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Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts

The New England journal of medicine, 2011-10, Vol.365 (15), p.1384-1395

2011

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The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

British journal of cancer, 2004-07, Vol.91 (2), p.355-358

2004

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SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repair

Oncogene, 2015-11, Vol.34 (46), p.5699-5708

2015

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COSMIC 2005

British journal of cancer, 2006-01, Vol.94 (2), p.318-322

2006

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Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

Oncogene, 2007-11, Vol.26 (50), p.7158-7162

2007

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Prevalence of BRCA1 and BRCA2 gene Mutations in patients with early-onset breast cancer

JNCI : Journal of the National Cancer Institute, 1999-06, Vol.91 (11), p.943-949

1999

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A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

British journal of cancer, 2002, Vol.86 (1), p.76-83

2002

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LKB1 KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition

British journal of cancer, 2009-01, Vol.100 (2), p.370-375

2009

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Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

Journal of medical genetics, 2005-02, Vol.42 (2), p.147-151

2005

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Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

Journal of medical genetics, 2010-05, Vol.47 (5), p.342-347

2010

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THE GENETICS OF BREAST CANCER SUSCEPTIBILITY

Annual review of genetics, 1998-01, Vol.32 (1), p.95-121

1998

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Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

American journal of human genetics, 1997-07, Vol.61 (1), p.120-128

1997

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Testicular microlithiasis as a familial risk factor for testicular germ cell tumour

British journal of cancer, 2007-12, Vol.97 (12), p.1701-1706

2007

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Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

Nature genetics, 1997-01, Vol.15 (1), p.103-105

1997

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JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis

The New England journal of medicine, 2007-02, Vol.356 (5), p.459-468

2007

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Instability of short tandem repeats (microsatellites) in human cancers

Nature genetics, 1994-02, Vol.6 (2), p.152-156

1994

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A census of human cancer genes

Nature reviews. Cancer, 2004-03, Vol.4 (3), p.177-183

2004

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Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours

Nature genetics, 2000-02, Vol.24 (2), p.197-200

2000

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The Catalogue of Somatic Mutations in Cancer (COSMIC)

Current Protocols in Human Genetics, 2008-04, Vol.57 (1), p.10.11.1-10.11.26

2008

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Cancer and genomics

Nature (London), 2001-02, Vol.409 (6822), p.850-852

2001

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Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation

Nature genetics, 1995-12, Vol.11 (4), p.428-433

1995

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Germline Mutations in BRCA1 and BRCA2 in Breast-Ovarian Families From a Breast Cancer Risk Evaluation Clinic

Journal of clinical oncology, 2001-04, Vol.19 (8), p.2247-2253

2001

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BRCA2 mutations in primary breast and ovarian cancers

Nature genetics, 1996-06, Vol.13 (2), p.238-240

1996

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Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers

British journal of cancer, 1997, Vol.76 (9), p.1150-1156

1997

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The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

Journal of medical genetics, 2007-07, Vol.44 (7), p.472-477

2007

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Somatic SF3B1 Mutation in Myelodysplasia with Ring Sideroblasts

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repair

COSMIC 2005

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

Prevalence of BRCA1 and BRCA2 gene Mutations in patients with early-onset breast cancer

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

LKB1 KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition

Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour

Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

THE GENETICS OF BREAST CANCER SUSCEPTIBILITY

Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13

Testicular microlithiasis as a familial risk factor for testicular germ cell tumour

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis

Instability of short tandem repeats (microsatellites) in human cancers

A census of human cancer genes

Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours

The Catalogue of Somatic Mutations in Cancer (COSMIC)

Cancer and genomics

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation

Germline Mutations in BRCA1 and BRCA2 in Breast-Ovarian Families From a Breast Cancer Risk Evaluation Clinic

BRCA2 mutations in primary breast and ovarian cancers

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

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