| Childhood attention‐deficit/hyperactivity disorder symptoms and the development of adolescent alcohol problems: A prospective, population‐based study of Swedish twins |
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| Genetic and environmental influences on the relationship between ADHD symptoms and internalizing problems: A Chinese twin study |
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| Issue Information ‐ TOC |
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| Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population |
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Han Chinese; Chinese population |
| Genome‐wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness |
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| Symptoms of psychosis in schizophrenia, schizoaffective disorder, and bipolar disorder: A comparison of African Americans and Caucasians in the Genomic Psychiatry Cohort |
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| A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity |
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| A need for precision medicine to enable tailored special education |
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| What are the benefits of phenotype analyses to special education? |
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| Disorder‐specific genetic factors in obsessive‐compulsive disorder: A comprehensive meta‐analysis |
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ancestral groups (Asian vs. Caucasian) |
| Social cognition as an RDoC domain |
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| Transcranial direct current stimulation reduces food‐craving and measures of hyperphagia behavior in participants with Prader‐Willi syndrome |
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| Telomere longitudinal shortening as a biomarker for dementia status of adults with Down syndrome |
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| RDoC and translational perspectives on the genetics of trauma‐related psychiatric disorders |
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| Does refining the phenotype improve replication rates? A review and replication of candidate gene studies on Major Depressive Disorder and Chronic Major Depressive Disorder |
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| Influence of family history of dementia in the development and progression of late‐onset Alzheimer's disease |
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| Genome‐wide association study with the risk of schizophrenia in a Korean population |
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| Association of the manganese superoxide dismutase gene Ala–9Val polymorphism with age of smoking initiation in male schizophrenia smokers |
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Chinese |
| Common variants in <i>QPCT</i> gene confer risk of schizophrenia in the Han Chinese population |
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| The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms |
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| A role for HLA‐DRB1*1101 and DRB1*0801 in cognitive ability and its decline with age |
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| Nicotine dependence and psychosis in Bipolar disorder and Schizoaffective disorder, Bipolar type |
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| The association between childhood autistic traits and adolescent psychotic experiences is explained by general neuropsychiatric problems |
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| Currently recognized genes for schizophrenia: High‐resolution chromosome ideogram representation |
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| Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population |
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Western populations |
| Copy number variation analysis of the 17q21.31 region and its role in neurodegenerative diseases |
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Spanish subjects |
| Genome‐wide significant linkage of schizophrenia‐related neuroanatomical trait to 12q24 |
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| No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects |
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a large healthy sample of European ancestry (ENIGMA sample, N=5,775); a healthy Chinese sample (N=1,013) |
| Common variants of <i>HTR1A</i> and <i>SLC6A4</i> confer the increasing risk of Schizophrenia susceptibility: A population‐based association and epistasis analysis |
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| The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome |
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| Genetic influences on the neural and physiological bases of acute threat: A research domain criteria (RDoC) perspective |
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| Attentional biases to emotional stimuli: Key components of the RDoC constructs of sustained threat and loss |
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| Working memory genetics in schizophrenia and related disorders: An RDoC perspective |
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| Genetic variation in the oxytocin receptor gene is associated with a social phenotype in autism spectrum disorders |
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| The influence of genes on “positive valence systems” constructs: A systematic review |
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| The genetics of alcohol dependence: Twin and SNP‐based heritability, and genome‐wide association study based on AUDIT scores |
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| TPH2 gene polymorphisms and bipolar disorder: A meta‐analysis |
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| Genetics of aggressive behavior: An overview |
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| Predictors of heroin relapse: Personality traits, impulsivity, COMT gene Val158met polymorphism in a 5‐year prospective study in Shanghai, China |
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| Substance use associated with short sleep duration in patients with schizophrenia or schizoaffective disorder |
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African–Americans |
| Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration |
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ethnicity; ancestry |
| A powerful phenotype for gene‐finding studies derived from trajectory analyses of symptoms of anxiety and depression between age seven and 18 |
