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Evidence for involvement of GNB1L in autism.
Not available
S-EPMC3270696
|
biostudies-literature
Cite
Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia.
Not available
S-EPMC3736834
|
biostudies-literature
Cite
A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population.
Not available
S-EPMC6722128
|
biostudies-literature
Cite
Negative Symptom Trajectories in Individuals at Clinical High Risk for Psychosis: Differences Based on Deficit Syndrome, Persistence, and Transition Status.
Not available
S-EPMC10287168
|
biostudies-literature
Cite
Association of Thalamic Dysconnectivity and Conversion to Psychosis in Youth and Young Adults at Elevated Clinical Risk.
Not available
S-EPMC4892891
|
biostudies-literature
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White matter changes in psychosis risk relate to development and are not impacted by the transition to psychosis.
Not available
S-EPMC8611104
|
biostudies-literature
Cite
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
Not available
S-EPMC4055488
|
biostudies-literature
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Rare coding variants in ten genes confer substantial risk for schizophrenia.
Not available
S-EPMC9805802
|
biostudies-literature
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Altered age-related trajectories of amygdala-prefrontal circuitry in adolescents at clinical high risk for psychosis: a preliminary study.
Not available
S-EPMC3245800
|
biostudies-literature
Cite
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.
Not available
S-EPMC4752855
|
biostudies-literature
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