Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE To determine the recurrence rate of exudative age-related macular degeneration (wet AMD) in patients on 12-week dosing interval anti-vascular endothelial growth factor (anti-VEGF) bevacizumab therapy. 30649077 2020
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE The authors review the recent NICE guideline for diagnosis and management of AMD, considerations for switching therapies and stopping treatment and need for regular monitoring of non-affected fellow eyes in patients with unilateral nAMD. 30926932 2019
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Moorfields AMD database report 2: fellow eye involvement with neovascular age-related macular degeneration. 31611234 2019
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 GeneticVariation disease BEFREE To investigate the association of treatment assignment (intravitreal aflibercept vs ranibizumab) and baseline characteristics with fellow eye conversion to nAMD in the VEGF (Vascular Endothelial Growth Factor) Trap-Eye: Investigation of Efficacy and Safety in Wet AMD (VIEW) studies. 31294771 2019
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 GeneticVariation disease BEFREE Choroidal neovascularization (CNV) is a hallmark of exudative age-related macular degeneration (exAMD) and a major cause of visual loss in AMD. 30917905 2019
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Plasma was prepared from EDTA blood that was collected from patients affected by dry AMD (n = 5), nAMD (n = 11), proliferative diabetic retinopathy (PDR; n = 9), and patients with an epiretinal membrane (ERM; n = 11). 29177891 2018
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Whether PCV is a subtype of AMD or a distinct entity from nAMD remains unknown. 29323771 2018
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Neovascular age-related macular degeneration (wet AMD) results from the pathological angiogenesis of choroidal capillaries, which leak fluid within or below the macular region of the retina. 29734810 2018
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE To explore the relationship between plasma C-reactive protein (CRP) levels, the main <i>ARMS2</i> gene single nucleotide polymorphism (SNP), and gender in patients with neovascular age-related macular degeneration (wet AMD). 30154790 2018
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Data on the VA of patients with intermediate AMD and VA at the time of nvAMD diagnosis suggest that patients are typically losing an average of 3 to 5 lines of vision and possibly more between the time that intermediate AMD progresses to nvAMD and the diagnosis of nvAMD is made. 28114653 2017
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE These findings highlight the need to address AMD awareness and the need for urgent treatment to prevent avoidable vision loss resulting from nvAMD. 29229653 2017
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 GeneticVariation disease BEFREE In this cross-sectional study, 162 subjects with nAMD from the Asian AMD Phenotyping Study and 105 randomly sampled age-matched and gender-matched controls from the population-based Singapore Chinese Eye Study were recruited. nAMD was categorised as either polypoidal choroidal vasculopathy (PCV) or 'typical' AMD (tAMD). 27485722 2017
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE To assess the safety of rAAV.sFlt-1 subretinal injection in neovascular age-related macular degeneration (wet AMD) over 36 months. 28245970 2017
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 GeneticVariation disease BEFREE To examine the association of systemic, ocular and genetic risk factors in neovascular age-related macular degeneration (nAMD) in a large cohort of Asian patients, and to further compare risk factors between those with typical AMD and polypoidal choroidal vasculoapthy (PCV) subtypes. 28120909 2017
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE To compare the genomic contribution of the ARMS2/HTRA1 region of chromosome 10q26 to typical neovascular age-related macular degeneration (nAMD) (also known as typical exudative AMD) and to polypoidal choroidal vasculopathy (PCV) METHODS: DNA samples were prepared from 84 patients with typical nAMD, 181 patients with PCV, and 276 control participants. 21191724 2010
Entrez Id: 263
Gene Symbol: AMD1P2
AMD1P2
0.100 Biomarker disease BEFREE Exudative age-related macular degeneration (exudative AMD) is a common vision-threatening disease, with both environmental and genetic factors contributing to its development. 19223990 2009