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Abstract
We searched for genetic causes of major psychiatric disorders (bipolar disorder, schizoaffective disorder, and schizophrenia) in a large, densely affected pedigree from Northern Sweden that originated with three pairs of founders born around 1650. We applied a systematic genomic approach to the pedigree via karyotyping (N = 9), genome-wide SNP arrays (N = 418), whole-exome sequencing (N = 26), and whole-genome sequencing (N = 10). Comprehensive analysis did not identify plausible variants of strong effect. Rather, pedigree cases had significantly higher genetic risk scores compared to pedigree and community controls.
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1 University of North Carolina at Chapel Hill, Department of Genetics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000000122483208)
2 University of Umeå, Department of Clinical Sciences and Psychiatry, Umeå, Sweden (GRID:grid.12650.30) (ISNI:0000 0001 1034 3451)
3 Virginia Commonwealth University, Center for Biomarker Research and Precision Medicine, Richmond, USA (GRID:grid.224260.0) (ISNI:0000 0004 0458 8737)
4 University of Antwerp and Antwerp University Hospital, Center of Medical Genetics, Antwerp, Belgium (GRID:grid.5284.b) (ISNI:0000 0001 0790 3681)
5 Broad Institute of MIT and Harvard, Cambridge, USA (GRID:grid.66859.34)
6 Universiteitsplein 1, Antwerp, Belgium and Multiplicom N.V., VIB Center for Molecular Neurology, Niel, Belgium (GRID:grid.436667.6)
7 University of North Carolina at Chapel Hill, Department of Genetics, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000000122483208); University of North Carolina at Chapel Hill, Department of Psychiatry, Chapel Hill, USA (GRID:grid.10698.36) (ISNI:0000000122483208); Karolinska Institutet, Department of Medical Epidemiology and Biostatistics, Stockholm, Sweden (GRID:grid.4714.6) (ISNI:0000 0004 1937 0626)