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ARVO Annual Meeting Abstract July 2019

Evidence for a cilia component in Axenfeld-Rieger Syndrome

Ordan J Lehmann; Paul Chrystal; Suey Van Baarle; Andrew Waskiewicz; Serhiy Havrylov

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):1617. doi:

ARVO Annual Meeting Abstract July 2019

Mutation of Bmp3 represents a novel cause of ocular coloboma

Lisa Prichard; Sonya Widen; Ordan J Lehmann; Andrew Waskiewicz

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):6028. doi:

ARVO Annual Meeting Abstract July 2018

Pigment Dispersion Syndrome and Pigmentary Glaucoma Associated Variants in Premelanosome Protein ( PMEL ) Cause Protein Processing and Fibrillogenesis Defects

Adrian Lahola-Chomiak; Baojian Fan; Tim Footz; David S Greenfield; Robert Ritch; Jamie E. Craig; Janey L Wiggs; Ordan J Lehmann; Michael A Walter

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3020. doi:

ARVO Annual Meeting Abstract July 2018

Targeted next generation amplicon sequencing for candidate genes of Pigment Dispersion Syndrome and Pigmentary Glaucoma

Tim Footz; Adrian Lahola-Chomiak; Ordan J Lehmann; Janey L Wiggs; Michael A Walter

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5140. doi:

ARVO Annual Meeting Abstract July 2018

Dissecting the Role of the Premelanosome Protein Gene ( PMEL ) in the Development of Pigmentary Glaucoma Using the Zebrafish Animal Model

Kim Nguyen-Phuoc; Gavin Neil; Tim Footz; Adrian Lahola-Chomiak; Ordan J Lehmann; Michael A Walter; W. Ted Allison

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5156. doi:

ARVO Annual Meeting Abstract June 2017

Genetic Etiology of Pigmentary Dispersion Syndrome/Pigmentary Glaucoma

Adrian Alexander Lahola-Chomiak; Tim Footz; Thien-Kim Nguyen-Phuoc; Ordan J Lehmann; Michael A Walter

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2131. doi:

ARVO Annual Meeting Abstract September 2016

Whole exome sequencing identifies new candidate genes for Pigment Dispersion Syndrome

Tim Footz; Ordan J Lehmann; Michael A Walter

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):795. doi:

ARVO Annual Meeting Abstract June 2015

Identification of a novel cause of ocular coloboma

Sonya Widen; Prajakta Desai; Mika Asai-Coakwell; Matthew Benson; Curtis French; Ordan J Lehmann; Andrew Waskiewicz

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):900. doi:

ARVO Annual Meeting Abstract April 2014

Additional complexities in Axenfeld-Rieger Syndrome - implications for pediatric glaucoma

Ordan J Lehmann; Mika Asai-Coakwell; Hardeep Singh; Erin Strachan

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3797. doi:

Retinal Cell Biology August 2013

Molecular Mechanisms Regulating Ocular Apoptosis in Zebrafish gdf6a Mutants

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Sameer D. Pant; Lindsey D. March; Jakub K. Famulski; Curtis R. French; Ordan J. Lehmann; Andrew J. Waskiewicz
TAGS: apoptosis, zebrafish, proteins, mitogen-activated protein kinase p38, caspase-3
Invest. Ophthalmol. Vis. Sci.. 2013; 54(8):5871-5879. doi: https://doi.org/10.1167/iovs.12-11315

Includes: Supplemental Content

Retinal Cell Biology July 2013

Apoptotic and Proliferative Defects Characterize Ocular Development in a Microphthalmic BMP Model

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Curtis R. French; Tara R. Stach; Lindsey D. March; Ordan J. Lehmann; Andrew J. Waskiewicz
TAGS: embryo, eye, eye development, genes, microphthalmos, zebrafish, apoptosis, stem cells, transcription factor
Invest. Ophthalmol. Vis. Sci.. 2013; 54(7):4636-4647. doi: https://doi.org/10.1167/iovs.13-11674

Includes: Supplemental Content

ARVO Annual Meeting Abstract March 2012

Molecular Mechanisms Underlying Increased Ocular Apoptosis Observed In gdf6a-/- Zebrafish During Development

Sameer D. Pant; Lindsey D. March; Curtis R. French; Andrew J. Waskiewicz; Ordan J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4529. doi:

ARVO Annual Meeting Abstract March 2012

Examining the contribution of Growth differentiation factor 6 (GDF6) to retinal dystrophies

Mika Asai-Coakwell; Xiao Hua Dai; Lindsey March; Elfride De Baere; Peter J. Francis; Yves Sauve; W Ted Allison; Robert K. Koenekoop; Andrew Waskiewicz; Ordan J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):4530. doi:

Glaucoma November 2006

Reduced Human and Murine Corneal Thickness in an Axenfeld-Rieger Syndrome Subtype

