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 2021-07-01 to 2025-07-01.)
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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Self‐reported medication use as an alternate phenotyping method for anxiety and depression in the UK Biobank16
Cover Image, Volume 189B, Number 6, September 202214
The role and molecular mechanisms of the early growth response 3 gene in schizophrenia13
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics13
William Boven's 1915 thesis “Similarity and Mendelism in the heredity of dementia praecox and manic‐depressive insanity”13
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort11
Novel genome‐wide associations for effort valuation and psychopathology in children and adults10
Appraising the Effects of Gut Microbiota on Insomnia Risk Through Genetic Causal Analysis10
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Transcriptional Patterns of Functional Connectivity Associated With Somatic Symptoms in Major Depressive Disorder10
Genome Sequencing Uncovers Additional Findings in Phelan‐McDermid Syndrome10
Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome9
Internalizing Psychiatric Symptoms in People With Mosaicism for Trisomy 218
The role of the gut microbiota in patients with Kleefstra syndrome8
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking8
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The beginnings of the debate between the Mendelians and the Biometricians in psychiatric genetics: David Heron, Karl Pearson, Abraham Rosanoff, and Charles Davenport 1913–19148
A Transcriptome‐Wide Mendelian Randomization Study in Isolated Human Immune Cells Highlights Risk Genes Involved in Viral Infections and Potential Drug Repurposing Opportunities for Schizophrenia7
Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis7
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Genome‐wide association study and polygenic risk score analysis for hearing measures in children6
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach6
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?6
LINC00665/miR–132–5p Reduces Inflammation in Epileptic Cells by Targeting MAPK36
Psychiatric Symptoms and Neuropsychological Findings in an Extremely Rare Case of 47,XXY Presenting With a Female Phenotype due to Deletion of the SRY Gene5
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Behavioral and transcriptomic analyses of mecp2 function in zebrafish5
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”5
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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 ideation4
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 Age4
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
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Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention4
Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia3
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome3
The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia3
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Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis2
Cover Image, Volume 186B, Number 8, December 20212
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population2
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Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit/Hyperactivity Disorder2
Identification of Transdiagnostic Childhood Externalizing Pathology Within an Electronic Medical Records Database and Application to the Analysis of Rare Copy Number Variation2
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 study2
The nature of hereditary influences on insanity from research on asylum records in Western Europe in the mid‐19th century2
A Systematic Review of the Application of Graph Neural Networks to Extract Candidate Genes and Biological Associations2
Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood2
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Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits1
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Causal Relationship Between Autism Spectrum Disorder and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study1
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies1
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Polygenic burden could explain high rates of affective disorders in a community with restricted founder population1
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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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
Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD1
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Influence of gut microbiota on the development of most prevalent neurodegenerative dementias and the potential effect of probiotics in elderly: A scoping review1
Sites of active gene regulation in the prenatal frontal cortex and their role in neuropsychiatric disorders1
Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants1
Associations between polygenic liability to psychopathology and non‐suicidal versus suicidal self‐injury1
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–19091
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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
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New Insights Into TRMT10A Syndrome: Case Report and Literature Review0
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Disentangling differing relationships between internalizing disorders and alcohol use0
Bruno Schulz's 1930 article “The Hereditary Relationships of Old‐Age Paranoid Psychosis”0
Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives0
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Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study0
A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes0
Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”0
The Role of SLC39A8.p.(Ala391Thr) in Schizophrenia Symptom Severity and Cognitive Ability: Cross‐Sectional Studies of Schizophrenia and the General UK Population0
De novo mutations disturb early brain development more frequently than common variants in schizophrenia0
Polygene by environment interactions predicting depressive outcomes0
The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops0
Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”0
Circadian Rhythms Correlated in DNA Methylation and Gene Expression Identified in Human Blood and Implicated in Psychiatric Disorders0
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children0
Cover Image, Volume 186B, Number 7, October 20210
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol0
Ethical concerns relating to genetic risk scores for suicide0
Novel characterization of the multivariate genetic architecture of internalizing psychopathology and alcohol use0
