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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 1
2007 2
2008 3
2009 1
2011 4
2012 6
2013 5
2014 5
2015 4
2016 4
2017 9
2018 8
2019 13
2020 12
2021 13
2022 13
2023 5
2024 5
2025 9
2026 11

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122 results

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Page 1
Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants.
Ishikawa T, Kimoto H, Seki A, Shirai M, Uto K, Makiyama T, Kitai T, Mishima H, Trujillano D, Simonet F, Baron E, Lindenbaum P, Kyndt F, Goudal A, Fukushima N, Fujita T, Hatakeyama K, Hagiwara N, Yoshiura KI, Redon R, Dina C, Estivill X, Ossowski S, Courtheix M, Probst V, Barc J, Schott JJ, Makita N. Ishikawa T, et al. Among authors: mishima h. Cardiovasc Res. 2025 Sep 29;121(11):1712-1721. doi: 10.1093/cvr/cvaf135. Cardiovasc Res. 2025. PMID: 40757694 Free article.
Clonal hematopoiesis related to ionizing radiation in atomic bomb survivors.
Taguchi M, Sato S, Nannya Y, Mishima H, Horai M, Ando K, Kinoshita A, Saiki R, Ochi Y, Nagai K, Yokota K, Hamada K, Miyata J, Maeda T, Namba S, Okada Y, Matsuda K, Ogawa S, Yoshiura KI, Miyazaki Y. Taguchi M, et al. Among authors: mishima h. Leukemia. 2026 Aug 12. doi: 10.1038/s41375-026-03101-2. Online ahead of print. Leukemia. 2026. PMID: 42587025 No abstract available.
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Matsumoto M, Oyake M, Itonaga T, Maeda M, Suenobu S, Sato D, Sasahara Y, Mishima H, Yoshiura KI, Ihara K. Matsumoto M, et al. Among authors: mishima h. Eur J Med Genet. 2024 Jun;69:104939. doi: 10.1016/j.ejmg.2024.104939. Epub 2024 Apr 15. Eur J Med Genet. 2024. PMID: 38614309 Free article. Review.
HLA-DRB3/4/5-based susceptibility profiles in nivolumab-induced type 1 diabetes and interstitial lung disease.
Nishikido S, Mishima H, Yoshiura KI, Sakamoto N, Ishimoto H, Morimoto S, Horie I, Akazawa S, Haraguchi A, Tsujiguchi H, Hara A, Tajima A, Hosomichi K, Mukae H, Kawakami A, Abiru N. Nishikido S, et al. Among authors: mishima h. Front Immunol. 2026 Jun 2;17:1840622. doi: 10.3389/fimmu.2026.1840622. eCollection 2026. Front Immunol. 2026. PMID: 42311662 Free PMC article.
Maternal copy number variations detected by noninvasive prenatal testing in Japanese women.
Masuda K, Mishima H, Yoshiura KI, Kitajima Y, Miura S, Hasegawa Y, Ichizuka K, Tominaga M, Komatsu R, Kondo T, Wada S, Sago H, Ito Y, Samura O, Suzumori N, Sawai H, Katagiri Y, Maeda Y, Morisaki H, Namba A, Kamei Y, Yotsumoto J, Shirato N, Nakayama S, Kawaguchi S, Hamanoue H, Mimura K, Matsubara Y, Okamoto Y, Fujiwara A, Maeda K, Watanabe T, Ida A, Hayakawa H, Goto K, Sekizawa A, Miura K. Masuda K, et al. Among authors: mishima h. J Hum Genet. 2026 Jun;71(6):335-342. doi: 10.1038/s10038-025-01444-9. Epub 2026 Jan 13. J Hum Genet. 2026. PMID: 41530548
Germline mutations causing familial lung cancer.
Tomoshige K, Matsumoto K, Tsuchiya T, Oikawa M, Miyazaki T, Yamasaki N, Mishima H, Kinoshita A, Kubo T, Fukushima K, Yoshiura K, Nagayasu T. Tomoshige K, et al. Among authors: mishima h. J Hum Genet. 2015 Oct;60(10):597-603. doi: 10.1038/jhg.2015.75. Epub 2015 Jul 16. J Hum Genet. 2015. PMID: 26178433
122 results