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 2020-11-01 to 2024-11-01.)
ArticleCitations
Genetic overlap and causality between substance use disorder and attention‐deficit and hyperactivity disorder26
Psychiatric phenotypes associated with hyperprolinemia: A systematic review20
Exploring the genetic overlap of suicide‐related behaviors and substance use disorders19
Genetics and epigenetics of self‐injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations14
Genomics and epigenomics of addiction13
Ethical concerns relating to genetic risk scores for suicide13
Rare protein‐coding variants implicate genes involved in risk of suicide death12
The shared genetic basis of mood instability and psychiatric disorders: A cross‐trait genome‐wide association analysis12
Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis12
Recommendations to encourage participation of individuals from diverse backgrounds in psychiatric genetic studies10
Julius Wagner von Jauregg, Otto Diem and research methods for assessing the contributions of hereditary burden to mental illness risk: 1902–190610
Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation9
CELSR1 variants are associated with partial epilepsy of childhood9
Application of animal experimental models in the research of schizophrenia9
Sites of active gene regulation in the prenatal frontal cortex and their role in neuropsychiatric disorders9
Mechanism of METTL3‐mediated m6A modification in depression‐induced cognitive deficits9
Changes in DNA methylation persist over time in males with severe alcohol use disorder—A longitudinal follow‐up study8
Functional variants fine‐mapping and gene function characterization provide insights into the role of ZNF323 in schizophrenia pathogenesis8
Mapping relationships between ADHD genetic liability, stressful life events, and ADHD symptoms in healthy adults8
Psychiatric genomics research during the COVID‐19 pandemic: A survey of Psychiatric Genomics Consortium researchers8
The nature of hereditary influences on insanity from research on asylum records in Western Europe in the mid‐19th century8
Within subject cross‐tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood8
Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder7
Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores7
Influence of antidepressant treatment on SLC6A4 methylation in Korean patients with major depression7
Investigating perceived heritability of mental health disorders and attitudes toward genetic testing in the United States, United Kingdom, and Australia7
Genetic study ofyoung‐onsetdementia using targeted gene panel sequencing in Taiwan7
Genome‐wide association study and polygenic risk score analysis for hearing measures in children7
Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences7
Polygenic risk for major depression is associated with lifetime suicide attempt in US soldiers independent of personal and parental history of major depression6
Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”6
“The Heidelberg Five” personality dimensions: Genome‐wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment6
The place of Franz Kallmann's 1938 “the genetics of schizophrenia” in the history of psychiatric genetics6
Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood6
Integrative multi‐omics analysis of genomic, epigenomic, and metabolomics data leads to new insights for Attention‐Deficit/Hyperactivity Disorder5
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
Candidate pharmacological treatments for substance use disorder and suicide identified by gene co‐expression network‐based drug repositioning5
Effects of polygenic risk for suicide attempt and risky behavior on brain structure in young people with familial risk of bipolar disorder5
Influence of gut microbiota on the development of most prevalent neurodegenerative dementias and the potential effect of probiotics in elderly: A scoping review5
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
Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide5
An integrative systems‐based analysis of substance use: eQTL‐informed gene‐based tests, gene networks, and biological mechanisms5
Prosper Lucas and his 1850 “Philosophical and Physiological Treatise on Natural Heredity”5
Machine learning and bioinformatic analysis of brain and blood mRNA profiles in major depressive disorder: A case–control study4
Increasing the resolution and precision of psychiatric genome‐wide association studies by re‐imputing summary statistics using a large, diverse reference panel4
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
Self‐reported medication use as an alternate phenotyping method for anxiety and depression in the UK Biobank4
