OOIR: Observatory of International Research

Papers

(The median citation count of Psychiatric Genetics is 1. 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 2021-11-01 to 2025-11-01.)

Article	Citations
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	32
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	19
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	11
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
Association of NTRK2 gene with suicidality: a meta-analysis	8
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort	7
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?	7
Familial KCNQ2 mutation: a psychiatric perspective	6
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature	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 new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder	6
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder	6
Mapping, clustering, and analysis of research in psychiatric genomics	6
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study	5
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	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
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
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	4
Genetics of social anxiety disorder: a systematic review	4
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	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
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder	4
How the human genome project has increased the prevalence of pseudoschizophrenia and decreased the prevalence of true schizophrenia?	4
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype	4
Whole-exome sequencing implicates 16p13.2 as a risk locus for attention-deficit/hyperactivity disorder in the Faroese population	3
Pathoclinical associations between panic disorders and the brain-derived neurotrophic factor Val66Met polymorphism: an updated meta-analysis	3
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by stressful events	3
Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay	2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review	2
Discriminative features in White-Sutton syndrome: literature review and first report in Iran	2
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia	2
Morphine may have a role in telomere shortening	2
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots	2
Genome-wide DNA methylation profiles of autism spectrum disorder	2
A rare case report of Huntington’s disease with severe psychiatric symptoms as initial manifestations	2
Diagnostic significance and potential function of miR-320d in schizophrenia	2
Effects of DNA methylation and polygenic scores on self-reported suicidal ideation in psychoses: no evidence of epigenetic basis of polygenic risk	2
Depression and sarcopenia: a Mendelian randomization analysis	2
Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders	2
Reflections on schizophrenia and genetics: a response to Gama Marques and Finsterer	1
Genetics of nonpharmacological treatments of depression	1
Whole-exome-based single nucleotide variants and copy number analysis for prenatal diagnosis of compound heterozygosity of SMPD4	1
Prenatal diagnosis and genetic counselling of a de-novo 11p13p11.2 duplication with normal phenotype	1
Investigation of cytochrome B mutations, and UCP2 and STC1 gene expressions in patients with bipolar disorder	1
Mechanism of electroconvulsive therapy in schizophrenia: a bioinformatics analysis study of RNA-seq data	1
Genomics and pharmacogenomics of cluster headache: implications for personalized management? A systematic review	1
‘A child with Malpuech–Michels–Mingarelli–Carnevale syndrome and ADHD and major depressive disorder’	1
Investigation of the forkhead box protein P2 gene by the next-generation sequence analysis method in children diagnosed with specific learning disorder	1
Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?	1
Treatment-resistant manic episode in a patient diagnosed with bipolar affective disorder	1
Phenotypic heterogeneity and genomic findings in psychiatry: do not throw the baby out with the bathwater	1
A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia	1
Integrated multi-omics analysis identifies epigenetic alteration related to neurodegeneration development in post-traumatic stress disorder patients	1
Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation	1