Publications by authors named "David Dimasi"

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No Strong Association between the Apolipoprotein E E4 Allele and Glaucoma: A Multicohort Study.
Sean Mullany, Santiago Diaz-Torres, Joshua M Schmidt, Daniel Thomson, Ayub Qassim, David Dimasi

Ophthalmol Sci· September 2023

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The E4 Allele Is Associated with Faster Rates of Neuroretinal Thinning in a Prospective Cohort Study of Suspect and Early Glaucoma.
Sean Mullany, Henry Marshall, Santiago Diaz-Torres, Ella C Berry, Joshua M Schmidt, David Dimasi

Ophthalmol Sci· June 2022

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RNA Sequencing of Lens Capsular Epithelium Implicates Novel Pathways in Pseudoexfoliation Syndrome.
Sean Mullany, Henry Marshall, Tiger Zhou, Daniel Thomson, Joshua M Schmidt, David Dimasi

Invest Ophthalmol Vis Sci· March 2022

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Colonic migrating motor complexes are inhibited in acute tri-nitro benzene sulphonic acid colitis.
Ben R Hofma, Hannah R Wardill, Chris Mavrangelos, Melissa A Campaniello, David Dimasi

PLoS One· April 2019

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Fluid-induced lung injury-role of TRPV4 channels.
Shailesh Bihari, Dani-Louise Dixon, Mark D Lawrence, Dylan De Bellis, Claudine S Bonder, David P Dimasi

Pflugers Arch· September 2017

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Topical Application of Fingolimod Perturbs Cutaneous Inflammation.
Wai Y Sun, David P Dimasi, Melissa R Pitman, YiZhong Zhuang, Robert Heddle

J Immunol· May 2016

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Examining the Role of Sphingosine Kinase-2 in the Regulation of Endothelial Cell Barrier Integrity.
David P Dimasi, Stuart M Pitson, Claudine S Bonder

Microcirculation· April 2016

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Dengue Virus Infection of Primary Endothelial Cells Induces Innate Immune Responses, Changes in Endothelial Cells Function and Is Restricted by Interferon-Stimulated Responses.
Julie K Calvert, Karla J Helbig, David Dimasi, Michaelia Cockshell, Michael R Beard

J Interferon Cytokine Res· August 2015

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Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region.
Glyn Chidlow, John P M Wood, Shiwani Sharma, David P Dimasi, Kathryn P Burdon

PLoS One· June 2014

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Neutrophil interactions with the vascular endothelium.
David Dimasi, Wai Y Sun, Claudine S Bonder

Int Immunopharmacol· December 2013

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The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in caucasians with primary open angle glaucoma.
Janey L Wiggs, Alex W Hewitt, Bao Jian Fan, Dan Yi Wang, Dayse R Figueiredo Sena, David P Dimasi

PLoS One· May 2013

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Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
Yi Lu, Veronique Vitart, Kathryn P Burdon, Chiea Chuen Khor, Yelena Bykhovskaya, David P Dimasi

Nat Genet· February 2013

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Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma.
David P Dimasi, Kathryn P Burdon, Alex W Hewitt, Jude Fitzgerald, Jie Jin Wang

Am J Ophthalmol· November 2012

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Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye.
Shiwani Sharma, Kathryn P Burdon, Glyn Chidlow, Sonja Klebe, April Crawford, David P Dimasi

Invest Ophthalmol Vis Sci· July 2012

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Ethnic and mouse strain differences in central corneal thickness and association with pigmentation phenotype.
David P Dimasi, Alex W Hewitt, Kenneth Kagame, Sam Ruvama, Ludovica Tindyebwa

PLoS One· December 2011

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Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
Yi Lu, David P Dimasi, Pirro G Hysi, Alex W Hewitt, Kathryn P Burdon

PLoS Genet· May 2010

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Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.
David P Dimasi, Kathryn P Burdon, Alex W Hewitt, Ravi Savarirayan, Paul R Healey

Mol Vis· March 2010

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Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.
David P Dimasi, Jern Y Chen, Alex W Hewitt, Sonja Klebe, Richard Davey

Hum Genet· January 2010

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Heritability of central corneal thickness in nuclear families.
John A Landers, Alex W Hewitt, David P Dimasi, Jac C Charlesworth, Tania Straga

Invest Ophthalmol Vis Sci· September 2009

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Functional and structural implications of the complement factor H Y402H polymorphism associated with age-related macular degeneration.
Rebecca J Ormsby, Shoba Ranganathan, Joo Chuan Tong, Kim M Griggs, David P Dimasi

Invest Ophthalmol Vis Sci· May 2008

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Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.
Alex W Hewitt, Shiwani Sharma, Kathryn P Burdon, Jie Jin Wang, Paul N Baird, David P Dimasi

Hum Mol Genet· March 2008

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Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma.
Chandrakumar Balaratnasingam, William H Morgan, John Nelson, David A Mackey, David P Dimasi

Ophthalmic Genet· September 2007

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A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site.
Kathryn P Burdon, Shiwani Sharma, Celia S Chen, David P Dimasi, David A Mackey

Hum Mutat· July 2007

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Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epithelium.
Shiwani Sharma, David Dimasi, Stefan Bröer, Raman Kumar, Neil G Della

Exp Cell Res· April 2007

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Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals.
Alex W Hewitt, Sonya L Bennett, Julia E Richards, David P Dimasi, Adam P Booth

Arch Ophthalmol· January 2007

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