Role of the Hepatocyte Growth Factor Gene in Refractive Error von Veerappan, Sundar, Pertile, Kelly K, Islam, Amirul F.M., PhD, Schäche, Maria, PhD, Chen, Christine Y., PhD, MBBS, Mitchell, Paul, MD, PhD, Dirani, Mohamed, PhD, Baird, Paul N., PhD

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The GEnes in Myopia (GEM) study in understanding the aetiology of refractive errors von Baird, Paul N., Schäche, Maria, Dirani, Mohamed

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Association of the hepatocyte growth factor gene with keratoconus in an Australian population von Sahebjada, Srujana, Schache, Maria, Richardson, Andrea J, Snibson, Grant, Daniell, Mark, Baird, Paul N

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Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort von Schache, Maria, Baird, Paul N

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Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci von Simpson, Claire L, Wojciechowski, Robert, Oexle, Konrad, Murgia, Federico, Portas, Laura, Li, Xiaohui, Verhoeven, Virginie J M, Vitart, Veronique, Schache, Maria, Hosseini, S Mohsen, Hysi, Pirro G, Raffel, Leslie J, Cotch, Mary Frances, Chew, Emily, Klein, Barbara E K, Klein, Ronald, Wong, Tien Yin, van Duijn, Cornelia M, Mitchell, Paul, Saw, Seang Mei, Fossarello, Maurizio, Wang, Jie Jin, Polašek, Ozren, Campbell, Harry, Rudan, Igor, Oostra, Ben A, Uitterlinden, André G, Hofman, Albert, Rivadeneira, Fernando, Amin, Najaf, Karssen, Lennart C, Vingerling, Johannes R, Döring, Angela, Bettecken, Thomas, Bencic, Goran, Gieger, Christian, Wichmann, H-Erich, Wilson, James F, Venturini, Cristina, Fleck, Brian, Cumberland, Phillippa M, Rahi, Jugnoo S, Hammond, Chris J, Hayward, Caroline, Wright, Alan F, Paterson, Andrew D, Baird, Paul N, Klaver, Caroline C W, Rotter, Jerome I, Pirastu, Mario, Meitinger, Thomas, Bailey-Wilson, Joan E, Stambolian, Dwight

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High Glucose-Induced Thioredoxin-Interacting Protein in Renal Proximal Tubule Cells Is Independent of Transforming Growth Factor-β1 von Qi, Weier, Chen, Xinming, Gilbert, Richard E, Zhang, Yuan, Waltham, Mark, Schache, Maria, Kelly, Darren J, Pollock, Carol A

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The Australian Twin Registry as a Resource For Genetic Studies into Ophthalmic Traits von Schache, Maria, Baird, Paul N.

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Genetic Association of Refractive Error and Axial Length with 15q14 but Not 15q25 in the Blue Mountains Eye Study Cohort von Schache, Maria, BSc(Hons), PhD, Richardson, Andrea J., BSc(Hons), Mitchell, Paul, MD, PhD, Wang, Jie Jin, MMed, PhD, Rochtchina, Elena, BSc, MApplStat, Viswanathan, Ananth C., MD, PhD, Wong, Tien Y., MD, PhD, Saw, Seang Mei, MBBS, PhD, Topouzis, Fotis, MD, PhD, Xie, Jing, MD, PhD, Sim, Xueling, BSc, PhD, Holliday, Elizabeth G., MBiostatistics, PhD, Attia, John, MD, PhD, Scott, Rodney J., BSc, PhD, Baird, Paul N., BSc, PhD

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Assessment of TGIF as a Candidate Gene for Myopia von Pertile, Kelly K, Schache, Maria, Islam, F. M. Amirul, Chen, Christine Y, Dirani, Mohamed, Mitchell, Paul, Baird, Paul N

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Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12 von Schäche, Maria, Chen, Christine Y, Pertile, Kelly Kathleen, Richardson, Andrea Jane, Dirani, Mohamed, Mitchell, Paul, Baird, Paul Nigel

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Genetic Mapping of Myopia Susceptibility Loci von Schache, Maria, Richardson, Andrea J, Pertile, Kelly K, Dirani, Mohamed, Scurrah, Katrina, Baird, Paul N

