11, Vol.91 (11), p.1911-1915

2004

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UHRF1 is a novel molecular marker for diagnosis and the prognosis of bladder cancer

British journal of cancer, 2009-07, Vol.101 (1), p.98-105

2009

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Germline Homozygous Mutations at Codon 804 in the RET Protooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients

The journal of clinical endocrinology and metabolism, 2005-06, Vol.90 (6), p.3454-3457

2005

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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer

British journal of cancer, 2006-12, Vol.95 (12), p.1689-1695

2006

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Paternal origin of new mutations in Von Recklinghausen neurofibromatosis

Nature (London), 1990-02, Vol.343 (6258), p.558-559

1990

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A clonal marker induced by mutation in mouse intestinal epithelium

Nature (London), 1988-06, Vol.333 (6172), p.463-466

1988

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Interactions between genes involved in the antioxidant defence system and breast cancer risk

British journal of cancer, 2006-08, Vol.95 (4), p.525-531

2006

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Common BRCA1 Variants and Susceptibility to Breast and Ovarian Cancer in the General Population

Human molecular genetics, 1997-02, Vol.6 (2), p.285-289

1997

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Clonal Origin of Epithelial Ovarian Carcinoma: Analysis by Loss of Heterozygosity, p53 Mutation, and X-Chromosome Inactivation

JNCI : Journal of the National Cancer Institute, 1992-12, Vol.84 (23), p.1793-1798

1992

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Common Polymorphisms in Checkpoint Kinase 2 Are not Associated with Breast Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2003-08, Vol.12 (8), p.809-812

2003

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MRI breast screening in high-risk women: cancer detection and survival analysis

Breast cancer research and treatment, 2014-06, Vol.145 (3), p.663-672

2014

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Common germ-line polymorphism of C1QA and breast cancer survival

British journal of cancer, 2010-04, Vol.102 (8), p.1294-1299

2010

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Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay

Human genetics, 1998-05, Vol.102 (5), p.591-597

1998

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Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

British journal of cancer, 2009-03, Vol.100 (6), p.993-1001

2009

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Further evidence for an HLA-related recessive mutation in nasopharyngeal carcinoma among the Chinese

British journal of cancer, 2005-03, Vol.92 (5), p.967-970

2005

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Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

Journal of internal medicine, 1995-10, Vol.238 (4), p.343-346

1995

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Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours

British journal of cancer, 2002-11, Vol.87 (10), p.1162-1165

2002

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Comparison of prophylactic oophorectomy specimens from carriers and noncarriers of a BRCA1 or BRCA2 gene mutation

JNCI : Journal of the National Cancer Institute, 1999-04, Vol.91 (7), p.626-628

1999

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Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population

British journal of cancer, 2006-06, Vol.94 (12), p.1921-1926

2006

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Polygenic inherited predisposition to breast cancer

Cold Spring Harbor Symposia on Quantitative Biology, 2005, Vol.70, p.35-41

2005

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Mutation testing in melanoma families: INK4A, CDK4 and INK4D

British Journal of Cancer, 1999-04, Vol.80 (1-2), p.295-300

1999

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Cancers in BRCA1 and BRCA2 carriers and in women at high risk for breast cancer: MR imaging and mammographic features

Radiology, 2009-08, Vol.252 (2), p.358-368

2009

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Polymorphisms Associated With Circulating Sex Hormone Levels in Postmenopausal Women

JNCI : Journal of the National Cancer Institute, 2004-06, Vol.96 (12), p.936-945

2004

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Stem-cell organization in mouse small intestine

Proceedings of the Royal Society. B, Biological sciences, 1990-07, Vol.241 (1300), p.13-18

1990

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

Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations

UHRF1 is a novel molecular marker for diagnosis and the prognosis of bladder cancer

Germline Homozygous Mutations at Codon 804 in the RET Protooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients

HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer

Paternal origin of new mutations in Von Recklinghausen neurofibromatosis

A clonal marker induced by mutation in mouse intestinal epithelium

Interactions between genes involved in the antioxidant defence system and breast cancer risk

Common BRCA1 Variants and Susceptibility to Breast and Ovarian Cancer in the General Population

Clonal Origin of Epithelial Ovarian Carcinoma: Analysis by Loss of Heterozygosity, p53 Mutation, and X-Chromosome Inactivation

Common Polymorphisms in Checkpoint Kinase 2 Are not Associated with Breast Cancer Risk

MRI breast screening in high-risk women: cancer detection and survival analysis

Common germ-line polymorphism of C1QA and breast cancer survival

Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay

Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

Further evidence for an HLA-related recessive mutation in nasopharyngeal carcinoma among the Chinese

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours

Comparison of prophylactic oophorectomy specimens from carriers and noncarriers of a BRCA1 or BRCA2 gene mutation

Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population

Polygenic inherited predisposition to breast cancer

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

Cancers in BRCA1 and BRCA2 carriers and in women at high risk for breast cancer: MR imaging and mammographic features

Polymorphisms Associated With Circulating Sex Hormone Levels in Postmenopausal Women

Stem-cell organization in mouse small intestine

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