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| Re: Sulovari A, Kranzler HR, Farrer LA, Gelernter J, Li D. 2015. Eye color: A potential indicator of alcohol dependence risk in European Americans. Am J Med Genet B Neuropsychiatr Genet. 168(5):347–53 |
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European Americans |
| Genetic analysis of <i>SLC41A1</i> in Chinese Parkinson's disease patients |
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Han Chinese |
| Genetics of cognitive control: Implications for Nimh's research domain criteria initiative |
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| Genetic architecture for human aggression: A study of gene–phenotype relationship in OMIM |
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| X‐linked intellectual disability related genes disrupted by balanced X‐autosome translocations |
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| Further analyses support the association between light eye color and alcohol dependence |
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| Aggression in non‐human vertebrates: Genetic mechanisms and molecular pathways |
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| Antipsychotic drugs attenuate aberrant DNA methylation of <i>DTNBP1</i> (dysbindin) promoter in saliva and post‐mortem brain of patients with schizophrenia and Psychotic bipolar disorder |
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| Genetic and environmental contributions to the inverse association between specific autistic traits and experience seeking in adults |
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| Rigorous tests of gene–environment interactions in a lab study of the oxytocin receptor gene (<i>OXTR</i>), alcohol exposure, and aggression |
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| Genetic analysis of SNPs in <i>CACNA1C</i> and <i>ANK3</i> gene with schizophrenia: A comprehensive meta‐analysis |
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four European decent samples; Asian samples |
| A magnetic resonance imaging family study of cortical thickness in schizophrenia |
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| Parental age effects on odor sensitivity in healthy subjects and schizophrenia patients |
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| ADHD across the lifespan—IMpACT on genetics of adult ADHD |
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| Traumatic brain injury and bipolar psychosis in the Genomic Psychiatry Cohort |
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| Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis |
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| Genome‐wide association study of schizophrenia in Ashkenazi Jews |
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Ashkenazi Jews; AJ ancestry; founder population |
| Paternal age effect: Replication in schizophrenia with intriguing dissociation between bipolar with and without psychosis |
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| Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At‐Risk Individuals |
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European-ancestry |
| Gene‐set and multivariate genome‐wide association analysis of oppositional defiant behavior subtypes in attention‐deficit/hyperactivity disorder |
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| Oxytocin system social function impacts in children with attention‐deficit/hyperactivity disorder |
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| Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder |
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| Associations of common copy number variants in glutathione S‐transferase mu 1 and D‐dopachrome tautomerase‐like protein genes with risk of schizophrenia in a Japanese population |
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| Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE |
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| New suggestive genetic loci and biological pathways for attention function in adult attention‐deficit/hyperactivity disorder |
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| Heritability of attention‐deficit hyperactivity disorder in adults |
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| Fine mapping and whole‐exome sequencing of a familial cortical myoclonic tremor with epilepsy family |
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| Brain calcification process and phenotypes according to age and sex: Lessons from <i>SLC20A2</i>, <i>PDGFB</i>, and <i>PDGFRB</i> mutation carriers |
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| The role of candidate‐gene <i>CNTNAP2</i> in childhood apraxia of speech and specific language impairment |
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| Junctophilin 3 (<i>JPH3</i>) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype |
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African ancestry; African origin; black; white (used as racial category) |
| Significant association between rare <i>IPO11‐HTR1A</i> variants and attention deficit hyperactivity disorder in Caucasians |
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subjects of European descent; subjects of African descent |
| Quantifying naturalistic social gaze in fragile X syndrome using a novel eye tracking paradigm |
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| A genome‐wide association study of suicidal behavior |
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| On the role of <i>NOS1</i> ex1f‐VNTR in ADHD—allelic, subgroup, and meta‐analysis |
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| A genome‐wide approach to children's aggressive behavior: <i>The EAGLE consortium</i> |
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| Gene set analysis: A step‐by‐step guide |
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| Converging evidence does not support <i>GIT1</i> as an ADHD risk gene |
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| Investigation of the role of <i>TCF4</i> rare sequence variants in schizophrenia |
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379 European participants of the 1000 Genomes Project; German schizophrenia patients / German sample |
| Social support and the serotonin transporter genotype (5‐HTTLPR) moderate levels of resilience, sense of coherence, and depression |
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| A genome‐wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful faces |
