Items where authors include "Hooning, M.J."

Article

Yiangou, K., Mavaddat, N., Dennis, J. et al. (124 more authors) (2024) Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction. Breast Cancer Research, 26. 189. ISSN 1465-5411

Kentistou, K.A. orcid.org/0000-0002-5816-664X, Kaisinger, L.R. orcid.org/0000-0002-0849-3191, Stankovic, S. orcid.org/0000-0002-6602-1379 et al. (220 more authors) (2024) Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7). pp. 1397-1411. ISSN 1061-4036

Morra, A. orcid.org/0000-0003-4983-7883, Schreurs, M.A.C. orcid.org/0000-0002-1826-5344, Andrulis, I.L. et al. (114 more authors) (2023) Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival. Cancer Medicine, 12 (15). pp. 16142-16162. ISSN 2045-7634

Dixon-Suen, S.C. orcid.org/0000-0003-3714-8386, Lewis, S.J., Martin, R.M. et al. (155 more authors) (2022) Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study. British Journal of Sports Medicine, 56 (20). pp. 1157-1170. ISSN 0306-3674

Opstal-van Winden, A.W.J., de Haan, H.G. orcid.org/0000-0003-1126-4776, Hauptmann, M. et al. (27 more authors) (2019) Genetic susceptibility to radiation-induced breast cancer after Hodgkin Lymphoma. Blood, 133 (10). pp. 1130-1139. ISSN 0006-4971

Escala-Garcia, M., Guo, Q., Dörk, T. et al. (234 more authors) (2019) Genome-wide association study of germline variants and breast cancer-specific mortality. British Journal of Cancer, 120. pp. 647-657. ISSN 0007-0920

Jiao, X., Aravidis, C., Marikkannu, R. et al. (103 more authors) (2017) PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1. Oncotarget, 8. pp. 102769-102782. ISSN 1949-2553

Day, F.R., Thompson, D.J., Helgason, H. et al. (219 more authors) (2017) Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, 49 (6). pp. 834-841. ISSN 1061-4036

Ghoussaini, M, French, J.D., Michailidou, K. et al. (122 more authors) (2016) Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen receptor positive breast cancer through FGF10 and MRPS30 regulation. American Journal of Human Genetics, 99 (4). pp. 903-911. ISSN 0002-9297

Shi, J., Zhang, Y., Zheng, W. et al. (125 more authors) (2016) Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer. International Journal of Cancer, 139 (6). pp. 1303-1317. ISSN 0020-7136

Guo, Y., Warren Andersen, S., Shu, X.O. et al. (108 more authors) (2016) Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. PLoS Medicine, 13 (8). e1002105. ISSN 1549-1277

Wyszynski, A., Hong, C.C., Lam, K. et al. (107 more authors) (2016) An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Human Molecular Genetics , 25 (17). pp. 3863-3876. ISSN 0964-6906

Hollestelle, A., van der Baan, F.H., Berchuck, A. et al. (355 more authors) (2016) No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. Gynecologic Oncology, 141 (2). pp. 386-401. ISSN 0090-8258

Zhao, Z., Wen, W., Michailidou, K. et al. (115 more authors) (2016) Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry. Cancer Causes and Control. pp. 1-15. ISSN 0957-5243

Dunning, A.M., Michailidou, K., Kuchenbaecker, K.B. et al. (245 more authors) (2016) Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics. ISSN 1061-4036

Easton, D.F., Lesueur, F., Decker, B. et al. (126 more authors) (2016) No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Journal of Medical Genetics . ISSN 0022-2593

Hamdi, Y., Soucy, P., Adoue, V. et al. (93 more authors) (2016) Association of Breast Cancer Risk with Genetic Variants Showing Differential Allelic Expression: Identification of a Novel Breast Cancer Susceptibility Locus at 4q21. Oncotarget, 7. pp. 80140-80163. ISSN 1949-2553

Jamshidi, M., Fagerholm, R., Khan, S. et al. (55 more authors) (2015) SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival. Oncotarget, 6 (35). pp. 37979-37994. ISSN 1949-2553

Orr, N., Dudbridge, F., Dryden, N. et al. (213 more authors) (2015) Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Human Molecular Genetics, 24 (10). 2966 - 2984. ISSN 0964-6906

Guo, Q., Schmidt, M.K., Kraft, P. et al. (143 more authors) (2015) Identification of Novel Genetic Markers of Breast Cancer Survival. Journal of the National Cancer Institute, 107 (5). ISSN 0027-8874

Mavaddat, N., Pharoah, P.D.P., Michailidou, K. et al. (209 more authors) (2015) Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants. JNCI-Journal of the National Cancer Institute, 107 (5). ISSN 0027-8874

Pirie, A., Guo, Q., Kraft, P. et al. (146 more authors) (2015) Common germline polymorphisms associated with breast cancer-specific survival. Breast Cancer Research, 17. 58. ISSN 1465-5411

Michailidou, K., Beesley, J., Lindstrom, S. et al. (245 more authors) (2015) Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nature Genetics, 47. pp. 373-380. ISSN 1061-4036

Spurdle, A.B., Couch, F.J., Parsons, M.T. et al. (195 more authors) (2014) Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia. Breast Cancer Research, 16. 3419. ISSN 1465-5411

Milne, R.L., Burwinkel, B., Michailidou, K. et al. (178 more authors) (2014) Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. Human Molecular Genetics, 23 (22). pp. 6096-6111. ISSN 0964-6906

Khan, S., Greco, D., Michailidou, K. et al. (161 more authors) (2014) MicroRNA Related Polymorphisms and Breast Cancer Risk. PLOS ONE, 9 (11). e109973. ISSN 1932-6203

Sawyer, E., Roylance, R., Petridis, C. et al. (151 more authors) (2014) Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast. PLoS Genetics, 10 (4). e1004285. ISSN 1553-7390

Agarwal, D., Pineda, S., Michailidou, K. et al. (179 more authors) (2014) FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium. British Journal of Cancer, 110 (4). pp. 1088-1100. ISSN 0007-0920

Gaudet, M.M., Kuchenbaecker, K.B., Vijai, J. et al. (129 more authors) (2013) Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk. PLoS Genetics, 9 (3). e1003173. ISSN 1553-7390

Kirchhoff, T., Gaudet, M.M., Antoniou, A.C. et al. (133 more authors) (2012) Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2. PLoS ONE, 7 (6). e35706. ISSN 1932-6203

Garcia-Closas, M., Hall, P., Nevanlinna, H. et al. (110 more authors) (2008) Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics. PLoS Genetics, 4 (4). e1000054. ISSN 1553-7404