American Journal of Medical Genetics Part B-Neuropsychiatric Genetics

Article	Citations
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Irma Weinberg's 1928 paper “on the problem of the determination of heredity prognosis: The risk in the cousins of schizophrenics”	20
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Self‐reported medication use as an alternate phenotyping method for anxiety and depression in the UK Biobank	16
Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism	15
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Cover Image, Volume 189B, Number 6, September 2022	13
William Boven's 1915 thesis “Similarity and Mendelism in the heredity of dementia praecox and manic‐depressive insanity”	13
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics	12
The role and molecular mechanisms of the early growth response 3 gene in schizophrenia	11
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort	11
Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome	10
Novel genome‐wide associations for effort valuation and psychopathology in children and adults	10
Appraising the Effects of Gut Microbiota on Insomnia Risk Through Genetic Causal Analysis	10
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A Transcriptome‐Wide Mendelian Randomization Study in Isolated Human Immune Cells Highlights Risk Genes Involved in Viral Infections and Potential Drug Repurposing Opportunities for Schizophrenia	9
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking	8
Internalizing Psychiatric Symptoms in People With Mosaicism for Trisomy 21	8
Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis	8
The beginnings of the debate between the Mendelians and the Biometricians in psychiatric genetics: David Heron, Karl Pearson, Abraham Rosanoff, and Charles Davenport 1913–1914	8
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The role of the gut microbiota in patients with Kleefstra syndrome	8

Do Influential Articles on the Genetics of Autism Show Evidence of Engagement With the Autistic Community?	7
LINC00665/miR–132–5p Reduces Inflammation in Epileptic Cells by Targeting MAPK3	7
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach	6
Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review	6
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”	6
Genome‐wide association study and polygenic risk score analysis for hearing measures in children	6
Behavioral and transcriptomic analyses of mecp2 function in zebrafish	6
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Pharmacogenetic Testing for Predicting Methylphenidate Treatment Outcomes in Childhood Attention Deficit Hyperactivity Disorder in Turkey: Focus on Carboxylesterase 1, Latrophilin‐3, and Catechol‐O‐Me	5
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Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention	5
Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation	5
Depression Symptom Trajectories in Mothers With the FMR1 Premutation Vary by CGG Repeat Length: A Longitudinal Study of 73 Women Spanning 20–75 Years of Age	4
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The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia	4
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Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia	4
The nature of hereditary influences on insanity from research on asylum records in Western Europe in the mid‐19th century	3
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome	3
Identification of Transdiagnostic Childhood Externalizing Pathology Within an Electronic Medical Records Database and Application to the Analysis of Rare Copy Number Variation	3
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Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis	3
Cover Image, Volume 186B, Number 8, December 2021	2
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Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood	2
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The era of the Dawn of Mendelian research in the field of psychiatry: Rüdin's 1922 review paper “regarding the heredity of mental disturbances”	2
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Association of BDNF risk variant and dorsolateral cortical thickness with long‐term treatment response to valproate in type I bipolar disorder: An exploratory study	2
A Systematic Review of the Application of Graph Neural Networks to Extract Candidate Genes and Biological Associations	2
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome‐wide association meta‐analysis	2
Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit/Hyperactivity Disorder	2
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population	2
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RETRACTED: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population	1
Polygenic burden could explain high rates of affective disorders in a community with restricted founder population	1
Influence of gut microbiota on the development of most prevalent neurodegenerative dementias and the potential effect of probiotics in elderly: A scoping review	1
Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD	1
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Causal Relationship Between Autism Spectrum Disorder and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study	1
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Associations between polygenic liability to psychopathology and non‐suicidal versus suicidal self‐injury	1
Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits	1
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies	1
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–1909	1

