• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在中国汉族人群中,GNB1L 与三种主要精神障碍的关联研究。

Association study between GNB1L and three major mental disorders in Chinese Han populations.

机构信息

Bio-X Center and Affiliated Changning Mental Health Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200030, China.

出版信息

Psychiatry Res. 2011 May 30;187(3):457-9. doi: 10.1016/j.psychres.2010.04.019. Epub 2010 Jun 9.

DOI:10.1016/j.psychres.2010.04.019
PMID:20538345
Abstract

We carried out an association study between GNB1L and three mental disorders (major depressive disorder, bipolar disorder, schizophrenia) in Chinese Han population. Among 1135 cases and 1135 controls, findings suggests that GNB1L is linked with bipolar disorder and schizophrenia and not with major depressive disorder.

摘要

我们在中国汉族人群中进行了 GNB1L 与三种精神障碍(重度抑郁症、双相情感障碍、精神分裂症)之间的关联研究。在 1135 例病例和 1135 例对照中,研究结果表明 GNB1L 与双相情感障碍和精神分裂症有关,而与重度抑郁症无关。

相似文献

1
Association study between GNB1L and three major mental disorders in Chinese Han populations.在中国汉族人群中,GNB1L 与三种主要精神障碍的关联研究。
Psychiatry Res. 2011 May 30;187(3):457-9. doi: 10.1016/j.psychres.2010.04.019. Epub 2010 Jun 9.
2
No association of the YWHAE gene with schizophrenia, major depressive disorder or bipolar disorder in the Han Chinese population.YWHAE 基因与汉族人群精神分裂症、重性抑郁障碍或双相情感障碍无关。
Behav Genet. 2011 Jul;41(4):557-64. doi: 10.1007/s10519-010-9426-1. Epub 2010 Dec 24.
3
Common SNPs and haplotypes in DGKH are associated with bipolar disorder and schizophrenia in the Chinese Han population.DGKH基因中的常见单核苷酸多态性(SNPs)和单倍型与中国汉族人群的双相情感障碍和精神分裂症相关。
Mol Psychiatry. 2011 May;16(5):473-5. doi: 10.1038/mp.2010.86. Epub 2010 Aug 24.
4
FGFR2 is associated with bipolar disorder: a large-scale case-control study of three psychiatric disorders in the Chinese Han population.成纤维细胞生长因子受体 2 与双相情感障碍相关:中国汉族人群三种精神障碍的大规模病例对照研究。
World J Biol Psychiatry. 2012 Dec;13(8):599-604. doi: 10.3109/15622975.2011.650203. Epub 2012 Mar 9.
5
FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population.FoxP2 与中国汉族人群的精神分裂症和重度抑郁症显著相关。
World J Biol Psychiatry. 2013 Mar;14(2):146-50. doi: 10.3109/15622975.2011.615860. Epub 2012 Mar 9.
6
Association of the trace amine associated receptor 6 (TAAR6) gene with schizophrenia and bipolar disorder in a Korean case control sample.韩国病例对照样本中痕量胺相关受体6(TAAR6)基因与精神分裂症和双相情感障碍的关联
J Psychiatr Res. 2008 Jan;42(1):35-40. doi: 10.1016/j.jpsychires.2006.09.011. Epub 2006 Nov 9.
7
Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia.TPH2 变体对重性抑郁障碍、双相情感障碍和精神分裂症患者诊断和治疗反应的影响。
Psychiatry Res. 2011 Aug 30;189(1):26-32. doi: 10.1016/j.psychres.2011.02.001. Epub 2011 Mar 10.
8
Positive association between GRIN2B gene and bipolar disorder in the Chinese Han Population.GRIN2B 基因与中国汉族人群双相情感障碍的正相关关系。
Psychiatry Res. 2011 Jan 30;185(1-2):290-2. doi: 10.1016/j.psychres.2009.11.026. Epub 2010 May 26.
9
Gene expression and association analyses of LIM (PDLIM5) in bipolar disorder and schizophrenia.双相情感障碍和精神分裂症中LIM(PDLIM5)的基因表达及关联分析
Mol Psychiatry. 2005 Nov;10(11):1045-55. doi: 10.1038/sj.mp.4001719.
10
SNAP25 is associated with schizophrenia and major depressive disorder in the Han Chinese population.SNAP25 与汉族人群中的精神分裂症和重度抑郁症有关。
J Clin Psychiatry. 2015 Jan;76(1):e76-82. doi: 10.4088/JCP.13m08962.

引用本文的文献

1
A 31-bp indel in the 5' UTR region of GNB1L is significantly associated with chicken body weight and carcass traits.一个位于 GNB1L 基因 5'UTR 区的 31 碱基对缺失与鸡的体重和体尺性状显著相关。
BMC Genet. 2020 Aug 26;21(1):91. doi: 10.1186/s12863-020-00900-z.
2
Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder.22q11.2缺失综合征患者外周血转录组分析揭示了与精神病和自闭症谱系障碍相关的功能通路。
PLoS One. 2015 Jul 22;10(7):e0132542. doi: 10.1371/journal.pone.0132542. eCollection 2015.
3
The schizophrenia/bipolar disorder candidate gene GNB1L is regulated in human temporal cortex by a cis-acting element located within the 3'-region.
精神分裂症/双相情感障碍候选基因GNB1L在人类颞叶皮质中受位于3'区域内的顺式作用元件调控。
Neurosci Bull. 2015 Feb;31(1):43-52. doi: 10.1007/s12264-014-1461-0. Epub 2014 May 15.
4
Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.22q11.2 拷贝数变异:从罕见变异到发育性神经精神疾病的常见机制
Mol Psychiatry. 2013 Nov;18(11):1153-65. doi: 10.1038/mp.2013.92. Epub 2013 Aug 6.
5
Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken.对智利斗鸡无尾和耳羽性状的全基因组关联作图及候选基因鉴定。
PLoS One. 2012;7(7):e40974. doi: 10.1371/journal.pone.0040974. Epub 2012 Jul 23.
6
Evidence for involvement of GNB1L in autism.GNB1L 参与自闭症的证据。
Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):61-71. doi: 10.1002/ajmg.b.32002. Epub 2011 Nov 16.