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Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays.
BMC Cancer. 2023 Apr 21;23(1):368. doi: 10.1186/s12885-023-10790-w.
BMC Cancer. 2023.
PMID: 37085799
Free PMC article.
Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort.
Jarhelle E, Riise Stensland HM, Mæhle L, Van Ghelue M.
Jarhelle E, et al.
Fam Cancer. 2017 Jan;16(1):1-16. doi: 10.1007/s10689-016-9916-2.
Fam Cancer. 2017.
PMID: 27495310
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Trans-activation-based risk assessment of BRCA1 BRCT variants with unknown clinical significance.
Langerud J, Jarhelle E, Van Ghelue M, Ariansen SL, Iversen N.
Langerud J, et al. Among authors: jarhelle e.
Hum Genomics. 2018 Nov 20;12(1):51. doi: 10.1186/s40246-018-0183-1.
Hum Genomics. 2018.
PMID: 30458859
Free PMC article.
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Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.
Jarhelle E, Riise Stensland HMF, Hansen GÅM, Skarsfjord S, Jonsrud C, Ingebrigtsen M, Strømsvik N, Van Ghelue M.
Jarhelle E, et al.
Sci Rep. 2019 Dec 27;9(1):19986. doi: 10.1038/s41598-019-55515-x.
Sci Rep. 2019.
PMID: 31882575
Free PMC article.
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