American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - 2020

43 articles | Last updated: 2025-12-03 14:12:55

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Article Title	T	A	T	A	T	A	T	A	Phrases Used
An integrative systems‐based analysis of substance use: <scp>eQTL</scp>‐informed gene‐based tests, gene networks, and biological mechanisms
Mapping relationships between <scp>ADHD</scp> genetic liability, stressful life events, and <scp>ADHD</scp> symptoms in healthy adults
Genetic overlap and causality between substance use disorder and <scp>attention‐deficit</scp> and hyperactivity disorder
Issue Information ‐ TOC
Cover Image, Volume 183B, Number 8, December 2020
Attention‐deficit/hyperactivity disorder symptoms and dietary habits in adulthood: A large population‐based twin study in Sweden
Induced pluripotent stem cell reprogramming‐associated methylation at the <scp><i>GABRA2</i></scp> promoter and chr4p12 <scp>GABA<sub>A</sub></scp> subunit gene expression in the context of alcohol us
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Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders
Effects of complement gene‐set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls
<scp>TWAS</scp> pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders
Investigating genetic correlation and causality between nicotine dependence and <scp>ADHD</scp> in a broader psychiatric context
Why does age of onset predict clinical severity in schizophrenia? A multiplex extended pedigree study
De novo <scp>STXBP1</scp> mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin <scp>1A</scp>
Epigenome‐wide analysis uncovers a blood‐based DNA methylation biomarker of lifetime cannabis use
The turn to controls and the refinement of the concept of hereditary burden: The 1895 study of Jenny Koller
A polygenic risk score analysis of <scp>ASD</scp> and <scp>ADHD</scp> across emotion recognition subtypes
Genetic feedback for psychiatric conditions: Where are we now and where are we going
Cover Image, Volume 183B, Number 6, September 2020
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Genes regulated by <scp>BCL11B</scp> during T‐cell development are enriched for de novo mutations found in schizophrenia patients
Early language measures associated with later psychosis features in 22q11.2 deletion syndrome
Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression
Genome‐wide admixture mapping of<scp>DSM‐IV</scp>alcohol dependence, criterion count, and the self‐rating of the effects of ethanol in African American populations						✓			European Americans
Huntingtin gene<scp>CAG</scp>repeat size affects autism risk: Family‐based and case–control association study
Language characterization in 16p11.2 deletion and duplication syndromes
The association between newborn screening analytes as measured on a second screen and childhood autism in a Texas Medicaid population
Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort							✓	✓	Taiwanese; Asian; ethnicities
A Mendelian randomization study of the causal association between anxiety phenotypes and schizophrenia
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Sodium hydrogen exchanger 9 <scp>NHE9</scp> (<scp><i>SLC9A9</i></scp>) and its emerging roles in neuropsychiatric comorbidity
Cover Image, Volume 183B, Number 4, June 2020
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Segregating patterns of copy number variations in extended autism spectrum disorder (<scp>ASD</scp>) pedigrees
Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature
Maternal and paternal effects on offspring internalizing problems: Results from genetic and family‐based analyses
<scp><i>MYT1L</i></scp>: A systematic review of genetic variation encompassing schizophrenia and autism
<scp><i>KTN1</i></scp> variants and risk for attention deficit hyperactivity disorder		✓
Cover Image, Volume 183B, Number 3, April 2020
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Issue Information ‐ TOC
Cover Image, Volume 183B, Number 2, March 2020
Refining critical regions in 15q24 microdeletion syndrome pertaining to autism