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Compiler Construction: Theory and Practice, , , and . SRA Inc., 2nd edition, (1985)A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity, , , , , , , , , and 5 other author(s). Cancer research, 73 (1): 265–275 (2013)Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers, , , , , , , , , and 201 other author(s). American journal of human genetics, 92 (4): 489–503 (2013)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)Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers, , , , , , , , , and 63 other author(s). Breast cancer research : BCR, 12 (6): R102 (2010)Split Euler tours in 4-regular planar graphs., , , and . Discussiones Mathematicae Graph Theory, 36 (1): 23-30 (2016)Automated discovery of drug treatment patterns for endocrine therapy of breast cancer within an electronic medical record., , , , , , , , , and . JAMIA, (2012)Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA), , , , , , , , , and 123 other author(s). British journal of cancer, 101 (12): 2048–2054 (2009)Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers, , , , , , , , , and 171 other author(s). Breast cancer research : BCR, 14 (1): R33 (2012)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)