OOIR: Observatory of International Research

Papers

(The TQCC of Psychiatric Genetics is 3. 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.)

Article	Citations
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	34
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	10
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders	8
A 19q13 microdeletion syndrome presenting with punding, frangophilia, hypermetamorphosis, frontal lobe and vermal hypoplasia, and depression, misdiagnosed as schizophrenia, and treated with mirtazapin	8
Elucidation of crucial metabolic pathways in the etiology of autism spectrum disorder through whole exome sequencing and chromosomal microarray	8
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
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress	7
Association of NTRK2 gene with suicidality: a meta-analysis	7
Familial KCNQ2 mutation: a psychiatric perspective	6
The clinical significance of miR-484 in depression of older people with Alzheimer’s disease and its potential role on depressive behavior	6
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder	6
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature	6
Mapping, clustering, and analysis of research in psychiatric genomics	6
A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder	6
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder	5
Case of twin achondroplasia and autism coexistence and literature review	5
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits	5
Prenatal diagnosis and genetic counselling of a rare de-novo 12p13.33p13.32 deletion and 15q26.2q26.3 duplication in a Chinese family	4
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study	4
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	4
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder	4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	4
How the human genome project has increased the prevalence of pseudoschizophrenia and decreased the prevalence of true schizophrenia?	4
Whole-exome sequencing implicates 16p13.2 as a risk locus for attention-deficit/hyperactivity disorder in the Faroese population	3

Mediating effect of genome-wide DNA methylation on suicidal ideation induced by stressful events	3
Pathoclinical associations between panic disorders and the brain-derived neurotrophic factor Val66Met polymorphism: an updated meta-analysis	3
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype	3
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	3
Diagnostic significance and potential function of miR-320d in schizophrenia	3
Familial co-occurrence of autism spectrum disorder and 47 XYY syndrome: revisiting the role of Y chromosome dosage in neurodevelopment	3
Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay	3