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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

Mapping of a familial essential tremor gene, FET1, to chromosome 3q13.

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.

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.