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 0. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
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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
Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism18
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Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort14
Cover Image, Volume 189B, Number 6, September 202214
William Boven's 1915 thesis “Similarity and Mendelism in the heredity of dementia praecox and manic‐depressive insanity”14
The role and molecular mechanisms of the early growth response 3 gene in schizophrenia14
Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome12
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Novel genome‐wide associations for effort valuation and psychopathology in children and adults11
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics10
Transcriptional Patterns of Functional Connectivity Associated With Somatic Symptoms in Major Depressive Disorder9
Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome7
Appraising the Effects of Gut Microbiota on Insomnia Risk Through Genetic Causal Analysis7
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Causal Relationship Between Gut Microbiota and Non‐Suicidal Self‐Injury: A Two‐Sample Mendelian Randomization Study7
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking6
Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis6
Challenging Behavior Domains in Individuals With Neurodevelopmental Genetic Syndromes: The Role of Psychological Features6
The role of the gut microbiota in patients with Kleefstra syndrome6
A Transcriptome‐Wide Mendelian Randomization Study in Isolated Human Immune Cells Highlights Risk Genes Involved in Viral Infections and Potential Drug Repurposing Opportunities for Schizophrenia6
LINC00665/miR–132–5p Reduces Inflammation in Epileptic Cells by Targeting MAPK36
Internalizing Psychiatric Symptoms in People With Mosaicism for Trisomy 216
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Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review6
Do Influential Articles on the Genetics of Autism Show Evidence of Engagement With the Autistic Community?5
Behavioral and transcriptomic analyses of mecp 2 function in zebrafish5
Genetic Underpinnings of Obsessive–Compulsive Disorder With and Without Tics: Implications of Genetic Heterogeneity on Clinical Management4
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach4
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”4
Psychiatric Symptoms and Neuropsychological Findings in an Extremely Rare Case of 47, XXY Presenting With a Female Phenotype due to Deletion of the 4
Pharmacogenetic Testing for Predicting Methylphenidate Treatment Outcomes in Childhood Attention Deficit Hyperactivity Disorder in Turkey: Focus on Carboxylesterase 1, Latrophilin‐3, and Catechol‐O‐Me3
Pseudo‐Schizophrenia Should Always Be Considered in Genetic Studies Regarding Psychosis3
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention3
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Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation3
A Systematic Review of Adverse Childhood Experiences and Epigenetic Age Acceleration in Later Adult Life Measured With Second and Third‐Generation Epigenetic Clocks3
Appraisal of Gene Expression‐Based Classifiers for Neuropsychiatric Disorders: A Meta‐Regression2
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The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia2
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 Age2
A Systematic Review of the Application of Graph Neural Networks to Extract Candidate Genes and Biological Associations2
Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit /Hyperactivity Disorder2
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Identification of Transdiagnostic Childhood Externalizing Pathology Within an Electronic Medical Records Database and Application to the Analysis of Rare Copy Number Variation2
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome2
Equitable Collaboration Between LMIC and HIC Researchers, Part I: A Preliminary Framework for Capa2
Mental Health Diagnoses Associated With Sex Chromosome Anomalies2
Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis2
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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Schizophrenia Genetics Modulates Clinical Depressive Features2
Genetic and Environmental Factors of Nicotine Addiction: Examination of Multiple Substance Addictions2
Deep Phenotyping at Scale: Study Protocol for the Korean Mood Disorder Genetic Study‐Depression (KOMOGEN‐D)2
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population2
Association of BDNF risk variant and dorsolateral cortical thickness with long‐term treatment response to valproate in type I bipolar disorder: An exploratory study2
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Ludvig Dahl's psychiatric genetic studies in his 1859 monograph: “Contribution to the knowledge of insanity in Norway”1
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Characterization of Two Novel PNKP Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations1
Causal Relationship Between Autism Spectrum Disorder and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study1
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 study1
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–19091
COMT rs4680 and DAOA rs947267 Polymorphism Interact to Influence Cognition and Psychiatric Symptoms in Chronic Schizop1
RETRACTED: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population1
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Polygene by environment interactions predicting depressive outcomes1
Influence of gut microbiota on the development of most prevalent neurodegenerative dementias and the potential effect of probiotics in elderly: A scoping review1
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Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits1
Associations between polygenic liability to psychopathology and non‐suicidal versus suicidal self‐injury1
Ryssia Wolfsohn's 1907 dissertation on “the heredity of dementia praecox”1
Circadian Rhythms Correlated in DNA Methylation and Gene Expression Identified in Human Blood and Implicated in Psychiatric Disorders1
Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants1
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Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD1
A Pilot Study to Assess the Impact of a Multifactorial Explanation for Mental Illness on Prejudicial Attitudes Towards People With Mental Illness1
Functional characterization of the schizophrenia associated gene AS3MT identifies a role in neuronal development1
Cover Image, Volume 198, Number 7, October 20251
The Multifaceted Etiology of Mental Disorders With a Focus on Trace Elements, a Review of Recent Literature0
De novo mutations disturb early brain development more frequently than common variants in schizophrenia0
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Comprehensive Analysis of Genomic Instability Derived lncRNAs Prognostic Signature and the Associated Tumor Microenvironment in Glioma0
Influence of antidepressant treatment on SLC6A4 methylation in Korean patients with major depression0
Network‐based meta‐analysis and the candidate gene association studies reveal novel ethnicity‐specific variants in MFSD3 and MRPL43 associated with dementia with Le0
The Impact of Brain‐Derived Neurotrophic Factor Polymorphism and Stimulation Parameters on the Response to Repetitive Transcranial Magnetic Stimulation: A Systematic Review0
How do experts in psychiatric genetics view the clinical utility of polygenic risk scores for schizophrenia?0
