A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

David A. van Heel(Queen Mary University of London), Lude Franke(Utrecht University), Karen A. Hunt(Queen Mary University of London), Rhian Gwilliam(Wellcome Sanger Institute), Alexandra Zhernakova(Utrecht University), Mike Inouye(Wellcome Sanger Institute), Martin C. Wapenaar(University Medical Center Groningen), Martin Barnardo(Churchill Hospital), Graeme Bethel(Wellcome Sanger Institute), Geoffrey Holmes(Royal Derby Hospital), C. Feighery(Trinity College Dublin), Derek P. Jewell(Centre for Human Genetics), Dermot Kelleher(Trinity College Dublin), Parveen Kumar(Queen Mary University of London), Simon Travis(University of Oxford), Julian R.F. Walters(Hammersmith Hospital), David S. Sanders(Royal Hallamshire Hospital), P D Howdle(St James's University Hospital), Jill Swift(University Hospital Llandough), Raymond J. Playford(Queen Mary University of London), William McLaren(Wellcome Sanger Institute), M. Luisa Mearin(Leiden University Medical Center), Chris J. Mulder(Vrije Universiteit Amsterdam), Ross McManus(Trinity College Dublin), Ralph McGinnis(Wellcome Sanger Institute), Lon R. Cardon(Centre for Human Genetics), Panos Deloukas(Wellcome Sanger Institute), Cisca Wijmenga(University Medical Center Groningen)
Nature Genetics
June 10, 2007
Cited by 672Open Access
Full Text

Abstract


Related Papers

No related papers found

Powered by citation graph analysis