The impact of a “Psychiatric Genetics for Genetic Counselors” workshop on genetic counselor attendees: An exploratory study4
Multi‐polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives3
RETRACTED: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population3
Schizophrenia risk alleles often affect the expression of many genes and each gene may have a different effect on the risk: A mediation analysis3
Neonatal DNA methylation and childhood low prosocial behavior: An epigenome‐wide association meta‐analysis3
Functional characterization of the schizophrenia associated gene AS3MT identifies a role in neuronal development3
The impact of receiving polygenic risk scores for alcohol use disorder on psychological distress, risk perception, and intentions to reduce drinking3
The relationship between case–control differential gene expression from brain tissue and genetic associations in schizophrenia3
Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis2
How do experts in psychiatric genetics view the clinical utility of polygenic risk scores for schizophrenia?2
A polygenic resilience score moderates the genetic risk for schizophrenia: Replication in 18,090 cases and 28,114 controls from the Psychiatric Genomics Consortium2
Genetic versus stress and mood determinants of sleep in the Amish2
The role of the gut microbiota in patients with Kleefstra syndrome2
Henri Legrand du Saulle's 1873 book: “La Folie Héréditaire” (hereditary madness)2
FOXO4 alleviates hippocampal neuronal damage in epileptic mice via the miR‐138‐5p/ROCK2 axis2
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–19092
The actions and interactions of family genetic risk scores for alcohol use disorder and major depression on the risk for these two disorders2
ADHD‐associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient‐derived cell lines2
Multivariate analyses of molecular genetic associations between childhood psychopathology and adult mood disorders and related traits2
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS‐by‐subtraction study in the UK Biobank2
Behavioral and transcriptomic analyses of mecp2 function in zebrafish2
Ryssia Wolfsohn's 1907 dissertation on “the heredity of dementia praecox”1
1
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children1
The era of the Dawn of Mendelian research in the field of psychiatry: Rüdin's 1922 review paper “regarding the heredity of mental disturbances”1
The examination of Kraepelin's diagnoses of dementia praecox and manic‐depressive insanity in pedigrees: Studies of Schuppius in 1912 and Wittermann in 19131
The role and molecular mechanisms of the early growth response 3 gene in schizophrenia1
A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data1
Leveraging DNA methylation to predict treatment response in major depressive disorder: A critical review1
Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants1
Family‐based genetic analysis in schizophrenia by whole‐exome sequence to identify rare pathogenic variants1
Issue Information ‐ TOC0
Mental health, coping, and protective factors in mothers of children with 22q11.2 deletion syndrome0
Circadian Rhythms Correlated in DNA Methylation and Gene Expression Identified in Human Blood and Implicated in Psychiatric Disorders0
0
Issue Information ‐ TOC0
Issue Information ‐ TOC0
Cover Image, Volume 186B, Number 6, September 20210
Issue Information ‐ TOC0
Causal Relationship Between Autism Spectrum Disorder and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study0
Issue Information ‐ TOC0
0
0
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies0
0
0
0
Cover Image, Volume 186B, Number 7, October 20210
Mediational pathways between aggregate genetic liability and nonfatal suicide attempt: A Swedish population‐based cohort0
Epigenetic underpinnings of the autistic mind: Histone modifications and prefrontal excitation/inhibition imbalance0
Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan0
Parenting Stress Index in Caregivers of Individuals With Noonan Syndrome0
Cover Image, Volume 189B, Number 6, September 20220
Retraction: Population features of alleles and genotypes frequency distribution of polymorphic genetic markers of antipsychotic medications pharmacokinetics in the Kazakh population0
0
Issue Information ‐ TOC0
Erratum0
Sex Differences in Cortical Thickness and Neuropsychiatric Symptom Burden Based on APOE4 Homozygosity in Alzheimer's Disease0
Life is pain: Fibromyalgia as a nexus of multiple liability distributions0
Polygenic burden could explain high rates of affective disorders in a community with restricted founder population0
Issue Information ‐ TOC0
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention0
De novo mutations disturb early brain development more frequently than common variants in schizophrenia0
