American Journal of Medical Genetics Part B-Neuropsychiatric Genetics

Papers
(The TQCC of American Journal of Medical Genetics Part B-Neuropsychiatric Genetics is 2. 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 2022-05-01 to 2026-05-01.)
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”22
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Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism17
Cover Image, Volume 189B, Number 6, September 202217
William Boven's 1915 thesis “Similarity and Mendelism in the heredity of dementia praecox and manic‐depressive insanity”16
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort14
Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome14
Issue Information ‐ TOC12
Commentary on Immune‐Genomic Approaches to Schizophrenia: Highlighting IRF3 , L3HYPDH , and Drug R10
10
Transcriptional Patterns of Functional Connectivity Associated With Somatic Symptoms in Major Depressive Disorder10
Novel genome‐wide associations for effort valuation and psychopathology in children and adults9
The role and molecular mechanisms of the early growth response 3 gene in schizophrenia9
Causal Relationship Between Gut Microbiota and Non‐Suicidal Self‐Injury: A Two‐Sample Mendelian Randomization Study8
Appraising the Effects of Gut Microbiota on Insomnia Risk Through Genetic Causal Analysis8
Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome8
Issue Information ‐ TOC7
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking7
Patient Perspectives on Psychiatric Polygenic Risk Scores in Reproductive Decision‐Making and Polygenic Embryo Screening7
Internalizing Psychiatric Symptoms in People With Mosaicism for Trisomy 216
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
Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review5
Issue Information ‐ TOC5
LINC00665/miR–132–5p Reduces Inflammation in Epileptic Cells by Targeting MAPK35
Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis5
Discrepancy in Combined Genotype Distribution Data Between Two Related Studies of 5‐ HTTLPR and Posttraumatic Stress Disorder Risk4
Psychiatric Symptoms and Neuropsychological Findings in an Extremely Rare Case of 47, XXY Presenting With a Female Phenotype due to Deletion of the 4
4
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention4
Do Influential Articles on the Genetics of Autism Show Evidence of Engagement With the Autistic Community?4
Behavioral and transcriptomic analyses of mecp 2 function in zebrafish4
Pharmacogenetic Testing for Predicting Methylphenidate Treatment Outcomes in Childhood Attention Deficit Hyperactivity Disorder in Turkey: Focus on Carboxylesterase 1, Latrophilin‐3, and Catechol‐O‐Me4
Pseudo‐Schizophrenia Should Always Be Considered in Genetic Studies Regarding Psychosis4
Challenging Behavior Domains in Individuals With Neurodevelopmental Genetic Syndromes: The Role of Psychological Features4
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”4
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach4
Issue Information ‐ TOC4
Genetic Underpinnings of Obsessive–Compulsive Disorder With and Without Tics: Implications of Genetic Heterogeneity on Clinical Management4
A Systematic Review of Adverse Childhood Experiences and Epigenetic Age Acceleration in Later Adult Life Measured With Second and Third‐Generation Epigenetic Clocks3
The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia3
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome3
Issue Information ‐ TOC3
Schizophrenia Genetics Modulates Clinical Depressive Features3
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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 Age3
Mental Health Diagnoses Associated With Sex Chromosome Anomalies3
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Equitable Collaboration Between LMIC and HIC Researchers, Part I: A Preliminary Framework for Capa3
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
Appraisal of Gene Expression‐Based Classifiers for Neuropsychiatric Disorders: A Meta‐Regression2
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population2
A Systematic Review of the Application of Graph Neural Networks to Extract Candidate Genes and Biological Associations2
Association of BDNF risk variant and dorsolateral cortical thickness with long‐term treatment response to valproate in type I bipolar disorder: An exploratory study2
Black EquaLity in OCD NeuroGenomics ( BELONG ):2
Genetic and Environmental Factors of Nicotine Addiction: Examination of Multiple Substance Addictions2
Issue Information ‐ TOC2
Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit /Hyperactivity Disorder2
Expanding the Phenotype of TLK2 ‐Related Neurodevelopmental Disorder: Longitudinal Presentation in2
Identification of Transdiagnostic Childhood Externalizing Pathology Within an Electronic Medical Records Database and Application to the Analysis of Rare Copy Number Variation2
Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis2
Deep Phenotyping at Scale: Study Protocol for the Korean Mood Disorder Genetic Study‐Depression ( KOMOGEN ‐D)2
Psychiatric and Cognitive Features in Italian Women With the FMR1 Premutation: A Comprehensive Ass2
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