Ordan J. Lehmann

University of Alberta — Canada

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index4.2kcitations105works0.82yr avg
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Research Topics

Ocular Disorders and Treatments(20), Glaucoma and retinal disorders(18), Corneal Surgery and Treatments(16), Retinal Development and Disorders(9), Congenital heart defects research(8)

Publications104 total

Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival
2025Open Access
Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival
2025Open Access
Author Response: Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival
2025Open Access
Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival
2025
Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling
Scientific Reports·2024· 4 citedOpen Access
FoxC1 activates limbal epithelial stem cells following corneal epithelial debridement
Experimental Eye Research·2023· 9 citedOpen Access
BMP3 is a novel locus involved in the causality of ocular coloboma
Human Genetics·2022· 5 cited
Analysis of BMP3 Variants In The Causality of Ocular Coloboma
Research Square (Research Square)·2021Open Access
Analysis of BMP3 variants in the causality of ocular coloboma
2021Open Access
Genetics and therapy for pediatric eye diseases
EBioMedicine·2021· 12 citedOpen Access
The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning
Genes·2021· 8 citedOpen Access
Ocular coloboma: Genetic variants reveal a dynamic model of eye development
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2020· 30 cited
Pleiotropy in <i>FOXC1</i> -attributable phenotypes involves altered ciliation and cilia-dependent signaling
2020Open Access
The Axenfeld-Rieger syndrome gene <i>FOXC1</i> contributes to left-right patterning
2020Open Access
Evidence for a cilia component in Axenfeld-Rieger Syndrome
Investigative Ophthalmology & Visual Science·2019· 1 citedOpen Access
Mutation of Bmp3 represents a novel cause of ocular coloboma
Investigative Ophthalmology & Visual Science·2019Open Access
foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish
Developmental Biology·2019· 68 cited
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Human Molecular Genetics·2018· 66 citedOpen Access
Morphogenesis and differentiation of embryonic vascular smooth muscle cells in zebrafish
2018· 1 citedOpen Access
Targeted next generation amplicon sequencing for candidate genes of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Investigative Ophthalmology & Visual Science·2018Open Access
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Frequent Co-authors

Andrew J. Waskiewicz(12), Curtis R. French(9), Shomi S. Bhattacharya(8), Roger A. Hitchings(7), Tim Jordan(6), Neil D. Ebenezer(6), Louise Ocaka(6), Mika Asai-Coakwell(5), Michael A. Walter(5), Peng T. Khaw(5), W. Ted Allison(4), Sue Povey(4), Anne H. Child(4), Glen Brice(4), Jane C. Sowden(3), Periasamy Sundaresan(3), Philip J. Gage(3), Tsutomu Kume(3), Tin Aung(3), J I McGill(3)