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Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits0
Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome0
The impact of a “Psychiatric Genetics for Genetic Counselors” workshop on genetic counselor attendees: An exploratory study0
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal0
Cover Image, Volume 186B, Number 6, September 20210
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The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter0
Luxenburger's 1939 Essay on “Schizophrenia and its Hereditary Circle”0
Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation0
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A Randomized Double‐Blind Placebo‐Controlled Trial of Guanfacine Extended Release for Aggression and Self‐Injurious Behavior Associated With Prader‐Willi Syndrome0
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Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide0
Henri Legrand du Saulle's 1873 book: “La Folie Héréditaire” (hereditary madness)0
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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 disorders0
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing0
Leveraging DNA methylation to predict treatment response in major depressive disorder: A critical review0
Exploring the genetic architecture of brain structure and ADHD using polygenic neuroimaging‐derived scores0
Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan0
Genetic polymorphism data support a relationship between schizophrenia and microsatellite variability in PLA2G4A in Northern Europeans not Han Chinese0
Association Between Polygenic Risk and Symptom Severity Change After Cognitive Behavioral Therapy for Obsessive‐Compulsive Disorder0
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Medical genetics in the 19th century as background to the development of psychiatric genetics0
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Life is pain: Fibromyalgia as a nexus of multiple liability distributions0
Characterization of Two Novel PNKP Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations0
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FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development0
Ryssia Wolfsohn's 1907 dissertation on “the heredity of dementia praecox”0
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS‐by‐subtraction study in the UK Biobank0
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Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis0
Genomic Analysis of Trichotillomania0
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Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences0
Polygenic risk for major depression is associated with lifetime suicide attempt in US soldiers independent of personal and parental history of major depression0
Psychiatric phenotypes associated with hyperprolinemia: A systematic review0
The shared genetic basis of mood instability and psychiatric disorders: A cross‐trait genome‐wide association analysis0
Phenotypic Manifestations of a New Variant in HDAC4 Gene0
CELSR1 variants are associated with partial epilepsy of childhood0
The examination of Kraepelin's diagnoses of dementia praecox and manic‐depressive insanity in pedigrees: Studies of Schuppius in 1912 and Wittermann in 19130
FOXO4 alleviates hippocampal neuronal damage in epileptic mice via the miR‐138‐5p/ROCK2 axis0
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations0
Independent inheritance of cognition and bipolar disorder in a family sample0
A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium0
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
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines0
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Network‐based artificial intelligence approaches for advancing personalized psychiatry0
Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome0
Correction to “Disentangling Differing Relationships Between Internalizing Disorders and Alcohol Use”0
Apples, Oranges, and Biobanks: Ascertainment Bias in Population‐Based Studies of Neurodevelopmental Psychiatric Disorders0
Exploring the genetic overlap of suicide‐related behaviors and substance use disorders0
Network‐based meta‐analysis and the candidate gene association studies reveal novel ethnicity‐specific variants in MFSD3 and MRPL43 associated with dementia with Le0
Interview with Stephen Glatt. Editor‐in‐Chief, American Journal of Medical Genetics: Neuropsychiatric Genetics0
Systematic exploration of a decade of publications on psychiatric genetics in Latin America0
Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder0
Potential New Expression Biomarkers for Anorexia Nervosa0
Genome‐Wide Insights and Polygenic Risk Scores in Common Epilepsies: A Narrative Review0
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Genetics of Response to ECT, TMS, Ketamine and Esketamine0
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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
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Sex Differences in Cortical Thickness and Neuropsychiatric Symptom Burden Based on APOE4 Homozygosity in Alzheimer's Disease0
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RYR3 Variants Are Potentially Associated With Idiopathic (Non‐Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene‐Disease Association by Genetic Dependent Natur0
Ludvig Dahl's psychiatric genetic studies in his 1859 monograph: “Contribution to the knowledge of insanity in Norway”0
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies0
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Genetic Variants ε2 and ε4 of APOE Predict Mortality and Poor Outcome Independently in Spontaneous Intracerebral Hemorrhage Within the Chinese Han Population0
Polygenic prediction of bipolar disorder in a Latin American sample0
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder0
Prosper Lucas and his 1850 “Philosophical and Physiological Treatise on Natural Heredity”0
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
Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood0
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Influence of antidepressant treatment on SLC6A4 methylation in Korean patients with major depression0
How do experts in psychiatric genetics view the clinical utility of polygenic risk scores for schizophrenia?0
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Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants0
Cover Image, Volume 189B, Number 5, July 20220
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Reconsidering the Genetic Overlap Between Cognition and Bipolar Disorder: A Commentary on D'Amico et al.'s Family Study0
Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (VHIR), Barcelona Spain0
Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance0
Cover Image, Volume 186B, Number 5, July 20210
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