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Results by year

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

Year Number of Results
1957 1
1958 3
1959 2
1961 2
1963 5
1964 1
1965 4
1966 5
1967 2
1968 3
1969 5
1970 2
1971 6
1972 1
1973 6
1974 3
1975 4
1976 1
1977 9
1978 3
1979 7
1980 4
1981 4
1982 3
1983 4
1984 5
1985 11
1986 6
1987 9
1988 9
1989 16
1990 10
1991 13
1992 19
1993 8
1994 10
1995 17
1996 11
1997 17
1998 14
1999 16
2000 14
2001 10
2002 7
2003 14
2004 13
2005 18
2006 20
2007 18
2008 17
2009 16
2010 16
2011 22
2012 16
2013 14
2014 26
2015 13
2016 15
2017 22
2018 27
2019 20
2020 27
2021 34
2022 34
2023 6
Text availability
Article attribute
Article type
Publication date

Search Results

673 results
Results by year
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Page 1
Genetic characteristics of retinitis pigmentosa in 1204 Japanese patients.
Koyanagi Y, Akiyama M, Nishiguchi KM, Momozawa Y, Kamatani Y, Takata S, Inai C, Iwasaki Y, Kumano M, Murakami Y, Omodaka K, Abe T, Komori S, Gao D, Hirakata T, Kurata K, Hosono K, Ueno S, Hotta Y, Murakami A, Terasaki H, Wada Y, Nakazawa T, Ishibashi T, Ikeda Y, Kubo M, Sonoda KH. Koyanagi Y, et al. Among authors: hotta y. J Med Genet. 2019 Oct;56(10):662-670. doi: 10.1136/jmedgenet-2018-105691. Epub 2019 Jun 17. J Med Genet. 2019. PMID: 31213501
Exophthalmos associated with chronic progressive external ophthalmoplegia.
Takeda Y, Suzuki H, Hosono K, Hikoya A, Komori M, Inagaki R, Haseoka T, Arai S, Takagi Y, Hotta Y, Sato M. Takeda Y, et al. Among authors: hotta y. Jpn J Ophthalmol. 2022 May;66(3):314-319. doi: 10.1007/s10384-022-00920-5. Epub 2022 Apr 19. Jpn J Ophthalmol. 2022. PMID: 35438395
Familial Mediterranean Fever without Fever.
Hotta Y, Kawasaki T, Kotani T, Okada H, Ikeda K, Yamane S, Yamada N, Sekoguchi S, Isozaki Y, Nagao Y, Murotani M, Oyamada H. Hotta Y, et al. Intern Med. 2020 May 15;59(10):1267-1270. doi: 10.2169/internalmedicine.3175-19. Epub 2020 Feb 12. Intern Med. 2020. PMID: 32051376 Free PMC article.
Coenzyme Q10 in the eye isomerizes by sunlight irradiation.
Mamun MA, Nabi MM, Sato T, Aramaki S, Takanashi Y, Sakamoto T, Hizume K, Mori C, Yasue M, Ozaki M, Islam A, Kahyo T, Horikawa M, Takahashi Y, Okazaki S, Ohishi K, Nagashima Y, Seno K, Hotta Y, Setou M. Mamun MA, et al. Among authors: hotta y. Sci Rep. 2022 Jul 15;12(1):12104. doi: 10.1038/s41598-022-16343-8. Sci Rep. 2022. PMID: 35840805 Free PMC article.
De novo heterozygous variants in KIF5B cause kyphomelic dysplasia.
Itai T, Wang Z, Nishimura G, Ohashi H, Guo L, Wakano Y, Sugiura T, Hayakawa H, Okada M, Saisu T, Kitta A, Doi H, Kurosawa K, Hotta Y, Hosono K, Sato M, Shimizu K, Takikawa K, Watanabe S, Ikeda N, Suzuki M, Fujita A, Uchiyama Y, Tsuchida N, Miyatake S, Miyake N, Matsumoto N, Ikegawa S. Itai T, et al. Among authors: hotta y. Clin Genet. 2022 Jul;102(1):3-11. doi: 10.1111/cge.14133. Epub 2022 Apr 5. Clin Genet. 2022. PMID: 35342932
673 results