Khanh-Nhat Tran-Viet
Publications by Year
Research Areas
Ophthalmology and Visual Impairment Studies, Corneal surgery and disorders, Glaucoma and retinal disorders, Ocular Disorders and Treatments, Retinopathy of Prematurity Studies
Most-Cited Works
- → Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity(2016)286 cited
- → Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31(2006)241 cited
- → Multiple rare SAPAP3 missense variants in trichotillomania and OCD(2008)199 cited
- → REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31(2008)180 cited
- → Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia(2013)115 cited
- → SLITRK1 mutations in trichotillomania(2006)104 cited
- → CYP1B1, MYOC, and LTBP2 Mutations in Primary Congenital Glaucoma Patients in the United States(2012)83 cited
- → Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia(2009)71 cited
- → Genetic Association of Insulin-like Growth Factor-1 Polymorphisms with High-Grade Myopia in an International Family Cohort(2010)69 cited
- → COL1A1andCOL2A1Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to theCOL2A1Locus(2009)60 cited