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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18.
Nature. 2014.
PMID: 24352232
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.
Ulfarsson MO, Walters GB, Gustafsson O, Steinberg S, Silva A, Doyle OM, Brammer M, Gudbjartsson DF, Arnarsdottir S, Jonsdottir GA, Gisladottir RS, Bjornsdottir G, Helgason H, Ellingsen LM, Halldorsson JG, Saemundsen E, Stefansdottir B, Jonsson L, Eiriksdottir VK, Eiriksdottir GR, Johannesdottir GH, Unnsteinsdottir U, Jonsdottir B, Magnusdottir BB, Sulem P, Thorsteinsdottir U, Sigurdsson E, Brandeis D, Meyer-Lindenberg A, Stefansson H, Stefansson K.
Ulfarsson MO, et al. Among authors: arnarsdottir s.
Transl Psychiatry. 2017 Apr 25;7(4):e1109. doi: 10.1038/tp.2017.77.
Transl Psychiatry. 2017.
PMID: 28440815
Free PMC article.
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A sequence variant associating with educational attainment also affects childhood cognition.
Gunnarsson B, Jónsdóttir GA, Björnsdóttir G, Konte B, Sulem P, Kristmundsdóttir S, Kehr B, Gústafsson Ó, Helgason H, Iordache PD, Ólafsson S, Frigge ML, Þorleifsson G, Arnarsdóttir S, Stefánsdóttir B, Giegling I, Djurovic S, Sundet KS, Espeseth T, Melle I, Hartmann AM, Thorsteinsdottir U, Kong A, Guðbjartsson DF, Ettinger U, Andreassen OA, Dan Rujescu, Halldórsson JG, Stefánsson H, Halldórsson BV, Stefánsson K.
Gunnarsson B, et al. Among authors: arnarsdottir s.
Sci Rep. 2016 Nov 4;6:36189. doi: 10.1038/srep36189.
Sci Rep. 2016.
PMID: 27811963
Free PMC article.
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Truncating mutations in RBM12 are associated with psychosis.
Steinberg S, Gudmundsdottir S, Sveinbjornsson G, Suvisaari J, Paunio T, Torniainen-Holm M, Frigge ML, Jonsdottir GA, Huttenlocher J, Arnarsdottir S, Ingimarsson O, Haraldsson M, Tyrfingsson T, Thorgeirsson TE, Kong A, Norddahl GL, Gudbjartsson DF, Sigurdsson E, Stefansson H, Stefansson K.
Steinberg S, et al. Among authors: arnarsdottir s.
Nat Genet. 2017 Aug;49(8):1251-1254. doi: 10.1038/ng.3894. Epub 2017 Jun 19.
Nat Genet. 2017.
PMID: 28628109
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Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome.
Vangkilde A, Jepsen JR, Schmock H, Olesen C, Arnarsdóttir S, Baaré WF, Plessen KJ, Didriksen M, Siebner HR, Werge T, Olsen L.
Vangkilde A, et al. Among authors: arnarsdottir s.
J Neurodev Disord. 2016 Nov 16;8:42. doi: 10.1186/s11689-016-9175-4. eCollection 2016.
J Neurodev Disord. 2016.
PMID: 27891188
Free PMC article.
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