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Lack of association between NCAM1 and early onset schizophrenia in a family based study in Shandong peninsula of China.
Chen, Xing; Tang, Jian; Liu, Yang; Luan, Meng; An, Kun; Zhang, Yan; Li, Fuhui; Zhou, Peng; Liu, Wenmin; Liu, Jintong; Chen, Gang.
Afiliación
  • Chen X; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • Tang J; Affiliated Hospital of Shandong University, Shandong University, Jinan, Shandong, China.
  • Liu Y; The Center for Clinical Laboratory, The Third Affiliated Hospital of Liao Ning Medical College, Jinzhou, Liao Ning, China.
  • Luan M; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • An K; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • Zhang Y; Childhood Psychiatry Unit, Shandong Mental Health Center, Jinan, Shandong, China.
  • Li F; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • Zhou P; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • Liu W; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
  • Liu J; Childhood Psychiatry Unit, Shandong Mental Health Center, Jinan, Shandong, China; Department of Psychiatry, Shandong University School of Medicine, Jinan, Shandong, China.
  • Chen G; Department of Medical Genetics, Institute of Basic Medicine, Shandong Academy of Medical Sciences, Jinan, Shandong, China.
J Pediatr Genet ; 1(1): 39-45, 2012 Mar.
Article en En | MEDLINE | ID: mdl-27625800
The neural cell adhesion molecule (NCAM1) gene plays important roles in cellular migration, synaptic integrity and neurodevelopment. Multiple NCAM1 proteins are differentially altered in schizophrenia (SZ). A whole genome association study was first carried out on Affymetrix genome-wide human single-nucleotide polymorphism (SNP) Array 6.0 and two pooled DNA samples consisting of 89 early onset SZ (EOS) cases and 1,000 controls. Association between rs10891495 and EOS was detected (χ(2) = 2 3.66, P = 1.15E-06). The position of this SNP is just within the NCAM1 gene. Since several previous studies reported that NCAM1 was a candidate gene for SZ, we further performed a family based association study and genotyped six SNPs (rs10891495, rs1245133, rs1821693, rs686050, rs12794326, rs674246) within NCAM1 gene in 100 EOS nuclear families. We found no evidence for association with SZ status either for SNP or for haplotype. Therefore, the NCAM1 gene is unlikely to play a major role in the etiology of early-onset SZ in the Chinese population.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Año: 2012 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: J Pediatr Genet Año: 2012 Tipo del documento: Article País de afiliación: China