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

D Stambolian, R Wojciechowski, K Oexle, M Pirastu, XH Li, LJ Raffel, MF Cotch, EY Chew, B Klein, R Klein, TY (Tien Yin) Wong, CL Simpson, Caroline Klaver, Cornelia Duijn, Virginie Verhoeven, PN Baird, V Vitart, AD Paterson, P Mitchell, SM SawM Fossarello, K Kazmierkiewicz, F Murgia, L Portas, M Schache, A Richardson, J Xie, JJ Wang, E Rochtchina, AC Viswanathan, C Hayward, AF Wright, O Polasek, H Campbell, I Rudan, Ben Oostra, André Uitterlinden, Bert Hofman, Fernando Rivadeneira, Najaf Amin, Lennart Karssen, Hans Vingerling, SM Hosseini, A Doring, T Bettecken, Z Vatavuk, C Gieger, HE Wichmann, JF Wilson, B Fleck, PJ Foster, F Topouzis, P McGuffin, XL Sim, M Inouye, EG Holliday, J Attia, RJ Scott, JI Rotter, T Meitinger, JE Bailey-Wilson

Research output: Contribution to journalArticleAcademicpeer-review

53 Citations (Scopus)
Original languageUndefined/Unknown
Pages (from-to)2754-2764
Number of pages11
JournalHuman Molecular Genetics
Volume22
Issue number13
DOIs
Publication statusPublished - 2013

Research programs

  • EMC MGC-02-96-01
  • EMC MM-01-39-09-A
  • EMC NIHES-01-64-01
  • EMC OR-01-60-01

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