Gardar Sveinbjornsson

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Publications (90)

• A frameshift variant in PKP2 can be associated with a complex phenotype in sudden cardiac death: a case report
  European Heart Journal - Case Reports 2026 DOI: 10.1093/ehjcr/ytag067
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• Sequence variants affecting fetal globin expression pointing to potential drug targets
  2026 DOI: 10.21203/rs.3.rs-9225158/v1
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• Missense variants in FRS3 affect body mass index in populations of diverse ancestries
  Nature Communications 2025 DOI: 10.1038/s41467-025-57753-2
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• Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder
  Nature Genetics 2025 DOI: 10.1038/s41588-025-02141-1
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• Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
  Nature Genetics 2025 DOI: 10.1038/s41588-025-02074-9
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• Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
  Nature Genetics 2025 DOI: 10.1038/s41588-024-02072-3
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• Sequence variants associated with BMI affect disease risk through BMI itself
  Nature Communications 2024 DOI: 10.1038/s41467-024-53568-9
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• Gene-based burden tests of rare germline variants identify six cancer susceptibility genes
  Nature Genetics 2024 DOI: 10.1038/s41588-024-01966-6
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• Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency
  Nature Genetics 2024 DOI: 10.1038/s41588-024-01885-6
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• Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease
  npj Parkinson's Disease 2024 DOI: 10.1038/s41531-024-00752-9
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