Olli Pietiläinen

Researcher Next ID · RN-019611

Researcher · Health Professions

Cambridge, Finland

Not currently recruitingFunding unknown

Research interests

Health Professions

Biochemistry, Genetics and Molecular Biology

Workplace Health and Well-being

Genetic Associations and Epidemiology

Genomic variations and chromosomal abnormalities

Employment and Welfare Studies

Genomics and Rare Diseases

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Nature Neuroscience · 2016 · https://doi.org/10.1038/nn.4267
Genetic background of extreme violent behavior
Molecular Psychiatry · 2014 · https://doi.org/10.1038/mp.2014.130
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Human Molecular Genetics · 2011 · https://doi.org/10.1093/hmg/ddr325
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort
Journal of Psychiatric Research · 2010 · https://doi.org/10.1016/j.jpsychires.2010.02.002
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
Molecular Psychiatry · 2009 · https://doi.org/10.1038/mp.2009.101
Common variants conferring risk of schizophrenia
Nature · 2009 · https://doi.org/10.1038/nature08186
Disruption of the neurexin 1 gene is associated with schizophrenia
Human Molecular Genetics · 2008 · https://doi.org/10.1093/hmg/ddn351
Large recurrent microdeletions associated with schizophrenia
Nature · 2008 · https://doi.org/10.1038/nature07229

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