日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?

莱伯遗传性视神经病变的患病风险和外显率真的低吗？

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2022.11.014
Mackey, David A; Ong, Jue-Sheng; MacGregor, Stuart; Whiteman, David C; Craig, Jamie E; Lopez Sanchez, M Isabel G; Kearns, Lisa S; Staffieri, Sandra E; Clarke, Linda; McGuinness, Myra B; Meteoukki, Wafaa; Samuel, Sona; Ruddle, Jonathan B; Chen, Celia; Fraser, Clare L; Harrison, John; Howell, Neil; Hewitt, Alex W
发表日期：2023
文献求助 收藏

Keratoconus International Consortium (KIC)- advancing keratoconus research

圆锥角膜国际联盟 (KIC)——推进圆锥角膜研究

期刊:BMC Ophthalmology
影响因子:1.7
doi:10.1186/s12886-023-03087-w
Sahebjada, Srujana; Chan, Elsie; Sutton, Gerard; Pang, Chi Pui Calvin; Kerdraon, Yves; Natarajan, Sundaram; Meteoukki, Wafaa; Ang, Andrea; Daniell, Mark; Baird, Paul N
发表日期：2023
文献求助 收藏

Establishing risk of vision loss in Leber hereditary optic neuropathy

确定莱伯遗传性视神经病变患者的视力丧失风险

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2021.09.015
Lopez Sanchez, M Isabel G; Kearns, Lisa S; Staffieri, Sandra E; Clarke, Linda; McGuinness, Myra B; Meteoukki, Wafaa; Samuel, Sona; Ruddle, Jonathan B; Chen, Celia; Fraser, Clare L; Harrison, John; Hewitt, Alex W; Howell, Neil; Mackey, David A
发表日期：2021
文献求助 收藏

Association of IL4 rs2070874, FoxP3 rs3761548 Polymorphisms with Keratoconus in Algeria

IL4 rs2070874、FoxP3 rs3761548 多态性与阿尔及利亚圆锥角膜的关联

期刊:Journal of Ophthalmic & Vision Research
影响因子:1.5
doi:10.18502/jovr.v16i4.9745
Meteoukki, Wafaa; Fodil, Mostefa; Negaz, Nawel Adda; Rahmoun, Nesrine; Hetraf, Sarah Lardjam; Djellouli, Hadjira Ouhaibi; Messal, Ahlem Djelti; Abdi, Meriem; Aberkane, Meriem Samia; Chiali, Abdelillah; Derdour, Amine; Idder, Aicha; -Fodil, Faouzia Zemani
IL4
发表日期：2021
文献求助 收藏