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

Year Number of Results
2002 3
2003 4
2004 5
2005 7
2006 1
2007 2
2008 3
2009 5
2010 7
2011 4
2012 2
2013 6
2014 7
2015 10
2016 9
2017 6
2018 2
2019 2
2020 2
2021 5
2022 4
2023 3
2024 1

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83 results

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Page 1
Complete sequencing and characterization of 21,243 full-length human cDNAs.
Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, Wakamatsu A, Hayashi K, Sato H, Nagai K, Kimura K, Makita H, Sekine M, Obayashi M, Nishi T, Shibahara T, Tanaka T, Ishii S, Yamamoto J, Saito K, Kawai Y, Isono Y, Nakamura Y, Nagahari K, Murakami K, Yasuda T, Iwayanagi T, Wagatsuma M, Shiratori A, Sudo H, Hosoiri T, Kaku Y, Kodaira H, Kondo H, Sugawara M, Takahashi M, Kanda K, Yokoi T, Furuya T, Kikkawa E, Omura Y, Abe K, Kamihara K, Katsuta N, Sato K, Tanikawa M, Yamazaki M, Ninomiya K, Ishibashi T, Yamashita H, Murakawa K, Fujimori K, Tanai H, Kimata M, Watanabe M, Hiraoka S, Chiba Y, Ishida S, Ono Y, Takiguchi S, Watanabe S, Yosida M, Hotuta T, Kusano J, Kanehori K, Takahashi-Fujii A, Hara H, Tanase TO, Nomura Y, Togiya S, Komai F, Hara R, Takeuchi K, Arita M, Imose N, Musashino K, Yuuki H, Oshima A, Sasaki N, Aotsuka S, Yoshikawa Y, Matsunawa H, Ichihara T, Shiohata N, Sano S, Moriya S, Momiyama H, Satoh N, Takami S, Terashima Y, Suzuki O, Nakagawa S, Senoh A, Mizoguchi H, Goto Y, Shimizu F, Wakebe H, Hishigaki H, Watanabe T, Sugiyama A, Takemoto M, Kawakami B, Yamazaki M, Watanabe K, Kumagai A, Itakura S, Fukuzumi Y, Fujimori Y, Komiyama M, Tashiro H, Tanigami… See abstract for full author list ➔ Ota T, et al. Among authors: nomura y. Nat Genet. 2004 Jan;36(1):40-5. doi: 10.1038/ng1285. Epub 2003 Dec 21. Nat Genet. 2004. PMID: 14702039
Rett syndrome: revised diagnostic criteria and nomenclature.
Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK; RettSearch Consortium. Neul JL, et al. Ann Neurol. 2010 Dec;68(6):944-50. doi: 10.1002/ana.22124. Ann Neurol. 2010. PMID: 21154482 Free PMC article.
Preface.
Nomura Y, Kerr A, Engerström IW. Nomura Y, et al. Brain Dev. 2005 Nov;27 Suppl 1:S1. doi: 10.1016/j.braindev.2005.07.001. Epub 2005 Sep 22. Brain Dev. 2005. PMID: 16182493 No abstract available.
Two-step nationwide epidemiological survey of myasthenia gravis in Japan 2018.
Yoshikawa H, Adachi Y, Nakamura Y, Kuriyama N, Murai H, Nomura Y, Sakai Y, Iwasa K, Furukawa Y, Kuwabara S, Matsui M; Taskforce of Validation of Evidence-based Diagnosis and Guidelines, and Impact on Quality of Life (QOL) in Patients with Neuroimmunological Diseases. Yoshikawa H, et al. Among authors: nomura y. PLoS One. 2022 Sep 21;17(9):e0274161. doi: 10.1371/journal.pone.0274161. eCollection 2022. PLoS One. 2022. PMID: 36129914 Free PMC article.
Rett syndrome.
Segawa M, Nomura Y. Segawa M, et al. Among authors: nomura y. Curr Opin Neurol. 2005 Apr;18(2):97-104. doi: 10.1097/01.wco.0000162848.99154.9a. Curr Opin Neurol. 2005. PMID: 15791137 Review.
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution.
Jagota P, Ugawa Y, Aldaajani Z, Ibrahim NM, Ishiura H, Nomura Y, Tsuji S, Diesta C, Hattori N, Onodera O, Bohlega S, Al-Din A, Lim SY, Lee JY, Jeon B, Pal PK, Shang H, Fujioka S, Kukkle PL, Phokaewvarangkul O, Lin CH, Shambetova C, Bhidayasiri R. Jagota P, et al. Among authors: nomura y. J Mov Disord. 2023 Sep;16(3):231-247. doi: 10.14802/jmd.23065. Epub 2023 Jun 13. J Mov Disord. 2023. PMID: 37309109 Free PMC article.
Natural history of Rett syndrome.
Nomura Y, Segawa M. Nomura Y, et al. J Child Neurol. 2005 Sep;20(9):764-8. doi: 10.1177/08830738050200091201. J Child Neurol. 2005. PMID: 16225833 Review.
83 results