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

Author Correction: The failure mechanism of the Baishi landslide in Beichuan County, Sichuan, China

作者更正：中国四川省北川县白石滑坡的破坏机制

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-90716-7
Tang, Ran; Ren, Suichuan; Li, Juntao; Feng, Peng; Li, Huajin; Deng, Ren; Li, Daxin; Kasama, Kiyonobu
发表日期：2025
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The failure mechanism of the Baishi landslide in Beichuan County, Sichuan, China

中国四川省北川县白石滑坡的破坏机制

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-67402-1
Tang, Ran; Ren, Suichuan; Li, Juntao; Feng, Peng; Li, Huajin; Deng, Ren; Li, Daxin; Kasama, Kiyonobu
发表日期：2024
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Comparing forceps and self-assembled intraocular rare earth magnet in removing metallic intraocular foreign bodies in 25-guage vitrectomy

比较镊子和自组装眼内稀土磁铁在25号玻璃体切除术中取出金属眼内异物的效果

期刊:BMC Ophthalmology
影响因子:1.7
doi:10.1186/s12886-024-03343-7
Li, Huajin; Zheng, Kailing; Wang, Huihang; Xie, Maosong
发表日期：2024
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The geographical pension gap: Understanding the causes of inequality in China's pension funds

地域养老金差距：了解中国养老基金不平等的原因

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0288754
Zhang, Songbiao; Wang, Xining; Li, Huajin; Wang, Huilin
发表日期：2023
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Clinical and genetic features of eight Chinese autosomal-dominant optic atrophy pedigrees with six novel OPA1 pathogenic variants

八个中国常染色体显性遗传性视神经萎缩家系的临床和遗传特征及六个新的OPA1致病变异

期刊:Ophthalmic Genetics
影响因子:1
doi:10.1080/13816810.2018.1466337
Li, Huajin; Jones, Evan M; Li, Hui; Yang, Lizhu; Sun, Zixi; Yuan, Zhisheng; Chen, Rui; Dong, Fangtian; Sui, Ruifang
OPA1
发表日期：2018
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The phenotypic variability of HK1-associated retinal dystrophy

HK1相关视网膜营养不良的表型变异性

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-017-07629-3
Yuan, Zhisheng; Li, Baiyu; Xu, Mingchu; Chang, Emmanuel Y; Li, Huajin; Yang, Lizhu; Wu, Shijing; Soens, Zachry T; Li, Yumei; Wong, Lee-Jun C; Lewis, Richard A; Sui, Ruifang; Chen, Rui
发表日期：2017
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CEP78 is mutated in a distinct type of Usher syndrome

CEP78基因突变与一种特殊的Usher综合征有关。

期刊:Journal of Medical Genetics
影响因子:3.7
doi:10.1136/jmedgenet-2016-104166
Fu, Qing; Xu, Mingchu; Chen, Xue; Sheng, Xunlun; Yuan, Zhisheng; Liu, Yani; Li, Huajin; Sun, Zixi; Li, Huiping; Yang, Lizhu; Wang, Keqing; Zhang, Fangxia; Li, Yumei; Zhao, Chen; Sui, Ruifang; Chen, Rui
CEP78
发表日期：2017
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Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions

对 Stargardt 黄斑营养不良患者的全面分析揭示了新的基因型-表型相关性和意想不到的诊断修正

期刊:Genetics in Medicine
影响因子:6.2
doi:10.1038/gim.2014.174
Zaneveld, Jacques; Siddiqui, Sorath; Li, Huajin; Wang, Xia; Wang, Hui; Wang, Keqing; Li, Hui; Ren, Huanan; Lopez, Irma; Dorfman, Allison; Khan, Ayesha; Wang, Feng; Salvo, Jason; Gelowani, Violet; Li, Yumei; Sui, Ruifang; Koenekoop, Robert; Chen, Rui
发表日期：2015
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Mutations in human IFT140 cause non-syndromic retinal degeneration.

人类 IFT140 基因突变会导致非综合征性视网膜变性

期刊:Human Genetics
影响因子:3.6
doi:10.1007/s00439-015-1586-x
Xu Mingchu, Yang Lizhu, Wang Feng, Li Huajin, Wang Xia, Wang Weichen, Ge Zhongqi, Wang Keqing, Zhao Li, Li Hui, Li Yumei, Sui Ruifang, Chen Rui
其它
Human
发表日期：2015
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A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.

NEUROD1 基因的纯合错义突变与非综合征型常染色体隐性遗传性视网膜色素变性相关

期刊:Investigative Ophthalmology & Visual Science
影响因子:4.7
doi:10.1167/iovs.14-15382
Wang Feng, Li Huajin, Xu Mingchu, Li Hui, Zhao Li, Yang Lizhu, Zaneveld Jacques E, Wang Keqing, Li Yumei, Sui Ruifang, Chen Rui
其它
发表日期：2014
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