OOIR: Observatory of International Research

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 2021-04-01 to 2025-04-01.)

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”	16
Issue Information ‐ TOC	13
Cover Image, Volume 189B, Number 5, July 2022	13
Rare protein‐coding variants implicate genes involved in risk of suicide death	13
Bruno Schulz's 1936 book “Methodology of medical genetic research particularly with regard to psychiatry”	12
Association of BDNF risk variant and dorsolateral cortical thickness with long‐term treatment response to valproate in type I bipolar disorder: An exploratory study	12
Ernst Rüdin's, 1911 vision of a Mendelian psychiatric genetics research program: His paper “Methods and goals of family research in psychiatry”	11
Genetic propensity for risky behavior and depression and risk of lifetime suicide attempt among urban African Americans in adolescence and young adulthood	9
	9
The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops	9
Behavioral and transcriptomic analyses of mecp2 function in zebrafish	9
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Erratum	8
Meet the Editors. An interview with Marta Ribasés, Vall d'Hebron Research Institute (VHIR), Barcelona Spain	8
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	8
A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co‐expression network module eigengenes	7
	7
Potential New Expression Biomarkers for Anorexia Nervosa	7
Issue Information ‐ TOC	7
Associations of Polygenic Risk for Depression, Traditional Chinese Medicine Constitution, and Depression: A Population‐Based Study in Taiwan	7
Issue Information ‐ TOC	7
Optimizing the Prediction of Depression Remission: A Longitudinal Machine Learning Approach	7

Genomics and epigenomics of substance use disorders: An introduction	6
	6
A Pilot Study to Assess the Impact of a Multifactorial Explanation for Mental Illness on Prejudicial Attitudes Towards People With Mental Illness	6
The beginnings of biometrical psychiatric genetics: Studies of the insane diathesis 1905–1909	6
Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies	6
Issue Information ‐ TOC	5
Genetic liability for gastrointestinal inflammation disorders and association with gastrointestinal symptoms in children with and without autism	5
Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol	5
Issue Information ‐ TOC	5
Application of animal experimental models in the research of schizophrenia	5
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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 data	3
KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing	3
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	3
	3
	3
Issue Information ‐ TOC	3
Self‐reported medication use as an alternate phenotyping method for anxiety and depression in the UK Biobank	2
Suicidal ideation and planning among Mexican adolescents are associated with depression polygenic risk scores	2
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children	2
Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”	2
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development	2
RYR3 Variants Are Potentially Associated With Idiopathic (Non‐Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene‐Disease Association by Genetic Dependent Natur	2
Neanderthal‐derived genetic variation in living humans relates to schizophrenia diagnosis, to psychotic symptom severity, and to dopamine synthesis	2
	2
	2
Distinguishing happiness and meaning in life from depressive symptoms: A GWAS‐by‐subtraction study in the UK Biobank	2
Polygenic risk scores for neuropsychiatric, inflammatory, and cardio‐metabolic traits highlight possible genetic overlap with suicide attempt and treatment‐emergent suicidal ideation	2
Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention	2