Abstract
王梦莹,刘冬静,黄辉,李文咏,周仁,朱洪平,周治波,吴涛.非综合征型唇腭裂二代测序研究进展[J].Chinese journal of Epidemiology,2018,39(3):387-390
非综合征型唇腭裂二代测序研究进展
Progress in next-generation sequencing research of non-syndromic oral clefts
Received:July 23, 2017  
DOI:10.3760/cma.j.issn.0254-6450.2018.03.026
KeyWord: 非综合征型唇腭裂  遗传易感因素  二代测序研究
English Key Word: Non-syndromic oral clefts  Genetic risk factors  Next-generation sequencing research
FundProject:国家自然科学基金(81102178,81573225);北京市自然科学基金(7172115)
Author NameAffiliationE-mail
Wang Mengying Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Liu Dongjing Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Huang Hui Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Li Wenyong Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Zhou Ren Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China  
Zhu Hongping Department of Oral and Maxillofacial Surgery, School of Stomatology, Peking University, Beijing 100081, China  
Zhou Zhibo Department of Oral and Maxillofacial Surgery, School of Stomatology, Peking University, Beijing 100081, China  
Wu Tao Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China twu@bjmu.edu.cn 
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Abstract:
      非综合征型唇腭裂(NSOC)是一种常见的出生缺陷。中国活产儿NSOC患病率为1.13/1 000活产儿~1.30/1 000活产儿,高于其他种族人群。NSOC是受基因和环境因素共同作用的复杂疾病,虽然全基因组关联研究发现了NSOC的多个遗传致病位点,但目前发现的遗传位点只能解释NSOC一小部分遗传度,未被解释的遗传度可能来自罕见遗传变异、拷贝数变异以及交互作用等。二代测序研究为进一步探索NSOC遗传危险因素提供了新的方法和思路,本文将对NSOC二代测序研究进行综述。
English Abstract:
      Non-syndromic oral clefts (NSOC) are among the most common birth defects. The prevalence of NSOC is 1.13-1.30 per 1 000 live births in China, which is higher than those in other major ethnic groups. The etiology of NSOC is complex and heterogeneous, which involves both genetic and environmental risk factors. Although genome-wide association studies have identified a number of risk loci, these loci can only account for a small proportion of the heritability of NSOC. The next-generation sequencing research provides new ideas for further exploring the genetic risk factors of NSOC. This paper summaries the progress in the next-generation sequencing research of NSOC.
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