Publication | Open Access

Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity

Whole Genome SequencingPsychiatryRisk PredictionNext-generation SequencingGeneticsPsychiatric GeneticsSchizophreniaGenome AnalysisSchizophrenia ProbandsGenetic HeterogeneityGenomicsMedicinePsychotic DisorderVariant Interpretation