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

Selective deletion of Slc2a1 from the RPE reveals that rods but not cones depend on glucose transport across the outer blood-retinal barrier

选择性敲除视网膜色素上皮细胞(RPE)中的Slc2a1基因表明,视杆细胞而非视锥细胞依赖于葡萄糖跨越外血视网膜屏障的转运。

Daniele, Lauren L; Han, John Y S; Yu, Minzhong; Sangani, Ravi A; Beight, Craig D; Rostami, Cyrus; Kiser, Philip D; Peachey, Neal S; Philp, Nancy J

Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma

PTPRB基因的罕见遗传变异与中心性浆液性脉络膜视网膜病变、静脉曲张和青光眼相关。

Rämö, Joel T; Gorman, Bryan R; Weng, Lu-Chen; Jurgens, Sean J; Singhanetr, Panisa; Tieger, Marisa G; van Dijk, Elon HC; Halladay, Christopher W; Wang, Xin; Hauser, Blake M; Kim, Soo Hyun; Brinks, Joost; Choi, Seung Hoan; Luo, Yuyang; Pyarajan, Saiju; Nealon, Cari L; Gorin, Michael B; Wu, Wen-Chih; Anthony, Scott A; Roncone, David P; Sobrin, Lucia; Kaarniranta, Kai; Yzer, Suzanne; Palotie, Aarno; Peachey, Neal S; Turunen, Joni A; Boon, Camiel JF; Ellinor, Patrick T; Iyengar, Sudha K; Daly, Mark J; Rossin, Elizabeth J

Performance of Polygenic Risk Scores for Primary Open-Angle Glaucoma in Populations of African Descent

多基因风险评分在非洲裔人群中对原发性开角型青光眼的预测性能

Chang-Wolf, Jennifer M; Kinzy, Tyler G; Driessen, Sjoerd J; Cruz, Lauren A; Iyengar, Sudha K; Peachey, Neal S; Aung, Tin; Khor, Chiea Chuen; Williams, Susan E; Ramsay, Michele; Olawoye, Olusola; Ashaye, Adeyinka; Klaver, Caroline C W; Hauser, Michael A; Thiadens, Alberta A H J; Cooke Bailey, Jessica N; Bonnemaijer, Pieter W M

Characterization of Hepatotropic Small Molecule Inhibitors of Hypoxia Inducible Factor Prolyl Hydroxylase in the Prevention of Oxygen-Induced Retinopathy

肝脏嗜性小分子缺氧诱导因子脯氨酰羟化酶抑制剂在预防氧诱导视网膜病变中的作用特征分析

Campla, Christie; Hoppe, George; Yu, Minzhong; Woda, Juliana; Peachey, Neal S; Josyula, Vara Prasad; Stauffer, Shaun R; Sears, Jonathan E

Identifying genetic determinants of outer retinal function in mice using a large-scale gene-targeted screen

利用大规模基因靶向筛选鉴定小鼠外层视网膜功能的遗传决定因素

Wotton, Janine M; Krebs, Mark P; Sangermano, Riccardo; Wong, Jessica K; Smith, Cynthia; Willett, Amelia M; Howell, Douglas; Jones, Abby; Witmeyer, Catherine; Lowy, Jacob P; McFarland, Michael; Murray, Stephan A; Braun, Robert E; Nishina, Patsy M; Pierce, Eric A; Place, Emily M; Bujakowska, Kinga M; Peachey, Neal S; White, Jacqueline K

Genome-wide association study of dry eye disease reveals shared heritability with systemic comorbidities

全基因组关联研究揭示干眼症与全身性合并症具有共同的遗传性

Gorman, Bryan R; Huang, Jaxon J; Barr, Peter B; Halladay, Christopher W; Nealon, Cari L; Chatzinakos, Chris; Francis, Michael; Jiang, Chen; Greenberg, Paul B; Wu, Wen-Chih; Pyarajan, Saiju; Choquet, Hélène; Bigdeli, Tim B; Iyengar, Sudha K; Peachey, Neal S; Galor, Anat

