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

Year Number of Results
1947 1
1951 1
1952 1
1953 2
1954 1
1957 3
1958 1
1959 2
1960 5
1961 9
1962 14
1963 17
1964 18
1965 31
1966 31
1967 19
1968 26
1969 26
1970 27
1971 21
1972 28
1973 20
1974 23
1975 35
1976 43
1977 31
1978 50
1979 52
1980 44
1981 54
1982 74
1983 70
1984 73
1985 101
1986 87
1987 102
1988 97
1989 131
1990 122
1991 161
1992 159
1993 166
1994 193
1995 236
1996 205
1997 204
1998 226
1999 251
2000 239
2001 273
2002 314
2003 311
2004 292
2005 347
2006 344
2007 357
2008 434
2009 471
2010 478
2011 498
2012 537
2013 594
2014 582
2015 571
2016 598
2017 607
2018 631
2019 576
2020 694
2021 706
2022 677
2023 587
2024 523
2025 508
2026 2

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14,523 results

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Page 1
Formation of I2+III2 supercomplex rescues respiratory chain defects.
Liang C, Padavannil A, Zhang S, Beh S, Robinson DRL, Meisterknecht J, Cabrera-Orefice A, Koves TR, Watanabe C, Watanabe M, Illescas M, Lim R, Johnson JM, Ren S, Wu YJ, Kappei D, Ghelli AM, Funai K, Osaka H, Muoio D, Ugalde C, Wittig I, Stroud DA, Letts JA, Ho L. Liang C, et al. Among authors: watanabe m. Cell Metab. 2025 Feb 4;37(2):441-459.e11. doi: 10.1016/j.cmet.2024.11.011. Epub 2025 Jan 8. Cell Metab. 2025. PMID: 39788125
[Lumpy Skin Disease].
Watanabe M, Ikezawa M, Kokuho T, Morioka K. Watanabe M, et al. Uirusu. 2025;75(1):1-12. doi: 10.2222/jsv.75.1. Uirusu. 2025. PMID: 41016798 Free article. Review. Japanese.
Contribution of germline and somatic mutations to risk of neuromyelitis optica spectrum disorder.
Yata T, Sato G, Ogawa K, Naito T, Sonehara K, Saiki R, Edahiro R, Namba S, Watanabe M, Shirai Y, Yamamoto K, NamKoong H, Nakanishi T, Yamamoto Y, Hosokawa A, Yamamoto M; Japan MS/NMOSD biobank; BioBank Japan Project; Japan COVID-19 Task Force; Oguro-Igashira E, Nii T, Maeda Y, Nakajima K, Nishikawa R, Tanaka H, Nakayamada S, Matsuda K, Nishigori C, Sano S, Kinoshita M, Koike R, Kimura A, Imoto S, Miyano S, Fukunaga K, Mihara M, Shimizu Y, Kawachi I, Miyamoto K, Tanaka Y, Kumanogoh A, Niino M, Nakatsuji Y, Ogawa S, Matsushita T, Kira JI, Mochizuki H, Isobe N, Okuno T, Okada Y. Yata T, et al. Among authors: watanabe m. Cell Genom. 2025 Mar 12;5(3):100776. doi: 10.1016/j.xgen.2025.100776. Epub 2025 Feb 21. Cell Genom. 2025. PMID: 39986280 Free PMC article.
Impact of myelodysplasia-related gene mutations and residual mutations at remission in venetoclax/azacitidine for AML.
Ikoma Y, Nakamura N, Kaneda Y, Takamori H, Seki T, Hiramoto N, Kitagawa J, Kanda J, Fujita K, Morishita T, Ochi Y, Chiba S, Sasaki N, Ichii M, Imada K, Watanabe M, Hishizawa M, Miyahara Y, Maesako Y, Tanaka Y, Oka S, Tsuji M, Yoshihara S, Mitani K, Ueda Y, Kitano T, Watanabe M, Sezaki N, Kondo T, Kasahara S, Takaori-Kondo A, Kanemura N, Ogawa S, Nannya Y. Ikoma Y, et al. Among authors: watanabe m. Leukemia. 2025 Jun;39(6):1362-1367. doi: 10.1038/s41375-025-02625-3. Epub 2025 Apr 21. Leukemia. 2025. PMID: 40259101 Free PMC article.
