Genetic susceptibility and mechanisms for refractive error.

Genetic susceptibility and mechanisms for refractive error.
复制标题

DOI:
10.1111/cge.12180
复制
发表时间:
2013-08
期刊:
影响因子:
3.5
通讯作者:
Stambolian D
Stambolian D
中科院分区:
医学2区
文献类型:
--
作者:
Stambolian D

文献摘要

参考文献

被引文献

相似文献

屈光不正,近视和远视,是世界范围内视力损害的最常见原因。遗传学的最新进展已被用于鉴定大量被认为含有屈光不正易感基因的遗传基因座。目前的遗传学证据证实,屈光不正受到常见和罕见变异的影响,并具有显著的环境成分。这些研究认为,只有通过将遗传知识与生物状态的体内测量相结合,才有可能了解屈光不正的潜在生物学,这将导致新的治疗靶点和准确的遗传预测。
Refractive errors, myopia and hyperopia, are the most common causes of visual impairment worldwide. Recent advances in genetics have been utilized to identify a wealth of genetic loci believed to contain susceptibility genes for refractive error. The current genetic evidence confirms that refractive error is influenced by both common and rare variants with a significant environmental component. These studies argue that only by combining genetic knowledge with in vivo measurements of biological states will it be possible to understand the underlying biology of refractive error that will lead to novel therapeutic targets and accurate genetic predictions.
DOI: 10.1126/science.1150021
发表时间: 2008-04-18
期刊: SCIENCE
影响因子: 56.9
作者:
Hillenmeyer, Maureen E.;Fung, Eula;Giaever, Guri
通讯作者: Giaever, Guri
DOI: 10.1167/iovs.10-6210
发表时间: 2011-05-01
影响因子: 4.4
作者:
Pan, Chen-Wei;Wong, Tien-Yin;Saw, Seang-Mei
通讯作者: Saw, Seang-Mei
DOI: 10.1371/journal.pgen.1000660
发表时间: 2009-09
期刊: PLoS genetics
影响因子: 4.5
作者:
Nakanishi H;Yamada R;Gotoh N;Hayashi H;Yamashiro K;Shimada N;Ohno-Matsui K;Mochizuki M;Saito M;Iida T;Matsuo K;Tajima K;Yoshimura N;Matsuda F
通讯作者: Matsuda F
DOI: 10.1167/iovs.11-7914
发表时间: 2011-10-01
影响因子: 4.4
作者:
Lu, Boyu;Jiang, Dan;Zhang, Qingjiong
通讯作者: Zhang, Qingjiong
DOI: 10.1167/iovs.09-3612
发表时间: 2010-01-01
影响因子: 4.4
作者:
Lin, Hui-Ju;Kung, Yung-Jen;Tsai, Fuu Jen
通讯作者: Tsai, Fuu Jen