Ordan J. Lehmann

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 · 282 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

Cherry Radford, Ordan J. Lehmann, John Dart · PubMed · 1998 · 245 citations

Medicine, Dermatology, Ophthalmology +14

Mutations in PIK3R1 Cause SHORT Syndrome

David A. Dyment, Amanda Smith, Diana Alcantara et al. · The American Journal of Human Genetics · 2013 · 197 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 161 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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 · 151 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17