16 research outputs found
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract
Nuclear cataract is the most common type of age-related cataract and a leading cause of blindness worldwide. Age-related nuclear cataract is heritable (h2 = 0.48), but little is known about specific genetic factors underlying this condition. Here we report findings from the largest to date multi-ethnic meta-analysis of genome-wide association studies (discovery cohort N = 14,151 and replication N = 5299) of the International Cataract Genetics Consortium. We confirmed the known genetic association of CRYAA (rs7278468, P = 2.8 × 10−16) with nuclear cataract and identified five new loci associated with this disease: SOX2-OT (rs9842371, P = 1.7 × 1
Quality of reporting of cranial irradiation techniques in randomized controlled trials of primary brain tumors: A systematic review
10.1371/journal.pone.0241566PLoS ONE1511-Nove024156
Quality of radiotherapy reporting in randomized controlled trials of prostate cancer
10.1186/s13014-018-1053-7Radiation Oncology13110
Impact of epidermal growth factor receptor sensitizing mutations on outcomes of patients with non-small cell lung cancer treated with definitive thoracic radiation therapy: A systematic review and meta-analysis
10.18632/oncotarget.21019Oncotarget865109712-10972
A cross-sectional study of knowledge, attitude and barriers to colorectal cancer screening among cancer survivors
10.31557/APJCP.2019.20.6.1817Asian Pacific Journal of Cancer Prevention2061817-182
EGFR kinase inhibitors and gastric acid suppressants in EGFR-mutant NSCLC: A retrospective database analysis of potential drug interaction
10.18632/oncotarget.13458Oncotarget75185542-8555
Adoption of prophylactic cranial irradiation (PCI) for extensive stage small cell lung cancer (ES-SCLC): A population based outcome study
10.1186/s13014-018-1184-xRadiation Oncology13124
Endothelial-immune crosstalk contributes to vasculopathy in nonalcoholic fatty liver disease.
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