Daianne N.M. Torres, M.Sc.
Affiliations: | UFRJ, Rio de Janeiro, Rio de Janeiro, Brazil |
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Publications
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Rebbeck TR, Friebel TM, Friedman E, et al. (2018) Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations. Human Mutation |
Michailidou K, Lindström S, Dennis J, et al. (2017) Association analysis identifies 65 new breast cancer risk loci. Nature |
Milne RL, Kuchenbaecker KB, Michailidou K, et al. (2017) Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Nature Genetics |
Liu J, Lončar I, Collée JM, et al. (2016) rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk. Scientific Reports. 6: 36874 |
Lawrenson K, Kar S, McCue K, et al. (2016) Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus. Nature Communications. 7: 12675 |
Southey MC, Goldgar DE, Winqvist R, et al. (2016) PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Journal of Medical Genetics |
Pelttari LM, Khan S, Vuorela M, et al. (2016) RAD51B in Familial Breast Cancer. Plos One. 11: e0153788 |
Zhao Z, Wen W, Michailidou K, et al. (2016) Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry. Cancer Causes & Control : Ccc |
Dunning AM, Michailidou K, Kuchenbaecker KB, et al. (2016) Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics |
Meeks HD, Song H, Michailidou K, et al. (2016) BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers. Journal of the National Cancer Institute. 108 |