Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

M.B. Trynka; K.A. Hunt; [No Value] Spanish Consortium on the Genetics of Coeliac Disease; [No Value] PreventCD Study Group; [No Value] Welcome trust Case Control Consortium; V.M. Wolters; D.A. van Heel

doi:10.1038/ng.998

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

M.B. Trynka, K.A. Hunt, [No Value] Spanish Consortium on the Genetics of Coeliac Disease, [No Value] PreventCD Study Group, [No Value] Welcome trust Case Control Consortium, V.M. Wolters, D.A. van Heel

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

Original language	English
Pages (from-to)	1193-1201
Number of pages	9
Journal	Nature Genetics
Volume	43
Issue number	12
DOIs	https://doi.org/10.1038/ng.998
Publication status	Published - 2011

Access to Document

10.1038/ng.998

http://www.ncbi.nlm.nih.gov/pubmed/22057235

Cite this

Trynka, M. B., Hunt, K. A., Spanish Consortium on the Genetics of Coeliac Disease, N. V., PreventCD Study Group, N. V., Welcome trust Case Control Consortium, N. V., Wolters, V. M., & van Heel, D. A. (2011). Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nature Genetics, 43(12), 1193-1201. https://doi.org/10.1038/ng.998

@article{8f296e516e90474899c034eddb32bfaf,

title = "Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.",

author = "M.B. Trynka and K.A. Hunt and {Spanish Consortium on the Genetics of Coeliac Disease}, {[No Value]} and {PreventCD Study Group}, {[No Value]} and {Welcome trust Case Control Consortium}, {[No Value]} and V.M. Wolters and {van Heel}, D.A.",

year = "2011",

doi = "10.1038/ng.998",

language = "English",

volume = "43",

pages = "1193--1201",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Research",

number = "12",

}

Trynka, MB, Hunt, KA, Spanish Consortium on the Genetics of Coeliac Disease, NV, PreventCD Study Group, NV, Welcome trust Case Control Consortium, NV, Wolters, VM & van Heel, DA 2011, 'Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.', Nature Genetics, vol. 43, no. 12, pp. 1193-1201. https://doi.org/10.1038/ng.998

TY - JOUR

T1 - Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

AU - Trynka, M.B.

AU - Hunt, K.A.

AU - Spanish Consortium on the Genetics of Coeliac Disease, [No Value]

AU - PreventCD Study Group, [No Value]

AU - Welcome trust Case Control Consortium, [No Value]

AU - Wolters, V.M.

AU - van Heel, D.A.

PY - 2011

Y1 - 2011

U2 - 10.1038/ng.998

DO - 10.1038/ng.998

M3 - Article

C2 - 22057235

SN - 1061-4036

VL - 43

SP - 1193

EP - 1201

JO - Nature Genetics

JF - Nature Genetics

IS - 12

ER -