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 2021-09-01 to 2025-09-01.)

Article	Citations
Exploring the utility of current polygenic scores in capturing resilience	29
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	19
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	10
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	8
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders	7
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort	7
A 19q13 microdeletion syndrome presenting with punding, frangophilia, hypermetamorphosis, frontal lobe and vermal hypoplasia, and depression, misdiagnosed as schizophrenia, and treated with mirtazapin	7
Familial KCNQ2 mutation: a psychiatric perspective	6
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series	6
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress	6
Mapping, clustering, and analysis of research in psychiatric genomics	6
Association of NTRK2 gene with suicidality: a meta-analysis	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
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?	6
Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder	5
A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder	5
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder	5
Co-existing bipolar disease and 17q12 deletion: a rare case report	5
Case of twin achondroplasia and autism coexistence and literature review	5
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature	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	4
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study	4
Genetics of social anxiety disorder: a systematic review	4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	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
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	3
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	3
A scoping review and comparison of approaches for measuring genetic heterogeneity in psychiatric disorders	3
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype	3
Pathoclinical associations between panic disorders and the brain-derived neurotrophic factor Val66Met polymorphism: an updated meta-analysis	2
Effects of DNA methylation and polygenic scores on self-reported suicidal ideation in psychoses: no evidence of epigenetic basis of polygenic risk	2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review	2
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms	2
Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay	2
Whole-exome sequencing implicates 16p13.2 as a risk locus for attention-deficit/hyperactivity disorder in the Faroese population	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
Depression and sarcopenia: a Mendelian randomization analysis	2
Diagnostic significance and potential function of miR-320d in schizophrenia	2
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by stressful events	2
Morphine may have a role in telomere shortening	2
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication	2
Genomics and pharmacogenomics of cluster headache: implications for personalized management? A systematic review	1
A rare case report of Huntington’s disease with severe psychiatric symptoms as initial manifestations	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
Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?	1
Discriminative features in White-Sutton syndrome: literature review and first report in Iran	1
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia	1
Treatment-resistant manic episode in a patient diagnosed with bipolar affective disorder	1
Mechanism of electroconvulsive therapy in schizophrenia: a bioinformatics analysis study of RNA-seq data	1
Whole-exome-based single nucleotide variants and copy number analysis for prenatal diagnosis of compound heterozygosity of SMPD4	1
Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders	1
Reflections on schizophrenia and genetics: a response to Gama Marques and Finsterer	1
Genetics of nonpharmacological treatments of depression	1
‘A child with Malpuech–Michels–Mingarelli–Carnevale syndrome and ADHD and major depressive disorder’	1
Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation	1