Ordan J. Lehmann
Edmonton, AB, Canada
Last Updated: 09/26/2026
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Found 26 publications
Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival.
Journal: eLife
Published: July 06, 2026
Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.
Journal: Scientific reports
Published: February 23, 2024
FoxC1 activates limbal epithelial stem cells following corneal epithelial debridement.
Journal: Experimental eye research
Published: July 17, 2023
BMP3 is a novel locus involved in the causality of ocular coloboma.
Journal: Human genetics
Published: September 03, 2021
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Journal: Genes
Published: December 24, 2020
Ocular coloboma: Genetic variants reveal a dynamic model of eye development.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: May 17, 2020
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish.
Journal: Developmental biology
Published: April 08, 2019
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma.
Journal: Human molecular genetics
Published: September 26, 2018
Genetic background-dependent role of Egr1 for eyelid development.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 06, 2017
Last Updated: 09/26/2026