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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error von Tedja, Milly S., Wojciechowski, Robert, Hysi, Pirro G., Eriksson, Nicholas, Furlotte, Nicholas A., Verhoeven, Virginie J. M., Iglesias, Adriana I., Meester-Smoor, Magda A., Tompson, Stuart W., Fan, Qiao, Khawaja, Anthony P., Cheng, Ching-Yu, Höhn, René, Yamashiro, Kenji, Wenocur, Adam, Grazal, Clare, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Jonas, Jost B., Wang, Ya Xing, Xie, Jing, Mitchell, Paul, Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Paterson, Andrew D., Hosseini, S. Mohsen, Shah, Rupal L., Williams, Cathy, Teo, Yik Ying, Tham, Yih Chung, Gupta, Preeti, Zhao, Wanting, Shi, Yuan, Saw, Woei-Yuh, Tai, E-Shyong, Sim, Xue Ling, Huffman, Jennifer E., Polašek, Ozren, Hayward, Caroline, Bencic, Goran, Rudan, Igor, Wilson, James F., Joshi, Peter K., Tsujikawa, Akitaka, Matsuda, Fumihiko, Whisenhunt, Kristina N., Zeller, Tanja, van der Spek, Peter J., Haak, Roxanna, Meijers-Heijboer, Hanne, van Leeuwen, Elisabeth M., Iyengar, Sudha K., Lass, Jonathan H., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, André G., Vingerling, Johannes R., Lehtimäki, Terho, Raitakari, Olli T., Biino, Ginevra, Concas, Maria Pina, Schwantes-An, Tae-Hwi, Igo, Robert P., Cuellar-Partida, Gabriel, Martin, Nicholas G., Craig, Jamie E., Gharahkhani, Puya, Williams, Katie M., Nag, Abhishek, Rahi, Jugnoo S., Cumberland, Phillippa M., Delcourt, Cécile, Bellenguez, Céline, Ried, Janina S., Bergen, Arthur A., Meitinger, Thomas, Gieger, Christian, Wong, Tien Yin, Hewitt, Alex W., Mackey, David A., Simpson, Claire L., Pfeiffer, Norbert, Pärssinen, Olavi, Baird, Paul N., Vitart, Veronique, Amin, Najaf, van Duijn, Cornelia M., Bailey-Wilson, Joan E., Young, Terri L., Saw, Seang-Mei, Stambolian, Dwight, MacGregor, Stuart, Guggenheim, Jeremy A., Tung, Joyce Y., Hammond, Christopher J., Klaver, Caroline C. W.

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia von Verhoeven, Virginie J M, Hysi, Pirro G, Wojciechowski, Robert, Guggenheim, Jeremy A, Höhn, René, MacGregor, Stuart, Hewitt, Alex W, Nag, Abhishek, Cheng, Ching-Yu, Yonova-Doing, Ekaterina, Zhou, Xin, Ikram, M Kamran, McMahon, George, Kemp, John P, Pourcain, Beate St, Simpson, Claire L, Mäkelä, Kari-Matti, Lehtimäki, Terho, Kähönen, Mika, Paterson, Andrew D, Hosseini, S Mohsen, Wong, Hoi Suen, Xu, Liang, Wedenoja, Juho, Yip, Shea Ping, Ho, Daniel W H, Pang, Chi Pui, Chen, Li Jia, Burdon, Kathryn P, Craig, Jamie E, Klein, Barbara E K, Klein, Ronald, Haller, Toomas, Metspalu, Andres, Khor, Chiea-Chuen, Tai, E-Shyong, Aung, Tin, Vithana, Eranga, Tay, Wan-Ting, Barathi, Veluchamy A, Chen, Peng, Li, Ruoying, Liao, Jiemin, Zheng, Yingfeng, Ong, Rick T, Döring, Angela, Evans, David M, Timpson, Nicholas J, Verkerk, Annemieke J M H, Meitinger, Thomas, Raitakari, Olli, Hawthorne, Felicia, Spector, Tim D, Pirastu, Mario, Murgia, Federico, Ang, Wei, Mishra, Aniket, Montgomery, Grant W, Pennell, Craig E, Cumberland, Phillippa M, Cotlarciuc, Ioana, Mitchell, Paul, Wang, Jie Jin, Schache, Maria, Janmahasatian, Sarayut, Jr, Robert P Igo, Lass, Jonathan H, Chew, Emily, Iyengar, Sudha K, Gorgels, Theo G M F, Rudan, Igor, Hayward, Caroline, Wright, Alan F, Polasek, Ozren, Vatavuk, Zoran, Wilson, James F, Fleck, Brian, Zeller, Tanja, Mirshahi, Alireza, Müller, Christian, Uitterlinden, André G, Rivadeneira, Fernando, Vingerling, Johannes R, Hofman, Albert, Oostra, Ben A, Amin, Najaf, Bergen, Arthur A B, Teo, Yik-Ying, Rahi, Jugnoo S, Vitart, Veronique, Williams, Cathy, Baird, Paul N, Oexle, Konrad, Pfeiffer, Norbert, Mackey, David A, Young, Terri L, Saw, Seang-Mei, Stambolian, Dwight, Klaver, Caroline C, Hammond, Christopher J

