Concepedia

Ordan J. Lehmann

OJ

37

Publications

3.1K

Citations

29

H-Index

1988

Active since

Affiliations

University of Alberta(Current)

University College London

Moorfields Eye Hospital

Southampton General Hospital

Institute of Ophthalmology

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

ORCID

Top concepts

Publications per year

1988–2019

37

Publications

37

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 et al. · Nature Genetics · 2009 · 280 citations · Full text

, , +8

Acanthamoeba keratitis: multicentre survey in England 1992-6. National Acanthamoeba Keratitis Study Group.

Cherry Radford, Ordan J. Lehmann, John Dart · PubMed · 1998 · 244 citations

Mutations in PIK3R1 Cause SHORT Syndrome

David A. Dyment, Amanda Smith, Diana Alcantara et al. · The American Journal of Human Genetics · 2013 · 191 citations · Full text

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

M. Ye, Karyn M. Berry-Wynne, Mika Asai-Coakwell et al. · Human Molecular Genetics · 2009 · 160 citations · Full text

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

Curtis R. French, Sudha Seshadri, Anita L. DeStefano et al. · Journal of Clinical Investigation · 2014 · 149 citations · Full text

Rows per page

1–5 of 37