| Genome‐wide association study of shared liability to anxiety disorders in Army STARRS |
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European ancestry |
| Genetic meta‐analysis of obsessive–compulsive disorder and self‐report compulsive symptoms |
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| Genome‐wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder |
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✓ |
European American; African American |
| Identification of <i>TMC1</i> as a relatively common cause for nonsyndromic hearing loss in the Saudi population |
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Saudi population; consanguineous populations; Saudi HL cases |
| Targeted sequencing of the <i>LRRTM</i> gene family in suicide attempters with bipolar disorder |
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| Evaluation of the relationships of the <scp><i>WBP1L</i></scp> gene with schizophrenia and the general psychopathology scale based on a case–control study |
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✓ |
✓ |
Chinese Han |
| Issue Information ‐ TOC |
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| Cover Image, Volume 183B, Number 1, January 2020 |
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| <i>5‐HT2AR</i> and <i>BDNF</i> gene variants in eating disorders susceptibility |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 180B, Number 8, December 2019 |
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| Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain‐related functional pathways |
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| The need for attention to the ethical, legal, and social implications of advances in psychiatric genomics |
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| Genetic variability of serotonin pathway associated with schizophrenia onset, progression, and treatment |
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| Tyrosinemia Type 1 and symptoms of ADHD: Biochemical mechanisms and implications for treatment and prognosis |
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| Region‐specific insular volumetric decreases in drug‐naive, first‐episode schizophrenia and their unaffected siblings |
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| Genetics of resilience: Implications from genome‐wide association studies and candidate genes of the stress response system in posttraumatic stress disorder and depression |
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| Clinical highlights of a very rare phospolipid remodeling disease due to MBOAT7 gene defect |
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| A screen of 1,049 schizophrenia and 30 Alzheimer's‐associated variants for regulatory potential |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 180B, Number 7, October 2019 |
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| AHRR methylation predicts smoking status and smoking intensity in both saliva and blood DNA |
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| Maternal environmental risk factors and the development of internalizing and externalizing problems in childhood: The complex role of genetic factors |
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| Corrigendum |
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| Nordic OCD & Related Disorders Consortium: Rationale, design, and methods |
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✓ |
✓ |
Nordic |
| A novel eye‐tracking paradigm for indexing social avoidance‐related behavior in fragile X syndrome |
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| Exploratory analysis of genetic variants influencing molecular traits in cerebral cortex of suicide completers |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 180B, Number 6, September 2019 |
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| Differentially methylated regions in bipolar disorder and suicide |
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| A look into the future? Patients' and health care staff's perception and evaluation of genetic information and the right not to know |
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| Expanding the phenotypic spectrum of MBOAT7‐related intellectual disability |
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| Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese |
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✓ |
✓ |
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Europeans; European samples |
| The new science of sex differences in neuropsychiatric traits |
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| Examining sex differences in pleiotropic effects for depression and smoking using polygenic and gene‐region aggregation techniques |
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| Psychiatric genetic counseling: A mapping exercise |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 180B, Number 5, July 2019 |
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| Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression |
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| International Society of Psychiatric Genetics Ethics Committee: Issues facing us |
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| <i>KCNJ6</i> variants modulate reward‐related brain processes and impact executive functions in attention‐deficit/hyperactivity disorder |
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| Genome‐wide analyses of psychological resilience in U.S. Army soldiers |
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✓ |
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European (EUR) ancestry soldiers |
| Improving access to genetic testing for adults with intellectual disability: A literature review and lessons from a quality improvement project in East London |
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| Issue Information ‐ TOC |
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| Cover Image, Volume 180B, Number 4, June 2019 |
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| Identification of gene ontology and pathways implicated in suicide behavior: Systematic review and enrichment analysis of GWAS studies |
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| Study of C677T variant of methylene tetrahydrofolate reductase gene in autistic spectrum disorder Egyptian children |
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| Improving the classification of neuropsychiatric conditions using gene ontology terms as features |
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| The association between newborn screening analytes and childhood autism in a Texas Medicaid population, 2010–2012 |
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| The role of glutamate receptors in attention‐deficit/hyperactivity disorder: From physiology to disease |
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| Erratum |
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| Attitudes toward the right to autonomous decision‐making in psychiatric genetic testing: Controversial and context‐dependent |
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| Clinical relevance of heterozygosis for aceruloplasminemia |
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| Cover Image, Volume 180B, Number 3, April 2019 |
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| Genetic association and functional characterization of <i>MCPH1</i> gene variation in bipolar disorder and schizophrenia |
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| Issue Information ‐ TOC |
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| Parent‐offspring transmission of drug abuse and alcohol use disorder: Application of the multiple parenting relationships design |
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| Cover Image, Volume 180B, Number 2, March 2019 |
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| Issue Information ‐ TOC |
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| Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia |
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✓ |
✓ |
Irish |
| Identification of symbol digit modality test score extremes in Huntington's disease |
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| Fine‐mapping scan of bipolar disorder susceptibility loci in Latino pedigrees |
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| Ethical implications of using biobanks and population databases for genetic suicide research |
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| Co‐shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome |
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| Quantifying between‐cohort and between‐sex genetic heterogeneity in major depressive disorder |
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| The genetic and environmental structure of fear and anxiety in juvenile twins |
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| ADHD risk genes involved in dopamine signaling and metabolism are associated with reduced estimated life expectancy at young adult follow‐up in hyperactive and control children |
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