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Results by year

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

Year Number of Results
1896 1
1897 1
1899 1
1900 2
1902 2
1903 1
1906 2
1907 2
1908 2
1912 1
1913 1
1915 1
1916 1
1917 1
1920 1
1921 1
1923 1
1924 1
1925 2
1926 1
1927 2
1935 1
1950 1
1956 3
1957 2
1959 1
1960 4
1961 4
1962 1
1967 1
1968 1
1969 2
1971 5
1972 2
1973 2
1974 2
1975 2
1976 2
1977 2
1979 4
1980 5
1981 4
1982 5
1983 7
1984 3
1985 3
1986 7
1987 3
1988 4
1989 5
1990 8
1991 11
1992 8
1993 10
1994 5
1995 15
1996 7
1997 9
1998 8
1999 7
2000 12
2001 12
2002 10
2003 9
2004 17
2005 10
2006 20
2007 12
2008 11
2009 12
2010 6
2011 12
2012 11
2013 12
2014 1
2015 4
2016 3
2017 4
2018 9
2019 9
2020 4
2021 8
2022 3
2023 2
2024 2

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404 results

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Page 1
Exome sequencing reveals genetic heterogeneity and clinically actionable findings in children with cerebral palsy.
Wang Y, Xu Y, Zhou C, Cheng Y, Qiao N, Shang Q, Xia L, Song J, Gao C, Qiao Y, Zhang X, Li M, Ma C, Fan Y, Peng X, Wu S, Lv N, Li B, Sun Y, Zhang B, Li T, Li H, Zhang J, Su Y, Li Q, Yuan J, Liu L, Moreno-De-Luca A, MacLennan AH, Gecz J, Zhu D, Wang X, Zhu C, Xing Q. Wang Y, et al. Among authors: maclennan ah. Nat Med. 2024 May 1. doi: 10.1038/s41591-024-02912-z. Online ahead of print. Nat Med. 2024. PMID: 38693247
The Presence of Women in the Dental Profession: A Global Survey.
Campus G, Maclennan A, von Hoyningen-Huene J, Wolf TG; FDI Section Women Dentists Worldwide Collaboration Group; Aerden M, Benyahya I, Bonaventura J, Brolese ELK, Linton JL, Gogilashvili K, Marron-Tarrazi I, Ilhan D, Iwasaki M, Grzech-Lesniak K, Perlea P, Thabet N. Campus G, et al. Among authors: maclennan a. Int Dent J. 2024 Feb;74(1):110-118. doi: 10.1016/j.identj.2023.07.010. Epub 2023 Sep 24. Int Dent J. 2024. PMID: 37748962 Free PMC article.
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants.
Kayumi S, Pérez-Jurado LA, Palomares M, Rangu S, Sheppard SE, Chung WK, Kruer MC, Kharbanda M, Amor DJ, McGillivray G, Cohen JS, García-Miñaúr S, van Eyk CL, Harper K, Jolly LA, Webber DL, Barnett CP, Santos-Simarro F, Pacio-Míguez M, Pozo AD, Bakhtiari S, Deardorff M, Dubbs HA, Izumi K, Grand K, Gray C, Mark PR, Bhoj EJ, Li D, Ortiz-Gonzalez XR, Keena B, Zackai EH, Goldberg EM, Perez de Nanclares G, Pereda A, Llano-Rivas I, Arroyo I, Fernández-Cuesta MÁ, Thauvin-Robinet C, Faivre L, Garde A, Mazel B, Bruel AL, Tress ML, Brilstra E, Fine AS, Crompton KE, Stegmann APA, Sinnema M, Stevens SCJ, Nicolai J, Lesca G, Lion-François L, Haye D, Chatron N, Piton A, Nizon M, Cogne B, Srivastava S, Bassetti J, Muss C, Gripp KW, Procopio RA, Millan F, Morrow MM, Assaf M, Moreno-De-Luca A, Joss S, Hamilton MJ, Bertoli M, Foulds N, McKee S, MacLennan AH, Gecz J, Corbett MA. Kayumi S, et al. Among authors: maclennan ah. Genet Med. 2022 Nov;24(11):2351-2366. doi: 10.1016/j.gim.2022.08.006. Epub 2022 Sep 9. Genet Med. 2022. PMID: 36083290 Free PMC article.
Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss.
Richard EM, Bakhtiari S, Marsh APL, Kaiyrzhanov R, Wagner M, Shetty S, Pagnozzi A, Nordlie SM, Guida BS, Cornejo P, Magee H, Liu J, Norton BY, Webster RI, Worgan L, Hakonarson H, Li J, Guo Y, Jain M, Blesson A, Rodan LH, Abbott MA, Comi A, Cohen JS, Alhaddad B, Meitinger T, Lenz D, Ziegler A, Kotzaeridou U, Brunet T, Chassevent A, Smith-Hicks C, Ekstein J, Weiden T, Hahn A, Zharkinbekova N, Turnpenny P, Tucci A, Yelton M, Horvath R, Gungor S, Hiz S, Oktay Y, Lochmuller H, Zollino M, Morleo M, Marangi G, Nigro V, Torella A, Pinelli M, Amenta S, Husain RA, Grossmann B, Rapp M, Steen C, Marquardt I, Grimmel M, Grasshoff U, Korenke GC, Owczarek-Lipska M, Neidhardt J, Radio FC, Mancini C, Claps Sepulveda DJ, McWalter K, Begtrup A, Crunk A, Guillen Sacoto MJ, Person R, Schnur RE, Mancardi MM, Kreuder F, Striano P, Zara F, Chung WK, Marks WA, van Eyk CL, Webber DL, Corbett MA, Harper K, Berry JG, MacLennan AH, Gecz J, Tartaglia M, Salpietro V, Christodoulou J, Kaslin J, Padilla-Lopez S, Bilguvar K, Munchau A, Ahmed ZM, Hufnagel RB, Fahey MC, Maroofian R, Houlden H, Sticht H, Mane SM, Rad A, Vona B, Jin SC, Haack TB, Makowski C, Hirsch Y, Riazuddin S, Kruer MC. Richard EM, et al. Among authors: maclennan ah. Am J Hum Genet. 2021 Oct 7;108(10):2006-2016. doi: 10.1016/j.ajhg.2021.08.003. Am J Hum Genet. 2021. PMID: 34626583 Free PMC article.
All cases of cerebral palsy warrant genomic screening.
Maclennan AH. Maclennan AH. Dev Med Child Neurol. 2021 Dec;63(12):1369. doi: 10.1111/dmcn.14951. Epub 2021 Jun 10. Dev Med Child Neurol. 2021. PMID: 34114233 Free article. No abstract available.
404 results