Items where authors include "Hillemanns, P."

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Number of items: 16.

Article

Levi, H., Carmi, S., Rosset, S. et al. (135 more authors) (2023) Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. Journal of Medical Genetics. ISSN 0022-2593

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

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

O'Mara, T.A. orcid.org/0000-0002-5436-3232, Glubb, D.M. orcid.org/0000-0002-2184-7708, Amant, F. et al. (122 more authors) (2018) Identification of nine new susceptibility loci for endometrial cancer. Nature Communications, 9. 3166.

Painter, J.N., O'Mara, T.A., Morris, A.P. et al. (73 more authors) (2018) Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Medicine, 7 (5). pp. 1978-1987. ISSN 2045-7634

Zeng, C., Guo, X., Long, J. et al. (234 more authors) (2016) Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18 (1). 64. ISSN 1465-542X

Schmidt, M.J., Cox, A. orcid.org/0000-0002-5138-1099, Hogervorst, F. et al. (81 more authors) (2016) Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers. Journal of Clinical Oncology, 34 (23). pp. 2750-2760. ISSN 0732-183X

Cheng, T.H.T., Thompson, D., Painter, J. et al. (98 more authors) (2015) Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Scientific Reports, 5. 17369. ISSN 2045-2322

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

Painter, J.N., O'Mara, T.A., Batra, J. et al. (116 more authors) (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 (5). pp. 1478-1492. ISSN 0964-6906

Carvajal-Carmona, L.G., O'Mara, T.A., Painter, J.N.. et al. (91 more authors) (2015) Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. Human Genetics, 134 (2). pp. 231-245. ISSN 0340-6717

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

Hein, R., Maranian, M., Hopper, J.L. et al. (168 more authors) (2012) Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC). PLoS ONE, 7 (8). e42380. ISSN 1932-6203

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

Stevens, K.N., Garcia-Closas, M., Fredericksen, Z. et al. (101 more authors) (2011) Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk. British Journal of Cancer, 105. pp. 1934-1939. ISSN 0007-0920

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

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