OOIR: Observatory of International Research

Papers

(The median citation count of Psychiatric Genetics is 2. 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 2020-11-01 to 2024-11-01.)

Article	Citations
Applications of Mendelian randomization in psychiatry: a comprehensive systematic review	25
Epigenetics in bipolar disorder: a critical review of the literature	25
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	11
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach	8
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity	7
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders	7
Genetic neuroimaging of bipolar disorder: a systematic 2017–2020 update	6
The characterization of psychotic symptoms in succinic semialdehyde dehydrogenase deficiency: a review	5
Genetics of social anxiety disorder: a systematic review	5
Understanding the role of gut microbiota in the pathogenesis of schizophrenia	5
The influence of regression models on genome-wide association studies of alcohol dependence: a comparison of binary and quantitative analyses	5
Epigenetic studies in suicidal ideation and behavior	5
Genome-wide DNA methylation profiles of autism spectrum disorder	5
Mendelian randomization study on the effect of tumor necrosis factor on schizophrenia	4
Alexithymia is associated with reduced vitamin D levels, but not polymorphisms of the vitamin D binding-protein gene	4
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review	4
Explore the role of CR1 genetic variants in late-onset Alzheimer’s disease susceptibility	4
Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder	4
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series	4
The OPRD1 rs678849 variant influences outcome of disulfiram treatment for cocaine dependency in methadone-maintained patients	4
Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia	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
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits	3
Ethnicity-dependent effects of Zinc finger 804A variant on schizophrenia: a systematic review and meta-analysis	3
The functional polymorphisms linked with interleukin-1β gene expression are associated with bipolar disorder	3

A case of White–Sutton syndrome arising from a maternally-inherited mutation in POGZ	3
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	3
Psychosis symptoms associated with Niemann-Pick disease type C	3
Morphine may have a role in telomere shortening	3
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by perceived stress	3
Variants of Th17 pathway-related genes influence brain morphometric changes and the risk of schizophrenia through epistatic interactions	3
Genome-wide association study of antisocial personality disorder diagnostic criteria provides evidence for shared risk factors across disorders	3
CYP2C19 polymorphisms are associated with severity of depression at initial evaluation and after the treatment independently of the prescribed medications: 4 weeks prospective study	3
Genome-wide methylation analysis of early-onset schizophrenia	3
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency	3
Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders	3
Effects of vitamin D-related gene polymorphisms on attempted suicide	3
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	3
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication	3
Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China	3
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	3
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	2
Re-analysis of genetic polymorphism data supports a relationship between schizophrenia and microsatellite variability in PLA2G4A	2
Co-existing bipolar disease and 17q12 deletion: a rare case report	2
Mapping, clustering, and analysis of research in psychiatric genomics	2
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms	2
Exploring the utility of current polygenic scores in capturing resilience	2
Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequences	2
Effects of CYP2C19*17 genetic polymorphisms on plasma and saliva concentrations of diazepam in patients with alcohol withdrawal syndrome	2
Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation	2
Epigenetic marks in suicide: a review	2
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia	2
Copy number variations in Japanese children with autism spectrum disorder	2
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots	2
Schizophreniform presentation and abrupt neurologic decline in a patient with late-onset mucopolysaccharidosis type IIIB	2
Global DNA methylation in suicidal ideation and suicide attempt in schizophrenia	2