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

A longitudinal study of the 5xFAD mouse retina delineates Amyloid beta (Aβ)-mediated retinal pathology from age-related changes.

对 5xFAD 小鼠视网膜的纵向研究区分了淀粉样蛋白β (Aβ) 介导的视网膜病变与年龄相关的变化

期刊:Alzheimers Research & Therapy
影响因子:7.6
doi:10.1186/s13195-025-01784-w
Lynn Savannah A, Pandi Sudha Priya Soundara, Sanchez-Bretano Aida, Muir Anna-Marie, Parker Lidia, Chatelet David S, Newall Tutte, Scott Jennifer A, Keeling Eloise, Smyth Neil R, Self Jay E, Lotery Andrew J, Lee Helena, Ratnayaka J Arjuna
其它
Mouse
发表日期：2025
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Can a Portable Flash Visual Evoked Potential (VEP) Device Identify Chiasmal Decussation Anomalies in Albinism?

便携式闪光视觉诱发电位（VEP）设备能否识别白化病患者的视交叉异常？

期刊:Diagnostics
影响因子:3.3
doi:10.3390/diagnostics15111395
Keeling, Eloise; Carter, Perry; Musa, Abdi Malik; Shawkat, Fatima; Lee, Helena; Self, Jay E
发表日期：2025
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Genetic insights into foveal morphology and its associations with pigmentation and age-related macular degeneration

遗传学视角下的黄斑形态及其与色素沉着和年龄相关性黄斑变性的关系

期刊:
影响因子:
doi:10.1101/2025.06.27.25330434
Green, David J; Romero-Bascones, David; Julian, Thomas H; Torchia, Sofia; Joisher, Heer N V; Ayala, Unai; Barrenechea, Maitane; Self, Jay E; Black, Graeme C; Fitzgerald, Tomas; Birney, Ewan; Cepko, Constance L; Carroll, Joseph; Sergouniotis, Panagiotis I
发表日期：2025
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Could a hand-held, visual electrophysiology device theoretically reduce diagnostic waiting times for complex eye conditions in the NHS? A Discrete Event Simulation (DES) modelling study

手持式视觉电生理设备能否在理论上缩短英国国民医疗服务体系（NHS）中复杂眼病的诊断等待时间？一项离散事件仿真（DES）建模研究

期刊:BMC Health Services Research
影响因子:
doi:10.1186/s12913-025-12551-w
Bayer, Steffen; Garillo, Daniel; Penn, Marion; Chorozoglou, Maria; Brailsford, Sally; Keeling, Eloise; Shawkat, Fatima; Carter, Perry; Lee, Helena; Self, Jay E
发表日期：2025
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Author Correction: Minimal reporting guideline for research involving eye tracking (2023 edition)

作者更正：涉及眼动追踪的研究的最低报告指南（2023版）

期刊:Behavior Research Methods
影响因子:3.9
doi:10.3758/s13428-024-02438-9
Dunn, Matt J; Alexander, Robert G; Amiebenomo, Onyekachukwu M; Arblaster, Gemma; Atan, Denize; Erichsen, Jonathan T; Ettinger, Ulrich; Giardini, Mario E; Gilchrist, Iain D; Hamilton, Ruth; Hessels, Roy S; Hodgins, Scott; Hooge, Ignace T C; Jackson, Brooke S; Lee, Helena; Macknik, Stephen L; Martinez-Conde, Susana; Mcilreavy, Lee; Muratori, Lisa M; Niehorster, Diederick C; Nyström, Marcus; Otero-Millan, Jorge; Schlüssel, Michael M; Self, Jay E; Singh, Tarkeshwar; Smyrnis, Nikolaos; Sprenger, Andreas
发表日期：2024
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Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia

对成纤维细胞生长因子14 (FGF14) 结构变异的分析揭示了早发性眼球震颤基因座NYS4和变异性共济失调的遗传基础。

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-022-01197-5
Ceroni, Fabiola; Osborne, Daniel; Clokie, Samuel; Bax, Dorine A; Cassidy, Emma J; Dunn, Matt J; Harris, Christopher M; Self, Jay E; Ragge, Nicola K
成纤维细胞
细胞生物学
FGF1
发表日期：2023
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Children's visual acuity tests without professional supervision: a prospective repeated measures study

儿童视力测试（无专业人员监督）：一项前瞻性重复测量研究

期刊:
影响因子:
doi:10.1038/s41433-023-02597-7
Osborne, Daniel; Steele, Aimee; Evans, Megan; Ellis, Helen; Pancholi, Roshni; Harding, Tomos; Dee, Jessica; Leary, Rachel; Bradshaw, Jeremy; O'Flynn, Elizabeth; Self, Jay E
发表日期：2023
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Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)

有证据表明，顺式酪氨酸酶基因单倍型 Ser192Tyr/Arg402Gln 是眼皮肤白化病 1B 型 (OCA1B) 的致病等位基因。

期刊:npj Genomic Medicine
影响因子:4.8
doi:10.1038/s41525-021-00275-9
Lin, Siying; Sanchez-Bretaño, Aida; Leslie, Joseph S; Williams, Katie B; Lee, Helena; Thomas, N Simon; Callaway, Jonathan; Deline, James; Ratnayaka, J Arjuna; Baralle, Diana; Schmitt, Melanie A; Norman, Chelsea S; Hammond, Sheri; Harlalka, Gaurav V; Ennis, Sarah; Cross, Harold E; Wenger, Olivia; Crosby, Andrew H; Baple, Emma L; Self, Jay E
发表日期：2022
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Novel therapeutics in nystagmus: what has the genetics taught us so far?

眼球震颤的新疗法：遗传学迄今为止教会了我们什么？

期刊:Therapeutic Advances in Rare Disease
影响因子:
doi:10.1177/2633004021998714
Self, Jay E; Lee, Helena
发表日期：2021
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Comprehensive sequencing of the myocilin gene in a selected cohort of severe primary open-angle glaucoma patients

对一组选定的重度原发性开角型青光眼患者进行肌纤蛋白基因的全面测序

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-019-38760-y
O'Gorman, Luke; Cree, Angela J; Ward, Daniel; Griffiths, Helen L; Sood, Roshan; Denniston, Alastair K; Self, Jay E; Ennis, Sarah; Lotery, Andrew J; Gibson, Jane
青光眼
神经科学
发表日期：2019
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