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Ómar Gústafsson

Researcher Next ID · RN-016984

Researcher · Biochemistry, Genetics and Molecular Biology

deCODE Genetics (Iceland)

, Iceland

Not currently recruitingFunding unknown
Works count
46
Citation count
8,403
H-index
31
i10-index
35

Research interests

Biochemistry, Genetics and Molecular Biology
Genomic variations and chromosomal abnormalities
Genetic Associations and Epidemiology
Genetics and Neurodevelopmental Disorders
Genomics and Rare Diseases
Congenital heart defects research

Publications

  • Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

    Proceedings of the National Academy of Sciences · 2014 · 10.1073/pnas.1318306111

  • Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

    The Lancet · 2010 · 10.1016/s0140-6736(10)61109-9

  • Common variants conferring risk of schizophrenia

    Nature · 2009 · 10.1038/nature08186

  • Disruption of the neurexin 1 gene is associated with schizophrenia

    Human Molecular Genetics · 2008 · 10.1093/hmg/ddn351

Current projects

    No projects listed.