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Ordan Lehmann
Ordan Lehmann
Professor of Ophthalmology and Medical Genetics, University of Alberta
Verified email at ualberta.ca
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Cited by
Year
Fox's in development and disease
OJ Lehmann, JC Sowden, P Carlsson, T Jordan, SS Bhattacharya
TRENDS in Genetics 19 (6), 339-344, 2003
4652003
Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
SL Sawyer, T Hartley, DA Dyment, CL Beaulieu, J Schwartzentruber, ...
Clinical genetics 89 (3), 275-284, 2016
4172016
Acanthamoeba keratitis: multicentre survey in England 1992–6
CF Radford, OJ Lehmann, JKG Dart
British journal of ophthalmology 82 (12), 1387-1392, 1998
2871998
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
KA Aldinger, OJ Lehmann, L Hudgins, VV Chizhikov, AG Bassuk, ...
Nature genetics 41 (9), 1037-1042, 2009
2652009
Mutations in PIK3R1 cause SHORT syndrome
DA Dyment, AC Smith, D Alcantara, JA Schwartzentruber, ...
The American Journal of Human Genetics 93 (1), 158-166, 2013
1762013
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene
T Aung, L Ocaka, ND Ebenezer, AG Morris, M Krawczak, DL Thiselton, ...
Human genetics 110, 52-56, 2002
1732002
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies
M Ye, KM Berry-Wynne, M Asai-Coakwell, P Sundaresan, T Footz, ...
Human molecular genetics 19 (2), 287-298, 2010
1682010
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
OJ Lehmann, ND Ebenezer, T Jordan, M Fox, L Ocaka, A Payne, ...
The American Journal of Human Genetics 67 (5), 1129-1135, 2000
1642000
Polymerase chain reaction analysis of corneal epithelial and tear samples in the diagnosis of Acanthamoeba keratitis.
OJ Lehmann, SM Green, N Morlet, S Kilvington, MF Keys, MM Matheson, ...
Investigative ophthalmology & visual science 39 (7), 1261-1265, 1998
1611998
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene
T Aung, T Rezaie, K Okada, AC Viswanathan, AH Child, G Brice, ...
Investigative ophthalmology & visual science 46 (8), 2816-2822, 2005
1542005
Risk factors for development of post-trabeculectomy endophthalmitis
OJ Lehmann, C Bunce, MM Matheson, V Maurino, PT Khaw, R Wormald, ...
British journal of ophthalmology 84 (12), 1349-1353, 2000
1472000
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
CR French, S Seshadri, AL Destefano, M Fornage, CR Arnold, PJ Gage, ...
The Journal of clinical investigation 124 (11), 4877-4881, 2014
1452014
GDF6, a novel locus for a spectrum of ocular developmental anomalies
M Asai-Coakwell, CR French, KM Berry, M Ye, R Koss, M Somerville, ...
The American Journal of Human Genetics 80 (2), 306-315, 2007
1262007
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies
G Chauhan, CR Arnold, AY Chu, M Fornage, A Reyahi, JC Bis, ...
The Lancet Neurology 15 (7), 695-707, 2016
1212016
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes
M Asai-Coakwell, CR French, M Ye, K Garcha, K Bigot, AG Perera, ...
Human molecular genetics 18 (6), 1110-1121, 2009
1162009
Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth
S Seo, HP Singh, PM Lacal, A Sasman, A Fatima, T Liu, KM Schultz, ...
Proceedings of the National Academy of Sciences 109 (6), 2015-2020, 2012
1122012
Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions
OJ Lehmann, ND Ebenezer, R Ekong, L Ocaka, AJ Mungall, S Fraser, ...
Investigative ophthalmology & visual science 43 (6), 1843-1849, 2002
1012002
Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing
T Aung, ND Ebenezer, G Brice, AH Child, Q Prescott, OJ Lehmann, ...
Journal of Medical Genetics 40 (8), e101-e101, 2003
882003
Axenfeld–Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome
K Maclean, J Smith, LS Heaps, N Chia, R Williams, GB Peters, E Onikul, ...
American Journal of Medical Genetics Part A 132 (4), 381-385, 2005
842005
Regional localization of the autosomal dominant polycystic kidney disease locus
ST Reeders, T Keith, P Green, GG Germino, NJ Barton, OJ Lehmann, ...
Genomics 3 (2), 150-155, 1988
831988
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