American Journal of Medical Genetics Part B-Neuropsychiatric Genetics

Papers
(The TQCC of American Journal of Medical Genetics Part B-Neuropsychiatric Genetics is 5. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression32
Genetic overlap and causality between substance use disorder and attention‐deficit and hyperactivity disorder25
Genetic feedback for psychiatric conditions: Where are we now and where are we going18
MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism18
Language characterization in 16p11.2 deletion and duplication syndromes17
Maternal and paternal effects on offspring internalizing problems: Results from genetic and family‐based analyses16
Exploring the genetic overlap of suicide‐related behaviors and substance use disorders15
TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders15
Psychiatric phenotypes associated with hyperprolinemia: A systematic review15
Epigenome‐wide analysis uncovers a blood‐based DNA methylation biomarker of lifetime cannabis use14
Genomics and epigenomics of addiction13
Investigating genetic correlation and causality between nicotine dependence and ADHD in a broader psychiatric context13
Ethical concerns relating to genetic risk scores for suicide13
The turn to controls and the refinement of the concept of hereditary burden: The 1895 study of Jenny Koller13
Attention‐deficit/hyperactivity disorder symptoms and dietary habits in adulthood: A large population‐based twin study in Sweden12
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations11
Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis11
Why does age of onset predict clinical severity in schizophrenia? A multiplex extended pedigree study11
Rare protein‐coding variants implicate genes involved in risk of suicide death11
Genome‐wide admixture mapping ofDSM‐IValcohol dependence, criterion count, and the self‐rating of the effects of ethanol in African American populations11
Early language measures associated with later psychosis features in 22q11.2 deletion syndrome10
Julius Wagner von Jauregg, Otto Diem and research methods for assessing the contributions of hereditary burden to mental illness risk: 1902–190610
A Mendelian randomization study of the causal association between anxiety phenotypes and schizophrenia10
The shared genetic basis of mood instability and psychiatric disorders: A cross‐trait genome‐wide association analysis9
A polygenic risk score analysis of ASD and ADHD across emotion recognition subtypes9
Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits8
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies8
CELSR1 variants are associated with partial epilepsy of childhood8
Functional variants fine‐mapping and gene function characterization provide insights into the role of ZNF323 in schizophrenia pathogenesis8
Sites of active gene regulation in the prenatal frontal cortex and their role in neuropsychiatric disorders8
Psychiatric genomics research during the COVID‐19 pandemic: A survey of Psychiatric Genomics Consortium researchers8
Changes in DNA methylation persist over time in males with severe alcohol use disorder—A longitudinal follow‐up study7
Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood7
Mapping relationships between ADHD genetic liability, stressful life events, and ADHD symptoms in healthy adults7
Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores7
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees7
Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation7
Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders6
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics6
Effects of complement gene‐set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls6
Genome‐wide association study and polygenic risk score analysis for hearing measures in children6
The nature of hereditary influences on insanity from research on asylum records in Western Europe in the mid‐19th century6
Application of animal experimental models in the research of schizophrenia6
Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”6
De novo STXBP1 mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1A6
Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia6
“The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment6
Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity6
Sex differences in anxiety and depression in children with attention deficit hyperactivity disorder: Investigating genetic liability and comorbidity5
Polygenic risk for major depression is associated with lifetime suicide attempt in US soldiers independent of personal and parental history of major depression5
Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood5
An integrative systems‐based analysis of substance use: eQTL‐informed gene‐based tests, gene networks, and biological mechanisms5
Prosper Lucas and his 1850 “Philosophical and Physiological Treatise on Natural Heredity”5
Novel characterization of the multivariate genetic architecture of internalizing psychopathology and alcohol use5
Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature5
Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences5
Philipp Jolly and his 1913 “the heredity of psychosis”: Homogeneity versus heterogeneity of familial transmission and an early look at Mendelian models for manic‐depressive illne5
0.026012182235718