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| <i>NCAM1‐TTC12‐ANKK1‐DRD2</i> gene cluster and the clinical and genetic heterogeneity of adults with ADHD |
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| Cumulative role of rare and common putative functional genetic variants at <i>NPAS3</i> in schizophrenia susceptibility |
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| Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
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| The predictive power of family history measures of alcohol and drug problems and internalizing disorders in a college population |
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| Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment |
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| Boymaw, Overexpressed in Brains With Major Psychiatric Disorders, May Encode a Small Protein to Inhibit Mitochondrial Function and Protein Translation |
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| Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia |
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| An angiotensin‐converting enzyme (ACE) polymorphism may mitigate the effects of angiotensin‐pathway medications on posttraumatic stress symptoms |
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| Association between genetic variants in <i>SLC25A12</i> and risk of autism spectrum disorders: An integrated meta‐analysis |
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| Eye color: A potential indicator of alcohol dependence risk in European Americans |
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European‐ancestry; European‐Americans; European Americans |
| ZNF804A rs1344706 is associated with cortical thickness, surface area, and cortical volume of the unmedicated first episode schizophrenia and healthy controls |
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| The impact of genome wide supported microRNA‐137 (MIR137) risk variants on frontal and striatal white matter integrity, neurocognitive functioning, and negative symptoms in schizophrenia |
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Chinese |
| Rare de novo deletion of metabotropic glutamate receptor 7 (<i>GRM7</i>) gene in a patient with autism spectrum disorder |
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| Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies |
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| MicroRNA hsa‐miR‐4717‐5p regulates RGS2 and may be a risk factor for anxiety‐related traits |
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| <i>ABCB1</i> gene variants and antidepressant treatment outcome: A meta‐analysis |
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ethnicity |
| Causal discovery in an adult ADHD data set suggests indirect link between <i>DAT1</i> genetic variants and striatal brain activation during reward processing |
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| ACN9 and alcohol dependence: Family‐based association analysis in multiplex alcohol dependence families |
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HapMap CEU population |
| Differential hippocampal gene expression and pathway analysis in an etiology‐based mouse model of major depressive disorder |
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| Case history and genome‐wide scans for copy number variants in a family with patient having 15q11.1–q11.2 duplication and 22q11.2 deletion, and schizophrenia |
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| Cadherin‐13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder |
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| Genomewide association analyses of electrophysiological endophenotypes for schizophrenia and psychotic bipolar disorders: A preliminary report |
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| <i>RGS2</i> genetic variation: Association analysis with panic disorder and dimensional as well as intermediate phenotypes of anxiety |
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| The neurocognitive impact of Fabry disease on pediatric patients |
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| Response to “DRD2 Ser311Cys polymorphism and risk of schizophrenia” |
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| The effect of <i>ANK3</i> bipolar‐risk polymorphisms on the working memory circuitry differs between loci and according to risk‐status for bipolar disorder |
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| Genetic and environmental contributions to the association between attention deficit hyperactivity disorder and alcohol dependence in adulthood: A large population‐based twin study |
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Swedish |
| <i>DRD2</i> Ser311Cys polymorphism and risk of schizophrenia |
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| Duplications in ADHD patients harbour neurobehavioural genes that are co‐expressed with genes associated with hyperactivity in the mouse |
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| Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease |
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Portuguese origin; Portuguese population; in Portugal; families of Portuguese origin; ancestral chro |
| The Neuropsychological profile of patients with 3‐Methylglutaconic aciduria type III, Costeff syndrome |
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| The relationship between schizophrenia and rheumatoid arthritis revisited: Genetic and epidemiological analyses |
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| An association between a dopamine transporter gene (<i>SLC6A3</i>) haplotype and ADHD symptom measures in nonclinical adults |
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| A preliminary analysis of microRNA as potential clinical biomarker for schizophrenia |
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| Alpha‐synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta‐analysis |
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various ethnic populations |
| Revisiting mendelian randomization studies of the effect of body mass index on depression |
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| Genome‐wide association study of lymphoblast cell viability after clozapine exposure |
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| Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population |
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| The role of age in association analyses of ADHD and related neurocognitive functioning: A proof of concept for dopaminergic and serotonergic genes |
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