Phonon triggered rhombohedral lattice distortion in vanadium at high pressure von Antonangeli, Daniele, Farber, Daniel L., Bosak, Alexei, Aracne, Chantel M., Ruddle, David G., Krisch, Michael

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Elasticity of hexagonal-closed-packed cobalt at high pressure and temperature: a quasiharmonic case von Antonangeli, Daniele, Krisch, Michael, Farber, Daniel L, Ruddle, David G, Fiquet, Guillaume

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Gas transport across the low-permeability containment zone of an underground nuclear explosion von Carrigan, Charles R., Sun, Yunwei, Hunter, Steven L., Ruddle, David G., Simpson, Matthew D., Obi, Curtis M., Huckins-Gang, Heather E., Prothro, Lance B., Townsend, Margaret J.

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Delayed signatures of underground nuclear explosions von Carrigan, Charles R., Sun, Yunwei, Hunter, Steven L., Ruddle, David G., Wagoner, Jeffrey L., Myers, Katherine B. L., Emer, Dudley F., Drellack, Sigmund L., Chipman, Veraun D.

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Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness von Lu, Yi, Dimasi, David P, Hysi, Pirro G, Hewitt, Alex W, Burdon, Kathryn P, Toh, Tze'Yo, Ruddle, Jonathan B, Li, Yi Ju, Mitchell, Paul, Healey, Paul R, Montgomery, Grant W, Hansell, Narelle, Spector, Timothy D, Martin, Nicholas G, Young, Terri L, Hammond, Christopher J, Macgregor, Stuart, Craig, Jamie E, Mackey, David A

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Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma von MacGregor, Stuart, Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Zhou, Tiger, Siggs, Owen M., Law, Matthew H., Souzeau, Emmanuelle, Sharma, Shiwani, Lynn, David J., Beesley, Jonathan, Sheldrick, Bronwyn, Mills, Richard A., Landers, John, Ruddle, Jonathan B., Graham, Stuart L., Healey, Paul R., White, Andrew J. R., Casson, Robert J., Best, Stephen, Grigg, John R, Goldberg, Ivan, Powell, Joseph E., Whiteman, David C., Radford-Smith, Graham L., Martin, Nicholas G., Montgomery, Grant W., Burdon, Kathryn P., Mackey, David A., Gharahkhani, Puya, Craig, Jamie E., Hewitt, Alex W.

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Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma von Gharahkhani, Puya, Burdon, Kathryn P, Fogarty, Rhys, Sharma, Shiwani, Hewitt, Alex W, Martin, Sarah, Law, Matthew H, Cremin, Katie, Bailey, Jessica N Cooke, Loomis, Stephanie J, Pasquale, Louis R, Haines, Jonathan L, Hauser, Michael A, Viswanathan, Ananth C, McGuffin, Peter, Topouzis, Fotis, Foster, Paul J, Graham, Stuart L, Casson, Robert J, Chehade, Mark, White, Andrew J, Zhou, Tiger, Souzeau, Emmanuelle, Landers, John, Fitzgerald, Jude T, Klebe, Sonja, Ruddle, Jonathan B, Goldberg, Ivan, Healey, Paul R, Mills, Richard A, Wang, Jie Jin, Montgomery, Grant W, Martin, Nicholas G, Radford-Smith, Graham, Whiteman, David C, Brown, Matthew A, Wiggs, Janey L, Mackey, David A, Mitchell, Paul, MacGregor, Stuart, Craig, Jamie E

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Patient experiences and perceived value of genetic testing in inherited retinal diseases: a cross-sectional survey von Britten-Jones, Alexis Ceecee, Schultz, Joshua, Mack, Heather G., Kearns, Lisa S., Huq, Aamira J., Ruddle, Jonathan B., Mackey, David A., Hewitt, Alex W., Edwards, Thomas L., Ayton, Lauren N.

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Establishing risk of vision loss in Leber hereditary optic neuropathy von Lopez Sanchez, M. Isabel G., Kearns, Lisa S., Staffieri, Sandra E., Clarke, Linda, McGuinness, Myra B., Meteoukki, Wafaa, Samuel, Sona, Ruddle, Jonathan B., Chen, Celia, Fraser, Clare L., Harrison, John, Hewitt, Alex W., Howell, Neil, Mackey, David A.

