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UnknownShared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Not available
S-EPMC5898828 | biostudies-literature
UnknownA Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
Not available
S-EPMC5294886 | biostudies-literature
UnknownGenetic imaging consortium for addiction medicine: From neuroimaging to genes.
Not available
S-EPMC4820288 | biostudies-literature
UnknownIRF2BPL Is Associated with Neurological Phenotypes.
Not available
S-EPMC6081494 | biostudies-literature
UnknownIdentification of common variants associated with human hippocampal and intracranial volumes.
Not available
S-EPMC3635491 | biostudies-literature
UnknownMega-Analysis of Gray Matter Volume in Substance Dependence: General and Substance-Specific Regional Effects.
Not available
S-EPMC6427822 | biostudies-literature
UnknownContribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Not available
S-EPMC5737772 | biostudies-literature
UnknownIdentification of common genetic risk variants for autism spectrum disorder.
Not available
S-EPMC6454898 | biostudies-literature
UnknownDiscovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Not available
S-EPMC6481311 | biostudies-literature
UnknownPartial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.
Not available
S-EPMC6925349 | biostudies-literature
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