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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

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Bettecken,  Thomas
Max Planck Institute of Psychiatry, Max Planck Society;

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Binder,  Elisabeth B.
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80291

Czamara,  Darina
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80372

Holsboer,  Florian
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80379

Ising,  Marcus
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80405

Kohli,  Martin A.
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80426

Lucae,  Susanne
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80450

Müller-Myhsok,  Bertram
Max Planck Institute of Psychiatry, Max Planck Society;

/persons/resource/persons80563

Uhr,  Manfred
Max Planck Institute of Psychiatry, Max Planck Society;

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Citation

O'Dushlaine, C., Rossin, L., Lee, P. H., Duncan, L., Parikshak, N. N., Newhouse, S., et al. (2015). Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. NATURE NEUROSCIENCE, 18(2), 199-209. doi:10.1038/nn.3922.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0028-FF5D-1
Abstract
Genome-wide association studies (GWAS) of psychiatric disorders have identified multiple genetic associations with such disorders, but better methods are needed to derive the underlying biological mechanisms that these signals indicate. We sought to identify biological pathways in GWAS data from over 60,000 participants from the Psychiatric Genomics Consortium. We developed an analysis framework to rank pathways that requires only summary statistics. We combined this score across disorders to find common pathways across three adult psychiatric disorders: schizophrenia, major depression and bipolar disorder. Histone methylation processes showed the strongest association, and we also found statistically significant evidence for associations with multiple immune and neuronal signaling pathways and with the postsynaptic density. Our study indicates that risk variants for psychiatric disorders aggregate in particular biological pathways and that these pathways are frequently shared between disorders. Our results confirm known mechanisms and suggest several novel insights into the etiology of psychiatric disorders.