目前，多数研究是全基因组关联研究。
At the moment, most of the studies are genome-wide association studies.
本文就近年来全基因组关联分析技术研究RA易感基因的进展做一综述。
This review summarizes the progress in using GWAS for screening of RA susceptible genes.
国际糖尿病：重新回到基因的话题上，对于我们理解糖尿病从全基因组关联分析的研究中会获得哪些便利呢？
International diabetes: Switching back to the discussion in genes, what advantage have been gained into the insight to diabetes from the Whole-Genome Association Study?
人群全基因组关联研究（GWAS）和极端表型患者针对性研究均在理解动脉粥样硬化遗传理论方面取得了进步。
Progress in understanding the genetic basis of atherosclerosis has come both from genome-wide association studies (GWAS) in populations and from focused studies of patients with extreme phenotypes.
在冰岛，瑞士和荷兰的同事的协助下，研究人员对1125名患有男性型秃发的白人男子进行了全基因组关联研究。
Along with colleagues in Iceland, Switzerland and the Netherlands, the researchers conducted a genome-wide association study of 1,125 Caucasian men who had been assessed for male pattern baldness.
用传统的家系连锁分析无法对精神分裂症这样的复杂疾病进行基因定位，而全基因组关联分析则为最终发现这些基因提供了较好的策略。
After linkage analysis failed to locate susceptible genes of complex diseases like schizophrenia, it is a better way to process whole-genome association studies.
这种方法称为全基因组关联研究(genomewide association study)，尽管许多人最初持怀疑态度，它已被证明在技术上是成功的。
This method, called a genomewide association study, has proved technically successful despite many skeptics' initial doubts.
威廉姆斯的研究小组进行了“全基因组关联研究”(genomewide association study)，他们将近4000名老年痴呆症患者的遗传密码与近8000名健康人的基因组进行了对比。
Williams's team conducted a "genome wide association study", in which the genetic codes of nearly 4, 000 Alzheimer's patients were compared with the genomes of almost 8, 000 healthy individuals.
全基因组学关联研究所产生的数据结果是巨大的，但是很少能直接鉴别出突变和病症之间的功能关系。
The output of genome-wide association studies is vast, yet it is rarely straightforward to identify the functional connection between a variant and a disorder.
全基因组学关联研究所产生的数据结果是巨大的，但是很少能直接鉴别出突变和病症之间的功能关系。
The output of genome-wide association studies is vast, yet it is rarely straightforward to identify the functional connection between a variant and a disorder.
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