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Browsing by Subject "Intellectual Disability"

Browsing by Subject "Intellectual Disability"

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  • Einarsson, Ingi; Daly, Daniel; Arngrímsson, Sigurbjörn Árni; Jóhannsson, Erlingur (Læknafélag Íslands, Læknafélag Reykjavíkur, 2015-04-01)
    Lítið er vitað um hreyfingu, holdafar og áhættuþætti fyrir ýmsum hjarta-, æða- og efnaskiptasjúkdómum á meðal barna með þroskahömlun. Tilgangur þessarar rannsóknar var að kanna líkamlegt ástand grunnskólabarna með þroskahömlun. Efniviður og ...
  • Reynisdottir, Tinna; Anderson, Kimberley Jade; Boukas, Leandros; Bjornsson, Hans Tomas (2022-06-21)
    Wiedemann-Steiner syndrome (WDSTS) is a neurodevelopmental disorder caused by de novo variants in KMT2A, which encodes a multi-domain histone methyltransferase. To gain insight into the currently unknown pathogenesis of WDSTS, we examined the spatial ...
  • Arnadottir, Gudny A.; Oddsson, Asmundur; Jensson, Brynjar O.; Gisladottir, Svanborg; Simon, Mariella T.; Arnthorsson, Asgeir O.; Katrinardottir, Hildigunnur; Fridriksdottir, Run; Ivarsdottir, Erna V.; Jonasdottir, Adalbjorg; Jonasdottir, Aslaug; Barrick, Rebekah; Saemundsdottir, Jona; le Roux, Louise; Oskarsson, Gudjon R.; Asmundsson, Jurate; Steffensen, Thora; Gudmundsson, Kjartan R.; Ludvigsson, Petur; Jonsson, Jon J.; Masson, Gisli; Jonsdottir, Ingileif; Holm, Hilma; Jonasson, Jon G.; Magnusson, Olafur Th; Thorarensen, Olafur; Abdenur, Jose; Norddahl, Gudmundur L.; Gudbjartsson, Daniel F.; Bjornsson, Hans T.; Thorsteinsdottir, Unnur; Sulem, Patrick; Stefansson, Kari (2022-02-04)
    Predicting the pathogenicity of biallelic missense variants can be challenging. Here, we use a deficit of observed homozygous carriers of missense variants, versus an expected number in a set of 153,054 chip-genotyped Icelanders, to identify potentially ...