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Copy number variation characteristics in subpopulations of patients with autism spectrum disorders
“Replicated” genome wide association for dependence on illegal substances: Genomic regions identified by overlapping clusters of nominally positive SNPs
Parent-of-origin effects of the serotonin transporter gene associated with autism
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects
Cognitive effects of genetic variation in monoamine neurotransmitter systems: A population-based study of COMT , MAOA , and 5HTTLPR
Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q
Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder
Linkage and association on 8p21.2-p21.1 in schizophrenia
Evaluation of risk loci for schizophrenia derived from genome-wide association studies in a German population
Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia
Methylenetetrahydrofolate reductase ( MTHFR ) C677T and A1298C polymorphisms and age of onset in schizophrenia: A combined analysis of independent samples
Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family
Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders
Genome-wide association study of hoarding traits
Narrowing the critical deletion region for autism spectrum disorders on 16p11.2