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

Single-Cell Gene Expression and eQTL Analyses in the Human Retina, RPE, and Choroid in Macular Degeneration

黄斑变性患者视网膜、视网膜色素上皮和脉络膜的单细胞基因表达和eQTL分析

Voigt, Andrew P; Mullin, Nathaniel K; Mulfaul, Kelly; Lozano, Lola P; Navratil, Emma M; Flamme-Wiese, Miles J; Lavine, Jeremy A; Fingert, John H; Tucker, Budd A; Stone, Edwin M; Scheetz, Todd E; Mullins, Robert F

Prevalence of Myocilin Mutations in a Cohort of Patients with Juvenile Open-Angle Glaucoma from sub-Saharan Africa

撒哈拉以南非洲青少年开角型青光眼患者队列中肌纤蛋白突变的患病率

Olawoye, Olusola; Young, Brian P; Nyunt, Angela W; Fafowora, Oluwatoyin F; Ajani, Magdalene; Sarimiye, Tarela; Creemer, Brendan A; Roos, Ben R; Coleman, Anne L; Gorin, Michael B; Hauser, Michael A; Scheetz, Todd E; Ashaye, Adeyinka; Fingert, John H

A Retrospective Longitudinal Study of 460 Patients with ABCA4-Associated Retinal Disease

一项对460例ABCA4相关视网膜疾病患者的回顾性纵向研究

Fenner, Beau J; Whitmore, S Scott; DeLuca, Adam P; Andorf, Jean L; Daggett, Heather T; Luse, Meagan A; Haefeli, Lorena M; Riley, Janet B; Critser, Douglas B; Wilkinson, Mark E; Dumitrescu, Alina V; Drack, Arlene V; Boyce, Timothy M; Russell, Jonathan F; Binkley, Elaine M; Sohn, Elliott H; Russell, Stephen R; Boldt, H Culver; Mullins, Robert F; Tucker, Budd A; Scheetz, Todd E; Han, Ian C; Stone, Edwin M

METTL23 Variants and Patients With Normal-Tension Glaucoma

METTL23 变异与正常眼压性青光眼患者

Scheetz, Todd E; Tollefson, Mallory R; Roos, Ben R; Boese, Erin A; Pouw, Andrew E; Stone, Edwin M; Schnieders, Michael J; Fingert, John H

GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery

GJA3基因变异与常染色体显性遗传性先天性白内障和白内障手术后青光眼有关

Boese, Erin A; Drack, Arlene V; Roos, Benjamin R; Alward, Wallace L M; Tollefson, Mallory R; Schnieders, Michael J; Scheetz, Todd E; Boldt, H Culver; Stone, Edwin M; Fingert, John H

Using Goldmann Visual Field Volume to Track Disease Progression in Choroideremia

利用戈尔德曼视野容积法追踪脉络膜萎缩症的疾病进展

DeLuca, Adam P; Whitmore, S Scott; Tatro, Nicole J; Andorf, Jeaneen L; Faga, Ben P; Faga, Laurel A; Colins, Malia M; Luse, Meagan A; Fenner, Beau J; Stone, Edwin M; Scheetz, Todd E

GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICS

利用空间转录组学研究人脉络膜新生血管膜内的基因表达

Voigt, Andrew P; Mullin, Nathaniel K; Navratil, Emma M; Flamme-Wiese, Miles J; Lin, Li-Chun; Scheetz, Todd E; Han, Ian C; Stone, Edwin M; Tucker, Budd A; Mullins, Robert F

Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degeneration

萎缩性和新生血管性黄斑变性中脉络膜内皮细胞和巨噬细胞的基因表达

Voigt, Andrew P; Mullin, Nathaniel K; Mulfaul, Kelly; Lozano, Lola P; Wiley, Luke A; Flamme-Wiese, Miles J; Boese, Erin A; Han, Ian C; Scheetz, Todd E; Stone, Edwin M; Tucker, Budd A; Mullins, Robert F

Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptoms

对非视网膜组织中m.3243A>G突变比例进行灵敏定量分析及其与视觉症状的关系

Mullin, Nathaniel K; Anfinson, Kristin R; Riker, Megan J; Wieland, Kelsey L; Tatro, Nicole J; Scheetz, Todd E; Mullins, Robert F; Stone, Edwin M; Tucker, Budd A

AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY

自身免疫性视网膜病变在患有常见变异型免疫缺陷的患者中模拟遗传性视网膜变性

Wiley, Luke A; Binkley, Elaine M; DeLuca, Adam P; Workalemahu, Grefachew; Tatro, Nicole J; Luse, Meagan A; Kennedy, Elizabeth L; Folk, James C; Scheetz, Todd E; Ballas, Zuhair K; Tucker, Budd A; Mullins, Robert F; Han, Ian C; Stone, Edwin M