文章名稱引用次數(shù)

• Co-shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome14
• Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD9
• The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population9
• A comprehensive review of the genetic and biological evidence supports a role for MicroRNA-137 in the etiology of schizophrenia7
• The role of glutamate receptors in attention-deficit/hyperactivity disorder: From physiology to disease7
• Association of copy number variation across the genome with neuropsychiatric traits in the general population7
• The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 26
• Association of Alzheimer's genetic loci with mild behavioral impairment6
• Glucocerebrosidase mutations and neuropsychiatric phenotypes in Parkinson's disease and Lewy body dementias: Review and meta-analyses6
• Gene-level associations in suicide attempter families show overrepresentation of synaptic genes and genes differentially expressed in brain development5