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Page 1
Stakeholder Perception of the Implementation of Genetic Risk Testing for Twelve Multifactorial Diseases.
Genes (Basel). 2023 Dec 28;15(1):49. doi: 10.3390/genes15010049.
Genes (Basel). 2023.
PMID: 38254940
Free PMC article.
Significance of prostate/pancreatic/skin cancer family history for detecting BRCA2 pathogenic variant careers among patients with breast cancer.
Minoura Y, Takahashi M, Maeda H, Kuwahara S, Tachikawa H, Yamamoto M, Tomioka N, Watanabe K, Sakurai A.
Minoura Y, et al.
Breast Cancer. 2022 Sep;29(5):808-813. doi: 10.1007/s12282-022-01360-2. Epub 2022 May 31.
Breast Cancer. 2022.
PMID: 35641852
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Initial screening by immunohistochemistry is effective in universal screening for Lynch syndrome in endometrial cancer patients: a prospective observational study.
Tsuruta T, Todo Y, Yamada R, Kuwahara K, Kurosu H, Minowa K, Minoura Y, Minobe S, Suzuki H, Kato H.
Tsuruta T, et al. Among authors: minoura y.
Jpn J Clin Oncol. 2022 Jul 8;52(7):752-758. doi: 10.1093/jjco/hyac058.
Jpn J Clin Oncol. 2022.
PMID: 35438162
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Risk-reducing decisions regarding germline BRCA pathogenic variant: focusing on the timing of genetic testing and RRSO.
Abe A, Nomura H, Fusegi A, Yunokawa M, Ueki A, Habano E, Arakawa H, Kaneko K, Minoura Y, Inari H, Ueno T, Kanao H.
Abe A, et al. Among authors: minoura y.
J Med Genet. 2024 Mar 21;61(4):392-398. doi: 10.1136/jmg-2023-109549.
J Med Genet. 2024.
PMID: 38124001
Free PMC article.
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