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Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error von Fan, Qiao, Verhoeven, Virginie J. M., Wojciechowski, Robert, Barathi, Veluchamy A., Hysi, Pirro G., Guggenheim, Jeremy A., Höhn, René, Vitart, Veronique, Khawaja, Anthony P., Yamashiro, Kenji, Hosseini, S Mohsen, Lehtimäki, Terho, Lu, Yi, Haller, Toomas, Xie, Jing, Delcourt, Cécile, Pirastu, Mario, Wedenoja, Juho, Gharahkhani, Puya, Venturini, Cristina, Miyake, Masahiro, Hewitt, Alex W., Guo, Xiaobo, Mazur, Johanna, Huffman, Jenifer E., Williams, Katie M., Polasek, Ozren, Campbell, Harry, Rudan, Igor, Vatavuk, Zoran, Wilson, James F., Joshi, Peter K., McMahon, George, St Pourcain, Beate, Evans, David M., Simpson, Claire L., Schwantes-An, Tae-Hwi, Igo, Robert P., Mirshahi, Alireza, Bellenguez, Céline, Blettner, Maria, Raitakari, Olli, Kähönen, Mika, Seppälä, Ilkka, Zeller, Tanja, Meitinger, Thomas, Ried, Janina S., Gieger, Christian, Portas, Laura, van Leeuwen, Elisabeth M., Amin, Najaf, Uitterlinden, André G., Rivadeneira, Fernando, Hofman, Albert, Vingerling, Johannes R., Wang, Ya Xing, Wang, Xu, Tai-Hui Boh, Eileen, Ikram, M. Kamran, Sabanayagam, Charumathi, Gupta, Preeti, Tan, Vincent, Zhou, Lei, Ho, Candice E. H., Lim, Wan’e, Beuerman, Roger W., Siantar, Rosalynn, Tai, E-Shyong, Vithana, Eranga, Mihailov, Evelin, Khor, Chiea-Chuen, Hayward, Caroline, Luben, Robert N., Foster, Paul J., Klein, Barbara E. K., Klein, Ronald, Wong, Hoi-Suen, Metspalu, Andres, Aung, Tin, Young, Terri L., He, Mingguang, Pärssinen, Olavi, van Duijn, Cornelia M., Jin Wang, Jie, Williams, Cathy, Jonas, Jost B., Teo, Yik-Ying, Mackey, David A., Oexle, Konrad, Yoshimura, Nagahisa, Paterson, Andrew D., Pfeiffer, Norbert, Wong, Tien-Yin, Baird, Paul N., Stambolian, Dwight, Wilson, Joan E. Bailey, Cheng, Ching-Yu, Hammond, Christopher J., Klaver, Caroline C. W., Saw, Seang-Mei

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Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population von Sahebjada, Srujana, Schache, Maria, Richardson, Andrea J, Snibson, Grant, MacGregor, Stuart, Daniell, Mark, Baird, Paul N

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Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error von Ikram, M. Kamran, Barathi, Veluchamy A., Kemp, John P., Wang, Ya Xing, Wright, Alan F., Amin, Najaf, Tay, Wan-Ting, Hayward, Caroline, Polasek, Ozren, Vatavuk, Zoran, Pang, Chi Pui, Wegner, Aharon, Yip, Shea Ping, Murgia, Federico, Portas, Laura, Ang, Wei, Fan, Qiao, Zhou, Xin, Iyengar, Sudha K., Vital, Mark, Yoo, Sonia, Maguire, Leo, McCulley, James, Renucci, Ann, Oliva, Matt, Brown, Marlene, Reeves, Sherman, Hamilton, Stephen, Kelly, Kathleen, Shaughnessy, Michael, Steinemann, Thomas, Mifflin, Mark, Chodosh, James, Galentine, Paul G., Mannis, Mark, Varma, Rohit, Wedenoja, Juho, Mirshahi, Alireza, Brown, Matthew A., Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S., Rautanen, Anna, Viswanathan, Ananth C., Giannoulatou, Eleni, Donnelly, Peter, Hammond, Naomi, McCann, Owen T., Ricketts, Michelle, Widaa, Sara, Yonova-Doing, Ekaterina, Klein, Ronald, Miller, D., Whitehouse, F., McLellan, M., Golden, E., Arrigg, P., Gauthier-Kelly, C., Lopes-Virella, M., Colwell, J., Farr, A., Elsing, S., Kaminski, L., Lorenzi, G., Johnsonbaugh, S., Liss, R., Gordon, J., Martin, C.L., Pop-Busui, R., Smith, A., Gothrup, J., Prosser, L., Schwartz, S., Maschak-Carey, B.J., Morrison, A., Meyer, D., Strowig, S., Gordon, A., Hokanson, J., Ginsberg, J., Van Ottingham, L., Harth, J., May, M., Adkins, T., White, N., Fradkin, J., Siebert, C., Danis, R., Dingledine, J., Chavers, B., Burzuk, B., Low, P., Wong, N., Fox, M., Clark, C., Zhang, L., Pang, Chi Pui, Inoko, Hidetoshi, Mitchell, Paul, Stambolian, Dwight

