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Issue DateTitleAuthor(s)Citation
2013Visual Impairment and Subsequent Use of Support Services Among Older People: Longitudinal Findings From the Blue Mountains Eye StudyBurlutsky, George; Fong, Calvin; Hong, Thomas; Mitchell, Paul; Rochtchina, Elena; Wang, Jie Jin; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Westmead Millennium InstituteVisual Impairment and Subsequent Use of Support Services Among Older People: Longitudinal Findings From the Blue Mountains Eye Study, American Journal of Ophthalmology, vol.156, 2, 2013,pp 393-399
2013Genetic Loci for retinal arteriolar microcirculationMitchell, Paul; Rochtchina, Elena; Wang, Jie Jin; Boerwinkle, Eric; Cotch, Mary Frances; et al, Various; Ikram, M Kamran; Jensen, Richard A.; Li, Xiaohui; MacGregor, Stuart; Sim, Xueling; Smith, Albert Vernon; Xie, Jing; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Westmead Millennium InstituteGenetic Loci for retinal arteriolar microcirculation, PLoS One, vol.8, 6, 2013,pp 1-12
2013Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive errorMitchell, Paul; Rochtchina, Elena; Wang, Jie Jin; Chew, Emily Y; Cotch, Mary Frances; et al, Various; Klein, Barbara E.K.; Klein, Ronald; Li, Xiaohui; Oexle, Konrad; Pirastu, Mario; Raffel, Leslie; Stambolian, Dwight; Wojciechowski, Robert; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Clinical Ophthal & Eye Health; Western Clinical School: Westmead Millennium InstituteMeta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error, Human Molecular Genetics, vol.22, 13, 2013,pp 2754-2764