Cargando…
Association of NKAPL rs1635 With Cognitive Function in Early-Onset Schizophrenia
BACKGROUND: Schizophrenia is a severe mental disorder with high heritability, and cognitive dysfunction is one of the core features. Growing evidence suggests the genetic risk of schizophrenia may contribute to cognitive impairments. The variant rs1635 (nucleotide sequence: c.455C>A; amino acid s...
Autores principales: | Yang, Yang, Su, Yi, Wei, Guiming, Kang, Zhewei, Lu, Zhe, Liao, Yundan, Lu, Tianlan, Yan, Hao, Yue, Weihua, Qin, Ying, Zhang, Yuyanan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253766/ https://www.ncbi.nlm.nih.gov/pubmed/35801084 http://dx.doi.org/10.3389/fgene.2022.941171 |
Ejemplares similares
-
Oxidative Stress and Psychiatric Disorders: Evidence from the Bidirectional Mendelian Randomization Study
por: Lu, Zhe, et al.
Publicado: (2022) -
Pharmacological treatment strategies for antipsychotic-induced hyperprolactinemia: a systematic review and network meta-analysis
por: Lu, Zhe, et al.
Publicado: (2022) -
Genome-wide association study identified six loci associated with adverse drug reactions to aripiprazole in schizophrenia patients
por: Wang, Xueping, et al.
Publicado: (2023) -
Dissecting the causal association between social or physical inactivity and depression: a bidirectional two-sample Mendelian Randomization study
por: Zhao, Guorui, et al.
Publicado: (2023) -
ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study
por: Lu, Zhe, et al.
Publicado: (2022)