Items where authors include "Brenner, H"

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Number of items: 37.

Article

Niehues, JM, Quirke, P orcid.org/0000-0002-3597-5444, West, NP orcid.org/0000-0002-0346-6709 et al. (16 more authors) (2023) Generalizable biomarker prediction from cancer pathology slides with self-supervised deep learning: A retrospective multi-centric study. Cell Reports Medicine, 4 (4). 100980. ISSN 2666-3791

Saldanha, OL, Quirke, P orcid.org/0000-0002-3597-5444, West, NP orcid.org/0000-0002-0346-6709 et al. (24 more authors) (2022) Swarm learning for decentralized artificial intelligence in cancer histopathology. Nature Medicine, 28. pp. 1232-1239. ISSN 1078-8956

Tian, Y, Kim, AE, Bien, SA et al. (74 more authors) (2022) Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Journal of the National Cancer Institute. ISSN 0027-8874

West, N orcid.org/0000-0002-0346-6709, Echle, A, Laleh, NG et al. (35 more authors) (2022) Artificial intelligence for detection of microsatellite instability in colorectal cancer – a multicentric analysis of a pre-screening tool for clinical application. ESMO Open, 7 (2). ISSN 2059-7029

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.

Schrammen, PL, Laleh, NG, Echle, A et al. (16 more authors) (2022) Weakly supervised annotation-free cancer detection and prediction of genotype in routine histopathology. Journal of Pathology, 256 (1). pp. 50-60. ISSN 0022-3417

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

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.

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

Park, JY, Choi, JY, Choi, J et al. (90 more authors) (2021) Gene-environment interactions relevant to estrogen and risk of breast cancer: Can gene-environment interactions be detected only among candidate snps from genome-wide association studies? Cancers, 13 (10). 2370. ISSN 2072-6694

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

Ji, X, Mukherjee, S, Landi, MT et al. (108 more authors) (2020) Protein-altering germline mutations implicate novel genes related to lung cancer development. Nature Communications, 11 (1). 2220.

Murray, CJL, Aravkin, AY, Zheng, P et al. (937 more authors) (2020) Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, 396 (10258). pp. 1223-1249. ISSN 0140-6736

Echle, A, Grabsch, HI orcid.org/0000-0001-9520-6228, Quirke, P orcid.org/0000-0002-3597-5444 et al. (20 more authors) (2020) Clinical-grade Detection of Microsatellite Instability in Colorectal Tumors by Deep Learning. Gastroenterology, 159 (4). 1406-1416.e11. ISSN 0016-5085

Kather, JN, Heij, LR, Grabsch, H orcid.org/0000-0001-9520-6228 et al. (25 more authors) (2020) Pan-cancer image-based detection of clinically actionable genetic alterations. Nature Cancer, 1 (8). pp. 789-799. ISSN 2662-1347

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

Kather, JN, Pearson, AT, Halama, N et al. (14 more authors) (2019) Deep learning can predict microsatellite instability directly from histology in gastrointestinal cancer. Nature Medicine, 25 (7). pp. 1054-1056. ISSN 1078-8956

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

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

Huyghe, JR, Bien, SA, Harrison, TA et al. (196 more authors) (2019) Discovery of common and rare genetic risk variants for colorectal cancer. Nature Genetics, 51 (1). pp. 76-87. ISSN 1061-4036

Murray, CJL, Callender, CSKH, Kulikoff, XR et al. (985 more authors) (2018) Population and fertility by age and sex for 195 countries and territories, 1950–2017: a systematic analysis for the Global Burden of Disease Study 2017. The Lancet, 392 (10159). pp. 1995-2051. ISSN 0140-6736

Early Breast Cancer Trialists' Collaborative Group (EBCTCG), Alberro, JA, Ballester, B et al. (596 more authors) (2018) Long-term outcomes for neoadjuvant versus adjuvant chemotherapy in early breast cancer: meta-analysis of individual patient data from ten randomised trials. The Lancet Oncology, 19 (1). pp. 27-39. ISSN 1470-2045

Liu, J, Lončar, I, Collée, JM et al. (97 more authors) (2016) rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk. Scientific Reports, 6. p. 36874. ISSN 2045-2322

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

Darabi, H, McCue, K, Beesley, J et al. (126 more authors) (2015) Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. American Journal of Human Genetics .

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

Ghoussaini, M, Edwards, SL, Michailidou, K et al. (209 more authors) (2014) Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation. Nature Communications, 5. 4999. ISSN 2041-1723

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

Bojesen, SE, Pooley, KA, Johnatty, SE et al. (442 more authors) (2013) Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nature Genetics, 45 (4). pp. 371-384. ISSN 1061-4036

Ghoussaini, M, Fletcher, O, Michailidou, K et al. (184 more authors) (2012) Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nature Genetics, 44 (3). pp. 312-318. ISSN 1061-4036

This list was generated on Sat Mar 23 08:39:14 2024 GMT.