OOIR: Observatory of International Research

Papers

(The TQCC of Psychiatric Genetics is 4. 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 2021-10-01 to 2025-10-01.)

Article	Citations
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	30
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	19
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders	10
Association of NTRK2 gene with suicidality: a meta-analysis	8
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	8
A 19q13 microdeletion syndrome presenting with punding, frangophilia, hypermetamorphosis, frontal lobe and vermal hypoplasia, and depression, misdiagnosed as schizophrenia, and treated with mirtazapin	7
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?	7
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort	7
Mapping, clustering, and analysis of research in psychiatric genomics	6
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder	6
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits	6
Familial KCNQ2 mutation: a psychiatric perspective	6
A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder	6
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress	6
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series	6
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder	5
Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder	5
A nonsense variant in the C-terminal transactivation domain of the EBF3 gene in an individual with intellectual disability and behavioural disorder: case report and literature review	5
Case of twin achondroplasia and autism coexistence and literature review	5
Co-existing bipolar disease and 17q12 deletion: a rare case report	5
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	5
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature	5
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study	4
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	4
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype	4

How the human genome project has increased the prevalence of pseudoschizophrenia and decreased the prevalence of true schizophrenia?	4
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder	4
A scoping review and comparison of approaches for measuring genetic heterogeneity in psychiatric disorders	4
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	4
Genetics of social anxiety disorder: a systematic review	4
Psycho-cognitive assessment and quality of life in older adults with chronic obstructive pulmonary disease-carrying the rs4713916 gene polymorphism (G/A) of gene FKBP5 and response to pulmonary rehabi	4