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Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low? von Mackey, David A., Ong, Jue-Sheng, MacGregor, Stuart, Whiteman, David C., Craig, Jamie E., Lopez Sanchez, M. Isabel G., Kearns, Lisa S., Staffieri, Sandra E., Clarke, Linda, McGuinness, Myra B., Meteoukki, Wafaa, Samuel, Sona, Ruddle, Jonathan B., Chen, Celia, Fraser, Clare L., Harrison, John, Howell, Neil, Hewitt, Alex W.

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Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness von Davidson, Alice E, Cheong, Sek-Shir, Hysi, Pirro G, Venturini, Cristina, Plagnol, Vincent, Ruddle, Jonathan B, Ali, Hala, Carnt, Nicole, Gardner, Jessica C, Hassan, Hala, Gade, Else, Kearns, Lisa, Jelsig, Anne Marie, Restori, Marie, Webb, Tom R, Laws, David, Cosgrove, Michael, Hertz, Jens M, Russell-Eggitt, Isabelle, Pilz, Daniela T, Hammond, Christopher J, Tuft, Stephen J, Hardcastle, Alison J

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X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development von Webb, Tom R., Matarin, Mar, Gardner, Jessica C., Kelberman, Dan, Hassan, Hala, Ang, Wei, Michaelides, Michel, Ruddle, Jonathan B., Pennell, Craig E., Yazar, Seyhan, Khor, Chiea C., Aung, Tin, Yogarajah, Mahinda, Robson, Anthony G., Holder, Graham E., Cheetham, Michael E., Traboulsi, Elias I., Moore, Anthony T., Sowden, Jane C., Sisodiya, Sanjay M., Mackey, David A., Tuft, Stephen J., Hardcastle, Alison J.

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ProxTom Lymphatic Vessel Reporter Mice Reveal Prox1 Expression in the Adrenal Medulla, Megakaryocytes, and Platelets von Truman, Lucy A, Bentley, Kevin L, Smith, Elenoe C, Massaro, Stephanie A, Gonzalez, David G, Haberman, Ann M, Hill, Myriam, Jones, Dennis, Min, Wang, Krause, Diane S, Ruddle, Nancy H

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Genome-wide association identifies ATOH7 as a major gene determining human optic disc size von Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J., Mackey, David A.

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Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations von Ragge, Nicola K., Brown, Alison G., Poloschek, Charlotte M., Lorenz, Birgit, Henderson, R. Alex, Clarke, Michael P., Russell-Eggitt, Isabelle, Fielder, Alistair, Gerrelli, Dianne, Martinez-Barbera, Juan Pedro, Ruddle, Piers, Hurst, Jane, Collin, J. Richard O., Salt, Alison, Cooper, Simon T., Thompson, Pamela J., Sisodiya, Sanjay M., Williamson, Kathleen A., FitzPatrick, David R., Heyningen, Veronica van, Hanson, Isabel M.

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Effect of Display Resolution on Time to Diagnosis with Virtual Pathology Slides in a Systematic Search Task von Randell, Rebecca, Ambepitiya, Thilina, Mello-Thoms, Claudia, Ruddle, Roy A., Brettle, David, Thomas, Rhys G., Treanor, Darren

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Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins von Mackey, David A., MacKinnon, Jane R., Brown, Shayne A., Kearns, Lisa S., Ruddle, Jonathan B., Sanfilippo, Paul G., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G., Hewitt, Alex W.

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Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect von Shaaban, Sherin, MacKinnon, Sarah, Andrews, Caroline, Staffieri, Sandra E, Maconachie, Gail D E, Chan, Wai-Man, Whitman, Mary C, Morton, Sarah U, Yazar, Seyhan, MacGregor, Stuart, Elder, James E, Traboulsi, Elias I, Gottlob, Irene, Hewitt, Alex W, Hunter, David G, Mackey, David A, Engle, Elizabeth C

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Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey von Mack, Heather G, Chen, Fred K, Grigg, John, Jamieson, Robyn, De Roach, John, O’Hare, Fleur, Britten-Jones, Alexis Ceecee, McGuinness, Myra, Tindill, Nicole, Ayton, Lauren

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Incidence and predictors of glaucoma following surgery for congenital cataract in the first year of life in Victoria, Australia von Ruddle, Jonathan B, Staffieri, Sandra E, Crowston, Jonathan G, Sherwin, Justin C, Mackey, David A

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