Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy

• المؤلفون الرئيسيون: Graham, P.S, Kaidonis, G, Abhary, S, Gillies, M.C, Daniell, M, Essex, R.W, Chang, J.H, Lake, S.R, Pal, B, Jenkins, A.J, Hewitt, A.W, Lamoureux, E.L, Hykin, P.G, Petrovsky, N, Brown, M.A, Craig, J.E, Burdon, K.P
• مؤلفون آخرون: DUKE-NUS MEDICAL SCHOOL
• التنسيق: مقال
• منشور في: 2020
• الموضوعات: hemoglobin A1c; untranslated RNA; C10orf112 protein, human; low density lipoprotein receptor; PCSK2 protein, human; proprotein convertase 2; aged; Article; Australian; Caucasian; chromosome 14; chromosome 2; chromosome 5; clinical evaluation; clinical feature; cohort analysis; controlled study; diabetic macular edema; disease duration; female; gene; gene location; genetic risk; genome-wide association study; genotype; human; LINC00343 gene; LOC285626 gene; major clinical study; male; MALRD1 gene; MRPL19 gene; non insulin dependent diabetes mellitus; NRXN3 gene; PCSK2 gene; proliferative diabetic retinopathy; risk assessment; risk factor; single nucleotide polymorphism; Australia; case control study; complication; diabetic retinopathy; genetic predisposition; genetics; macular edema; middle aged; procedures; Aged; Case-Control Studies; Chromosomes, Human, Pair 2; Chromosomes, Human, Pair 5; Diabetes Mellitus, Type 2; Diabetic Retinopathy; European Continental Ancestry Group; Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Macular Edema; Male; Middle Aged; Polymorphism, Single Nucleotide; Proprotein Convertase 2; Receptors, LDL
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/181201
• المؤسسة: National University of Singapore

10.1186/s12881-018-0587-8