Adaptive selection at G6PD and disparities in diabetes complications

G6PD 的适应性选择与糖尿病并发症的差异

Breeyear, Joseph H; Hellwege, Jacklyn N; Schroeder, Philip H; House, John S; Poisner, Hannah M; Mitchell, Sabrina L; Charest, Brian; Khakharia, Anjali; Basnet, Til B; Halladay, Christopher W; Reaven, Peter D; Meigs, James B; Rhee, Mary K; Sun, Yang; Lynch, Mary G; Bick, Alexander G; Wilson, Otis D; Hung, Adriana M; Nealon, Cari L; Iyengar, Sudha K; Rotroff, Daniel M; Buse, John B; Leong, Aaron; Mercader, Josep M; Sobrin, Lucia; Brantley, Milam A Jr; Peachey, Neal S; Motsinger-Reif, Alison A; Wilson, Peter W; Sun, Yan V; Giri, Ayush; Phillips, Lawrence S; Edwards, Todd L

A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma.

一项针对非洲裔人群的多队列全基因组关联研究揭示了原发性开角型青光眼的风险位点

Verma Shefali S, Gudiseva Harini V, Chavali Venkata R M, Salowe Rebecca J, Bradford Yuki, Guare Lindsay, Lucas Anastasia, Collins David W, Vrathasha Vrathasha, Nair Rohini M, Rathi Sonika, Zhao Bingxin, He Jie, Lee Roy, Zenebe-Gete Selam, Bowman Anita S, McHugh Caitlin P, Zody Michael C, Pistilli Maxwell, Khachatryan Naira, Daniel Ebenezer, Murphy Windell, Henderer Jeffrey, Kinzy Tyler G, Iyengar Sudha K, Peachey Neal S, Taylor Kent D, Guo Xiuqing, Chen Yii-Der Ida, Zangwill Linda, Girkin Christopher, Ayyagari Radha, Liebmann Jeffrey, Chuka-Okosa Chimd M, Williams Susan E, Akafo Stephen, Budenz Donald L, Olawoye Olusola O, Ramsay Michele, Ashaye Adeyinka, Akpa Onoja M, Aung Tin, Wiggs Janey L, Ross Ahmara G, Cui Qi N, Addis Victoria, Lehman Amanda, Miller-Ellis Eydie, Sankar Prithvi S, Williams Scott M, Ying Gui-Shuang, Cooke Bailey Jessica, Rotter Jerome I, Weinreb Robert, Khor Chiea Chuen, Hauser Michael A, Ritchie Marylyn D, O'Brien Joan M

Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries

全基因组关联分析揭示了不同种族人群中与年龄相关性黄斑变性相关的独特遗传结构

Gorman, Bryan R; Voloudakis, Georgios; Igo, Robert P Jr; Kinzy, Tyler; Halladay, Christopher W; Bigdeli, Tim B; Zeng, Biao; Venkatesh, Sanan; Cooke Bailey, Jessica N; Crawford, Dana C; Markianos, Kyriacos; Dong, Frederick; Schreiner, Patrick A; Zhang, Wen; Hadi, Tamer; Anger, Matthew D; Stockwell, Amy; Melles, Ronald B; Yin, Jie; Choquet, Hélène; Kaye, Rebecca; Patasova, Karina; Patel, Praveen J; Yaspan, Brian L; Jorgenson, Eric; Hysi, Pirro G; Lotery, Andrew J; Gaziano, J Michael; Tsao, Philip S; Fliesler, Steven J; Sullivan, Jack M; Greenberg, Paul B; Wu, Wen-Chih; Assimes, Themistocles L; Pyarajan, Saiju; Roussos, Panos; Peachey, Neal S; Iyengar, Sudha K

A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation

一项针对 Fuchs 角膜营养不良的多种族全基因组关联研究 (GWAS) 突显了层粘连蛋白、胶原蛋白和内皮细胞调控的作用。

Gorman, Bryan R; Francis, Michael; Nealon, Cari L; Halladay, Christopher W; Duro, Nalvi; Markianos, Kyriacos; Genovese, Giulio; Hysi, Pirro G; Choquet, Hélène; Afshari, Natalie A; Li, Yi-Ju; Gaziano, J Michael; Hung, Adriana M; Wu, Wen-Chih; Greenberg, Paul B; Pyarajan, Saiju; Lass, Jonathan H; Peachey, Neal S; Iyengar, Sudha K