Irma Weinberg's 1928 paper “on the problem of the determination of heredity prognosis: The risk in the cousins of schizophrenics”0
Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”0
0
0
0
Network‐based meta‐analysis and the candidate gene association studies reveal novel ethnicity‐specific variants in MFSD3 and MRPL43 associated with dementia with Le0
Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study0
Cover Image, Volume 186B, Number 5, July 20210
Issue Information ‐ TOC0
Bruno Schulz's 1930 article “The Hereditary Relationships of Old‐Age Paranoid Psychosis”0
Independent inheritance of cognition and bipolar disorder in a family sample0
Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation0
Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism0
Ludvig Dahl's psychiatric genetic studies in his 1859 monograph: “Contribution to the knowledge of insanity in Norway”0
Novel genome‐wide associations for effort valuation and psychopathology in children and adults0
Luxenburger's 1939 Essay on “Schizophrenia and its Hereditary Circle”0
0
Genomics and epigenomics of substance use disorders: An introduction0
0
Issue Information ‐ TOC0
Issue Information ‐ TOC0
Systematic exploration of a decade of publications on psychiatric genetics in Latin America0
0
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
Issue Information ‐ TOC0
Polygenic prediction of bipolar disorder in a Latin American sample0
Network‐based artificial intelligence approaches for advancing personalized psychiatry0
A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes0
Cognitive, Social, and Emotional‐Behavioral Outcomes in Children and Adolescents With Beckwith–Wiedemann Syndrome0
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing0
Cover Image, Volume 186B, Number 8, December 20210
Issue Information ‐ TOC0
0
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”0
0
Cover Image, Volume 186B, Number 4, June 20210
Cover Image, Volume 189B, Number 5, July 20220
Issue Information ‐ TOC0
Cover Image, Volume 186B, Number 1, January 20210
Issue Information ‐ TOC0
Issue Information ‐ TOC0
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 study0
0
New Insights Into TRMT10A Syndrome: Case Report and Literature Review0
Issue Information ‐ TOC0
Issue Information ‐ TOC0
The genetic and environmental etiology of novel frequency‐driven regional parcellations of abnormal white matter0
Issue Information ‐ TOC0
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol0
Issue Information ‐ TOC0
Disentangling differing relationships between internalizing disorders and alcohol use0
Contribution of Rare and Potentially Functionally Relevant Sequence Variants in Schizophrenia Risk‐Locus Xq28,distal0
Issue Information ‐ TOC0
0
Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD0
Issue Information ‐ TOC0
William Boven's 1915 thesis “Similarity and Mendelism in the heredity of dementia praecox and manic‐depressive insanity”0
0
Polygene by environment interactions predicting depressive outcomes0
Issue Information ‐ TOC0
0
Genetic polymorphism data support a relationship between schizophrenia and microsatellite variability in PLA2G4A in Northern Europeans not Han Chinese0
Issue Information ‐ TOC0
Revolutionizing dementia detection: Leveraging vision and Swin transformers for early diagnosis0
Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (VHIR), Barcelona Spain0
Associations between polygenic liability to psychopathology and non‐suicidal versus suicidal self‐injury0
0
Exploring the genetic architecture of brain structure and ADHD using polygenic neuroimaging‐derived scores0
The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops0
Low‐grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis‐like syndrome0
Interview with Stephen Glatt. Editor‐in‐Chief, American Journal of Medical Genetics: Neuropsychiatric Genetics0
Genetic Variants ε2 and ε4 of APOE Predict Mortality and Poor Outcome Independently in Spontaneous Intracerebral Hemorrhage Within the Chinese Han Population0
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach0
Issue Information ‐ TOC0
Association of BDNF risk variant and dorsolateral cortical thickness with long‐term treatment response to valproate in type I bipolar disorder: An exploratory study0
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development0
Psychiatric and neurological manifestations in adults with Smith–Magenis syndrome: A scoping review0
0
0
Cover Image, Volume 183B, Number 8, December 20200
Issue Information ‐ TOC0
0
0
Medical genetics in the 19th century as background to the development of psychiatric genetics0
Characterization of Two Novel PNKP Splice‐Site Variants in a Proband With Microcephaly, Intellectual Disability, and Multiple Malformations0
Cover Image, Volume 186B, Number 3, April 20210
0.042066097259521