Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe
Author:
Funder
Polish Ministry of Science and Higher Education
National Institutes of Health
Publisher
Elsevier BV
Subject
General Medicine
Reference76 articles.
1. Complex trait genetics of refractive error;Young;Arch Ophthalmol,2007
2. Prevalence of refractive error in Europe: the European eye epidemiology (E(3)) consortium;Williams;Eur J Epidemiol,2015
3. A review on the epidemiology of myopia in school children worldwide;Grzybowski;BMC Ophthalmol,2020
4. Myopia;Morgan;Lancet,2012
5. Risk factors for high myopia: a 22-year follow-up study from childhood to adulthood;Pärssinen;Acta Ophthalmol,2019
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Crosstalk between heredity and environment in myopia: An overview;Heliyon;2024-04
2. Whole-Exome Sequencing of 21 Families: Candidate Genes for Early-Onset High Myopia;International Journal of Molecular Sciences;2023-10-27
3. Epitranscriptomic investigation of myopia-associated RNA editing in the retina;Frontiers in Neuroscience;2023-06-28
4. Differential methylation of microRNA encoding genes may contribute to high myopia;Frontiers in Genetics;2023-01-04
5. Decreased Levels of DNA Methylation in the PCDHA Gene Cluster as a Risk Factor for Early-Onset High Myopia in Young Children;Investigative Opthalmology & Visual Science;2022-08-29
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3