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 2021-04-01 to 2025-04-01.)
ArticleCitations
Unresolved ethical issues of genetic counseling and testing in clinical psychiatry28
Identification of de-novo CREBBP gene variants in patients with Rubinstein–Taybi syndrome11
Haploinsufficiency of the HIRA gene may not always produce severe neurodevelopmental consequences9
Re-analysis of genetic polymorphism data supports a relationship between schizophrenia and microsatellite variability in PLA2G4A7
Diverse clinical manifestations of X-linked adrenoleukodystrophy in a Chinese family with identical multisite variants of ABCD1 gene6
Morphine may have a role in telomere shortening6
Analysis of convergence of linkage and association studies in autism spectrum disorders5
Rare copy number variants in ASTN2 gene in patients with neurodevelopmental disorders5
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 di5
Genome-wide by environment interaction studies of maternal smoking and educational score in UK biobank5
Identification of rare missense mutations in the glutamate ionotropic receptor AMPA type subunit genes in schizophrenia5
Case of twin achondroplasia and autism coexistence and literature review4
A novel risk variant block across introns 36–45 of CACNA1C for schizophrenia: a cohort-wise replication and cerebral region-wide validation study4
Exploring the utility of current polygenic scores in capturing resilience4
Association analysis of risk genes identified by SCHEMA with schizophrenia in the Chinese Han population4
Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization4
Mendelian randomization study on the effect of tumor necrosis factor on schizophrenia4
Novel RPS6KA3 mutations cause Coffin-Lowry syndrome in two patients and concurrent compulsive eyebrow-pulling behavior in one of them4
Study protocol of DIVERGE, the first genetic epidemiological study of major depressive disorder in Pakistan4
A pathogenic P4HTM gene variant in two brothers with autism spectrum disorder4
Treatment-resistant manic episode in a patient diagnosed with bipolar affective disorder3
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
Psychiatric symptoms in an adolescent reveal a novel compound heterozygous mutation of the PANK2 gene in the atypical PKAN syndrome3
Brain differential gene expression and blood cross-validation of a molecular signature of patients with major depressive disorder3
UK Biobank subjects carrying protein truncating variants in HERC1 are not at substantially increased risk of minor psychiatric disorders3
Nucks1 gene polymorphism rs823114 is associated with the positive symptoms and neurocognitive function of patients with schizophrenia in parts of southern China3
Clinical features of UK Biobank subjects carrying protein-truncating variants in genes implicated in schizophrenia pathogenesis3
Genetic association of SLC6A3 (dopamine transporter) gene polymorphisms with personality disorders and substance abuse disorders: a systematic review and meta-analysis3
Pathophysiology and management of neuropsychiatric symptoms in succinic semialdehyde dehydrogenase deficiency3
Schizophrenia polygenic risk score and type 2 diabetes onset in older adults with no schizophrenia diagnosis3
Genome-wide methylation analysis of early-onset schizophrenia3
Explore the role of CR1 genetic variants in late-onset Alzheimer’s disease susceptibility3
Further evidence of the role of microRNA in schizophrenia: a case report3
The therapygenetics of anxiety disorders3
The OPRD1 rs678849 variant influences outcome of disulfiram treatment for cocaine dependency in methadone-maintained patients3
Psychosis symptoms associated with Niemann-Pick disease type C3
Influence of 5-HTTLPR polymorphism on postpartum depressive and posttraumatic symptoms2
Genome-wide DNA methylation profiles of autism spectrum disorder2
The association among multiple-site chronic pain, sedentary behavior, and major depressive disorders: a mendelian randomization study2
Two siblings with autism spectrum disorder and two different genetic abnormalities: paternal 16p11.2 microdeletion and maternal 17q12 microduplication2
Genetics of nonpharmacological treatments of depression2
Evaluation of hsa-let-7d-5p, hsa-let-7g-5p and hsa-miR-15b-5p plasma levels in patients with Alzheimer’s disease2
Prenatal diagnosis and molecular cytogenetic analyses of a homozygous Robertsonian translocation family with novel mosaic Robertsonian fission karyotype2
White matter volume and myelin oligodendrocyte glycoprotein (MOG) microsatellites in pediatric obsessive-compulsive disorder2
CYP2C19 polymorphisms are associated with severity of depression at initial evaluation and after the treatment independently of the prescribed medications: 4 weeks prospective study2
Psychosis and autism without functional regression in a patient with Kleefstra syndrome2
Epigenetic marks in suicide: a review2
Association of NTRK2 gene with suicidality: a meta-analysis2
Genetics of social anxiety disorder: a systematic review2
Genetic determinants associated with response to clozapine in schizophrenia: an umbrella review2
Chromosomal rearrangement in the 22q11.2 region: a critical locus for sociability and attentional skills2
A case of White–Sutton syndrome arising from a maternally-inherited mutation in POGZ1
‘A child with Malpuech–Michels–Mingarelli–Carnevale syndrome and ADHD and major depressive disorder’1
Mechanism of electroconvulsive therapy in schizophrenia: a bioinformatics analysis study of RNA-seq data1
Analysis of 200 000 exome-sequenced UK Biobank subjects fails to identify genes influencing probability of developing a mood disorder resulting in psychiatric referral1
The functional polymorphisms linked with interleukin-1β gene expression are associated with bipolar disorder1
A case of CHD2 variant-associated psychosis and response to treatment1
A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia1
Differential effect of panic on the DNA methylation of the glucocorticoid receptor gene exon 1F in chronic subjective tinnitus with distress1
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 rehabi1
Genomics and pharmacogenomics of cluster headache: implications for personalized management? A systematic review1
Evaluating the genetic interaction effects of gut microbiome and diet on the risk of neuroticism in the UK Biobank cohort1
Effects of vitamin D-related gene polymorphisms on attempted suicide1
A scoping review and comparison of approaches for measuring genetic heterogeneity in psychiatric disorders1
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