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Results by year

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

Year Number of Results
1965 1
1970 1
1973 6
1974 3
1975 2
1978 2
1979 1
1982 2
1983 5
1984 2
1985 5
1986 2
1987 1
1988 3
1991 6
1992 1
1993 2
1994 4
1995 9
1996 4
1997 1
1998 6
1999 7
2000 4
2001 2
2002 8
2003 6
2004 11
2005 6
2006 11
2007 9
2008 11
2009 16
2010 11
2011 17
2012 31
2013 17
2014 26
2015 20
2016 19
2017 28
2018 21
2019 30
2020 35
2021 39
2022 30
2023 22
2024 9

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Search Results

446 results

Results by year

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Page 1
Heterozygous loss-of-function DHX9 variants are associated with neurodevelopmental disorders: Human genetic and experimental evidences.
Yamada M, Nitta Y, Uehara T, Suzuki H, Miya F, Takenouchi T, Tamura M, Ayabe S, Yoshiki A, Maeno A, Saga Y, Furuse T, Yamada I, Okamoto N, Kosaki K, Sugie A. Yamada M, et al. Among authors: takenouchi t. Eur J Med Genet. 2023 Aug;66(8):104804. doi: 10.1016/j.ejmg.2023.104804. Epub 2023 Jun 25. Eur J Med Genet. 2023. PMID: 37369308
Vanishing basal ganglia in ATP1A3-related polymicrogyria.
Ogawa E, Sakaguchi Y, Enokizono M, Yoshihashi H, Yamada M, Suzuki H, Kosaki K, Miyama S, Takenouchi T. Ogawa E, et al. Among authors: takenouchi t. Am J Med Genet A. 2022 Feb;188(2):665-667. doi: 10.1002/ajmg.a.62531. Epub 2021 Oct 11. Am J Med Genet A. 2022. PMID: 34633143 No abstract available.
Protection against neurodegenerative disease on Earth and in space.
Takamatsu Y, Koike W, Takenouchi T, Sugama S, Wei J, Waragai M, Sekiyama K, Hashimoto M. Takamatsu Y, et al. Among authors: takenouchi t. NPJ Microgravity. 2016 Apr 7;2:16013. doi: 10.1038/npjmgrav.2016.13. eCollection 2016. NPJ Microgravity. 2016. PMID: 28725728 Free PMC article.
446 results