Eranga N. Vithana

A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)

Eranga N. Vithana, Leen Abu‐Safieh, Maxine Allen et al. · Molecular Cell · 2001 · 333 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

Pirro G. Hysi, Ching‐Yu Cheng, Henriët Springelkamp et al. · Nature Genetics · 2014 · 249 citations · Full text

Life Sciences, Genetics, Ophthalmology +10

Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers

Juliet D. French, Maya Ghoussaini, Stacey L. Edwards et al. · The American Journal of Human Genetics · 2013 · 214 citations · Full text

Medicine, Genetics, Molecular Genetics +16