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Contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriers

, , , , , , , , , , , , , , , , , and . Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 27 (35): 5887–5892 (2009)

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Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk, , , , , , , , , and 4 other author(s). Breast cancer research and treatment, 118 (2): 407–413 (2009)Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers, , , , , , , , , and 99 other author(s). Human molecular genetics, 20 (23): 4732–4747 (2011)Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 169 other author(s). Human molecular genetics, 20 (16): 3304–3321 (2011)Identification of a DMBT1 polymorphism associated with increased breast cancer risk and decreased promoter activity, , , , , , , , , and 17 other author(s). Human mutation, 31 (1): 60–66 (2010)A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population, , , , , , , , , and 168 other author(s). Nature genetics, 42 (10): 885–892 (2010)High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas, , , , , , , , , and 8 other author(s). Genes, chromosomes & cancer, 52 (2): 150–155 (2013)Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 58 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 19 (11): 2859–2868 (2010)Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 127 other author(s). Human molecular genetics, 18 (22): 4442–4456 (2009)GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma, , , , , , , , , and 7 other author(s). British journal of haematology, 144 (3): 317–331 (2009)Recurrent loss of the Y chromosome and homozygous deletions within the pseudoautosomal region 1: association with male predominance in mantle cell lymphoma, , , , , , , , , and 4 other author(s). Haematologica, 93 (6): 949–950 (2008)