Items where authors include "Kraft, P"

Article

Bjornsdottir, G, Stefansdottir, L, Thorleifsson, G et al. (119 more authors) (2022) Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Nature Communications, 13 (1). 634. ISSN 2041-1723

Dennis, J, Tyrer, JP, Walker, LC et al. (121 more authors) (2022) Rare germline copy number variants (CNVs) and breast cancer risk. Communications Biology, 5. 65. ISSN 2399-3642

Ahearn, TU, Zhang, H, Michailidou, K et al. (202 more authors) (2022) Common variants in breast cancer risk loci predispose to distinct tumor subtypes. Breast Cancer Research, 24 (1). 2.

Park, HA, Neumeyer, S, Michailidou, K et al. (274 more authors) (2021) Mendelian randomisation study of smoking exposure in relation to breast cancer risk. British Journal of Cancer, 125. pp. 1135-1145. ISSN 0007-0920

Boer, CG, Hatzikotoulas, K, Southam, L et al. (63 more authors) (2021) Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Cell, 184 (18). 4784-4818.e17. ISSN 0092-8674

Ruth, KS, Day, FR, Hussain, J et al. (265 more authors) (2021) Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872). pp. 393-397. ISSN 0028-0836

Morra, A, Escala-Garcia, M, Beesley, J et al. (175 more authors) (2021) Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. Breast Cancer Research, 23 (1). 86.

Chen, H, Majumdar, A, Wang, L et al. (75 more authors) (2021) Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals. HGG advances, 2 (3). 100041. ISSN 2666-2477

Baxter, JS, Johnson, N, Tomczyk, K et al. (180 more authors) (2021) Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element. The American Journal of Human Genetics, 108 (7). pp. 1190-1203. ISSN 0002-9297

Johnson, N, Maguire, S, Morra, A et al. (145 more authors) (2021) CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers. British Journal of Cancer, 124 (4). pp. 842-854. ISSN 0007-0920

Zhang, YD, Hurson, AN, Zhang, H et al. (102 more authors) (2020) Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers. Nature Communications, 11. 3353.

Feng, H, Gusev, A, Pasaniuc, B et al. (249 more authors) (2020) Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status. Genetic Epidemiology, 44 (5). pp. 442-468. ISSN 0741-0395

Zhang, H, Ahearn, TU, Lecarpentier, J et al. (269 more authors) (2020) Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. Nature Genetics, 52 (6). pp. 572-581. ISSN 1061-4036

Kapoor, PM, Lindström, S, Behrens, S et al. (147 more authors) (2020) Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium. International Journal of Epidemiology, 49 (1). pp. 216-232. ISSN 0300-5771

Escala-Garcia, M, Abraham, J, Andrulis, IL et al. (142 more authors) (2020) A network analysis to identify mediators of germline-driven differences in breast cancer prognosis. Nature Communications, 11 (1). 312.

Fachal, L, Aschard, H, Beesley, J et al. (338 more authors) (2020) Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes. Nature Genetics, 52 (1). pp. 56-73. ISSN 1061-4036

Laskar, RS, Muller, DC, Li, P et al. (105 more authors) (2019) Sex specific associations in genome wide association analysis of renal cell carcinoma. European Journal of Human Genetics, 27. pp. 1589-1598. ISSN 1018-4813

Shu, X, Wu, L, Khankari, NK et al. (203 more authors) (2019) Associations of obesity and circulating insulin and glucose with breast cancer risk : a Mendelian randomization analysis. International Journal of Epidemiology, 48 (3). pp. 795-806. ISSN 0300-5771

Jiang, X, Finucane, HK orcid.org/0000-0003-3864-9828, Schumacher, FR orcid.org/0000-0002-3073-7463 et al. (330 more authors) (2019) Shared heritability and functional enrichment across six solid cancers. Nature Communications, 10. 431. ISSN 2041-1723

Duffy, DL, Zhu, G, Li, X et al. (42 more authors) (2019) Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10. 299. ISSN 2041-1723

Mavaddat, N, Michailidou, K, Dennis, J et al. (266 more authors) (2019) Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes. The American Journal of Human Genetics, 104 (1). pp. 21-34. ISSN 0002-9297

Duffy, DL, Zhu, G, Li, X et al. (42 more authors) (2018) Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9. 4774. ISSN 2041-1723

Fang, J, Jia, J, Makowski, M et al. (38 more authors) (2018) Publisher correction: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nature Communications, 9. p. 16159.

Machiela, MJ, Hofmann, JN, Carreras-Torres, R et al. (109 more authors) (2017) Genetic variants related to longer telomere length are associated with increased risk of renal cell carcinoma. European Urology, 72 (5). pp. 747-754. ISSN 0302-2838

Scelo, G, Purdue, MP, Brown, KM et al. (120 more authors) (2017) Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nature Communications, 8. 15724. ISSN 2041-1723

Fang, J, Jia, J, Makowski, M et al. (41 more authors) (2017) Functional characterisation of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nature Communications, 8. 15034. ISSN 2041-1723

Teumer, A, Qi, Q, Nethander, M et al. (85 more authors) (2016) Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. Aging Cell, 15 (5). pp. 811-824. ISSN 1474-9718

Gusev, A, Shi, H, Kichaev, G et al. (205 more authors) (2016) Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. NATURE COMMUNICATIONS, 7. ARTN 10979. ISSN 2041-1723

Day, FR, Ruth, KS, Thompson, DJ et al. (240 more authors) (2015) Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 (11). ISSN 1061-4036

Perry, JRB, Day, F, Elks, CE et al. (200 more authors) (2014) Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, 514 (7520). 92-+. ISSN 0028-0836

Garcia-Closas, M, Couch, FJ, Lindstrom, S et al. (271 more authors) (2013) Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nature Genetics, 45 (4). pp. 392-398. ISSN 1061-4036

Haiman, CA, Chen, GK, Vachon, CM et al. (128 more authors) (2011) A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nature Genetics, 43 (12). 1210. ISSN 1061-4036

Conference or Workshop Item

Lindstrom, S, Kar, S, Wang, L et al. (25 more authors) (2020) Cross-cancer GWAS meta-analysis of more than 370,000 cases and 530,000 controls identifies multiple novel cancer risk regions. In: AACR Annual Meeting 2020, 27 Apr - 24 Jun 2020, Philadelphia, PA, USA.

Feng, H, Majumdar, A, Pasaniuc, B et al. (20 more authors) (2020) Cross-cancer cross-tissue Transcriptome-wide Association Study (TWAS) of 11 cancers identifies 56 novel genes. In: AACR Annual Meeting 2020, 27 Apr 2020, Philadelphia, PA, USA.