Victor H. K. Yong

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

Eranga N. Vithana, Patricio E. Morgan, Periasamy Sundaresan et al. · Nature Genetics · 2006 · 296 citations

Life Sciences, Genetics, Molecular Genetics +3

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

Eranga N. Vithana, Patricio E. Morgan, Vedam L. Ramprasad et al. · Human Molecular Genetics · 2007 · 257 citations · Full text

Medicine, Genetics, Molecular Genetics +17

A common variant near TGFBR3 is associated with primary open angle glaucoma

Zheng Li, R. Rand Allingham, Masakazu Nakano et al. · Human Molecular Genetics · 2015 · 119 citations · Full text

Life Sciences, Genetics, Ophthalmology +14

Association Analysis of<i>CFH</i>,<i>C2</i>,<i>BF</i>, and<i>HTRA1</i>Gene Polymorphisms in Chinese Patients with Polypoidal Choroidal Vasculopathy

Kelvin Y. Lee, Eranga N. Vithana, Ranjana Mathur et al. · Investigative Ophthalmology & Visual Science · 2008 · 108 citations · Full text

Medicine, Genetics, Ophthalmology +14

Association of<i>LOXL1</i>Gene Polymorphisms with Pseudoexfoliation in the Japanese

Mineo Ozaki, Kelvin Y. C. Lee, Eranga N. Vithana et al. · Investigative Ophthalmology & Visual Science · 2008 · 96 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15