摘要
人类基因组计划的完成极大推动了人类疾病,尤其是复杂疾病遗传机制的研究。基因组学研究为发现与环境因素作用并最终导致疾病的遗传基础提供了有效的方法。基因组医学研究的突破尚需时日,它需要基础与临床医学研究的合作与共同努力,但同时也为我们提供了新的机遇和挑战。
The recent achievements of the Human Genome Project make it increasingly feasible to determine the genetic basis of human diseases, especially complex traits. Genomics will provide powerful means to discover hereditary elements that interact with environmental factors leading to diseases. However, the expected transformation toward genomics-based medicine will occur over decades, which requires the joint efforts of many scientists and physicians. Such transformation provides both opportunities and challenges to everyone involved in this field.
出处
《中国医学科学院学报》
CAS
CSCD
北大核心
2005年第3期263-264,共2页
Acta Academiae Medicinae Sinicae
关键词
遗传性疾病
复杂疾病
基因
genetic diseases
polygenic diseases
genomics
