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UnknownDISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness.
Not available
S-EPMC6127284 | biostudies-literature
UnknownBalanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function.
Not available
S-EPMC4994153 | biostudies-literature
UnknownRare chromosomal deletions and duplications increase risk of schizophrenia.
Not available
S-EPMC3912847 | biostudies-literature
UnknownRare coding variants in ten genes confer substantial risk for schizophrenia.
Not available
S-EPMC9805802 | biostudies-literature
UnknownGWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.
Not available
S-EPMC3443634 | biostudies-literature
UnknownCommon polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Not available
S-EPMC3912837 | biostudies-literature
UnknownNetwork-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia.
Not available
S-EPMC3390381 | biostudies-literature
UnknownTwo non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia.
Not available
S-EPMC4117700 | biostudies-literature
UnknownGenetic classification of populations using supervised learning.
Not available
S-EPMC3093382 | biostudies-literature
UnknownAdditive genetic variation in schizophrenia risk is shared by populations of African and European descent.
Not available
S-EPMC3845872 | biostudies-literature
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