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

Year Number of Results
1965 1
1966 1
1984 1
1998 1
1999 2
2000 2
2001 4
2002 2
2003 3
2004 4
2005 8
2006 11
2007 12
2008 13
2009 13
2010 18
2011 17
2012 8
2013 7
2014 12
2015 10
2016 12
2017 6
2018 7
2019 8
2020 7
2021 12
2022 5
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Search Results

168 results
Results by year
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Page 1
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: reid sm. Nat Genet. 2020 Oct;52(10):1046-1056. doi: 10.1038/s41588-020-0695-1. Epub 2020 Sep 28. Nat Genet. 2020. PMID: 32989326
Emergence and spread of novel H5N8, H5N5 and H5N1 clade 2.3.4.4 highly pathogenic avian influenza in 2020.
Lewis NS, Banyard AC, Whittard E, Karibayev T, Al Kafagi T, Chvala I, Byrne A, Meruyert Akberovna S, King J, Harder T, Grund C, Essen S, Reid SM, Brouwer A, Zinyakov NG, Tegzhanov A, Irza V, Pohlmann A, Beer M, Fouchier RAM, Akhmetzhan Akievich S, Brown IH. Lewis NS, et al. Among authors: reid sm. Emerg Microbes Infect. 2021 Dec;10(1):148-151. doi: 10.1080/22221751.2021.1872355. Emerg Microbes Infect. 2021. PMID: 33400615 Free PMC article.
Anxiety in children and adolescents with cerebral palsy.
McMahon J, Harvey A, Reid SM, May T, Antolovich G. McMahon J, et al. Among authors: reid sm. J Paediatr Child Health. 2020 Aug;56(8):1194-1200. doi: 10.1111/jpc.14879. Epub 2020 May 15. J Paediatr Child Health. 2020. PMID: 32412671
Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome.
Shepherd DA, Vos N, Reid SM, Godler DE, Guzys A, Moreno-Betancur M, Amor DJ. Shepherd DA, et al. Among authors: reid sm. Genes (Basel). 2020 Jul 2;11(7):736. doi: 10.3390/genes11070736. Genes (Basel). 2020. PMID: 32630716 Free PMC article.
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Among authors: reid sm. Nat Genet. 2021 Mar;53(3):412. doi: 10.1038/s41588-021-00780-8. Nat Genet. 2021. PMID: 33432185 No abstract available.
168 results