Guðrún A. Jónsdóttir

deCODE Genetics (Iceland) — IS

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index13.7kcitations28works8.82yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(8), Genetics and Neurodevelopmental Disorders(7), Genetic Associations and Epidemiology(6), Genomics and Rare Diseases(6), Epigenetics and DNA Methylation(4)

Publications28 total

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication
Biological Psychiatry Global Open Science·2025Open Access
Robust inference and widespread genetic correlates from a large-scale genetic association study of human personality
2025· 12 citedOpen Access
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder
Nature Genetics·2025· 7 citedOpen Access
Sequence variants associated with BMI affect disease risk through BMI itself
Nature Communications·2024· 6 citedOpen Access
Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease
npj Parkinson s Disease·2024· 11 citedOpen Access
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Communications Biology·2024· 17 citedOpen Access
Sequence variants affecting voice pitch in humans
Science Advances·2023· 18 citedOpen Access
Thirty novel sequence variants impacting human intracranial volume
Brain Communications·2022· 7 citedOpen Access
Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia
Intelligence·2021· 8 citedOpen Access
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Molecular Psychiatry·2019· 3 citedOpen Access
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Molecular Psychiatry·2018· 73 citedOpen Access
MAP1B mutations cause intellectual disability and extensive white matter deficit
Nature Communications·2018· 35 citedOpen Access
Truncating mutations in RBM12 are associated with psychosis
Nature Genetics·2017· 72 cited
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
Translational Psychiatry·2017· 83 citedOpen Access
Selection against variants in the genome associated with educational attainment
Proceedings of the National Academy of Sciences·2017· 186 citedOpen Access
A sequence variant associating with educational attainment also affects childhood cognition
Scientific Reports·2016· 2 citedOpen Access
CNVs conferring risk of autism or schizophrenia affect cognition in controls
Nature·2013· 713 citedOpen Access
Academic achievement in 4th and 7th grade: The contribution of gender, parental education, achievement goals and intelligence
2012· 2 cited
Addictions and their familiality in Iceland
Annals of the New York Academy of Sciences·2010· 29 cited
Erratum: Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor
Nature Genetics·2009· 2 citedOpen Access
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Frequent Co-authors

Hreinn Stefánsson(25), Gyða Björnsdóttir(15), Daníel F. Guðbjartsson(15), Kāri Stefánsson(13), Patrick Sulem(11), Thorgeir E. Thorgeirsson(10), G. Bragi Walters(9), Engilbert Sigurðsson(9), Ómar Gústafsson(8), Unnur Þorsteinsdóttir(8), Rósa S. Gísladóttir(8), Stacy Steinberg(7), Guðmar Þorleifsson(7), Hannes Helgason(7), Ástrós Skúladóttir(7), Garðar Sveinbjörnsson(6), Hilma Hólm(6), Augustine Kong(5), Magnús Ö. Úlfarsson(5), Shulan Tian(4)