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 Saw; M 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

doi:10.1093/hmg/ddt116

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 Saw

M 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 journal › Article › Academic › peer-review

54 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	2754-2764
Number of pages	11
Journal	Human Molecular Genetics
Volume	22
Issue number	13
DOIs	https://doi.org/10.1093/hmg/ddt116
Publication status	Published - 2013

Research programs

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

Access to Document

10.1093/hmg/ddt116

http://hdl.handle.net/1765/56920

Cite this

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., ... 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, 22(13), 2754-2764. https://doi.org/10.1093/hmg/ddt116

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title = "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",

author = "D Stambolian and R Wojciechowski and K Oexle and M Pirastu and XH Li and LJ Raffel and MF Cotch and EY Chew and B Klein and R Klein and Wong, \{TY (Tien Yin)\} and CL Simpson and Caroline Klaver and Cornelia Duijn and Virginie Verhoeven and PN Baird and V Vitart and AD Paterson and P Mitchell and SM Saw and M Fossarello and K Kazmierkiewicz and F Murgia and L Portas and M Schache and A Richardson and J Xie and JJ Wang and E Rochtchina and AC Viswanathan and C Hayward and AF Wright and O Polasek and H Campbell and I Rudan and Ben Oostra and Andr{\'e} Uitterlinden and Bert Hofman and Fernando Rivadeneira and Najaf Amin and Lennart Karssen and Hans Vingerling and SM Hosseini and A Doring and T Bettecken and Z Vatavuk and C Gieger and HE Wichmann and JF Wilson and B Fleck and PJ Foster and F Topouzis and P McGuffin and XL Sim and M Inouye and EG Holliday and J Attia and RJ Scott and JI Rotter and T Meitinger and JE Bailey-Wilson",

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doi = "10.1093/hmg/ddt116",

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volume = "22",

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journal = "Human Molecular Genetics",

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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

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. / Stambolian, D; Wojciechowski, R; Oexle, K et al.
In: Human Molecular Genetics, Vol. 22, No. 13, 2013, p. 2754-2764.

Research output: Contribution to journal › Article › Academic › peer-review

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T1 - 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

AU - Stambolian, D

AU - Wojciechowski, R

AU - Oexle, K

AU - Pirastu, M

AU - Li, XH

AU - Raffel, LJ

AU - Cotch, MF

AU - Chew, EY

AU - Klein, B

AU - Klein, R

AU - Wong, TY (Tien Yin)

AU - Simpson, CL

AU - Klaver, Caroline

AU - Duijn, Cornelia

AU - Verhoeven, Virginie

AU - Baird, PN

AU - Vitart, V

AU - Paterson, AD

AU - Mitchell, P

AU - Saw, SM

AU - Fossarello, M

AU - Kazmierkiewicz, K

AU - Murgia, F

AU - Portas, L

AU - Schache, M

AU - Richardson, A

AU - Xie, J

AU - Wang, JJ

AU - Rochtchina, E

AU - Viswanathan, AC

AU - Hayward, C

AU - Wright, AF

AU - Polasek, O

AU - Campbell, H

AU - Rudan, I

AU - Oostra, Ben

AU - Uitterlinden, André

AU - Hofman, Bert

AU - Rivadeneira, Fernando

AU - Amin, Najaf

AU - Karssen, Lennart

AU - Vingerling, Hans

AU - Hosseini, SM

AU - Doring, A

AU - Bettecken, T

AU - Vatavuk, Z

AU - Gieger, C

AU - Wichmann, HE

AU - Wilson, JF

AU - Fleck, B

AU - Foster, PJ

AU - Topouzis, F

AU - McGuffin, P

AU - Sim, XL

AU - Inouye, M

AU - Holliday, EG

AU - Attia, J

AU - Scott, RJ

AU - Rotter, JI

AU - Meitinger, T

AU - Bailey-Wilson, JE

PY - 2013

Y1 - 2013

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DO - 10.1093/hmg/ddt116

M3 - Article

C2 - 23474815

SN - 0964-6906

VL - 22

SP - 2754

EP - 2764

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 13

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