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 2020-03-01 to 2024-03-01.)

Article	Citations
Epigenetics in bipolar disorder: a critical review of the literature	21
Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children	17
Transient receptor potential vanilloid 1 antagonism in neuroinflammation, neuroprotection and epigenetic regulation: potential therapeutic implications for severe psychiatric disorders treatment	16
Applications of Mendelian randomization in psychiatry: a comprehensive systematic review	12
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	10
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders	7
The role of the gut microbiota in the pathophysiology of mental and neurological disorders	7
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: a case of pharmaco-synergistic heterozygosity	7
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach	6
Does 5-HTTLPR moderate the effect of the quality of environmental context on maternal sensitivity? Testing the differential susceptibility hypothesis	6
Genetic neuroimaging of bipolar disorder: a systematic 2017–2020 update	5
Understanding the role of gut microbiota in the pathogenesis of schizophrenia	4
Genome-wide DNA methylation profiles of autism spectrum disorder	4
Epigenetic studies in suicidal ideation and behavior	4
Positive association between PTN polymorphisms and schizophrenia in Northeast Chinese Han population	4
The OPRD1 rs678849 variant influences outcome of disulfiram treatment for cocaine dependency in methadone-maintained patients	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
The genetic variations in SAP97 gene and the risk of schizophrenia in the Chinese Han population: a further study	4
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
The effect of rs1076560 (DRD2) and rs4680 (COMT) on tardive dyskinesia and cognition in schizophrenia subjects	3
Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder	3
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series	3
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication	3
The influence of regression models on genome-wide association studies of alcohol dependence: a comparison of binary and quantitative analyses	3

Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	3
The characterization of psychotic symptoms in succinic semialdehyde dehydrogenase deficiency: a review	3
Effects of vitamin D-related gene polymorphisms on attempted suicide	3
Genetics of social anxiety disorder: a systematic review	3
Mendelian randomization study on the effect of tumor necrosis factor on schizophrenia	3
Morphine may have a role in telomere shortening	3
Ethnicity-dependent effects of Zinc finger 804A variant on schizophrenia: a systematic review and meta-analysis	3
A case of White–Sutton syndrome arising from a maternally-inherited mutation in POGZ	3
Anticipatory oculomotor responses in parents of children with attention deficit hyperactivity disorder	2
Co-existing bipolar disease and 17q12 deletion: a rare case report	2
The functional polymorphisms linked with interleukin-1β gene expression are associated with bipolar disorder	2
CYP2C19 polymorphisms are associated with severity of depression at initial evaluation and after the treatment independently of the prescribed medications: 4 weeks prospective study	2
A preliminary exome sequence in three patients with tardive dystonia	2
Psychosis symptoms associated with Niemann-Pick disease type C	2
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia	2
Schizophreniform presentation and abrupt neurologic decline in a patient with late-onset mucopolysaccharidosis type IIIB	2
Effects of CYP2C19*17 genetic polymorphisms on plasma and saliva concentrations of diazepam in patients with alcohol withdrawal syndrome	2
Alexithymia is associated with reduced vitamin D levels, but not polymorphisms of the vitamin D binding-protein gene	2
Hemizygous mutations in L1CAM in two unrelated male probands with childhood onset psychosis	2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review	2
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency	2
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	2
Explore the role of CR1 genetic variants in late-onset Alzheimer’s disease susceptibility	2
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by perceived stress	2
Identification of rare mutations of the vasoactive intestinal peptide receptor 2 gene in schizophrenia	2
Mapping, clustering, and analysis of research in psychiatric genomics	2
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms	2
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	2
Genome-wide methylation analysis of early-onset schizophrenia	2
Copy number variations in Japanese children with autism spectrum disorder	2
Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequences	2