Author: Jaana Suvisaari

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Preprints

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

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Patient iPSC-astrocytes show transcriptional and functional dysregulation in schizophrenia

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Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

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Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

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The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484

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Molecular signaling pathways underlying schizophrenia

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Circulating lipids associate with future weight gain in individuals with an at-risk mental state and in first-episode psychosis

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Functional characterization of six SLCO1B1 (OATP1B1) variants observed in Finnish individuals with a psychotic disorder

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