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19p13.1 is a triple-negative-specific breast cancer susceptibility locus, , , , , , , , , and 144 other author(s). Cancer research, 72 (7): 1795–1803 (2012)Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 34 other author(s). Human molecular genetics, 19 (14): 2886–2897 (2010)Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 180 other author(s). Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 21 (4): 645–657 (2012)Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer, , , , , , , , , and 427 other author(s). Nature genetics, 45 (4): 371-84, 384e1-2 (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 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)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)