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 2021-05-01 to 2025-05-01.)

Article	Citations
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population	29
Exploring the utility of current polygenic scores in capturing resilience	11
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome	10
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders	7
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	7
Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China	6
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder	6
Familial KCNQ2 mutation: a psychiatric perspective	5
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort	5
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress	5
Alexithymia is associated with reduced vitamin D levels, but not polymorphisms of the vitamin D binding-protein gene	5
Effects of vitamin D-related gene polymorphisms on attempted suicide	5
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series	5
Association of NTRK2 gene with suicidality: a meta-analysis	5
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?	5
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature	4
Co-existing bipolar disease and 17q12 deletion: a rare case report	4
Case of twin achondroplasia and autism coexistence and literature review	4
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease	4
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder	4
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits	4
Mapping, clustering, and analysis of research in psychiatric genomics	4
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
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder	4
A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder	4

Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder	4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis	4
Genetics of social anxiety disorder: a systematic review	4
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study	3
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
Diagnostic significance and potential function of miR-320d in schizophrenia	3
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by stressful events	3
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype	3
Psychosis and autism without functional regression in a patient with Kleefstra syndrome	3
Whole-exome sequencing implicates 16p13.2 as a risk locus for attention-deficit/hyperactivity disorder in the Faroese population	3
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder	3
A scoping review and comparison of approaches for measuring genetic heterogeneity in psychiatric disorders	3
Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay	3
Pathoclinical associations between panic disorders and the brain-derived neurotrophic factor Val66Met polymorphism: an updated meta-analysis	3
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: A case of pharmaco-synergistic heterozygosity: Erratum	2
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders	2
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication	2
Discriminative features in White-Sutton syndrome: literature review and first report in Iran	2
Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders	2
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots	2
Epigenetic marks in suicide: a review	2
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms	2
Depression and sarcopenia: a Mendelian randomization analysis	2
Morphine may have a role in telomere shortening	2
Genome-wide DNA methylation profiles of autism spectrum disorder	2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review	2
Genomics and pharmacogenomics of cluster headache: implications for personalized management? A systematic review	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
A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia	1
Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation	1
A rare case report of Huntington’s disease with severe psychiatric symptoms as initial manifestations	1
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency	1
Mechanism of electroconvulsive therapy in schizophrenia: a bioinformatics analysis study of RNA-seq data	1
Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?	1
Diverse clinical manifestations of X-linked adrenoleukodystrophy in a Chinese family with identical multisite variants of ABCD1 gene	1
Genetics of nonpharmacological treatments of depression	1
‘A child with Malpuech–Michels–Mingarelli–Carnevale syndrome and ADHD and major depressive disorder’	1
Whole-exome-based single nucleotide variants and copy number analysis for prenatal diagnosis of compound heterozygosity of SMPD4	1