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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.

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.

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.

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.

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.

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.

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.

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.

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.

Retinal Cell Biology August 2013

Molecular Mechanisms Regulating Ocular Apoptosis in Zebrafish gdf6a Mutants

PDF

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. 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

PDF

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. 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.

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.

ARVO Annual Meeting Abstract April 2009

Characterization of a Novel Bmp Ligand in Ocular Disease

M. Ye; K. Berry; M. Asai-Coakwell; A. J. Waskiewicz; O. J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):2327.

ARVO Annual Meeting Abstract April 2009

18q Deletion Syndrome: Finding the Causative Gene for Ocular Phenotypes

K. M. Berry; O. J. Lehmann; A. J. Waskiewicz

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):1652.

ARVO Annual Meeting Abstract May 2008

A Novel Mechanistic Spectrum Underlies Glaucoma-Associated Chromosome 6p25 Copy Number Variations

B. Chanda; M. Asai-Coakwell; J. C. Sowden; M. A. Walter; O. J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):1654.

ARVO Annual Meeting Abstract May 2008

Phenotypic Variability and Incomplete Penetrance Are Features of GDF6 Mutations

M. Asai-Coakwell; C. R. French; M. Ye; S. Mema; B. Chanda; P. Sundaresun; V. van Heyningen; A. Waskiewicz; O. J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):4008.

ARVO Annual Meeting Abstract May 2007

Progress Determining the Mechanism of Segmental Duplication and Deletion in Axenfeld Rieger Phenotypes

B. Chanda; M. Asai-Coakwell; M. Ye; J. C. Sowden; M. A. Walter; O. J. Lehmann

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5598.

Glaucoma November 2006

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

PDF

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. 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

PDF

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. https://doi.org/10.1167/iovs.04-1133

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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

Characterization of a Novel Bmp Ligand in Ocular Disease

18q Deletion Syndrome: Finding the Causative Gene for Ocular Phenotypes

A Novel Mechanistic Spectrum Underlies Glaucoma-Associated Chromosome 6p25 Copy Number Variations

Phenotypic Variability and Incomplete Penetrance Are Features of GDF6 Mutations

Progress Determining the Mechanism of Segmental Duplication and Deletion in Axenfeld Rieger Phenotypes

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

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