UB Paderborn / Katalog / Suche / in CDI

Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy

Nature Medicine, 2007-09, Vol.13 (9), p.1050-1059

2007

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Pregnancies, Breast-Feeding, and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study (IBCCS)

JNCI : Journal of the National Cancer Institute, 2006-04, Vol.98 (8), p.535-544

2006

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Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma

JNCI : Journal of the National Cancer Institute, 2002-06, Vol.94 (12), p.894-903

2002

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Melanocortin-1 Receptor (MC1R) Gene Variants and Dysplastic Nevi Modify Penetrance of CDKN2A Mutations in French Melanoma-Prone Pedigrees

Cancer epidemiology, biomarkers & prevention, 2005-10, Vol.14 (10), p.2384-2390

2005

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Role of Radiation Dose in the Risk of Secondary Leukemia After a Solid Tumor in Childhood Treated Between 1980 and 1999

International journal of radiation oncology, biology, physics, 2010-12, Vol.78 (5), p.1474-1482

2010

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Significant contribution of germline BRCA2 rearrangements in male breast cancer families

Cancer research (Chicago, Ill.), 2004-11, Vol.64 (22), p.8143-8147

2004

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Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations

Journal of medical genetics, 2010-02, Vol.47 (2), p.142-144

2010

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Risk of Secondary Leukemia After a Solid Tumor in Childhood According to the Dose of Epipodophyllotoxins and Anthracyclines: A Case-Control Study by the Société Française d’Oncologie Pédiatrique

Journal of clinical oncology, 2003-03, Vol.21 (6), p.1074-1081

2003

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Influence of Genes, Nevi, and Sun Sensitivity on Melanoma Risk in a Family Sample Unselected by Family History and in Melanoma-Prone Families

JNCI : Journal of the National Cancer Institute, 2004-05, Vol.96 (10), p.785-795

2004

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Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients

Human mutation, 2009-04, Vol.30 (4), p.564-574

2009

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Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene

Oncogene, 2003-02, Vol.22 (6), p.840-846

2003

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Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome

JAMA : the journal of the American Medical Association, 2011-06, Vol.305 (22), p.2304

2011

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Patients’ characteristics and rate of Internet use to obtain cancer information

Journal of public health (Oxford, England), 2006-09, Vol.28 (3), p.235-237

2006

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Radiation and genetic factors in the risk of second malignant neoplasms after a first cancer in childhood

The Lancet (British edition), 1997-07, Vol.350 (9071), p.91-95

1997

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Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

European journal of cancer (1990), 2006-05, Vol.42 (7), p.871-881

2006

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BRAF as a melanoma susceptibility candidate gene?

Cancer research (Chicago, Ill.), 2003-06, Vol.63 (12), p.3061-3065

2003

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BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma

Familial cancer, 2007-12, Vol.6 (4), p.453-461

2007

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Genetic epidemiology of neuroblastoma: A study of 426 cases at the Institut Gustave-Roussy in France

Pediatric Blood & Cancer, 2004-01, Vol.42 (1), p.99-105

2004

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New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment

Genes chromosomes & cancer, 2007-08, Vol.46 (8), p.751-760

2007

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The Li–Fraumeni syndrome

Biochimie, 2002, Vol.84 (1), p.75-82

Chompret, Agnès

2002

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Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome

Journal of medical genetics, 2006-06, Vol.43 (6), p.531-533

2006

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PDGFRA germline mutation in a family with multiple cases of gastrointestinal stromal tumor

Gastroenterology (New York, N.Y. 1943), 2004-01, Vol.126 (1), p.318-321

2004

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Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy

Pregnancies, Breast-Feeding, and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study (IBCCS)

Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma

Melanocortin-1 Receptor (MC1R) Gene Variants and Dysplastic Nevi Modify Penetrance of CDKN2A Mutations in French Melanoma-Prone Pedigrees

Role of Radiation Dose in the Risk of Secondary Leukemia After a Solid Tumor in Childhood Treated Between 1980 and 1999

Significant contribution of germline BRCA2 rearrangements in male breast cancer families

Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations

Risk of Secondary Leukemia After a Solid Tumor in Childhood According to the Dose of Epipodophyllotoxins and Anthracyclines: A Case-Control Study by the Société Française d’Oncologie Pédiatrique

Influence of Genes, Nevi, and Sun Sensitivity on Melanoma Risk in a Family Sample Unselected by Family History and in Melanoma-Prone Families

Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients

Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome

Patients’ characteristics and rate of Internet use to obtain cancer information

Radiation and genetic factors in the risk of second malignant neoplasms after a first cancer in childhood

Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing

Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors

BRAF as a melanoma susceptibility candidate gene?

BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma

Genetic epidemiology of neuroblastoma: A study of 426 cases at the Institut Gustave-Roussy in France

New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment

The Li–Fraumeni syndrome

Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome

PDGFRA germline mutation in a family with multiple cases of gastrointestinal stromal tumor

Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK)

Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families

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