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

Year Number of Results
1979 1
1980 1
1981 1
1982 3
1984 1
1985 1
1986 6
1987 5
1988 8
1989 5
1990 4
1991 6
1992 6
1993 5
1994 5
1995 1
1996 2
1997 2
1998 5
1999 5
2000 3
2001 9
2002 6
2003 4
2004 9
2005 5
2006 8
2007 5
2008 2
2009 5
2010 7
2011 1
2012 13
2013 6
2014 8
2015 4
2016 6
2017 4
2018 6
2019 6
2020 4
2021 5
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184 results
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Page 1
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
May P, Girard S, Harrer M, Bobbili DR, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad CE, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Guerrero-López R, Baulac S, Marini C, Thiele H, Altmüller J, Jabbari K, Ruppert AK, Jurkowski W, Lal D, Rusconi R, Cestèle S, Terragni B, Coombs ID, Reid CA, Striano P, Caglayan H, Siren A, Everett K, Møller RS, Hjalgrim H, Muhle H, Helbig I, Kunz WS, Weber YG, Weckhuysen S, Jonghe P, Sisodiya SM, Nabbout R, Franceschetti S, Coppola A, Vari MS, Kasteleijn-Nolst Trenité D, Baykan B, Ozbek U, Bebek N, Klein KM, Rosenow F, Nguyen DK, Dubeau F, Carmant L, Lortie A, Desbiens R, Clément JF, Cieuta-Walti C, Sills GJ, Auce P, Francis B, Johnson MR, Marson AG, Berghuis B, Sander JW, Avbersek A, McCormack M, Cavalleri GL, Delanty N, Depondt C, Krenn M, Zimprich F, Peter S, Nikanorova M, Kraaij R, van Rooij J, Balling R, Ikram MA, Uitterlinden AG, Avanzini G, Schorge S, Petrou S, Mantegazza M, Sander T, LeGuern E, Serratosa JM, Koeleman BPC, Palotie A, Lehesjoki AE, Nothnagel M, Nürnberg P, Maljevic S, Zara F, Cossette P, Krause R, Lerche H; Epicure Consortium; EuroEPINOMICS CoGIE Consortium; EpiPGX Consortium. May P, et al. Among authors: siren a. Lancet Neurol. 2018 Aug;17(8):699-708. doi: 10.1016/S1474-4422(18)30215-1. Epub 2018 Jul 17. Lancet Neurol. 2018. PMID: 30033060 Free article.
X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes.
Philips AK, Sirén A, Avela K, Somer M, Peippo M, Ahvenainen M, Doagu F, Arvio M, Kääriäinen H, Van Esch H, Froyen G, Haas SA, Hu H, Kalscheuer VM, Järvelä I. Philips AK, et al. Among authors: siren a. Orphanet J Rare Dis. 2014 Apr 11;9:49. doi: 10.1186/1750-1172-9-49. Orphanet J Rare Dis. 2014. PMID: 24721225 Free PMC article.
Cognition in adults with Williams syndrome-A 20-year follow-up study.
Sauna-Aho O, Bjelogrlic-Laakso N, Sirén A, Kangasmäki V, Arvio M. Sauna-Aho O, et al. Among authors: siren a. Mol Genet Genomic Med. 2019 Jun;7(6):e695. doi: 10.1002/mgg3.695. Epub 2019 Apr 29. Mol Genet Genomic Med. 2019. PMID: 31033253 Free PMC article.
Cohort Profile: The Danish Longitudinal Study of Ageing (DLSA).
Kjær AA, Siren A, Seestedt MH, Fridberg T, Casier F. Kjær AA, et al. Among authors: siren a. Int J Epidemiol. 2019 Aug 1;48(4):1050-1050g. doi: 10.1093/ije/dyz026. Int J Epidemiol. 2019. PMID: 30874730 No abstract available.
The life history of human foraging: Cross-cultural and individual variation.
Koster J, McElreath R, Hill K, Yu D, Shepard G Jr, van Vliet N, Gurven M, Trumble B, Bird RB, Bird D, Codding B, Coad L, Pacheco-Cobos L, Winterhalder B, Lupo K, Schmitt D, Sillitoe P, Franzen M, Alvard M, Venkataraman V, Kraft T, Endicott K, Beckerman S, Marks SA, Headland T, Pangau-Adam M, Siren A, Kramer K, Greaves R, Reyes-García V, Guèze M, Duda R, Fernández-Llamazares Á, Gallois S, Napitupulu L, Ellen R, Ziker J, Nielsen MR, Ready E, Healey C, Ross C. Koster J, et al. Among authors: siren a. Sci Adv. 2020 Jun 24;6(26):eaax9070. doi: 10.1126/sciadv.aax9070. eCollection 2020 Jun. Sci Adv. 2020. PMID: 32637588 Free PMC article.
Erythropoietin--a novel concept for neuroprotection.
Sirén AL, Ehrenreich H. Sirén AL, et al. Eur Arch Psychiatry Clin Neurosci. 2001 Aug;251(4):179-84. doi: 10.1007/s004060170038. Eur Arch Psychiatry Clin Neurosci. 2001. PMID: 11697582 Review.
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