Author: Unnur Thorsteinsdottir

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Preprints

Genetic insights into the biological mechanisms governing human ovarian ageing

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Early Spread of SARS-Cov-2 in the Icelandic Population

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  • Site-wide: 8,687
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Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

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The nature of nurture: effects of parental genotypes

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Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

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  • Site-wide: 3,227
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• Year to date:
  • Site-wide: 41,667
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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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  • Site-wide: 3,307
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Estimating heritability without environmental bias

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Recurrence of de novo mutations in families

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

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  • Site-wide: 12,032
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The genetic architecture of osteoarthritis: insights from UK Biobank

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Large-Scale Genome-Wide Meta Analysis of Polycystic Ovary Syndrome Suggests Shared Genetic Architecture for Different Diagnosis Criteria.

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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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  • Site-wide: 23,326
  • In genetic and genomic medicine: 61
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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Discovering patterns of pleiotropy in genome-wide association studies

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Genome-wide analysis yields new loci associating with aortic valve stenosis

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  • Site-wide: 43,906
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A rare missense mutation in MYH6 confers high risk of coarctation of the aorta

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Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

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  • Site-wide: 55,386
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