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

Interpretable Aging Signatures in Human Retinal Cell Types Revealed by Single-Cell RNA Sequencing and Sparse Logistic Regression

通过单细胞RNA测序和稀疏逻辑回归揭示人类视网膜细胞类型中可解释的衰老特征

期刊:Ophthalmology Science
影响因子:4.6
doi:10.1016/j.xops.2025.101062
Yang, Luning; Lin, Sen; Tao, Yiwen; Pan, Qi; Cai, Tengda; Ye, Yunyan; Liu, Jianhui; Zhou, Yang; Shao, Yongqing; Yi, Quanyong; Lu, Zen Huat; Chen, Lie; McKay, Gareth; Rankin, Richard; Li, Fan; Meng, Weihua
细胞生物学
衰老
Human
单细胞
发表日期：2026
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A genome-wide association study identifies EYA2 as a contributing gene for diabetic retinopathy in type 2 diabetes

全基因组关联研究发现，EYA2是2型糖尿病视网膜病变的一个致病基因。

期刊:
影响因子:
doi:10.1038/s43856-026-01465-1
Cai, Tengda; Pan, Qi; Tao, Yiwen; Nangia, Charvi; Rajendrakumar, Aravind L; Ye, Yunyan; Dottorini, Tania; Haque, Mainul; Palmer, Colin Na; Shao, Yongqing; Meng, Weihua
糖尿病视网膜病变
视网膜病变
神经科学
代谢
糖尿病
发表日期：2026
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Genome-Wide Association Study to Identify Genetic Variants Associated With Diabetic Maculopathy

全基因组关联研究旨在识别与糖尿病性黄斑病变相关的遗传变异。

期刊:Investigative Ophthalmology & Visual Science
影响因子:4.7
doi:10.1167/iovs.66.3.55
Gurung, Rajya L; Nangia, Charvi; Cai, Tengda; FitzGerald, Liesel M; McComish, Bennet J; Liu, Ebony; Kaidonis, Georgia; Ridge, Bronwyn; Hewitt, Alex W; Vote, Brendan; Verma, Nitin; Craig, Jamie E; Palmer, Colin N A; Burdon, Kathryn P; Meng, Weihua
代谢
糖尿病
发表日期：2025
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A scRNA-seq reference contrasting living and early post-mortem human retina across diverse donor states.

一项针对不同供体状态的活体和早期死后人类视网膜的单细胞RNA测序参考研究

期刊:Human Genomics
影响因子:4.3
doi:10.1186/s40246-025-00796-9
Yang Luning, Tao Yiwen, Pan Qi, Cai Tengda, Ye Yunyan, Liu Jianhui, Zhou Yang, Shao Yongqing, Yi Quanyong, Lu Zen Huat, Chen Lie, McKay Gareth, Rankin Richard, Meng Weihua
细胞生物学
Human
单细胞
发表日期：2025
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A genome-wide association study identifies genetic variants associated with hip pain in the UK Biobank cohort (N = 221,127)

一项全基因组关联研究在英国生物银行队列（N = 221,127）中发现了与髋关节疼痛相关的遗传变异。

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-025-85871-w
Pan, Qi; Tao, Yiwen; Cai, Tengda; Veluchamy, Abi; Hebert, Harry L; Zhu, Peixi; Haque, Mainul; Dottorini, Tania; Colvin, Lesley A; Smith, Blair H; Meng, Weihua
发表日期：2025
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Genetic variants associated with gout identified through a genome-wide study in the UK biobank (N = 150 542)

通过英国生物银行（N = 150 542）的全基因组研究，鉴定出与痛风相关的遗传变异

期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddaf151
Tao, Yiwen; Cai, Tengda; Pan, Qi; Yang, Luning; Lin, Sen; Haque, Mainul; Dottorini, Tania; Abhishek, Abhishek; Meng, Weihua
痛风
代谢
发表日期：2025
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A genome-wide association study identifies novel genetic variants associated with neck or shoulder pain in the UK biobank (N = 430,193)

一项全基因组关联研究在英国生物样本库（N = 430,193）中发现了与颈部或肩部疼痛相关的新基因变异。

期刊:Pain Reports
影响因子:3.1
doi:10.1097/PR9.0000000000001267
Tao, Yiwen; Pan, Qi; Cai, Tengda; Lu, Zen Huat; Haque, Mainul; Dottorini, Tania; Colvin, Lesley A; Smith, Blair H; Meng, Weihua
发表日期：2025
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Genome-wide association study identifies novel genetic variants associated with widespread pain in the UK Biobank (N = 172,230)

全基因组关联研究在英国生物银行（N = 172,230）中发现了与广泛性疼痛相关的新基因变异

期刊:Molecular Pain
影响因子:2.8
doi:10.1177/17448069251346603
Pan, Qi; Cai, Tengda; Tao, Yiwen; Yang, Luning; Compte, Roger; Naeini, Maryam Kazemi; Haque, Mainul; Dottorini, Tania; Williams, Frances Mk; Meng, Weihua
发表日期：2025
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