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Page 1
Genetic medicine in companion diagnostics of germline BRCA testing of Japanese pancreatic cancer patients.
Matsubayashi H, Todaka A, Kawakami T, Hamauchi S, Yokota T, Higashigawa S, Kiyozumi Y, Harada R, Kado N, Nishimura S, Ishiwatari H, Sato J, Niiya F, Ono H, Sugiura T, Sasaki K, Yasui H, Yamazaki K. Matsubayashi H, et al. Among authors: nishimura s. J Hum Genet. 2023 Feb;68(2):81-86. doi: 10.1038/s10038-022-01097-y. Epub 2022 Dec 8. J Hum Genet. 2023. PMID: 36482120
Prevalence of low-penetrant germline TP53 D49H mutation in Japanese cancer patients.
Yamaguchi K, Urakami K, Nagashima T, Shimoda Y, Ohnami S, Ohnami S, Ohshima K, Mochizuki T, Hatakeyama K, Serizawa M, Akiyama Y, Maruyama K, Katagiri H, Ishida Y, Takahashi K, Nishimura S, Terashima M, Kawamura T, Kinugasa Y, Yamakawa Y, Onitsuka T, Ohde Y, Sugino T, Ito I, Matsubayashi H, Horiuchi Y, Mizuguchi M, Yamazaki M, Inoue K, Wakamatsu K, Sugiyama M, Uesaka K, Kusuhara M. Yamaguchi K, et al. Among authors: nishimura s. Biomed Res. 2016;37(4):259-64. doi: 10.2220/biomedres.37.259. Biomed Res. 2016. PMID: 27545002 Free article.
Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.
Horiuchi Y, Matsubayashi H, Kiyozumi Y, Nishimura S, Higashigawa S, Kado N, Nagashima T, Mizuguchi M, Ohnami S, Arai M, Urakami K, Kusuhara M, Yamaguchi K. Horiuchi Y, et al. Among authors: nishimura s. Hum Genet. 2021 Feb;140(2):321-331. doi: 10.1007/s00439-020-02207-6. Epub 2020 Jul 24. Hum Genet. 2021. PMID: 32710294
Sharing genetic test results of germline pathogenic variants of hereditary cancer with relatives: A single-center cross-sectional study.
Fukuzaki N, Kiyozumi Y, Higashigawa S, Horiuchi Y, Mizuguchi M, Matsubayashi H, Nishimura S, Mori K, Notsu A, Suishu I, Ohnami S, Kusuhara M, Yamaguchi K, Doorenbos AZ, Takeda Y. Fukuzaki N, et al. Among authors: nishimura s. Jpn J Clin Oncol. 2021 Oct 5;51(10):1547-1553. doi: 10.1093/jjco/hyab110. Jpn J Clin Oncol. 2021. PMID: 34244736 Free PMC article.
Microsatellite instability is biased in Amsterdam II-defined Lynch-related cancer cases with family history but is rare in other cancers: a summary of 1000 analyses.
Matsubayashi H, Higashigawa S, Kiyozumi Y, Oishi T, Sasaki K, Ishiwatari H, Imai K, Hotta K, Yabuuchi Y, Ishikawa K, Satoh T, Ono H, Todaka A, Kawakami T, Shirasu H, Yasui H, Sugiura T, Uesaka K, Kagawa H, Shiomi A, Kado N, Hirashima Y, Kiyohara Y, Bando E, Niwakawa M, Nishimura S, Aramaki T, Mamesaya N, Kenmotsu H, Horiuchi Y, Serizawa M. Matsubayashi H, et al. Among authors: nishimura s. BMC Cancer. 2022 Jan 17;22(1):73. doi: 10.1186/s12885-022-09172-5. BMC Cancer. 2022. PMID: 35039004 Free PMC article.
Present status of germline findings in precision medicine for Japanese cancer patients: issues in the current system.
Higashigawa S, Matsubayashi H, Kiyozumi Y, Kado N, Nishimura S, Oishi T, Sugino T, Fushiki K, Shirasu H, Yasui H, Mamesaya N, Fukuzaki N, Kunitomo K, Horiuchi Y, Kenmotsu H, Serizawa M. Higashigawa S, et al. Among authors: nishimura s. Jpn J Clin Oncol. 2022 May 31;52(6):599-608. doi: 10.1093/jjco/hyac046. Jpn J Clin Oncol. 2022. PMID: 35411369
Discordance of microsatellite instability and mismatch repair immunochemistry occurs depending on the cancer type.
Matsubayashi H, Oishi T, Sasaki K, Abe M, Kiyozumi Y, Higashigawa S, Niiya F, Sato J, Ishiwatari H, Imai K, Hotta K, Kishida Y, Takada K, Ono H, Yamazaki K, Yasui H, Kenmotsu H, Kado N, Kagawa H, Shiomi A, Sugiura T, Bando E, Nishimura S, Hatakeyama K, Serizawa M, Harada R, Sugino T. Matsubayashi H, et al. Among authors: nishimura s. Hum Pathol. 2023 May;135:54-64. doi: 10.1016/j.humpath.2022.12.016. Epub 2022 Dec 31. Hum Pathol. 2023. PMID: 36596344
A Cross-sectional Study of Regret in Cancer Patients After Sharing Test Results for Pathogenic Germline Variants of Hereditary Cancers With Relatives.
Fukuzaki N, Kiyozumi Y, Higashigawa S, Horiuchi Y, Matsubayashi H, Nishimura S, Mori K, Notsu A, Suishu I, Ohnami S, Kusuhara M, Yamaguchi K, Doorenbos AZ, Takeda Y. Fukuzaki N, et al. Among authors: nishimura s. Cancer Nurs. 2023 Mar 7. doi: 10.1097/NCC.0000000000001224. Online ahead of print. Cancer Nurs. 2023. PMID: 36881649
A Japanese Family Meeting the Clinical Diagnostic Criteria for MEN1 with a MEN1 Variant of Uncertain Significance.
Matsubayashi H, Kiyozumi Y, Harada R, Mukaigawa T, Sugiura T, Ishiwatari H, Sato J, Niiya F, Nakashima K, Kado N, Nishimura S, Honda G, Ohike N. Matsubayashi H, et al. Among authors: nishimura s. Intern Med. 2024 Apr 15;63(8):1119-1123. doi: 10.2169/internalmedicine.2300-23. Epub 2023 Sep 1. Intern Med. 2024. PMID: 37661450 Free PMC article.
3,055 results