Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

Autor: Musolf, Anthony M., Haarman, Annechien E. G., Luben, Robert N., Ong, Jue-Sheng, Patasova, Karina, Trapero, Rolando Hernandez, Marsh, Joseph, Jain, Ishika, Jain, Riya, Wang, Paul Zhiping, Lewis, Deyana D., Tedja, Milly S., Iglesias, Adriana I., Li, Hengtong, Cowan, Cameron S., Baird, Paul Nigel, Veluchamy, Amutha Barathi, Burdon, Kathryn P., Campbell, Harry, Chen, Li Jia, Cheng, Ching-Yu, Chew, Emily Y., Craig, Jamie E., Cumberland, Phillippa M., Deangelis, Margaret M., Delcourt, Cécile, Ding, Xiaohu, Evans, David M., Fan, Qiao, Fossarello, Maurizio, Foster, Paul J., Gharahkhani, Puya, Guggenheim, Jeremy A., Guo, Xiaobo, Han, Xikun, He, Mingguang, Hewitt, Alex W., Hoang, Quan V., Iyengar, Sudha K., Jonas, Jost B., Kähönen, Mika, Kaprio, Jaakko, Klein, Barbara E., Lass, Jonathan H., Lee, Kris, Lehtimäki, Terho, Lewis, Deyana, Li, Qing, Li, Shi-Ming, Lyytikäinen, Leo-Pekka, MacGregor, Stuart, Mackey, David A., Martin, Nicholas G., Meguro, Akira, Middlebrooks, Candace, Miyake, Masahiro, Mizuki, Nobuhisa, Musolf, Anthony, Nickels, Stefan, Oexle, Konrad, Pang, Chi Pui, Paterson, Andrew D., Pennell, Craig, Pfeiffer, Norbert, Polasek, Ozren, Rahi, Jugnoo S., Raitakari, Olli, Rudan, Igor, Sahebjada, Srujana, Simpson, Claire L., Tai, E-Shyong, Tideman, J. Willem L., Tsujikawa, Akitaka, Wang, Ningli, Bin, Wei Wen, Williams, Cathy, Williams, Katie M., Wilson, James F., Wojciechowski, Robert, Wang, Ya Xing, Yamashiro, Kenji, Yam, Jason C. S., Yap, Maurice K. H., Yazar, Seyhan, Yip, Shea Ping, Young, Terri L., Zhou, Xiangtian, Biino, Ginevra, Klein, Alison P., Duggal, Priya, Hayward, Caroline, Haller, Toomas, Metspalu, Andres, Wedenoja, Juho, Pärssinen, Olavi, Saw, Seang-Mei, Stambolian, Dwight, Hysi, Pirro G., Khawaja, Anthony P., Vitart, Veronique, Hammond, Christopher J., van Duijn, Cornelia M., Verhoeven, Virginie J. M., Klaver, Caroline C. W., Bailey-Wilson, Joan E.

Refractive error, measured here as mean spherical equivalent (SER), is a complex eye condition caused by both genetic and environmental factors. Individuals with strong positive or negative values of SER require spectacles or other approaches for vis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1222::3def4718c026d2337b121878f5e3c487
http://urn.fi/URN:NBN:fi:jyu-202301041122

Genetic Association Study of KCNQ5 Polymorphisms with High Myopia.

Autor: Liao, Xuan¹, Yap, Maurice K. H.², Leung, Kim Hung³, Kao, Patrick Y. P.², Liu, Long Qian⁴, Yip, Shea Ping³

Publikováno v: BioMed Research International. 8/13/2017, Vol. 2017, p1-7. 7p.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Association of High Myopia with Crystallin Beta A4 (CRYBA4) Gene Polymorphisms in the Linkage-Identified MYP6 Locus.

Autor: Ho, Daniel W. H.^1,2, Yap, Maurice K. H.², Po Wah Ng^1,2, Wai Yan Fung², Shea Ping Yip² shea.ping.yip@inet.polyu.edu.hk

Publikováno v: PLoS ONE. Jun2012, Vol. 7 Issue 6, p1-10. 10p.

PAX6 Haplotypes Are Associated with High Myopia in Han Chinese.

Autor: Bo Jiang^1,2,3, Yap, Maurice K. H.³, Kim Hung Leung², Po Wah Ng^2,3, Wai Yan Fung², Wai Wa Lam², Yangshun Gu¹, Shea Ping Yip² shea.ping.yip@inet.polyu.edu.hk

Publikováno v: PLoS ONE. 2011, Vol. 6 Issue 5, p1-10. 10p.