| Issue Information ‐ TOC |
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| Genomics of body fat percentage may contribute to sex bias in anorexia nervosa |
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| Cover Image, Volume 180, Number 1, January 2019 |
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| Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populations |
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| A case–control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE) |
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| Genes known to escape X chromosome inactivation predict co‐morbid chronic musculoskeletal pain and posttraumatic stress symptom development in women following trauma exposure |
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| Putative contributions of the sex chromosome proteins SOX3 and SRY to neurodevelopmental disorders |
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| Solving for X: Evidence for sex‐specific autism biomarkers across multiple transcriptomic studies |
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| Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach |
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| Ethical issues in susceptibility genetic testing for late‐onset neurodegenerative diseases |
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| The ethics of global psychiatric genomics: Multilayered challenges to integrating genomics in global mental health and disability—A position paper of the Oxford Global Initiative in Neuropsychiatric G |
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| The array of clinical phenotypes of males with mutations in <i>Methyl‐CpG binding protein 2</i> |
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| Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy |
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| GWAS and network analysis of co‐occurring nicotine and alcohol dependence identifies significantly associated alleles and network |
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European Americans (EAs); African Americans (AAs) |
| Cover Image, Volume 177B, Number 8, December 2018 |
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| The involvement of the canonical Wnt‐signaling receptor <i>LRP5</i> and <i>LRP6</i> gene variants with ADHD and sexual dimorphism: Association study and meta‐analysis |
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| Issue Information ‐ TOC |
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| Italian validation of the functional difficulties questionnaire (FDQ‐9) and its correlation with major determinants of quality of life in adults with hypermobile Ehlers–Danlos syndrome/hypermobility s |
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| Sequence variants in muscle tissue‐related genes may determine the severity of muscle contractures in cerebral palsy |
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| Aberrant transcriptomes and DNA methylomes define pathways that drive pathogenesis and loss of brain laterality/asymmetry in schizophrenia and bipolar disorder |
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| Sex differences in the genetic architecture of obsessive–compulsive disorder |
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| <i>CNKSR1</i> gene defect can cause syndromic autosomal recessive intellectual disability |
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| Musical auditory processing, cognition, and psychopathology in 22q11.2 deletion syndrome |
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| <i>PSMD12</i> haploinsufficiency in a neurodevelopmental disorder with autistic features |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 177B, Number 7, October 2018 |
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| <i>DRD4</i> methylation as a potential biomarker for physical aggression: An epigenome‐wide, cross‐tissue investigation |
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| Biomarkers for major depressive and bipolar disorders using metabolomics: A systematic review |
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| Introduction to special section on Leveraging Electronic Health Records for psychiatric genetic research |
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| Gene‐level associations in suicide attempter families show overrepresentation of synaptic genes and genes differentially expressed in brain development |
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| Exome sequencing of sporadic childhood‐onset schizophrenia suggests the contribution of X‐linked genes in males |
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| Association of Alzheimer's genetic loci with mild behavioral impairment |
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| Characterization of speech and language phenotype in children with <i>NRXN1</i> deletions |
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| Psychiatric genetics researchers' views on offering return of results to individual participants |
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| Blood‐based dynamic genomic signature for obsessive–compulsive disorder |
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| Genotype–phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype |
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| Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature |
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| “Like parent, like child”: Attention deficit hyperactivity disorder‐like characteristics in parents of ADHD cases |
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| DNA methylation of FKBP5 and response to exposure‐based psychological therapy |
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| Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data |
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| Convergent analysis of genome‐wide genotyping and transcriptomic data suggests association of zinc finger genes with lithium response in bipolar disorder |
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| Ethnic variation of <i>IL‐4</i> intron 3 VNTR gene polymorphism; its association with type 2 diabetes mellitus and its complication (neuropathy) in Egyptian subjects |
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| Biobehavioral composite of social aspects of anxiety in young adults with fragile X syndrome contrasted to autism spectrum disorder |
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| Copy number variation and neuropsychiatric problems in females and males in the general population |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 177B, Number 6, September 2018 |
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| The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders |
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| A comparative study of magnetic resonance imaging on the gray matter and resting‐state function in prodromal and first‐episode schizophrenia |
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| microRNA and mRNA profiles in nucleus accumbens underlying depression versus resilience in response to chronic stress |
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| Metabolomics in patients with psychosis: A systematic review |
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| A rare exonic <i>NRXN3</i> deletion segregating with neurodevelopmental and neuropsychiatric conditions in a three‐generation Chinese family |
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| Exploring relationships between joint hypermobility and neurodevelopment in children (4–13 years) with hereditary connective tissue disorders and developmental coordination disorder |
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| A longitudinal approach to biological psychiatric research: The PsyCourse study |
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| Issue Information ‐ TOC |
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| Genome‐wide association study of cognitive flexibility assessed by the Wisconsin Card Sorting Test |
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| Chromosome 17q12 duplications: Further delineation of the range of psychiatric and clinical phenotypes |
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| Associations between risk factors for schizophrenia and concordance in four monozygotic twin samples |
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| Cover Image, Volume 177B, Number 5, July 2018 |
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| Cover Image, Volume 177B, Number 4, June 2018 |
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| Issue Information ‐ TOC |
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| Is BDNF‐Val66Met polymorphism associated with psychotic experiences and psychotic disorder outcome? Evidence from a 6 years prospective population‐based cohort study |
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| <i>MTHFR</i> regulatory effects on methylation of CG05575921 in response to smoking: Effects are also discernable using <i>MTHFR</i> expression |
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| Genome‐wide and digital polymerase chain reaction epigenetic assessments of alcohol consumption |
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| Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone <i>HIST1H1E</i> and literature review |
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| Voxel‐wise brain‐wide functional connectivity abnormalities in first‐episode, drug‐naive patients with major depressive disorder |
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| A molecule‐based genetic association approach implicates a range of voltage‐gated calcium channels associated with schizophrenia |
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| Machine learning in schizophrenia genomics, a case‐control study using 5,090 exomes |
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| Association of copy number variation across the genome with neuropsychiatric traits in the general population |
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| A data‐driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome‐wide significant genetic loci |
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| RASopathies are associated with a distinct personality profile |
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| Rubinstein–Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach |
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| Tumor necrosis factor‐alpha <i>−</i>1031T/C polymorphism is associated with cognitive deficits in chronic schizophrenia patients versus healthy controls |
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| Evidence for additionally increased apoptosis in the peripheral blood mononuclear cells of major depressive patients with a high risk for suicide |
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| Preventing discrimination based on psychiatric risk biomarkers |
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| Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications |
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| Genome‐wide analysis of adolescent psychotic‐like experiences shows genetic overlap with psychiatric disorders |
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| Cover Image, Volume 177B, Number 3, April 2018 |
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| Issue Information ‐ TOC |
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| The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population |
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| Cover Image, Volume 177B, Number 2, March 2018 |
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| Issue Information ‐ TOC |
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| Effects of MiR‐137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls |
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| Adaptive behavior in infants and toddlers with Down syndrome and fragile X syndrome |
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