Psychiatric Genetics

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 2021-07-01 to 2025-07-01.)
ArticleCitations
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population29
Exploring the utility of current polygenic scores in capturing resilience16
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome10
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders7
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 di7
Association of NTRK2 gene with suicidality: a meta-analysis6
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder6
A 19q13 microdeletion syndrome presenting with punding, frangophilia, hypermetamorphosis, frontal lobe and vermal hypoplasia, with depression misdiagnosed as schizophrenia, treated with mirtazapine5
Familial KCNQ2 mutation: a psychiatric perspective5
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress5
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort5
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series5
Effects of vitamin D-related gene polymorphisms on attempted suicide5
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?5
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder4
Co-existing bipolar disease and 17q12 deletion: a rare case report4
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis4
A new case with coexistence of mosaic 48,XYYY/47,XYY, and CACNA1E variant in autism spectrum disorder4
Telomere length and telomerase activity of leukocytes as biomarkers of selective serotonin reuptake inhibitor responses in patients with major depressive disorder4
Case of twin achondroplasia and autism coexistence and literature review4
Mapping, clustering, and analysis of research in psychiatric genomics4
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits4
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder4
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature4
Psychosis and autism without functional regression in a patient with Kleefstra syndrome3
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder3
A scoping review and comparison of approaches for measuring genetic heterogeneity in psychiatric disorders3
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 review3
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype3
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study3
Genetics of social anxiety disorder: a systematic review3
How the human genome project has increased the prevalence of pseudoschizophrenia and decreased the prevalence of true schizophrenia?3
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease3
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