Ordan J. Lehmann
University of Alberta(CA)
Publications by Year
Research Areas
Ocular Disorders and Treatments, Glaucoma and retinal disorders, Corneal Surgery and Treatments, Retinal Development and Disorders, Congenital heart defects research
Most-Cited Works
- → Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care(2015)391 cited
- → Fox's in development and disease(2003)349 cited
- → FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation(2009)282 cited
- → Acanthamoeba keratitis: multicentre survey in England 1992-6. National Acanthamoeba Keratitis Study Group.(1998)244 cited
- → Mutations in PIK3R1 Cause SHORT Syndrome(2013)196 cited
- → Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies(2009)160 cited
- → Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease(2014)