1. A genome‐wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes. Issue 7 (4th September 2018) Authors: Meng, Weihua; Shah, Kaanan P.; Pollack, Samuela; Toppila, Iiro; Hebert, Harry L.; McCarthy, Mark I.; Groop, Leif; Ahlqvist, Emma; Lyssenko, Valeriya; Agardh, Elisabet; Daniell, Mark; Kaidonis, Georgia; Craig, Jamie E.; Mitchell, Paul; Liew, Gerald; Kifley, Annette; Wang, Jie Jin; Christiansen, Ma... Journal: Acta ophthalmologica Issue: Volume 96:Issue 7(2018) Page Start: e811 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome. (May 2016) Authors: Sharma, Shiwani; Martin, Sarah; Sykes, Matthew J.; Dave, Alpana; Hewitt, Alex W.; Burdon, Kathryn P.; Ronci, Maurizio; Voelcker, Nicolas H.; Craig, Jamie E. Journal: Experimental eye research Issue: Volume 146(2016:May) Page Start: 212 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome. (May 2016) Authors: Sharma, Shiwani; Martin, Sarah; Sykes, Matthew J.; Dave, Alpana; Hewitt, Alex W.; Burdon, Kathryn P.; Ronci, Maurizio; Voelcker, Nicolas H.; Craig, Jamie E. Journal: Experimental eye research Issue: Volume 146(2016:May) Page Start: 212 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort. Issue 10 (19th August 2022) Authors: Souzeau, Emmanuelle; Siggs, Owen M.; Mullany, Sean; Schmidt, Joshua M.; Hassall, Mark M.; Dubowsky, Andrew; Chappell, Angela; Breen, James; Bae, Haae; Nicholl, Jillian; Hadler, Johanna; Kearns, Lisa S.; Staffieri, Sandra E.; Hewitt, Alex W.; Mackey, David A.; Gupta, Aanchal; Burdon, Kathryn P.; K... Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 10(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophy. (September 2021) Authors: Kuot, Abraham; Corbett, Mark A.; Mills, Richard A.; Snibson, Grant; Wiffen, Steven; Loh, Raymond; Burdon, Kathryn P.; Craig, Jamie E.; Sharma, Shiwani Journal: Experimental eye research Issue: Volume 210(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma. (4th March 2018) Authors: Burdon, Kathryn P.; Awadalla, Mona S.; Mitchell, Paul; Wang, Jie Jin; White, Andrew; Keane, Miriam C.; Souzeau, Emmanuelle; Graham, Stuart L.; Goldberg, Ivan; Healey, Paul R.; Landers, John; Mills, Richard A. D.; Best, Stephen; Hewitt, Alex W.; Sharma, Shiwani; Craig, Jamie E. Journal: Ophthalmic genetics Issue: Volume 39:Number 2(2018) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Epha2 genotype influences ultraviolet radiation induced cataract in mice. (November 2019) Authors: Dave, Alpana; Craig, Jamie E.; Skrzypiec, Karina; Quinn, Stephen; Barnes, Mary; Di Girolamo, Nick; Mackey, David A.; Burdon, Kathryn P.; de Iongh, Robb U.; Sharma, Shiwani Journal: Experimental eye research Issue: Volume 188(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome. (4th March 2017) Authors: Yazar, Seyhan; Franchina, Maria; Craig, Jamie E.; Burdon, Kathryn P.; Mackey, David A. Journal: Ophthalmic genetics Issue: Volume 38:Number 2(2017) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Human Lipoxygenase Pathway Gene Variation and Association with Markers of Subclinical Atherosclerosis in the Diabetes Heart Study. (31st May 2010) Authors: Burdon, Kathryn P.; Rudock, Megan E.; Lehtinen, Allison B.; Langefeld, Carl D.; Bowden, Donald W.; Register, Thomas C.; Liu, Yongmei; Freedman, Barry I.; Carr, J. Jeffrey; Hedrick, Catherine C.; Rich, Stephen S. Other Names: Gualillo Oreste Academic Editor. Journal: Mediators of inflammation Issue: Volume 2010(2010) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Identification of a Novel Oligomerization Disrupting Mutation in CRYΑA Associated with Congenital Cataract in a South Australian Family. Issue 3 (17th January 2013) Authors: Laurie, Kate J.; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy; Sykes, Matthew J.; Casey, Theresa; Teo, Theodosia; Pater, John; Craig, Jamie E.; Sharma, Shiwani; Burdon, Kathryn P. Journal: Human mutation Issue: Volume 34:Issue 3(2013:Mar.) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