American Journal of Medical Genetics Part B-Neuropsychiatric Genetics

Papers
(The median citation count of American Journal of Medical Genetics Part B-Neuropsychiatric Genetics is 1. 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 2020-03-01 to 2024-03-01.)
ArticleCitations
Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression31
Genetic overlap and causality between substance use disorder and attention‐deficit and hyperactivity disorder24
Genetic feedback for psychiatric conditions: Where are we now and where are we going18
MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism17
Maternal and paternal effects on offspring internalizing problems: Results from genetic and family‐based analyses16
Language characterization in 16p11.2 deletion and duplication syndromes16
TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders15
Exploring the genetic overlap of suicide‐related behaviors and substance use disorders15
Epigenome‐wide analysis uncovers a blood‐based DNA methylation biomarker of lifetime cannabis use14
Psychiatric phenotypes associated with hyperprolinemia: A systematic review14
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
Ethical concerns relating to genetic risk scores for suicide12
KTN1 variants and risk for attention deficit hyperactivity disorder12
Investigating genetic correlation and causality between nicotine dependence and ADHD in a broader psychiatric context12
Genomics and epigenomics of addiction11
Rare protein‐coding variants implicate genes involved in risk of suicide death11
Why does age of onset predict clinical severity in schizophrenia? A multiplex extended pedigree study11
Genome‐wide admixture mapping ofDSM‐IValcohol dependence, criterion count, and the self‐rating of the effects of ethanol in African American populations11
Julius Wagner von Jauregg, Otto Diem and research methods for assessing the contributions of hereditary burden to mental illness risk: 1902–190610
Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis10
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations10
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
Early language measures associated with later psychosis features in 22q11.2 deletion syndrome9
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
Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits8
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
A polygenic risk score analysis of ASD and ADHD across emotion recognition subtypes8
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies8
Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood7
Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation7
Mapping relationships between ADHD genetic liability, stressful life events, and ADHD symptoms in healthy adults7
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees7
Changes in DNA methylation persist over time in males with severe alcohol use disorder—A longitudinal follow‐up study6
Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia6
Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores6
Genome‐wide association study and polygenic risk score analysis for hearing measures in children6
Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders6
Application of animal experimental models in the research of schizophrenia6
Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity6
De novo STXBP1 mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1A6
The nature of hereditary influences on insanity from research on asylum records in Western Europe in the mid‐19th century6
“The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment6
Effects of complement gene‐set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls6
Psychosocial implications of living with familial risk of a psychiatric disorder and attitudes to psychiatric genetic testing: A systematic review of the literature5
Sex differences in anxiety and depression in children with attention deficit hyperactivity disorder: Investigating genetic liability and comorbidity5
Novel characterization of the multivariate genetic architecture of internalizing psychopathology and alcohol use5
Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood5
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics5
Prosper Lucas and his 1850 “Philosophical and Physiological Treatise on Natural Heredity”5
Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”5
An integrative systems‐based analysis of substance use: eQTL‐informed gene‐based tests, gene networks, and biological mechanisms5
Polygenic risk for major depression is associated with lifetime suicide attempt in US soldiers independent of personal and parental history of major depression5
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
Influence of antidepressant treatment on SLC6A4 methylation in Korean patients with major depression4
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder4
Genetic study ofyoung‐onsetdementia using targeted gene panel sequencing in Taiwan4
Candidate pharmacological treatments for substance use disorder and suicide identified by gene co‐expression network‐based drug repositioning4
Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder4
The beginnings of the debate between the Mendelians and the Biometricians in psychiatric genetics: David Heron, Karl Pearson, Abraham Rosanoff, and Charles Davenport 1913–19144
Huntingtin gene CAG repeat size affects autism risk: Family‐based and case–control association study4
Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit/Hyperactivity Disorder3
Influence of gut microbiota on the development of most prevalent neurodegenerative dementias and the potential effect of probiotics in elderly: A scoping review3
Increasing the resolution and precision of psychiatric genome‐wide association studies by re‐imputing summary statistics using a large, diverse reference panel3
Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide3
The impact of a “Psychiatric Genetics for Genetic Counselors” workshop on genetic counselor attendees: An exploratory study3
Schizophrenia risk alleles often affect the expression of many genes and each gene may have a different effect on the risk: A mediation analysis3
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking3
Self‐reported medication use as an alternate phenotyping method for anxiety and depression in the UK Biobank3
Machine learning and bioinformatic analysis of brain and blood mRNA profiles in major depressive disorder: A case–control study3
Genes regulated by BCL11B during T‐cell development are enriched for de novo mutations found in schizophrenia patients2
Induced pluripotent stem cell reprogramming‐associated methylation at the GABRA2 promoter and chr4p12 GABAA subunit gene expression in the context of alcohol us2
FOXO4 alleviates hippocampal neuronal damage in epileptic mice via the miR‐138‐5p/ROCK2 axis2
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome‐wide association meta‐analysis2
Henri Legrand du Saulle's 1873 book: “La Folie Héréditaire” (hereditary madness)2
Genetic versus stress and mood determinants of sleep in the Amish2
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines2
The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia2
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–19092
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS‐by‐subtraction study in the UK Biobank1
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The examination of Kraepelin's diagnoses of dementia praecox and manic‐depressive insanity in pedigrees: Studies of Schuppius in 1912 and Wittermann in 19131
Functional characterization of the schizophrenia associated gene AS3MT identifies a role in neuronal development1
A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium1
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The actions and interactions of family genetic risk scores for alcohol use disorder and major depression on the risk for these two disorders1
Ryssia Wolfsohn's 1907 dissertation on “the heredity of dementia praecox”1
Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits1
Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants1
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A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data1
Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort1
The association between newborn screening analytes as measured on a second screen and childhood autism in a Texas Medicaid population1
RETRACTED: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population1
Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants1
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