A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration

• Main Authors: Kawashima-Kumagai, K, Yamashiro, K, Yoshikawa, M, Miyake, M, Ming, G.C.C, Fan, Q, Koh, J.Y, Saito, M, Sugahara-Kuroda, M, Oishi, M, Akagi-Kurashige, Y, Nakata, I, Nakanishi, H, Gotoh, N, Oishi, A, Tamura, H, Ooto, S, Tsujikawa, A, Kurimoto, Y, Sekiryu, T, Matsuda, F, Khor, C.-C, Cheng, C.-Y, Wong, T.Y, Yoshimura, N
• Other Authors: SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
• Format: Article
• Published: Nature Publishing Group 2020
• Subjects: aged; Asian continental ancestry group; case control study; female; genetic predisposition; genetics; genome-wide association study; human; male; neovascularization (pathology); pathology; single nucleotide polymorphism; very elderly; wet macular degeneration; Aged; Aged, 80 and over; Asian Continental Ancestry Group; Case-Control Studies; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Male; Neovascularization, Pathologic; Polymorphism, Single Nucleotide; Wet Macular Degeneration
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/178596
• Institution: National University of Singapore

10.1038/s41598-017-07526-9