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

Article	Citations
Unresolved ethical issues of genetic counseling and testing in clinical psychiatry	28
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	11
Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequences	9
Re-analysis of genetic polymorphism data supports a relationship between schizophrenia and microsatellite variability in PLA2G4A	7
Morphine may have a role in telomere shortening	6
Diverse clinical manifestations of X-linked adrenoleukodystrophy in a Chinese family with identical multisite variants of ABCD1 gene	6
Genome-wide by environment interaction studies of maternal smoking and educational score in UK biobank	5
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia	5
Analysis of convergence of linkage and association studies in autism spectrum disorders	5
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders	5
Protocol for a pharmacogenetic study of antidepressants: characterization of drug-metabolizing profiles of cytochromes CYP2D6 and CYP2C19 in a Sardinian population of patients with major depressive di	5
Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization	4
Mendelian randomization study on the effect of tumor necrosis factor on schizophrenia	4
Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of them	4
Study protocol of DIVERGE, the first genetic epidemiological study of major depressive disorder in Pakistan	4
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder	4
Case of twin achondroplasia and autism coexistence and literature review	4
A novel risk variant block across introns 36–45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study	4
Exploring the utility of current polygenic scores in capturing resilience	4
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	3
Genetic association of SLC6A3 (dopamine transporter) gene polymorphisms with personality disorders and substance abuse disorders: a systematic review and meta-analysis	3
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency	3
Schizophrenia polygenic risk score and type 2 diabetes onset in older adults with no schizophrenia diagnosis	3
Genome-wide methylation analysis of early-onset schizophrenia	3

Explore the role of CR1 genetic variants in late-onset Alzheimer’s disease susceptibility	3
Further evidence of the role of microRNA in schizophrenia: a case report	3
The therapygenetics of anxiety disorders	3
The OPRD1 rs678849 variant influences outcome of disulfiram treatment for cocaine dependency in methadone-maintained patients	3
Psychosis symptoms associated with Niemann-Pick disease type C	3
Treatment-resistant manic episode in a patient diagnosed with bipolar affective disorder	3
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	3
Psychiatric symptoms in an adolescent reveal a novel compound heterozygous mutation of the PANK2 gene in the atypical PKAN syndrome	3
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	3
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders	3
Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China	3