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Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome.
Woltmann A, Chen B, Lascorz J, Johansson R, Eyfjörd JE, Hamann U, Manjer J, Enquist-Olsson K, Henriksson R, Herms S, Hoffmann P, Hemminki K, Lenner P, Försti A. Woltmann A, et al. Among authors: eyfjord je. PLoS One. 2014 Jun 2;9(6):e98229. doi: 10.1371/journal.pone.0098229. eCollection 2014. PLoS One. 2014. PMID: 24886783 Free PMC article.
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome.
Shi H, Bevier M, Johansson R, Grzybowska E, Chen B, Eyfjörd JE, Hamann U, Manjer J, Enquist K, Henriksson R, Carlson J, Brandt A, Lascorz J, Butkiewicz D, Pamula-Pilat J, Tecza K, Herms S, Hoffmann P, Hemminki K, Lenner P, Försti A. Shi H, et al. Among authors: eyfjord je. Breast Cancer Res Treat. 2011 Dec;130(3):905-16. doi: 10.1007/s10549-011-1600-5. Epub 2011 Jun 1. Breast Cancer Res Treat. 2011. PMID: 21630024
Inbreeding and homozygosity in breast cancer survival.
Thomsen H, Filho MI, Woltmann A, Johansson R, Eyfjörd JE, Hamann U, Manjer J, Enquist-Olsson K, Henriksson R, Herms S, Hoffmann P, Chen B, Huhn S, Hemminki K, Lenner P, Försti A. Thomsen H, et al. Among authors: eyfjord je. Sci Rep. 2015 Nov 12;5:16467. doi: 10.1038/srep16467. Sci Rep. 2015. PMID: 26558712 Free PMC article.
Combined effect of low-penetrant SNPs on breast cancer risk.
Harlid S, Ivarsson MI, Butt S, Grzybowska E, Eyfjörd JE, Lenner P, Försti A, Hemminki K, Manjer J, Dillner J, Carlson J. Harlid S, et al. Among authors: eyfjord je. Br J Cancer. 2012 Jan 17;106(2):389-96. doi: 10.1038/bjc.2011.461. Epub 2011 Nov 1. Br J Cancer. 2012. PMID: 22045194 Free PMC article.
A candidate CpG SNP approach identifies a breast cancer associated ESR1-SNP.
Harlid S, Ivarsson MI, Butt S, Hussain S, Grzybowska E, Eyfjörd JE, Lenner P, Försti A, Hemminki K, Manjer J, Dillner J, Carlson J. Harlid S, et al. Among authors: eyfjord je. Int J Cancer. 2011 Oct 1;129(7):1689-98. doi: 10.1002/ijc.25786. Epub 2011 Mar 11. Int J Cancer. 2011. PMID: 21105050
Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters.
Phelan CM, Borg A, Cuny M, Crichton DN, Baldersson T, Andersen TI, Caligo MA, Lidereau R, Lindblom A, Seitz S, Kelsell D, Hamann U, Rio P, Thorlacius S, Papp J, Olah E, Ponder B, Bignon YJ, Scherneck S, Barkardottir R, Borresen-Dale AL, Eyfjörd J, Theillet C, Thompson AM, Larsson C, et al. Phelan CM, et al. Cancer Res. 1998 Mar 1;58(5):1004-12. Cancer Res. 1998. PMID: 9500463
A DNA methylation-based definition of biologically distinct breast cancer subtypes.
Stefansson OA, Moran S, Gomez A, Sayols S, Arribas-Jorba C, Sandoval J, Hilmarsdottir H, Olafsdottir E, Tryggvadottir L, Jonasson JG, Eyfjord J, Esteller M. Stefansson OA, et al. Mol Oncol. 2015 Mar;9(3):555-68. doi: 10.1016/j.molonc.2014.10.012. Epub 2014 Nov 5. Mol Oncol. 2015. PMID: 25468711 Free PMC article.
151 results