Cross‐sectional and longitudinal associations between gut microbiota composition and cognition in the second year of life: Findings from the Child Health and Resident Microbes study	1
Functional characterization of the schizophrenia associated gene AS3MT identifies a role in neuronal development	1
Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants	1
Sites of active gene regulation in the prenatal frontal cortex and their role in neuropsychiatric disorders	1
Application of animal experimental models in the research of schizophrenia	1
A Pilot Study to Assess the Impact of a Multifactorial Explanation for Mental Illness on Prejudicial Attitudes Towards People With Mental Illness	1
Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide	0
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Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”	0
Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants	0
Exploring the genetic architecture of brain structure and ADHD using polygenic neuroimaging‐derived scores	0
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Reconsidering the Genetic Overlap Between Cognition and Bipolar Disorder: A Commentary on D'Amico et al.'s Family Study	0
The actions and interactions of family genetic risk scores for alcohol use disorder and major depression on the risk for these two disorders	0
Cover Image, Volume 186B, Number 6, September 2021	0
Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis	0
Henri Legrand du Saulle's 1873 book: “La Folie Héréditaire” (hereditary madness)	0
A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes	0
Potential New Expression Biomarkers for Anorexia Nervosa	0
Exploring the genetic overlap of suicide‐related behaviors and substance use disorders	0
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The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops	0
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development	0
Association Between Polygenic Risk and Symptom Severity Change After Cognitive Behavioral Therapy for Obsessive‐Compulsive Disorder	0
Characterization of Two Novel PNKP Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations	0
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children	0
Phenotypic Manifestations of a New Variant in HDAC4 Gene	0
Systematic exploration of a decade of publications on psychiatric genetics in Latin America	0
Ryssia Wolfsohn's 1907 dissertation on “the heredity of dementia praecox”	0
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies	0
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder	0
The shared genetic basis of mood instability and psychiatric disorders: A cross‐trait genome‐wide association analysis	0
Genetic Variants ε2 and ε4 of APOE Predict Mortality and Poor Outcome Independently in Spontaneous Intracerebral Hemorrhage Within the Chinese Han Population	0
The impact of a “Psychiatric Genetics for Genetic Counselors” workshop on genetic counselor attendees: An exploratory study	0
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Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives	0
Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood	0
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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	0
The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter	0
Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (VHIR), Barcelona Spain	0
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Network‐based artificial intelligence approaches for advancing personalized psychiatry	0
Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance	0
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Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation	0
De novo mutations disturb early brain development more frequently than common variants in schizophrenia	0
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing	0
Cover Image, Volume 186B, Number 4, June 2021	0
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Network‐based meta‐analysis and the candidate gene association studies reveal novel ethnicity‐specific variants in MFSD3 and MRPL43 associated with dementia with Le	0
Cover Image, Volume 189B, Number 5, July 2022	0
A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data	0
Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome	0
Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder	0
RYR3 Variants Are Potentially Associated With Idiopathic (Non‐Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene‐Disease Association by Genetic Dependent Natur	0
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Sex Differences in Cortical Thickness and Neuropsychiatric Symptom Burden Based on APOE4 Homozygosity in Alzheimer's Disease	0
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol	0
Disentangling differing relationships between internalizing disorders and alcohol use	0
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Novel characterization of the multivariate genetic architecture of internalizing psychopathology and alcohol use	0
Polygenic risk for major depression is associated with lifetime suicide attempt in US soldiers independent of personal and parental history of major depression	0
Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study	0
Ludvig Dahl's psychiatric genetic studies in his 1859 monograph: “Contribution to the knowledge of insanity in Norway”	0
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Luxenburger's 1939 Essay on “Schizophrenia and its Hereditary Circle”	0
Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences	0
Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome	0
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Apples, Oranges, and Biobanks: Ascertainment Bias in Population‐Based Studies of Neurodevelopmental Psychiatric Disorders	0
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal	0
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations	0
How do experts in psychiatric genetics view the clinical utility of polygenic risk scores for schizophrenia?	0
Cover Image, Volume 186B, Number 7, October 2021	0
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Independent inheritance of cognition and bipolar disorder in a family sample	0
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines	0
Correction to “Disentangling Differing Relationships Between Internalizing Disorders and Alcohol Use”	0
Influence of antidepressant treatment on SLC6A4 methylation in Korean patients with major depression	0
A Randomized Double‐Blind Placebo‐Controlled Trial of Guanfacine Extended Release for Aggression and Self‐Injurious Behavior Associated With Prader‐Willi Syndrome	0
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Medical genetics in the 19th century as background to the development of psychiatric genetics	0
A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium	0
Life is pain: Fibromyalgia as a nexus of multiple liability distributions	0
Interview with Stephen Glatt. Editor‐in‐Chief, American Journal of Medical Genetics: Neuropsychiatric Genetics	0
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Cover Image, Volume 186B, Number 5, July 2021	0
Bruno Schulz's 1930 article “The Hereditary Relationships of Old‐Age Paranoid Psychosis”	0
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Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”	0
New Insights Into TRMT10A Syndrome: Case Report and Literature Review	0
Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan	0
Erratum	0
FOXO4 alleviates hippocampal neuronal damage in epileptic mice via the miR‐138‐5p/ROCK2 axis	0
Polygene by environment interactions predicting depressive outcomes	0
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS‐by‐subtraction study in the UK Biobank	0
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Leveraging DNA methylation to predict treatment response in major depressive disorder: A critical review	0
Circadian Rhythms Correlated in DNA Methylation and Gene Expression Identified in Human Blood and Implicated in Psychiatric Disorders	0
Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores	0
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Prosper Lucas and his 1850 “Philosophical and Physiological Treatise on Natural Heredity”	0
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Ethical concerns relating to genetic risk scores for suicide	0
Polygenic prediction of bipolar disorder in a Latin American sample	0
Genetic polymorphism data support a relationship between schizophrenia and microsatellite variability in PLA2G4A in Northern Europeans not Han Chinese	0
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Psychiatric phenotypes associated with hyperprolinemia: A systematic review	0
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Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits	0
The examination of Kraepelin's diagnoses of dementia praecox and manic‐depressive insanity in pedigrees: Studies of Schuppius in 1912 and Wittermann in 1913	0
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CELSR1 variants are associated with partial epilepsy of childhood	0
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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	0
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