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Results by year

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

Year Number of Results
1950 1
1951 1
1952 4
1953 4
1954 5
1955 5
1956 4
1957 2
1958 3
1959 3
1960 5
1961 7
1962 15
1963 13
1964 15
1965 11
1966 9
1967 19
1968 13
1969 17
1970 20
1971 20
1972 33
1973 17
1974 41
1975 38
1976 42
1977 49
1978 55
1979 54
1980 53
1981 69
1982 88
1983 98
1984 120
1985 114
1986 107
1987 98
1988 122
1989 117
1990 93
1991 108
1992 119
1993 122
1994 126
1995 155
1996 144
1997 212
1998 166
1999 207
2000 213
2001 206
2002 223
2003 197
2004 238
2005 250
2006 259
2007 246
2008 267
2009 272
2010 266
2011 293
2012 351
2013 335
2014 362
2015 402
2016 399
2017 423
2018 385
2019 364
2020 438
2021 558
2022 485
2023 416
2024 367

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Publication date

Search Results

10,277 results

Results by year

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Page 1
Multiancestry genomic and transcriptomic analysis of gastric cancer.
Totoki Y, Saito-Adachi M, Shiraishi Y, Komura D, Nakamura H, Suzuki A, Tatsuno K, Rokutan H, Hama N, Yamamoto S, Ono H, Arai Y, Hosoda F, Katoh H, Chiba K, Iida N, Nagae G, Ueda H, Shihang C, Sekine S, Abe H, Nomura S, Matsuura T, Sakai E, Ohshima T, Rino Y, Yeoh KG, So J, Sanghvi K, Soong R, Fukagawa A, Yachida S, Kato M, Seto Y, Ushiku T, Nakajima A, Katai H, Tan P, Ishikawa S, Aburatani H, Shibata T. Totoki Y, et al. Among authors: yamamoto s. Nat Genet. 2023 Apr;55(4):581-594. doi: 10.1038/s41588-023-01333-x. Epub 2023 Mar 13. Nat Genet. 2023. PMID: 36914835
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, Terasaki H, Kominami T, Nao-I N, Mawatari G, Mizota A, Shinoda K, Kondo M, Kato K, Sekiryu T, Nakamura M, Kusuhara S, Yamamoto H, Yamamoto S, Mochizuki K, Kondo H, Matsushita I, Kameya S, Fukuchi T, Hatase T, Horiguchi M, Shimada Y, Tanikawa A, Yamamoto S, Miura G, Ito N, Murakami A, Fujimaki T, Hotta Y, Tanaka K, Iwata T. Suga A, et al. Among authors: yamamoto s. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
Identification of an Anti-Integrin αvβ6 Autoantibody in Patients With Ulcerative Colitis.
Kuwada T, Shiokawa M, Kodama Y, Ota S, Kakiuchi N, Nannya Y, Yamazaki H, Yoshida H, Nakamura T, Matsumoto S, Muramoto Y, Yamamoto S, Honzawa Y, Kuriyama K, Okamoto K, Hirano T, Okada H, Marui S, Sogabe Y, Morita T, Matsumori T, Mima A, Nishikawa Y, Ueda T, Matsumura K, Uza N, Chiba T, Seno H. Kuwada T, et al. Among authors: yamamoto s. Gastroenterology. 2021 Jun;160(7):2383-2394.e21. doi: 10.1053/j.gastro.2021.02.019. Epub 2021 Feb 12. Gastroenterology. 2021. PMID: 33582126 Free article.
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Among authors: yamamoto s. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.
Estimated Effect of Restarting Renin-Angiotensin System Inhibitors after Discontinuation on Kidney Outcomes and Mortality.
Hattori K, Sakaguchi Y, Oka T, Asahina Y, Kawaoka T, Doi Y, Hashimoto N, Kusunoki Y, Yamamoto S, Yamato M, Yamamoto R, Matsui I, Mizui M, Kaimori JY, Isaka Y. Hattori K, et al. Among authors: yamamoto s. J Am Soc Nephrol. 2024 Oct 1;35(10):1391-1401. doi: 10.1681/ASN.0000000000000425. Epub 2024 Jun 18. J Am Soc Nephrol. 2024. PMID: 38889205 No abstract available.
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Nil Z, Deshwar AR, Huang Y, Barish S, Zhang X, Choufani S, Le Quesne Stabej P, Hayes I, Yap P, Haldeman-Englert C, Wilson C, Prescott T, Tveten K, Vøllo A, Haynes D, Wheeler PG, Zon J, Cytrynbaum C, Jobling R, Blyth M, Banka S, Afenjar A, Mignot C, Robin-Renaldo F, Keren B, Kanca O, Mao X, Wegner DJ, Sisco K, Shinawi M; Undiagnosed Disease Network; Wangler MF, Weksberg R, Yamamoto S, Costain G, Bellen HJ. Nil Z, et al. Among authors: yamamoto s. Am J Hum Genet. 2023 Nov 2;110(11):1919-1937. doi: 10.1016/j.ajhg.2023.09.009. Epub 2023 Oct 11. Am J Hum Genet. 2023. PMID: 37827158 Free PMC article.
A red light-responsive photoswitch for deep tissue optogenetics.
Kuwasaki Y, Suzuki K, Yu G, Yamamoto S, Otabe T, Kakihara Y, Nishiwaki M, Miyake K, Fushimi K, Bekdash R, Shimizu Y, Narikawa R, Nakajima T, Yazawa M, Sato M. Kuwasaki Y, et al. Among authors: yamamoto s. Nat Biotechnol. 2022 Nov;40(11):1672-1679. doi: 10.1038/s41587-022-01351-w. Epub 2022 Jun 13. Nat Biotechnol. 2022. PMID: 35697806
Defining conversion therapy for esophageal squamous cell carcinoma.
Matsuda S, Tsushima T, Kato K, Hsu CH, Lee JM, Wong IY, Wang HC, Kang CH, Guo X, Yamamoto S, Tsuji T, Kawakubo H, Takeuchi H, Law S, Kitagawa Y. Matsuda S, et al. Among authors: yamamoto s. Ann Gastroenterol Surg. 2022 Oct 19;7(1):7-9. doi: 10.1002/ags3.12623. eCollection 2023 Jan. Ann Gastroenterol Surg. 2022. PMID: 36643357 Free PMC article.
10,277 results
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