| Longitudinal interplays of estrogen receptor alpha gene <i>rs9340799</i> with social‐environmental factors on post‐traumatic stress disorder in Chinese Han adolescents after Wenchuan earthquake |
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Chinese Han adolescents |
| Familial transmission of externalizing syndromes in extended Swedish families |
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| Emotional and behavioral problems in children and adolescents with neurofibromatosis type 1 |
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| A comprehensive review of genetic and epigenetic mechanisms that regulate <i>BDNF</i> expression and function with relevance to major depressive disorder |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 177B, Number 1, January 2018 |
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| Polygenic risk scores distinguish patients from non‐affected adult relatives and from normal controls in schizophrenia and bipolar disorder multi‐affected kindreds |
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| Mutation spectra and founder effect of <i>TMC1</i> in patients with non‐syndromic deafness in Xiamen area, China |
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| <i>SLC6A3</i> polymorphism and response to methylphenidate in children with ADHD: A systematic review and meta‐analysis |
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| Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population |
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| Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification |
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| Association of <i>IMMP2L</i> deletions with autism spectrum disorder: A trio family study and meta‐analysis |
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Han Chinese population; Chinese population |
| Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in <i>PTEN</i> hamartoma tumor syndrome |
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| Genome‐wide gene‐environment interaction in depression: A systematic evaluation of candidate genes |
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subjects of European ancestry |
| Association study of <i>NDST3</i> gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population |
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Han Chinese population; Chinese origin |
| Issue Information ‐ TOC |
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| Contribution of genes in the GABAergic pathway to bipolar disorder and its executive function deficit in the Chinese Han population |
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Chinese Han population |
| Cover Image, Volume 174B, Number 8, December 2017 |
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| Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences |
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| OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia |
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| Identification of a novel homozygous <i>TRAPPC9</i> gene mutation causing non‐syndromic intellectual disability, speech disorder, and secondary microcephaly |
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Pakistani descent |
| A functional polymorphism of the <i>OXTR</i> gene is associated with autistic traits in Caucasian and Asian populations |
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Asian, Chinese, ethnic/cultural groups |
| Genetic and molecular risk factors within the newly identified primate‐specific exon of the <i>SAP97/DLG1</i> gene in the 3q29 schizophrenia‐associated locus |
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Japanese cohort |
| Ancestry‐specific and sex‐specific risk alleles identified in a genome‐wide gene‐by‐alcohol dependence interaction study of risky sexual behaviors |
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European‐American (EA); African‐American (AA) |
| Exome sequencing reveals <i>NAA15</i> and <i>PUF60</i> as candidate genes associated with intellectual disability |
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| Nhe5 deficiency enhances learning and memory via upregulating Bdnf/TrkB signaling in mice |
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| The role of cadherin genes in five major psychiatric disorders: A literature update |
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| Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance |
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European‐American families |
| The role of <i>CLOCK</i> gene in psychiatric disorders: Evidence from human and animal research |
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| Cover Image, Volume 174B, Number 7, October 2017 |
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| Genomewide association studies of suicide attempts in US soldiers |
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ancestral group (European-, African-, Latino-American); European ancestry discovery samples; Europea |
| Issue Information ‐ TOC |
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| Phelan‐McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reports |
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| Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome |
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| The clinical features of alcohol use disorders in biological and step‐fathers that predict risk for alcohol use disorders in offspring |
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| A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains |
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| Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type |
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| Cover Image, Volume 174B, Number 6, September 2017 |
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| Issue Information ‐ TOC |
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| Role of 108 schizophrenia‐associated loci in modulating psychopathological dimensions in schizophrenia and bipolar disorder |
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| The regulation of tetraspanin 8 gene expression—A potential new mechanism in the pathogenesis of bipolar disorder |
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| Posterior column ataxia with retinitis pigmentosa coexisting with sensory‐autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser <i>FLVCR1</i> mutation |
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Italian woman |
| Lack of <i>TMEM230</i> mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population |
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| The dopamine transporter role in psychiatric phenotypes |
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| Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia |
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| The epigenomics of schizophrenia, in the mouse |
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| Optimizing the chances of success in the search for epigenetic biomarkers: Embracing genetic variation |
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| Microbiome, inflammation, epigenetic alterations, and mental diseases |
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| Epigenome‐wide association of PTSD from heterogeneous cohorts with a common multi‐site analysis pipeline |
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ancestry population stratification |
| National‐scale precision medicine for psychiatric disorders in Sweden |
