S
Soley Bjornsdottir
Researcher at deCODE genetics
Publications - 4
Citations - 2077
Soley Bjornsdottir is an academic researcher from deCODE genetics. The author has contributed to research in topics: Neuregulin 1 & Epigenetics of schizophrenia. The author has an hindex of 4, co-authored 4 publications receiving 2004 citations.
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Journal ArticleDOI
Neuregulin 1 and Susceptibility to Schizophrenia
Hreinn Stefansson,Engilbert Sigurdsson,Valgerdur Steinthorsdottir,Soley Bjornsdottir,Thordur Sigmundsson,Shyamali Ghosh,J Brynjolfsson,Steinunn Gunnarsdottir,Omar Ivarsson,Thomas T. Chou,Omar Hjaltason,Birgitta Birgisdottir,Helgi Jonsson,Vala G. Gudnadottir,Elsa Gudmundsdottir,Asgeir Björnsson,Brynjolfur Ingvarsson,Andres Ingason,Sigmundur Sigfusson,Hronn Hardardottir,Richard P. Harvey,Richard P. Harvey,Donna Lai,Mingdong Zhou,Daniela Brunner,Vincent Mutel,Acuna Gonzalo,Greg Lemke,Jesus Sainz,Gardar Johannesson,Thorkell Andresson,Daniel F. Gudbjartsson,Andrei Manolescu,Michael L. Frigge,Mark E. Gurney,Augustine Kong,Jeffrey R. Gulcher,Hannes Petursson,Kari Stefansson +38 more
TL;DR: The results of a genomewide scan of schizophrenia families in Iceland show that schizophrenia maps to chromosome 8p, and extensive fine-mapping of the 8p locus and haplotype-association analysis identifies neuregulin 1 (NRG1) as a candidate gene for schizophrenia.
Journal ArticleDOI
Mapping of a familial essential tremor gene, FET1, to chromosome 3q13.
Gulcher,Palmi V. Jonsson,Augustine Kong,Augustine Kong,Kristleifur Kristjansson,Mike Frigge,Mike Frigge,Ari Karason,Einarsdóttir Ie,Hreinn Stefansson,Anna S. Einarsdóttir,Sigurthoardóttir S,Baldursson S,Soley Bjornsdottir,Soffia M. Hrafnkelsdottir,Finnbogi Jakobsson,Benedickz J,Kari Stefansson +17 more
TL;DR: The scan for FET genes in 16 Icelandic families with 75 affected individuals revealed one locus on chromosome 3q13 to which FET mapped with genome-wide significance when the data were analysed either parametrically or non-parametrically, assuming an autosomal dominant model.
Journal ArticleDOI
Multiple novel transcription initiation sites for NRG1.
Valgerdur Steinthorsdottir,Hreinn Stefansson,Shyamali Ghosh,Birgitta Birgisdottir,Soley Bjornsdottir,Anne Charlotte Fasquel,Olafur Olafsson,Kari Stefansson,Jeffrey R. Gulcher +8 more
TL;DR: The discovery of nine novelNRG1 exons, including six alternative 5'-exons, increasing the number of potential promoters in NRG1 from three to nine, and three of the novel 5'- exons are well conserved in syntenic rat and mouse sequences; they encode proteins with novel amino-termini, here termed types IV-VI.
Patent
Inversion on chromosome 8p23 is a risk factor for anxiety disorders, depression and bipolar
TL;DR: In this paper, an association between psychiatric disorders and disorders comorbid with psychiatric disorders, and genetic markers in the 8p23 genomic region is described, and methods and surrogate markers for detecting the orientation of the Inv8p23 inversion fragment are also disclosed.