Skip to main content

and
  1. No Access

    Article

    Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33

    Myopia is one of the most common ocular disorders in the world, yet the genetic etiology of the disease remains poorly understood. Specialized founder populations, such as the Pennsylvania Amish, provide the o...

    Anthony M. Musolf, Claire L. Simpson, Theresa A. Alexander, Laura Portas in Human Genetics (2019)

  2. Article

    Open Access

    Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

    To identify genetic variants associated with refractive astigmatism in the general population, meta-analyses of genome-wide association studies were performed for: White Europeans aged at least 25 years (20 co...

    Qing Li, Robert Wojciechowski, Claire L. Simpson, Pirro G. Hysi in Human Genetics (2015)

  3. Article

    Open Access

    Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

    Myopia is a complex genetic disorder and a common cause of visual impairment among working age adults. Genome-wide association studies have identified susceptibility loci on chromosomes 15q14 and 15q25 in Cauc...

    Virginie J. M. Verhoeven, Pirro G. Hysi, Seang-Mei Saw, Veronique Vitart in Human Genetics (2012)