Author Rhiem, Kerstin
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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 |
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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2019 | Journal Article |
Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer
Weber-Lassalle, N.; Borde, J.; Weber-Lassalle, K.; Horváth, J.; Niederacher, D.; Arnold, N. & Kaulfuß, S. et al. (2019)
Breast Cancer Research, 21(1) art. 55. DOI: https://doi.org/10.1186/s13058-019-1137-9
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2021 | Journal Article
Ex Vivo Study of Artifacts Caused by Breast Tissue Markers with Different 1.5 Tesla and 3 Tesla MRI Scanners – A Bicentric Study
Puesken, M.; Unterberg-Buchwald, C. ; Rhiem, K.; Große Hokamp, N.; Maintz, D.; Lotz, J. & Wienbeck, S. (2021)
Academic Radiology, 28(1) pp. 77-84. DOI: https://doi.org/10.1016/j.acra.2019.12.006
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2023 | Journal Article
Prevalence of pathogenic germline variants in women with non-familial unilateral tri-ple-negative breast cancer
Rhiem, K.; Zachariae, S.; Waha, A.; Grill, S.; Hester, A.; Golatta, M. & van Mackelenbergh, M. et al. (2023)
Breast Care,. DOI: https://doi.org/10.1159/000528972
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