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Medical genetics in the 19th century as background to the development of psychiatric genetics0
Molecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations0
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Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan0
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A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium0
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies0
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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 data0
Genetic Variants ε2 and ε4 of APOE Predict Mortality and Poor Outcome Independently in Spontaneous Intracerebral Hemorrhage Within the Chinese Han Population0
The impact of a “Psychiatric Genetics for Genetic Counselors” workshop on genetic counselor attendees: An exploratory study0
Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation0
The rs11150601 Intron Variant of SETD1A Is Associated With Female Schizophrenia in the UK Biobank Cohort0
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Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood0
Henri Legrand du Saulle's 1873 book: “La Folie Héréditaire” (hereditary madness)0
Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences0
Improving Machine Learning Prediction of ADHD Using Gene Set Polygenic Risk Scores and Risk Scores From Genetically Correlated Phenotypes0
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Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome0
The examination of Kraepelin's diagnoses of dementia praecox and manic‐depressive insanity in pedigrees: Studies of Schuppius in 1912 and Wittermann in 19130
Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (VHIR), Barcelona Spain0
CELSR1 variants are associated with partial epilepsy of childhood0
Systematic exploration of a decade of publications on psychiatric genetics in Latin America0
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The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter0
Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder0
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Independent inheritance of cognition and bipolar disorder in a family sample0
Treg Cells Modulate Neuroinflammation and Behavioral Deficits in Autism: Evidence From MR‐Based Genetic Analyses and Experimental Models0
Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits0
Genetics of Response to ECT, TMS, Ketamine and Esketamine0
Network‐based artificial intelligence approaches for advancing personalized psychiatry0
Exploring the genetic architecture of brain structure and ADHD using polygenic neuroimaging‐derived scores0
Interview with Stephen Glatt. Editor‐in‐Chief, American Journal of Medical Genetics: Neuropsychiatric Genetics0
The shared genetic basis of mood instability and psychiatric disorders: A cross‐trait genome‐wide association analysis0
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing0
Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”0
Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review0
Disentangling differing relationships between internalizing disorders and alcohol use0
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Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance0
Neurodevelopmental Phenotyping and Genotyping in the Pediatric National Institute of Health Undiagnosed Disease Program0
FOXO4 alleviates hippocampal neuronal damage in epileptic mice via the miR‐138‐5p/ROCK2 axis0
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS ‐by‐subtraction study in the UK Biobank0
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Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol0
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations0
Polygenic prediction of bipolar disorder in a Latin American sample0
A Randomized Double‐Blind Placebo‐Controlled Trial of Guanfacine Extended Release for Aggression and Self‐Injurious Behavior Associated With Prader‐Willi Syndrome0
m6A Methylation‐Induced Autophagy Impairment by TFEB Regulation in SOD1 0
Genomic Analysis of Trichotillomania0
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The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops0
Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study0
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Association Between Polygenic Risk and Symptom Severity Change After Cognitive Behavioral Therapy for Obsessive‐Compulsive Disorder0
The Impact of the Parental Patterns of Morbidity and Comorbidity in the Cross‐Generational Transmission of Risk for Major Depression and Alcohol Use Disorder0
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines0
Bruno Schulz's 1930 article “The Hereditary Relationships of Old‐Age Paranoid Psychosis”0
Apples, Oranges, and Biobanks: Ascertainment Bias in Population‐Based Studies of Neurodevelopmental Psychiatric Disorders0
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Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide0
Life is pain: Fibromyalgia as a nexus of multiple liability distributions0
Luxenburger's 1939 Essay on “Schizophrenia and its Hereditary Circle”0
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The Role of SLC39A8 .p.( Ala391Thr ) in Schizophrenia Symptom Severity and Cognitive Ability: Cros0
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Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children0
Correction to “Disentangling Differing Relationships Between Internalizing Disorders and Alcohol Use”0
RYR3 Variants Are Potentially Associated With Idiopathic (Non‐Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene‐Disease Association by Genetic Dependent Natur0
The actions and interactions of family genetic risk scores for alcohol use disorder and major depression on the risk for these two disorders0
Potential New Expression Biomarkers for Anorexia Nervosa0
A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes0
Sex Differences in Cortical Thickness and Neuropsychiatric Symptom Burden Based on APOE4 Homozygosity in Alzheimer's Disease0
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FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development0
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 Heterogeneity0
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Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants0
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Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome0
The Genetic Landscape of Kynurenine Predicts Neurovascular Pathology and Disrupted White Matter Integrity in Patients With Mood Disorders0
Neurodevelopmental and Psychiatric Studies in Children and Adolescents With Neurofibromatosis Type I: A Comprehensive Scoping Review0
Phenotypic Manifestations of a New Variant in HDAC4 Gene0
Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives0
Functional Genomics Studies of Psychiatric Disorders in Individuals of Latin American Populations: A Scoping Review0
New Insights Into TRMT10A Syndrome: Case Report and Literature Review0
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal0
Cover Image, Volume 189B, Number 5, July 20220
Rüdin's Unpublished Family Study From the Early 1920s: “On the Inheritance of Manic‐Depressive Insanity”0
Reconsidering the Genetic Overlap Between Cognition and Bipolar Disorder: A Commentary on D'Amico et al.'s Family Study0
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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 Sample0
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Leveraging DNA methylation to predict treatment response in major depressive disorder: A critical review0
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