| Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia |
16 |
| Missing a beat: assessment of circadian rhythm abnormalities in bipolar disorder in the genomic era |
10 |
| Genetic risk factors and gene-environment interactions in adult and childhood attention-deficit/hyperactivity disorder |
9 |
| No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population |
6 |
| Brain-derived neurotrophic factor and schizophrenia |
6 |
| Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder: lessons from CNTNAP ADGRL and PARK2 |
5 |
| Lack of association between triggering receptor expressed on myeloid cells 2 polymorphism rs75932628 and late-onset Alzheimer's disease in a Chinese Han population |
5 |
| Association study of FGF18 with developmental dyslexia in Chinese population |
4 |
| The emerging pattern of shared polygenic architecture of psychiatric disorders, conceptual and methodological challenges |
4 |
| Integrated analysis of the genetic basis of suicidal behavior: what has been shown by structural genetic studies so far |
3 |
| Offspring of parents with schizophrenia, bipolar disorder, and depression: a review of familial high-risk and molecular genetics studies |
3 |
| Genomics of human aggression: current state of genome-wide studies and an automated systematic review tool |
3 |
| Shared genetic etiology between alcohol dependence and major depressive disorder |
3 |
| Candidate genes for novelty-seeking: a meta-analysis of association studies of DRD4 exon III and COMT Val158Met |
3 |
| Genetic analysis of common variants in the ZNF804A gene with schizophrenia and major depressive disorder |
3 |
| Investigation of differential HDAC4 methylation patterns in eating disorders |
2 |
| Understanding the schizophrenia phenotype in the first patient with the full SCN2A phenotypic spectrum |
2 |
| Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene |
2 |
| Association of functional polymorphisms in 3 '-untranslated regions of COMT, DISC and DTNBP1 with schizophrenia: a meta-analysis |
2 |
| Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals |
2 |
| Endophenotypes of executive functions in obsessive compulsive disorder? A meta-analysis in unaffected relatives |
2 |
| In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-d-aspartate receptor in schizophrenia |
2 |
| Familial association of attention-deficit hyperactivity disorder with autoimmune diseases in the population of Sweden |
2 |
| Buspirone for the treatment of anxiety-related symptoms in Angelman syndrome: a case series |
2 |
| MTHFR gene methylation is associated with perceived stress in healthy young adults |
2 |
| Association between COMT gene polymorphisms, clinical symptoms, and cognitive functions in Han Chinese patients with schizophrenia |
1 |
| High-functioning autism in a Sri Lankan youth with Langer-Giedion syndrome |
1 |
| Unravelling the GSK3 beta-related genotypic interaction network influencing hippocampal volume in recurrent major depressive disorder |
1 |
| Polygenic risk score for schizophrenia is not strongly associated with the expression of specific genes or gene sets |
1 |
| Anorexia nervosa is associated with Neuronatin variants |
1 |
| Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence |
1 |
| Decreased serum complement component 4 levels in patients with schizophrenia |
1 |
| Common variants in SATB2 are associated with schizophrenia in Uygur Chinese population |
1 |
| Genetic association of the human MAP3K5 gene with schizophrenia in a Chinese Han population |
1 |
| No association of GRIN2A polymorphisms with the major depressive disorder in the Chinese Han origin |
1 |
| Association between RELN polymorphisms and schizophrenia in a Han population from Northeast China |
1 |
| A case of intellectual disability reveals a novel mutation in IQSEC2 gene by whole exome sequencing |
1 |
| Schizophrenia in microcephalic osteodysplastic primordial dwarfism type II syndrome: supporting evidence for an association between the PCNT gene and schizophrenia |
1 |
| Association of polymorphisms in HTR2A, TPH and TPH2 genes with attempted suicide in rural China |
0 |
| Clinical association to FKBP5 rs1360780 in patients with depression |
0 |
| Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome |
0 |
| Association study of the PDE4D gene and obsessive-compulsive disorder in a Chinese Han population |
0 |
| The interaction between estradiol change and the serotonin transporter gene (5-HTTLPR) polymorphism is associated with postpartum depressive symptoms |
0 |
| Gene knockout animal models of depression, anxiety and obsessive compulsive disorders |
0 |
| New insights and perspectives on the genetics of obsessive-compulsive disorder |
0 |
| Zinc finger proteins in psychiatric disorders and response to psychotropic medications |
0 |
| Familial risk for psychiatric disorders in military veterans who have post-traumatic stress disorder with psychosis: a retrospective electronic record review |
0 |
| Assessment of a glyoxalase I frameshift variant, p.P122fs, in Japanese patients with schizophrenia |
0 |
