Polygenic risk scores distinguish patients from non-affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi-affected kindreds
Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China
SLC6A3 polymorphism and response to methylphenidate in children with ADHD: A systematic review and meta-analysis
Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes : The childhood trauma working-group of PGC-MDD
Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population
Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis
Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome
Association study of NDST3 gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population
Contribution of genes in the GABAergic pathway to bipolar disorder and its executive function deficit in the Chinese Han population
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences
OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia
A functional polymorphism of the OXTR gene is associated with autistic traits in Caucasian and Asian populations
Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly
Nhe5 deficiency enhances learning and memory via upregulating Bdnf/TrkB signaling in mice
The role of cadherin genes in five major psychiatric disorders: A literature update
Genomewide association studies of suicide attempts in US soldiers
Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance
The role of CLOCK gene in psychiatric disorders: Evidence from human and animal research
Phelan-McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reports
Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome
Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type
A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains
The clinical features of alcohol use disorders in biological and step-fathers that predict risk for alcohol use disorders in offspring
The dopamine transporter role in psychiatric phenotypes
eHealth provides a novel opportunity to exploit the advantages of the Nordic countries in psychiatric genetic research, building on the public health care system, biobanks, and registries
National-scale precision medicine for psychiatric disorders in Sweden
A comprehensive review of the genetic and biological evidence supports a role for MicroRNA-137 in the etiology of schizophrenia
Association between COMT Val158Met and psychiatric disorders: A comprehensive meta-analysis
The highly pleiotropic gene SLC39A8 as an opportunity to gain insight into the molecular pathogenesis of schizophrenia
The use of electronic health records for psychiatric phenotyping and genomics
Neuregulin 3 and its roles in schizophrenia risk and presentation
Glucocerebrosidase mutations and neuropsychiatric phenotypes in Parkinson's disease and Lewy body dementias: Review and meta-analyses
A gene-based review of RGS4 as a putative risk gene for psychiatric illness
ADH1B: From Alcoholism, Natural Selection, and Cancer to the Human Phenome
APOE gene and neuropsychiatric disorders and endophenotypes: A comprehensive review
The relationship between schizophrenia and rheumatoid arthritis revisited: Genetic and epidemiological analyses
An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults
Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse
Revisiting mendelian randomization studies of the effect of body mass index on depression
Genome-wide association study of lymphoblast cell viability after clozapine exposure
Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis
Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease
Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population
Genetic Association of The Tachykinin Receptor 1 TACR1 Gene in Bipolar Disorder, Attention Deficit Hyperactivity Disorder, and the Alcohol Dependence Syndrome
Adult Neuropsychiatric Expression and Familial Segregation of 2q13 Duplications
Genome Scan for Cognitive Trait Loci of Dyslexia: Rapid Naming and Rapid Switching of Letters, Numbers, and Colors
Allelic Association, DNA Resequencing and Copy Number Variation at the Metabotropic Glutamate Receptor GRM7 Gene Locus in Bipolar Disorder
ADHD Pharmacogenetics Across The Life Cycle: New Findings and Perspectives
Altered DNA Methylation Status of Human Brain Derived Neurotrophis Factor Gene Could be Useful as Biomarker of Depression
Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive–compulsive disorder: Results from the OCD Collaborative Genetics Study
The genetics of functional disability in schizophrenia and bipolar illness: Methods and initial results for VA cooperative study #572
Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity
Risk and information evaluation of prioritized genes for complex traits: Application to bipolar disorder
Screening Individuals with Intellectual Disability, Autism and Tourette's Syndrome for KCNK9 Mutations and Aberrant DNA Methylation within the 8q24 Imprinted Cluster.
Characterizing Runs of Homozygosity and Their Impact on Risk for Psychosis in a Population Isolate
Testing the role of circadian genes in conferring risk for psychiatric disorders
Erratum: Sequence analysis of 17 NRXN1 deletions
The interaction effect between BDNF val66met polymorphism and obesity on executive functions and frontal structure
The search for peripheral biomarkers for major depression: Benefiting from successes in the biology of smoking
Novel non-specific liquid fingerprint technology for wine analysis: a feasibility study