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Paper Details

Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disorders.
BMJ Open
2
2023
CNVs, cardiovascular disease, common variants, copy number variations, genome-wide genotyping chip, neoplasms, psychiatric morbidity, psychosis, psychotic depression, psychotic disorders, psychotic illness, rare variants, schizoaffective disorder, schizophrenia, type I or type II bipolar disorder
Author NameAffiliation
Benjamin M NealeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Benjamin M NealeMassachusetts General Hospital
Mark J DalyInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Mark J DalyInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Aarno PalotieInstitute for Molecular Medicine Finland (FIMM), University of Helsinki
Aarno PalotieStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Aarno PalotieMassachusetts General Hospital
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