| Bioinformatic analyses and conceptual synthesis of evidence linking <i>ZNF804A</i> to risk for schizophrenia and bipolar disorder |
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| Association between <i>DRD2</i> (rs1799732 and rs1801028) and <i>ANKK1</i> (rs1800497) polymorphisms and schizophrenia: A meta‐analysis |
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| Interactions between <i>MAOA</i> and <i>SYP</i> polymorphisms were associated with symptoms of attention—deficit/hyperactivity disorder in Chinese Han subjects |
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| Prevalence of Autism Spectrum Disorder symptoms in children with neurofibromatosis type 1 |
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| Behavioral phenotype in Costello syndrome with atypical mutation: A case report |
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| No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population |
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common European mitochondrial DNA variants; Spanish population |
| Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity |
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| Curvilinear association of CGG repeats and age at menopause in women with <i>FMR1</i> premutation expansions |
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| DNA extracted from saliva for methylation studies of psychiatric traits: Evidence tissue specificity and relatedness to brain |
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African Americans |
| Neuropsychological profiles of patients with 2q37.3 deletion associated with developmental dyspraxia |
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| Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol‐related phenotypes in a Native American community sample |
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Native American (NA) populations; NA ancestry; other ethnic groups; NA population; ancestry admixtur |
| A genome‐wide CNV analysis of schizophrenia reveals a potential role for a multiple‐hit model |
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| Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes |
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European Americans; African Americans |
| Obsessive compulsive symptom dimensions and neuroticism: An examination of shared genetic and environmental risk |
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| The ‐116C/G polymorphism in <i>XBP1</i> gene is associated with psychiatric illness in Asian population: A meta‐analysis |
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Asian population |
| Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population |
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Chinese population; Chinese dyslexic children |
| Synergistic association of <i>PI4KA</i> and <i>GRM3</i> genetic polymorphisms with poor antipsychotic response in south Indian schizophrenia patients with low severity of illness |
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south Indian |
| Mitochondrial DNA (mtDNA) variants in the European haplogroups HV, JT, and U do not have a major role in schizophrenia |
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European haplogroups |
| Family based genome‐wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics |
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Indian |
| Effects of negative stressors on DNA methylation in the brain: Implications for mood and anxiety disorders |
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| Risk and information evaluation of prioritized genes for complex traits: Application to bipolar disorder |
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| Hypomethylation of the paternally inherited <i>LRRTM1</i> promoter linked to schizophrenia |
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| Language and traits of autism spectrum conditions: Evidence of limited phenotypic and etiological overlap |
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| Identification of ANKK1 rs1800497 variant in schizophrenia: New data and meta‐analysis |
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Han Chinese |
| Diversity in the <i>androgen receptor</i> CAG repeat has been shaped by a multistep mutational mechanism |
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European and Asian ancestry |
| Differential hippocampal gene expression and pathway analysis in an etiology‐based mouse model of major depressive disorder |
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| A genome‐wide linkage scan of bipolar disorder in Latino families identifies susceptibility loci at 8q24 and 14q32 |
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| Aberrant parietal cortex developmental trajectories in girls with turner syndrome and related visual–spatial cognitive development: A preliminary study |
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| The miR‐137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals |
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| Polygenic scores associated with educational attainment in adults predict educational achievement and ADHD symptoms in children |
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| Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate |
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Oceanic population; Palauan |
| Glutamatergic copy number variants and their role in attention‐deficit/hyperactivity disorder |
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| Association of microcephalin 1, syntrophin‐beta 1, and other genes with automatic thoughts in the Japanese population |
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| Screening individuals with intellectual disability, autism and Tourette's syndrome for <i>KCNK9</i> mutations and aberrant DNA methylation within the 8q24 imprinted cluster. |
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| Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome‐wide association and polygenic scoring study |
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| Association of the T102C polymorphism in the <i>HTR2A</i> gene with major depressive disorder, bipolar disorder, and schizophrenia |
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Asian or Chinese populations |
| ADHD pharmacogenetics across the life cycle: New findings and perspectives |
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| Replication and cross‐phenotype study based upon schizophrenia GWASs data in the Japanese population: Support for association of MHC region with psychosis |
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| Exploring the indirect effects of catechol‐O‐methyltransferase (<i>COMT</i>) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children |
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| Association of <i>CDH11</i> with non‐syndromic ASD |
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| Maternal predictors of anxiety risk in young males with fragile X |
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| Genetic association of the tachykinin receptor 1 <i>TACR1</i> gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome |
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| Adult neuropsychiatric expression and familial segregation of 2q13 duplications |
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| Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor <i>GRM7</i> gene locus in bipolar disorder |
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| Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors |
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| Altered DNA methylation status of human brain derived neurotrophis factor gene could be useful as biomarker of depression |
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Japanese |
| Genetic variation at the <i>CELF1</i> (CUGBP, elav‐like family member 1 gene) locus is genome‐wide associated with Alzheimer's disease and obesity |
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| The genetics of functional disability in schizophrenia and bipolar illness: Methods and initial results for VA cooperative study #572 |
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| Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive–compulsive disorder: Results from the OCD Collaborative Genetics Study |
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| Prevalence and heritability of obsessive‐compulsive spectrum and anxiety disorder symptoms: A survey of the Australian Twin Registry |
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| Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes |
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North European descent |
| Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders |
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| Testing the role of circadian genes in conferring risk for psychiatric disorders |
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| Erratum: Sequence analysis of 17 NRXN1 deletions |
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| The interaction effect between BDNF <i>val66met</i> polymorphism and obesity on executive functions and frontal structure |
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| The search for peripheral biomarkers for major depression: Benefiting from successes in the biology of smoking |
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| Transposable elements and psychiatric disorders |
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| Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depression |
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| Genetic mutations in early‐onset Parkinson's disease Mexican patients: Molecular testing implications |
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Mexican Mestizo |
| Communication, cognitive development and behavior in children with Cornelia de Lange Syndrome (CdLS): Preliminary results |
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| A recessive genetic model and runs of homozygosity in major depressive disorder |
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| Arguments for the sake of endophenotypes: Examining common misconceptions about the use of endophenotypes in psychiatric genetics |
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| A variant within <i>FGF1</i> is associated with Alzheimer's disease in the Han Chinese population |
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| Reelin gene variants and risk of autism spectrum disorders: An integrated meta‐analysis |
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| Investigation of association of serotonin transporter and monoamine oxidase‐A genes with Alzheimer's disease and depression in the VITA study cohort: A 90‐month longitudinal study |
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| The effects of a<i>MAP2K5</i>microRNA target site SNP on risk for anxiety and depressive disorders |
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✓ |
European‐American (EA); African‐American (AA) |
| A family study of trichotillomania and chronic hair pulling |
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