Psychiatric Genetics

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.)
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 resilience11
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
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder6
Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China6
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort5
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress5
Alexithymia is associated with reduced vitamin D levels, but not polymorphisms of the vitamin D binding-protein gene5
Effects of vitamin D-related gene polymorphisms on attempted suicide5
Stimulant intolerance in children with Angelman syndrome with hyperactivity: a case series5
Association of NTRK2 gene with suicidality: a meta-analysis5
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?5
Familial KCNQ2 mutation: a psychiatric perspective5
Maternal 15q11.2-q13.1 duplication syndrome-associated psychosis and mania: a new case and review of the literature4
Co-existing bipolar disease and 17q12 deletion: a rare case report4
Case of twin achondroplasia and autism coexistence and literature review4
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease4
Causal association of attention-deficit/hyperactivity disorder and autism spectrum disorder with post-traumatic stress disorder4
Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits4
Mapping, clustering, and analysis of research in psychiatric genomics4
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 review4
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder4
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
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis4
Genetics of social anxiety disorder: a systematic review4
Mediating effect of genome-wide DNA methylation on suicidal ideation induced by stressful events3
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype3
Psychosis and autism without functional regression in a patient with Kleefstra syndrome3
Whole-exome sequencing implicates 16p13.2 as a risk locus for attention-deficit/hyperactivity disorder in the Faroese population3
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
Two novel variants of the STXBP1 and CHRNB2 genes identified in a Chinese boy with refractory seizures and developmental delay3
Pathoclinical associations between panic disorders and the brain-derived neurotrophic factor Val66Met polymorphism: an updated meta-analysis3
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study3
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 rehabi3
Diagnostic significance and potential function of miR-320d in schizophrenia3
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders2
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication2
Discriminative features in White-Sutton syndrome: literature review and first report in Iran2
Chromatin gatekeeper and modifier CHD proteins in development, and in autism and other neurological disorders2
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots2
Epigenetic marks in suicide: a review2
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms2
Depression and sarcopenia: a Mendelian randomization analysis2
Morphine may have a role in telomere shortening2
Genome-wide DNA methylation profiles of autism spectrum disorder2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review2
Metformin, valproic acid, and starvation induce seizures in a patient with partial SLC13A5 deficiency: A case of pharmaco-synergistic heterozygosity: Erratum2
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia1
Treatment-resistant manic episode in a patient diagnosed with bipolar affective disorder1
A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia1
Emerging trends in gene and bipolar disorder research: a bibliometric analysis and network visualisation1
A rare case report of Huntington’s disease with severe psychiatric symptoms as initial manifestations1
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency1
Mechanism of electroconvulsive therapy in schizophrenia: a bioinformatics analysis study of RNA-seq data1
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 gene1
Genetics of nonpharmacological treatments of depression1
‘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 SMPD41
Genomics and pharmacogenomics of cluster headache: implications for personalized management? A systematic review1
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