Determination of Genotype and Phenotypes in Pediatric Patients With Biventricular Noncompaction.
Hirono K, Hata Y, Imamura T, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Ichimata S, Nishida N, Iwasaki H, Urata S, Okada S, Hiratsuji T, Sakaguchi H, Takigiku K, Nakazawa M, Nishihara E, Harada M, Matsuo O, Yasuda K, Yoshida Y, Namiki H, Yasuda K, Ifuku T, Urayama K, Oka H, Ogino K, Kato A, Kan N, Seki S, Seki M, Odanaka Y, Iwashima S, Yoshida S, Miyata T, Miyamoto T, Watanabe K, Kuwabara N, Inuzuka R, Takahashi Y, Sakazaki H, Muneuchi J, Kogaki S, Numano F, Kido S, Nii M, Hoshino S, Ishida H, Maeda J, Hayabuchi Y, Otsubo Y, Ikeda K, Tsukano S, Watanabe M, Momoi N, Fujii T, Fujioka T, Fujino M, Uchiyama H, Baba S, Horigome H, Honda T, Suzuki K, Ichida F. Hirono K, et al. Among authors: watanabe m. J Am Heart Assoc. 2024 Nov 5;13(21):e035614. doi: 10.1161/JAHA.124.035614. Epub 2024 Nov 4. J Am Heart Assoc. 2024. PMID: 39494597 Free PMC article.
Herpes simplex virus 1 evades APOBEC1-mediated immunity via its uracil-DNA glycosylase in mice.
Kato A, Harima H, Tsunekawa Y, Igarashi M, Kitamura K, Wakae K, Nishiyama T, Morimoto S, Suzuki T, Kozuka-Hata H, Oyama M, Motooka D, Watanabe M, Takeshima K, Maruzuru Y, Koyanagi N, Okano H, Inada T, Okada T, Muramatsu M, Kawaguchi Y. Kato A, et al. Among authors: watanabe m. Nat Microbiol. 2025 Jul;10(7):1758-1774. doi: 10.1038/s41564-025-02026-3. Epub 2025 Jun 3. Nat Microbiol. 2025. PMID: 40461648
Genetic analysis of myeloid neoplasms with der(1;7)(q10;p10).
Okuda R, Ochi Y, Saiki R, Yamanaka T, Terao C, Yoshizato T, Nakagawa MM, Zhao L, Ohyashiki K, Hiramoto N, Sanada M, Handa H, Kasahara S, Miyazaki Y, Sezaki N, Shih LY, Kern W, Kanemura N, Kitano T, Imashuku S, Watanabe M, Creignou M, Chonabayashi K, Usuki K, Ishikawa T, Gotoh A, Atsuta Y, Shiraishi Y, Mitani K, Chiba S, Takaori-Kondo A, Miyano S, Kamatani Y, Haferlach T, Hellström-Lindberg E, Matsuda K, Yoshida Y, Makishima H, Nannya Y, Ogawa S. Okuda R, et al. Among authors: watanabe m. Leukemia. 2025 Mar;39(3):760-764. doi: 10.1038/s41375-024-02494-2. Epub 2024 Dec 23. Leukemia. 2025. PMID: 39715854 Free PMC article. No abstract available.
AI-based phenotyping of hepatic fiber morphology to inform molecular alterations in metabolic dysfunction-associated steatotic liver disease.
Fujiwara N, Matsushita Y, Tempaku M, Tachi Y, Kimura G, Izuoka K, Hayata Y, Kawamura S, Eguchi A, Nakatsuka T, Sato M, Ono A, Murakami E, Tsuge M, Oka S, Hayashi A, Hirokawa Y, Watanabe M, Parikh ND, Singal AG, Marrero JA, Hoshida Y, Mizuno S, Tateishi R, Koike K, Fujishiro M, Nakagawa H. Fujiwara N, et al. Among authors: watanabe m. Hepatology. 2025 Apr 22:10.1097/HEP.0000000000001360. doi: 10.1097/HEP.0000000000001360. Online ahead of print. Hepatology. 2025. PMID: 40262132
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