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Results by year

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

Year Number of Results
1949 1
1953 1
1954 2
1957 1
1958 3
1959 6
1960 8
1961 29
1962 14
1963 7
1964 10
1965 11
1966 12
1967 11
1968 13
1969 20
1970 21
1971 25
1972 18
1973 26
1974 20
1975 11
1976 9
1977 13
1978 13
1979 13
1980 30
1981 26
1982 19
1983 17
1984 11
1985 14
1986 14
1987 12
1988 15
1989 13
1990 12
1991 11
1992 12
1993 12
1994 8
1995 9
1996 11
1997 2
1998 2
1999 6
2000 3
2001 4
2002 5
2003 6
2004 11
2005 6
2006 11
2007 11
2008 8
2009 9
2010 6
2011 8
2012 11
2013 15
2014 10
2015 12
2016 23
2017 29
2018 32
2019 31
2020 27
2021 18
2022 10
2023 12
2024 8

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847 results

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Page 1
Response.
Holmes I, Shinn B, Mitsuhashi S, Boortalary T, Bashir M, Kowalski T, Loren D, Kumar A, Schlachterman A, Chiang A. Holmes I, et al. Among authors: mitsuhashi s. Gastrointest Endosc. 2022 Apr;95(4):815-816. doi: 10.1016/j.gie.2021.12.012. Gastrointest Endosc. 2022. PMID: 35303988 No abstract available.
Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.
Takata A, Nakashima M, Saitsu H, Mizuguchi T, Mitsuhashi S, Takahashi Y, Okamoto N, Osaka H, Nakamura K, Tohyama J, Haginoya K, Takeshita S, Kuki I, Okanishi T, Goto T, Sasaki M, Sakai Y, Miyake N, Miyatake S, Tsuchida N, Iwama K, Minase G, Sekiguchi F, Fujita A, Imagawa E, Koshimizu E, Uchiyama Y, Hamanaka K, Ohba C, Itai T, Aoi H, Saida K, Sakaguchi T, Den K, Takahashi R, Ikeda H, Yamaguchi T, Tsukamoto K, Yoshitomi S, Oboshi T, Imai K, Kimizu T, Kobayashi Y, Kubota M, Kashii H, Baba S, Iai M, Kira R, Hara M, Ohta M, Miyata Y, Miyata R, Takanashi JI, Matsui J, Yokochi K, Shimono M, Amamoto M, Takayama R, Hirabayashi S, Aiba K, Matsumoto H, Nabatame S, Shiihara T, Kato M, Matsumoto N. Takata A, et al. Among authors: mitsuhashi s. Nat Commun. 2019 Jun 7;10(1):2506. doi: 10.1038/s41467-019-10482-9. Nat Commun. 2019. PMID: 31175295 Free PMC article.
Large-scale discovery of novel neurodevelopmental disorder-related genes through a unified analysis of single-nucleotide and copy number variants.
Hamanaka K, Miyake N, Mizuguchi T, Miyatake S, Uchiyama Y, Tsuchida N, Sekiguchi F, Mitsuhashi S, Tsurusaki Y, Nakashima M, Saitsu H, Yamada K, Sakamoto M, Fukuda H, Ohori S, Saida K, Itai T, Azuma Y, Koshimizu E, Fujita A, Erturk B, Hiraki Y, Ch'ng GS, Kato M, Okamoto N, Takata A, Matsumoto N. Hamanaka K, et al. Among authors: mitsuhashi s. Genome Med. 2022 Apr 26;14(1):40. doi: 10.1186/s13073-022-01042-w. Genome Med. 2022. PMID: 35468861 Free PMC article.
Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy.
Ohori S, Miyauchi A, Osaka H, Lourenco CM, Arakaki N, Sengoku T, Ogata K, Honjo RS, Kim CA, Mitsuhashi S, Frith MC, Seyama R, Tsuchida N, Uchiyama Y, Koshimizu E, Hamanaka K, Misawa K, Miyatake S, Mizuguchi T, Saito K, Fujita A, Matsumoto N. Ohori S, et al. Among authors: mitsuhashi s. Life Sci Alliance. 2023 Jun 7;6(8):e202302025. doi: 10.26508/lsa.202302025. Print 2023 Aug. Life Sci Alliance. 2023. PMID: 37286232 Free PMC article.
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, Takeuchi H, Kawamoto M, Kohara N, Ando T, Ieda T, Kita Y, Kokubun N, Tsuboi Y, Katoh K, Kino Y, Katsuno M, Iwasaki Y, Yoshida M, Tanaka F, Suzuki IK, Frith MC, Matsumoto N, Sobue G. Sone J, et al. Among authors: mitsuhashi s. Nat Genet. 2019 Aug;51(8):1215-1221. doi: 10.1038/s41588-019-0459-y. Epub 2019 Jul 22. Nat Genet. 2019. PMID: 31332381
PRUNE1-related disorder: Expanding the clinical spectrum.
Imagawa E, Yamamoto Y, Mitsuhashi S, Isidor B, Fukuyama T, Kato M, Sasaki M, Tanabe S, Miyatake S, Mizuguchi T, Takata A, Miyake N, Matsumoto N. Imagawa E, et al. Among authors: mitsuhashi s. Clin Genet. 2018 Oct;94(3-4):362-367. doi: 10.1111/cge.13385. Epub 2018 Jun 26. Clin Genet. 2018. PMID: 29797509
Miller-Fisher Syndrome Following Influenza A Infection.
Mitsuhashi S, Suzuki A, Hayashi K, Sato M, Nakaya Y, Takaku N, Kobayashi Y. Mitsuhashi S, et al. Cureus. 2024 Mar 12;16(3):e56064. doi: 10.7759/cureus.56064. eCollection 2024 Mar. Cureus. 2024. PMID: 38618457 Free PMC article.
847 results