Divya Venkataraman

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

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese.

Kelvin Y. C. Lee, Su Ling Ho, Anbupalam Thalamuthu et al. · PubMed · 2009 · 53 citations

Life Sciences, Genetics, Molecular Genetics +17

Association of<i>TCF4</i>Gene Polymorphisms with Fuchs' Corneal Dystrophy in the Chinese

Anbupalam Thalamuthu, Chiea Chuen Khor, Divya Venkataraman et al. · Investigative Ophthalmology & Visual Science · 2011 · 52 citations

Life Sciences, Genetics, Molecular Genetics +17

Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population.

Eranga N. Vithana, Monisha E. Nongpiur, Divya Venkataraman et al. · PubMed · 2010 · 46 citations

Life Sciences, Genetics, Ophthalmology +13