Author Gehrig, Andrea
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2016 | Journal Article
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
Kast, K.; Rhiem, K.; Wappenschmidt, B.; Hahnen, E.; Hauke, J.; Bluemcke, B. & Zarghooni, V. et al. (2016)
Journal of Medical Genetics, 53(7) pp. 465-471. DOI: https://doi.org/10.1136/jmedgenet-2015-103672
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2017 | Journal Article
NGS-based multi-gene panel analysis in BRCA1/2 -negative breast and ovarian cancer families.
Pohl, E.; Hauke, J.; Horvath, J.; Dworniczak, B.; Gehrig, A.; Niederacher, D. & Arnold, N. et al. (2017)
Journal of Clinical Oncology, 35(15_suppl) pp. 1526-1526. DOI: https://doi.org/10.1200/JCO.2017.35.15_suppl.1526
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2018 | Journal Article
Gene panel testing of 5589 BRCA1/2 -negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Hauke, J.; Horvath, J.; Groß, E.; Gehrig, A.; Honisch, E.; Hackmann, K. & Schmidt, G. et al. (2018)
Cancer Medicine, 7(4) pp. 1349-1358. DOI: https://doi.org/10.1002/cam4.1376
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2018 | Journal Article |
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history
Engel, C. ; Rhiem, K.; Hahnen, E.; Loibl, S.; Weber, K. E.; Seiler, S. & Zachariae, S. et al. (2018)
BMC Cancer, 18(1) art. 265. DOI: https://doi.org/10.1186/s12885-018-4029-y
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2022 | Journal Article | Research Paper |
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Dumont, M.; Weber-Lassalle, N.; Joly-Beauparlant, C.; Ernst, C.; Droit, A.; Feng, B.-J. & Dubois, S. et al. (2022)
Cancers, 14(14). DOI: https://doi.org/10.3390/cancers14143363
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