| Meta‐Analysis of Transcriptomic Studies of Blood and Six Brain Regions Identifies a Consensus of 15 Cross‐Tissue Mechanisms in Alzheimer's Disease and Suggests an Origin of Cross‐Study Heterogeneity |
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| Potential New Expression Biomarkers for Anorexia Nervosa |
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| A Pilot Study to Assess the Impact of a Multifactorial Explanation for Mental Illness on Prejudicial Attitudes Towards People With Mental Illness |
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| Issue Information ‐ TOC |
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| Reconsidering the Genetic Overlap Between Cognition and Bipolar Disorder: A Commentary on D'Amico et al.'s Family Study |
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| Issue Information ‐ TOC |
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| Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal |
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controls of European ancestry |
| Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach |
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| New Insights Into <scp>TRMT10A</scp> Syndrome: Case Report and Literature Review |
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| Characterization of Two Novel <i>PNKP</i> Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations |
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| Genetic Variants ε2 and ε4 of <scp>APOE</scp> Predict Mortality and Poor Outcome Independently in Spontaneous Intracerebral Hemorrhage Within the Chinese Han Population |
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Chinese Han Population |
| Sex Differences in Cortical Thickness and Neuropsychiatric Symptom Burden Based on <i>APOE4</i> Homozygosity in Alzheimer's Disease |
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| Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome |
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| Causal Relationship Between Autism Spectrum Disorder and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study |
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| Circadian Rhythms Correlated in <scp>DNA</scp> Methylation and Gene Expression Identified in Human Blood and Implicated in Psychiatric Disorders |
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| Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome |
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| Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan |
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| Issue Information ‐ TOC |
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| The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter |
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| Issue Information ‐ TOC |
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| A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes |
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| Polygene by environment interactions predicting depressive outcomes |
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| Independent inheritance of cognition and bipolar disorder in a family sample |
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| Exploring the genetic architecture of brain structure and <scp>ADHD</scp> using polygenic neuroimaging‐derived scores |
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| Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study |
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| Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (<scp>VHIR</scp>), Barcelona Spain |
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| Interview with Stephen Glatt. Editor‐in‐Chief, <i>American Journal of Medical Genetics: Neuropsychiatric Genetics</i> |
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| Network‐based artificial intelligence approaches for advancing personalized psychiatry |
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| The impact of family‐genetic risk scores on social functioning in individuals affected with six major psychiatric and substance use disorders in a Swedish National Sample |
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| Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance |
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| Issue Information ‐ TOC |
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| Issue Information ‐ TOC |
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| Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation |
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| Leveraging <scp>DNA</scp> methylation to predict treatment response in major depressive disorder: A critical review |
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| Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis |
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| <scp><i>KCNJ3</i></scp> is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing |
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| Associations between polygenic liability to psychopathology and non‐suicidal versus suicidal self‐injury |
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participants of European ancestry |
| Behavioral and transcriptomic analyses of <scp><i>mecp</i>2</scp> function in zebrafish |
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| Mendelian randomization analysis using <scp>GWAS</scp> and <scp>eQTL</scp> data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis |
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| The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops |
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| Luxenburger's 1939 Essay on “Schizophrenia and its Hereditary Circle” |
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| <scp><i>FOXG1</i></scp> variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development |
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| Issue Information ‐ TOC |
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| Speech and language in <i>DDX3X</i>‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention |
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| Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome |
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| Disentangling differing relationships between internalizing disorders and alcohol use |
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Finnish and East Asian ancestry groups; Finnish and East Asian ancestry groups |
| Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population |
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Kazakh population |
| Low‐grade parental gonosomal mosaicism in <scp><i>CHD2</i></scp> siblings with <scp>Smith–Magenis</scp>‐like syndrome |
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| Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort |
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| Issue Information ‐ TOC |
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| The role and molecular mechanisms of the early growth response 3 gene in schizophrenia |
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| Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants |
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