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Page 1
Thirty novel sequence variants impacting human intracranial volume.
Nawaz MS, Einarsson G, Bustamante M, Gisladottir RS, Walters GB, Jonsdottir GA, Skuladottir AT, Bjornsdottir G, Magnusson SH, Asbjornsdottir B, Unnsteinsdottir U, Sigurdsson E, Jonsson PV, Palmadottir VK, Gudjonsson SA, Halldorsson GH, Ferkingstad E, Jonsdottir I, Thorleifsson G, Holm H, Thorsteinsdottir U, Sulem P, Gudbjartsson DF, Stefansson H, Thorgeirsson TE, Ulfarsson MO, Stefansson K. Nawaz MS, et al. Among authors: jonsdottir ga. Brain Commun. 2022 Oct 25;4(6):fcac271. doi: 10.1093/braincomms/fcac271. eCollection 2022. Brain Commun. 2022. PMID: 36415660 Free PMC article.
Recombination rate and reproductive success in humans.
Kong A, Barnard J, Gudbjartsson DF, Thorleifsson G, Jonsdottir G, Sigurdardottir S, Richardsson B, Jonsdottir J, Thorgeirsson T, Frigge ML, Lamb NE, Sherman S, Gulcher JR, Stefansson K. Kong A, et al. Nat Genet. 2004 Nov;36(11):1203-6. doi: 10.1038/ng1445. Epub 2004 Oct 3. Nat Genet. 2004. PMID: 15467721
Variant in the sequence of the LINGO1 gene confers risk of essential tremor.
Stefansson H, Steinberg S, Petursson H, Gustafsson O, Gudjonsdottir IH, Jonsdottir GA, Palsson ST, Jonsson T, Saemundsdottir J, Bjornsdottir G, Böttcher Y, Thorlacius T, Haubenberger D, Zimprich A, Auff E, Hotzy C, Testa CM, Miyatake LA, Rosen AR, Kristleifsson K, Rye D, Asmus F, Schöls L, Dichgans M, Jakobsson F, Benedikz J, Thorsteinsdottir U, Gulcher J, Kong A, Stefansson K. Stefansson H, et al. Among authors: jonsdottir ga. Nat Genet. 2009 Mar;41(3):277-9. doi: 10.1038/ng.299. Epub 2009 Feb 1. Nat Genet. 2009. PMID: 19182806 Free PMC article.
Addictions and their familiality in Iceland.
Tyrfingsson T, Thorgeirsson TE, Geller F, Runarsdóttir V, Hansdóttir I, Bjornsdottir G, Wiste AK, Jonsdottir GA, Stefansson H, Gulcher JR, Oskarsson H, Gudbjartsson D, Stefansson K. Tyrfingsson T, et al. Among authors: jonsdottir ga. Ann N Y Acad Sci. 2010 Feb;1187:208-17. doi: 10.1111/j.1749-6632.2009.05151.x. Ann N Y Acad Sci. 2010. PMID: 20201855 Review.
CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Stefansson H, Meyer-Lindenberg A, Steinberg S, Magnusdottir B, Morgen K, Arnarsdottir S, Bjornsdottir G, Walters GB, Jonsdottir GA, Doyle OM, Tost H, Grimm O, Kristjansdottir S, Snorrason H, Davidsdottir SR, Gudmundsson LJ, Jonsson GF, Stefansdottir B, Helgadottir I, Haraldsson M, Jonsdottir B, Thygesen JH, Schwarz AJ, Didriksen M, Stensbøl TB, Brammer M, Kapur S, Halldorsson JG, Hreidarsson S, Saemundsen E, Sigurdsson E, Stefansson K. Stefansson H, et al. Among authors: jonsdottir b, jonsdottir ga. Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18. Nature. 2014. PMID: 24352232
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: jonsdottir ga. Sci Rep. 2016 Nov 4;6:36189. doi: 10.1038/srep36189. Sci Rep. 2016. PMID: 27811963 Free PMC article.
Selection against variants in the genome associated with educational attainment.
Kong A, Frigge ML, Thorleifsson G, Stefansson H, Young AI, Zink F, Jonsdottir GA, Okbay A, Sulem P, Masson G, Gudbjartsson DF, Helgason A, Bjornsdottir G, Thorsteinsdottir U, Stefansson K. Kong A, et al. Among authors: jonsdottir ga. Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):E727-E732. doi: 10.1073/pnas.1612113114. Epub 2017 Jan 17. Proc Natl Acad Sci U S A. 2017. PMID: 28096410 Free PMC article.
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: jonsdottir b, jonsdottir ga. Transl Psychiatry. 2017 Apr 25;7(4):e1109. doi: 10.1038/tp.2017.77. Transl Psychiatry. 2017. PMID: 28440815 Free PMC article.
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: jonsdottir ga. Nat Genet. 2017 Aug;49(8):1251-1254. doi: 10.1038/ng.3894. Epub 2017 Jun 19. Nat Genet. 2017. PMID: 28628109
MAP1B mutations cause intellectual disability and extensive white matter deficit.
Walters GB, Gustafsson O, Sveinbjornsson G, Eiriksdottir VK, Agustsdottir AB, Jonsdottir GA, Steinberg S, Gunnarsson AF, Magnusson MI, Unnsteinsdottir U, Lee AL, Jonasdottir A, Sigurdsson A, Jonasdottir A, Skuladottir A, Jonsson L, Nawaz MS, Sulem P, Frigge M, Ingason A, Love A, Norddhal GL, Zervas M, Gudbjartsson DF, Ulfarsson MO, Saemundsen E, Stefansson H, Stefansson K. Walters GB, et al. Among authors: jonsdottir ga. Nat Commun. 2018 Aug 27;9(1):3456. doi: 10.1038/s41467-018-05595-6. Nat Commun. 2018. PMID: 30150678 Free PMC article.
28 results