Minghui Qin

Complexity of the genotype-phenotype correlation in familial exudative vitreoretinopathy with mutations in the<i>LRP5</i>and/or<i>FZD4</i>genes

Minghui Qin, Hideyuki Hayashi, Kenji Oshima et al. · Human Mutation · 2005 · 152 citations

Medicine, Genetics, Ophthalmology +17

A Homozygosity-Based Search for Mutations in Patients with Autosomal Recessive Retinitis Pigmentosa, Using Microsatellite Markers

Hiroyuki Kondo, Minghui Qin, Atsushi Mizota et al. · Investigative Ophthalmology & Visual Science · 2004 · 88 citations

Life Sciences, Genetics, Molecular Genetics +15

Novel Mutations in Norrie Disease Gene in Japanese Patients with Norrie Disease and Familial Exudative Vitreoretinopathy

Hiroyuki Kondo, Minghui Qin, Shunji Kusaka et al. · Investigative Ophthalmology & Visual Science · 2007 · 56 citations

Life Sciences, Genetics, Ophthalmology +16

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy

Minghui Qin, Hiroyuki Kondo, Tomoko Tahira et al. · Human Genetics · 2007 · 33 citations

Medicine, Genetics, Ophthalmology +13

Severe Form of Familial Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene

Hiroyuki Kondo, Minghui Qin, Tomoko Tahira et al. · Ophthalmic Genetics · 2007 · 30 citations

Medicine, Genetics, Ophthalmology +17