Ordan J. Lehmann - Concepedia

Author

Ordan J. Lehmann

Also Known As

Douglas J. Rhee, O J Lehmann, O Lehmann, O. J Lehmann, O. J. Lehmann, O. Lehmann, O.J. LEHMANN, O.J. Lehmann, Ordan J Lehmann, Ordan J. Lehmann

105

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

University of Alberta University College London Moorfields Eye Hospital Southampton General Hospital Institute of Ophthalmology

About

Ordan J. Lehmann is an author at University of Alberta specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.4K
2	Molecular Genetics	7	7	781
3	Cell Biology	4	4	290
4	Cellular Physiology	1	1	68
5	Nephrology	1	1	16

Ordan J. Lehmann

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation Kimberly A. Aldinger, Ordan J. Lehmann, Louanne Hudgins, Nature Genetics Neurobiology Of DiseaseDevelopmental BiologyGenetic DisorderDevelopmental GeneticsGenetics	2009	280
Acanthamoeba keratitis: multicentre survey in England 1992-6. National Acanthamoeba Keratitis Study Group. Cherry Radford, Ordan J. Lehmann, John Dart PubMed	1998	244
Mutations in PIK3R1 Cause SHORT Syndrome David A. Dyment, Amanda Smith, Diana Alcantara, The American Journal of Human Genetics	2013	191
Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies M. Ye, Karyn M. Berry-Wynne, Mika Asai-Coakwell, Human Molecular Genetics	2009	160
Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease Curtis R. French, Sudha Seshadri, Anita L. DeStefano, Journal of Clinical Investigation	2014	149
Chromosomal Duplication Involving the Forkhead Transcription Factor Gene FOXC1 Causes Iris Hypoplasia and Glaucoma Ordan J. Lehmann, Neil D. Ebenezer, Tim Jordan, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsGenomic MechanismGenetic Mechanism	2000	148
Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene Tin Aung, Tayebeh Rezaie, Koji Okada, Investigative Ophthalmology & Visual Science	2005	147
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Tin Aung, Louise Ocaka, Neil D. Ebenezer, Human Genetics Opa1 GeneOcular DiseaseOphthalmologyExperimental OphthalmologyGenetics	2001	139
Polymerase chain reaction analysis of corneal epithelial and tear samples in the diagnosis of Acanthamoeba keratitis. Ordan J. Lehmann, S. M. Green, Nigel Morlet, PubMed	1998	121
Risk factors for development of post-trabeculectomy endophthalmitis Ordan J. Lehmann British Journal of Ophthalmology	2000	117

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