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Mika Asai-Coakwell; Christopher Backhouse; Ronald J. Casey; Philip J. Gage; Ordan J. Lehmann
TAGS: cornea, syndrome, mutation, glaucoma
Invest. Ophthalmol. Vis. Sci.. 2006; 47(11):4905-4909. doi: https://doi.org/10.1167/iovs.06-0457

Glaucoma August 2005

Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene

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Tin Aung; Tayebeh Rezaie; Koji Okada; Ananth C. Viswanathan; Anne H. Child; Glen Brice; Shomi S. Bhattacharya; Ordan J. Lehmann; Mansoor Sarfarazi; Roger A. Hitchings
TAGS: genes, glaucoma, mutation, optn gene, visual fields
Invest. Ophthalmol. Vis. Sci.. 2005; 46(8):2816-2822. doi: https://doi.org/10.1167/iovs.04-1133

Glaucoma June 2003

Novel Anterior Segment Phenotypes Resulting from Forkhead Gene Alterations: Evidence for Cross-Species Conservation of Function

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Ordan J. Lehmann; Stephen Tuft; Glen Brice; Richard Smith; Åsa Blixt; Rachel Bell; Bengt Johansson; Tim Jordan; Roger A. Hitchings; Peng T. Khaw; Simon W. M. John; Peter Carlsson; Shomi S. Bhattacharya
TAGS: genes, phenotype, mutation, glaucoma, foxc2 gene, cornea
Invest. Ophthalmol. Vis. Sci.. 2003; 44(6):2627-2633. doi: https://doi.org/10.1167/iovs.02-0609

Glaucoma June 2002

Ocular Developmental Abnormalities and Glaucoma Associated with Interstitial 6p25 Duplications and Deletions

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Ordan J. Lehmann; Neil D. Ebenezer; Rosemary Ekong; Louise Ocaka; Andrew J. Mungall; Scott Fraser; James I. McGill; Roger A. Hitchings; Peng T. Khaw; Jane C. Sowden; Sue Povey; Michael A. Walter; Shomi S. Bhattacharya; Tim Jordan
TAGS: congenital abnormality, genetic pedigree, genotype determination, glaucoma, chromosome abnormality, immune reconstitution inflammatory syndrome, phenotype, genes
Invest. Ophthalmol. Vis. Sci.. 2002; 43(6):1843-1849. doi:

Biochemistry and Molecular Biology December 2001

A Novel Keratocan Mutation Causing Autosomal Recessive Cornea Plana

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Ordan J. Lehmann; Mohamed F. El-ashry; Neil D. Ebenezer; Louise Ocaka; Peter J. Francis; Susan E. Wilkie; Reshma J. Patel; Linda Ficker; Tim Jordan; Peng T. Khaw; Shomi S. Bhattacharya
TAGS: autosomal recessive inheritance, cornea, mutation, proteins
Invest. Ophthalmol. Vis. Sci.. 2001; 42(13):3118-3122. doi:

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Evidence for a cilia component in Axenfeld-Rieger Syndrome

Mutation of Bmp3 represents a novel cause of ocular coloboma

Pigment Dispersion Syndrome and Pigmentary Glaucoma Associated Variants in Premelanosome Protein ( PMEL ) Cause Protein Processing and Fibrillogenesis Defects

Targeted next generation amplicon sequencing for candidate genes of Pigment Dispersion Syndrome and Pigmentary Glaucoma

Dissecting the Role of the Premelanosome Protein Gene ( PMEL ) in the Development of Pigmentary Glaucoma Using the Zebrafish Animal Model

Genetic Etiology of Pigmentary Dispersion Syndrome/Pigmentary Glaucoma

Whole exome sequencing identifies new candidate genes for Pigment Dispersion Syndrome

Identification of a novel cause of ocular coloboma

Additional complexities in Axenfeld-Rieger Syndrome - implications for pediatric glaucoma

Molecular Mechanisms Regulating Ocular Apoptosis in Zebrafish gdf6a Mutants

Apoptotic and Proliferative Defects Characterize Ocular Development in a Microphthalmic BMP Model

Molecular Mechanisms Underlying Increased Ocular Apoptosis Observed In gdf6a-/- Zebrafish During Development

Examining the contribution of Growth differentiation factor 6 (GDF6) to retinal dystrophies

Reduced Human and Murine Corneal Thickness in an Axenfeld-Rieger Syndrome Subtype

Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene

Novel Anterior Segment Phenotypes Resulting from Forkhead Gene Alterations: Evidence for Cross-Species Conservation of Function

Ocular Developmental Abnormalities and Glaucoma Associated with Interstitial 6p25 Duplications and Deletions

A Novel Keratocan Mutation Causing Autosomal Recessive Cornea Plana

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