[go: up one dir, main page]

Follow
Ordan Lehmann
Ordan Lehmann
Professor of Ophthalmology and Medical Genetics, University of Alberta
Verified email at ualberta.ca
Title
Cited by
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
4782003
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
4772016
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
3072009
Acanthamoeba keratitis: multicentre survey in England 1992–6
CF Radford, OJ Lehmann, JKG Dart
British journal of ophthalmology 82 (12), 1387-1392, 1998
3051998
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
2032013
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
1832010
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 (1), 52-56, 2002
1832002
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
1742005
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
1741998
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
1722014
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
1682000
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
1632000
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
1532016
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
1362007
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
1192012
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
1192009
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
1042002
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
972003
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
872005
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies
M Asai-Coakwell, L March, XH Dai, M DuVal, I Lopez, CR French, ...
Human molecular genetics 22 (7), 1432-1442, 2013
852013
The system can't perform the operation now. Try again later.
Articles 1–20