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Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium von Fan, Qiao, Guo, Xiaobo, Tideman, J. Willem L., Williams, Katie M., Yazar, Seyhan, Hosseini, S. Mohsen, Howe, Laura D., Pourcain, Beaté St, Evans, David M., Timpson, Nicholas J., McMahon, George, Hysi, Pirro G., Krapohl, Eva, Wang, Ya Xing, Jonas, Jost B., Baird, Paul Nigel, Wang, Jie Jin, Cheng, Ching-Yu, Teo, Yik-Ying, Wong, Tien-Yin, Ding, Xiaohu, Wojciechowski, Robert, Young, Terri L., Pärssinen, Olavi, Oexle, Konrad, Pfeiffer, Norbert, Bailey-Wilson, Joan E., Paterson, Andrew D., Klaver, Caroline C. W., Plomin, Robert, Hammond, Christopher J., Mackey, David A., He, Mingguang, Saw, Seang-Mei, Williams, Cathy, Guggenheim, Jeremy A.

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The Australian Twin Register as a resource for genetic studies into ophthalmic traits von Maria Schache, Paul N. Baird

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Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia von Miyake, Masahiro, Yamashiro, Kenji, Tabara, Yasuharu, Suda, Kenji, Morooka, Satoshi, Nakanishi, Hideo, Khor, Chiea-Chuen, Chen, Peng, Qiao, Fan, Nakata, Isao, Akagi-Kurashige, Yumiko, Gotoh, Norimoto, Tsujikawa, Akitaka, Meguro, Akira, Kusuhara, Sentaro, Polasek, Ozen, Hayward, Caroline, Wright, Alan F., Campbell, Harry, Richardson, Andrea J., Schache, Maria, Takeuchi, Masaki, Mackey, David A., Hewitt, Alex W., Cuellar, Gabriel, Shi, Yi, Huang, Luling, Yang, Zhenglin, Leung, Kim Hung, Kao, Patrick Y.P., Yap, Maurice K.H., Yip, Shea Ping, Moriyama, Muka, Ohno-Matsui, Kyoko, Mizuki, Nobuhisa, MacGregor, Stuart, Vitart, Veronique, Aung, Tin, Saw, Seang-Mei, Tai, E-Shyong, Wong, Tien Yin, Cheng, Ching-Yu, Baird, Paul N., Yamada, Ryo, Matsuda, Fumihiko, Yoshimura, Nagahisa

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Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error von Stambolian, Dwight, Wojciechowski, Robert, Oexle, Konrad, Pirastu, Mario, Li, Xiaohui, Raffel, Leslie J, Cotch, Mary Frances, Chew, Emily Y, Klein, Barbara, Klein, Ronald, Wong, Tien Y, Simpson, Claire L, Klaver, Caroline C W, van Duijn, Cornelia M, Verhoeven, Virginie J M, Baird, Paul N, Vitart, Veronique, Paterson, Andrew D, Mitchell, Paul, Saw, Seang Mei, Fossarello, Maurizio, Kazmierkiewicz, Krista, Murgia, Federico, Portas, Laura, Schache, Maria, Richardson, Andrea, Xie, Jing, Wang, Jie Jin, Rochtchina, Elena, Viswanathan, Ananth C, Hayward, Caroline, Wright, Alan F, Polasek, Ozren, Campbell, Harry, Rudan, Igor, Oostra, Ben A, Uitterlinden, André G, Hofman, Albert, Rivadeneira, Fernando, Amin, Najaf, Karssen, Lennart C, Vingerling, Johannes R, Hosseini, S M, Döring, Angela, Bettecken, Thomas, Vatavuk, Zoran, Gieger, Christian, Wichmann, H-Erich, Wilson, James F, Fleck, Brian, Foster, Paul J, Topouzis, Fotis, McGuffin, Peter, Sim, Xueling, Inouye, Michael, Holliday, Elizabeth G, Attia, John, Scott, Rodney J, Rotter, Jerome I, Meitinger, Thomas, Bailey-Wilson, Joan E

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