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Hreinn Stefánsson

Researcher Next ID · RN-016857

Researcher · Biochemistry, Genetics and Molecular Biology

deCODE Genetics (Iceland)

, Iceland

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Not currently recruitingFunding unknown
Works count
467
Citation count
92,554
H-index
127
i10-index
315

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Genetic Associations and Epidemiology
Genomic variations and chromosomal abnormalities
Genetics and Neurodevelopmental Disorders
Genomics and Rare Diseases
Migraine and Headache Studies

Publications

  • Identification of common genetic risk variants for autism spectrum disorder

    Nature Genetics · 2019 · 10.1038/s41588-019-0344-8

  • Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

    Nature Genetics · 2019 · 10.1038/s41588-018-0311-9

  • Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Nature Genetics · 2018 · 10.1038/s41588-018-0269-7

  • Variant of TREM2 Associated with the Risk of Alzheimer's Disease

    New England Journal of Medicine · 2012 · 10.1056/nejmoa1211103

  • Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

    Nature Genetics · 2006 · 10.1038/ng1732

Current projects

    No projects listed.