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Familial breast-ovarian cancer locus on chromosome 17q12-q23

The Lancet (British edition), 1991-07, Vol.338 (8759), p.82-83

1991

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The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

The New England journal of medicine, 1994-08, Vol.331 (5), p.294-299

1994

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Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma

Journal of medical genetics, 2006-01, Vol.43 (1), p.39-47

2006

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Hereditary breast cancer : pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage

Cancer, 1996-02, Vol.77 (4), p.697-709

1996

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Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

Cancer research (Chicago, Ill.), 1999-01, Vol.59 (2), p.455-461

1999

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Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region

Oncogene, 1998-12, Vol.17 (24), p.3169-3176

1998

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A prospective evaluation of plasma phospholipid fatty acids and breast cancer risk in the EPIC study

Annals of oncology, 2017-11, Vol.28 (11), p.2836-2842

2017

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A 1-kb alu-mediated germ-line deletion removing BRCA1 exon 17

Cancer research (Chicago, Ill.), 1997-03, Vol.57 (5), p.828-831

1997

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An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation?

American journal of human genetics, 1999, Vol.64 (1), p.300-302

1999

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Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG→ATG) mutation

Surgery, 2000-07, Vol.128 (1), p.93-98

2000

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Family history of cancer and germline BRCA2 mutations in sporadic exocrine pancreatic cancer

Gut, 2002-05, Vol.50 (5), p.653-657

2002

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An estimate of the heritable fraction of childhood cancer

British journal of cancer, 1991-06, Vol.63 (6), p.993-999

1991

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Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

Nature genetics, 1996-03, Vol.12 (3), p.309-311

1996

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Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines

Oncogene, 1998-12, Vol.17 (22), p.2851-2861

1998

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Mutations in BRCA1 and BRCA2 in breast cancer families: Are there more breast cancer-susceptibility genes?

American journal of human genetics, 1997-03, Vol.60 (3), p.486-495

1997

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A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families

American journal of human genetics, 1996, Vol.58 (1), p.42-51

1996

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Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues

International journal of cancer, 2000-03, Vol.85 (6), p.877-881

2000

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A BRCA1 Nonsense Mutation Causes Exon Skipping

American journal of human genetics, 1998-03, Vol.62 (3), p.713-715

1998

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Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain

Oncogene, 1997-07, Vol.15 (4), p.393-402

1997

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Effect of Smoking on Breast Cancer in Carriers of Mutant BRCA1 or BRCA2 Genes

JNCI : Journal of the National Cancer Institute, 1998-05, Vol.90 (10), p.761-765

1998

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Psychosocial impact of genetic testing in familial medullary-thyroid carcinoma: A multicentric pilot-evaluation

Annals of oncology, 1999-01, Vol.10 (1), p.87-95

1999

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Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer

Nature genetics, 1994-01, Vol.6 (1), p.106-110

1994

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Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: Trends for future evaluations

Annals of oncology, 2001-10, Vol.12 (10), p.1461-1465

2001

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A prospective evaluation of plasma phospholipid fatty acids and breast cancer risk in the EPIC study

Annals of oncology, 2017-11, Vol.28 (11), p.2836

2017

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Stable transfection of Epstein-Barr virus (EBV) nuclear antigen 2 in lymphoma cells containing the EBV P3HR1 genome induces expression of B-cell activation molecules CD21 and CD23

Journal of Virology, 1990-03, Vol.64 (3), p.1002-1013

1990

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Familial breast-ovarian cancer locus on chromosome 17q12-q23

The Ewing Family of Tumors -- A Subgroup of Small-Round-Cell Tumors Defined by Specific Chimeric Transcripts

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanoma

Hereditary breast cancer : pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

Down-regulation of BRCA1 in human sporadic breast cancer; analysis of DNA methylation patterns of the putative promoter region

A prospective evaluation of plasma phospholipid fatty acids and breast cancer risk in the EPIC study

A 1-kb alu-mediated germ-line deletion removing BRCA1 exon 17

An Alu-Mediated 6-kb Duplication in the BRCA1 Gene: A New Founder Mutation?

Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG→ATG) mutation

Family history of cancer and germline BRCA2 mutations in sporadic exocrine pancreatic cancer

An estimate of the heritable fraction of childhood cancer

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines

Mutations in BRCA1 and BRCA2 in breast cancer families: Are there more breast cancer-susceptibility genes?

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families

Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues

A BRCA1 Nonsense Mutation Causes Exon Skipping

Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain

Effect of Smoking on Breast Cancer in Carriers of Mutant BRCA1 or BRCA2 Genes

Psychosocial impact of genetic testing in familial medullary-thyroid carcinoma: A multicentric pilot-evaluation

Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer

Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: Trends for future evaluations

A prospective evaluation of plasma phospholipid fatty acids and breast cancer risk in the EPIC study

Stable transfection of Epstein-Barr virus (EBV) nuclear antigen 2 in lymphoma cells containing the EBV P3HR1 genome induces expression of B-cell activation molecules CD21 and CD23

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