Stambolian, D, Wojciechowski, R, Oexle, K, Pirastu, M, Li, XH, Raffel, LJ, Cotch, MF, Chew, EY, Klein, B, Klein, R, Wong, TY, Simpson, CL
, Klaver, C, Duijn, C
, Verhoeven, V, Baird, PN, Vitart, V, Paterson, AD, Mitchell, P, Saw, SM, Fossarello, M, Kazmierkiewicz, K, Murgia, F, Portas, L, Schache, M, Richardson, A, Xie, J, Wang, JJ, Rochtchina, E, Viswanathan, AC, Hayward, C, Wright, AF, Polasek, O, Campbell, H, Rudan, I, Oostra, B
, Uitterlinden, A, Hofman, B, Rivadeneira, F, Amin, N, Karssen, L
, Vingerling, H, Hosseini, SM, Doring, A, Bettecken, T, Vatavuk, Z, Gieger, C, Wichmann, HE, Wilson, JF, Fleck, B, Foster, PJ, Topouzis, F, McGuffin, P, Sim, XL, Inouye, M, Holliday, EG, Attia, J, Scott, RJ, Rotter, JI, Meitinger, T & Bailey-Wilson, JE 2013, '
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',
Human Molecular Genetics, vol. 22, no. 13, pp. 2754-2764.
https://doi.org/10.1093/hmg/ddt116