Publications by authors named "Yale Guo"

Background: Work-related musculoskeletal disorders significantly impact the job performance and quality of life of nursing personnel in China, necessitating an understanding of their prevalence and risk factors to enhance occupational health and improve medical safety.

Objective: To systematically evaluate the prevalence and risk factors of work-related musculoskeletal disorders among clinical nurses in China.

Design: Systematic literature review and meta-analysis.

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Article Synopsis
  • Non-syndromic intellectual disability (NSID) refers to intellectual disabilities in individuals who appear physically normal but have significant cognitive and adaptive challenges, with most genetic causes remaining unidentified.
  • This study aimed to identify specific causal genes related to NSID by genotyping a cohort of 139 families from the Qinba mountain region in western China, using a specific set of genetic markers.
  • The researchers discovered four genetic markers within the LOC101928437 locus that showed a strong association with NSID, suggesting it could be a new candidate gene contributing to the condition in this population.
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Dopamine receptor D4 (DRD4) is activated by the neurotransmitter dopamine and links to many neurological and psychiatric conditions because of its close relationship with prefrontal cortex and other important brain regions. To explore the possibility that genetic variants of DRD4 gene predispose to children with mental retardation (MR), five target SNPs of DRD4 were selected and genotyped in the samples of 163 MR pedigrees from the Qinba region of China. Two SNPs (rs752306 and rs3758653) showed weak association with MR (the P values were 0.

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Deiodinase enzyme II (DIO2) has an important role in individuals' thyroid hormones' level, the development of central and peripheral nervous systems and characterized by mental retardation (MR). The DIO2 gene was genotyped by using five haplotype-tagging single-nucleotide polymorphisms (SNPs) in 157 Chinese MR high-density family pedigrees, including 452 nuclear families and >1460 persons. The single marker and haplotype analyses were performed by Family-based Association Tests (FBAT).

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Discs-large-related 3 (DLG3), a member of the membrane-associated guanylate kinases (MAGUKs) protein family, playing an important role in regulating NMDA signal pathway and contributing to synaptic plasticity, may have an influence on the susceptibility of non-syndromic mental retardation (NSMR). To investigate the possible genetic contribution of DLG3 gene to the NSMR of Chinese Han population, we performed an association study of 556 subjects (118 NSMR, 116 borderline NSMR, and 322 controls in 275 males and 281 females) from Qin-Ba mountain region of Shaanxi province in the northwest of China by five common SNPs in the gene. The results showed that there was no positive association between the genetic variations of DLG3 and NSMR.

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Objective: Neuroligin-4 is essential for proper brain function. Some studies indicate a close relationship between neuroligin-4 and several human psychiatric conditions.

Methods: The case-control method was used to study the association between nonspecific mental retardation (NSMR) and genetic variants of neuroligin-4 gene (NLGN4).

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Article Synopsis
  • Mental retardation (MR) is a common cognitive impairment in children, with diverse genetic factors contributing to its causes, including mutations in the FACL4 gene.
  • A study was conducted with 556 subjects from the Qin-Ba mountain region of China to investigate the link between FACL4 gene mutations and non-specific mental retardation, using five specific SNPs for analysis.
  • The results showed no significant differences in genotype or allele frequencies between children with non-specific mental retardation and the control group, indicating that FACL4 gene mutations do not increase susceptibility to MR in this population.
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To investigate the possible genetic association of nonsyndromic X-linked mental retardation (NS-XLMR) with FTSJ1 gene polymorphisms, a case-control association study was performed focusing on the Chinese Han population in the Qinba mountain region. Three common single nucleotide polymorphisms (SNPs) (rs2268954, rs2070991, rs5905692) in the gene were selected and genotyped using the polymerase chain reaction single-strand confirmation polymorphism (PCR-SSCP) method. Pairwise linkage disequilibrium (LD) analysis showed that the three SNPs were in strong LD (all D' > 0.

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Objective: Febrile seizure is a very common emergency in children. Although researchers home and abroad constantly pay close attention to studies on brain damage and lesion possibly caused by febrile seizure, studies of effects on motor, behavior, spatial learning and memory are relatively seldom. In our study, Sprague-Dawley rats were utilized for the purpose of the exploration of effects of febrile seizures on their motor, behavior, spatial learning and memory.

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