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As one of the leading causes of visual impairment and blindness, myopia poses a significant public health burden in Asia. The… Expand Genome-wide association studies (GWAS) have identified ten loci harboring common variants that influence risk of developing… Expand Systemic lupus erythematosus (SLE) is an autoimmune disease with a complex genetic basis that includes susceptibility gene(s… Expand With λs estimates of 10 to 20 and other evidence of familial aggregation, as well as a monozygotic twin concordance rate >20… Expand Abnormalities in cellular differentiation are frequent occurrences in human cancers. Treatment of human melanoma cells with… Expand DNA copy number changes were characterized by comparative genomic hybridization (CGH) in 18 breast cancer cell lines. In 5 of… Expand Usher syndrome type IIa (OMIM 276901), an autosomal recessive disorder characterized by moderate to severe sensorineural hearing… Expand Systemic lupus erythematosus (SLE) is an autoimmune disorder characterized by production of autoantibodies against intracellular… Expand Usher syndrome type II is associated with hearing loss and retinitis pigmentosa but not with any vestibular problems. It is known… Expand