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| 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 |
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| Single‐nucleotide polymorphisms in genes related to the hypothalamic‐pituitary‐adrenal axis as risk factors for posttraumatic stress disorder |
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| Genetically contextual effects of smoking on genome wide DNA methylation |
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| Shifting the focus toward rare variants in schizophrenia to close the gap from genotype to phenotype |
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| A comprehensive review of the genetic and biological evidence supports a role for MicroRNA‐137 in the etiology of schizophrenia |
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| Cover Image, Volume 174B, Number 5, July 2017 |
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| Imaging genetics in neurodevelopmental psychopathology |
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| Accuracy and utility of an epigenetic biomarker for smoking in populations with varying rates of false self‐report |
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| Issue Information ‐ TOC |
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| Serotonergic <i>5HTTLPR</i>/rs25531 s‐allele homozygosity associates with violent suicides in male citalopram users |
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| Genome‐wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders |
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| Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing |
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| Association between <i>COMT Val158Met</i> and psychiatric disorders: A comprehensive meta‐analysis |
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| The highly pleiotropic gene <i>SLC39A8</i> as an opportunity to gain insight into the molecular pathogenesis of schizophrenia |
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European populations; Europeans |
| The use of electronic health records for psychiatric phenotyping and genomics |
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| A genome‐wide quantitative trait locus (QTL) linkage scan of NEO personality factors in Latino families segregating bipolar disorder |
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Latino |
| Neuregulin 3 and its roles in schizophrenia risk and presentation |
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| A gene‐based review of <i>RGS4</i> as a putative risk gene for psychiatric illness |
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| Glucocerebrosidase mutations and neuropsychiatric phenotypes in Parkinson's disease and Lewy body dementias: Review and meta‐analyses |
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| Issue Information ‐ TOC |
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| Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene‐based tests, genome‐wide variation, and SNP heritability |
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990 individuals of European ancestry |
| Visuoperceptual processing in children with neurofibromatosis type 1: True deficit or artefact? |
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| Cover Image, Volume 174B, Number 4, June 2017 |
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| Genetic risk variants for social anxiety |
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| Delusional and psychotic disorders in juvenile myotonic dystrophy type‐1 |
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| Genome‐wide association study of HIV‐associated neurocognitive disorder (HAND): A CHARTER group study |
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| Genome‐wide meta‐analysis identifies a novel susceptibility signal at <i>CACNA2D3</i> for nicotine dependence |
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European (n = 14,713); African (n = 3,369) participants; 'ancestral groups' |
| Whole genome sequence association and ancestry‐informed polygenic profile of EEG alpha in a Native American population |
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higher degree European; Native American (NA) population; NA ancestry |
| Genetic and environmental contributions to the association between ADHD and affective problems in early childhood—A Swedish population‐based twin study |
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| A common genetic variant in <i>FOXP2</i> is associated with language‐based learning (dis)abilities: Evidence from two Italian independent samples |
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Italian |
| MTHFR methylation moderates the impact of smoking on DNA methylation at AHRR for African American young adults |
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| FMR1 genotype interacts with parenting stress to shape health and functional abilities in older age |
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| Vitamin D‐related genes are subjected to significant <i>de novo</i> mutation burdens in autism spectrum disorder |
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| Familial cases and male cases with <i>MECP2</i> mutations |
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| The genome‐wide expression effects of escitalopram and its relationship to neurogenesis, hippocampal volume, and antidepressant response |
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| Anxiety genetics: Dispatches from the frontier |
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| Developmental trajectories for young children with 16p11.2 copy number variation |
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| <i>ADH1B</i>: From alcoholism, natural selection, and cancer to the human phenome |
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| Investigation of <i>SHANK3</i> in schizophrenia |
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European controls; 2468 European Sanger‐sequenced controls; German controls |
| Can lncRNAs be indicators for the diagnosis of early onset or acute schizophrenia and distinguish major depressive disorder and generalized anxiety disorder?—A cross validation analysis |
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| Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum diso |
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| Copy number variation in 19 Italian multiplex families with autism spectrum disorder: Importance of synaptic and neurite elongation genes |
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Italian; single ethnic group |
| Issue Information ‐ TOC |
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| Predicting brain structure in population‐based samples with biologically informed genetic scores for schizophrenia |
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| Cover Image, Volume 174B, Number 3, April 2017 |
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| Genetic risk variants for social anxiety |
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EUR |
| Issue Information ‐ TOC |
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| Anxiety genetics: Dispatches from the frontier |
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| Cover Image, Volume 174B, Number 2, March 2017 |
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| miR‐149 and miR‐29c as candidates for bipolar disorder biomarkers |
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| Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome |
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