Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry

Hunt, Karen A., Smyth, Deborah J., Balschun, Tobias, Ban, Maria, Mistry, Vanisha, Ahmad, Tariq, Anand, Vidya, Barrett, Jeffrey C., Bhaw-Rosun, Leena, Bockett, Nicholas A., Brand, Oliver J., Brouwer, Elisabeth, Concannon, Patrick, Cooper, Jason D., Dias, Kerith-Rae M., van Diemen, Cleo C., Dubois, Patrick C., Edkins, Sarah, Foelster-Holst, Regina, Fransen, Karin, Glass, David N., Heap, Graham A. R., Hofmann, Sylvia, Huizinga, Tom W. J., Hunt, Sarah, Langford, Cordelia, Lee, James, Mansfield, John, Marrosu, Maria Giovanna, Mathew, Christopher G., Mein, Charles A., Mueller-Quernheim, Joachim, Nutland, Sarah, Onengut-Gumuscu, Suna, Ouwehand, Willem, Pearce, Kerra, Prescott, Natalie J., Posthumus, Marcel D., Potter, Simon, Rosati, Giulio, Sambrook, Jennifer, Satsangi, Jack, Schreiber, Stefan, Shtir, Corina, Simmonds, Matthew J., Sudman, Marc, Thompson, Susan D., Toes, Rene, Trynka, Gosia, Vyse, Timothy J., Walker, Neil M., Weidinger, Stephan, Zhernakova, Alexandra, Zoledziewska, Magdalena, Type 1 Diabetes Genetics Consortium, UK Inflammatory Bowel Disease (IBD) Genetics Consortium, Wellcome Trust Case Control Consortium, Weersma, Rinse K., Gough, Stephen C. L., Sawcer, Stephen, Wijmenga, Cisca, Parkes, Miles, Cucca, Francesco, Franke, Andre, Deloukas, Panos, Rich, Stephen S., Todd, John A., van Heel, David A. and Brown, Matthew A. (2012) Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nature Genetics, 44 1: 3-5. doi:10.1038/ng.1037


Author Hunt, Karen A.
Smyth, Deborah J.
Balschun, Tobias
Ban, Maria
Mistry, Vanisha
Ahmad, Tariq
Anand, Vidya
Barrett, Jeffrey C.
Bhaw-Rosun, Leena
Bockett, Nicholas A.
Brand, Oliver J.
Brouwer, Elisabeth
Concannon, Patrick
Cooper, Jason D.
Dias, Kerith-Rae M.
van Diemen, Cleo C.
Dubois, Patrick C.
Edkins, Sarah
Foelster-Holst, Regina
Fransen, Karin
Glass, David N.
Heap, Graham A. R.
Hofmann, Sylvia
Huizinga, Tom W. J.
Hunt, Sarah
Langford, Cordelia
Lee, James
Mansfield, John
Marrosu, Maria Giovanna
Mathew, Christopher G.
Mein, Charles A.
Mueller-Quernheim, Joachim
Nutland, Sarah
Onengut-Gumuscu, Suna
Ouwehand, Willem
Pearce, Kerra
Prescott, Natalie J.
Posthumus, Marcel D.
Potter, Simon
Rosati, Giulio
Sambrook, Jennifer
Satsangi, Jack
Schreiber, Stefan
Shtir, Corina
Simmonds, Matthew J.
Sudman, Marc
Thompson, Susan D.
Toes, Rene
Trynka, Gosia
Vyse, Timothy J.
Walker, Neil M.
Weidinger, Stephan
Zhernakova, Alexandra
Zoledziewska, Magdalena
Type 1 Diabetes Genetics Consortium
UK Inflammatory Bowel Disease (IBD) Genetics Consortium
Wellcome Trust Case Control Consortium
Weersma, Rinse K.
Gough, Stephen C. L.
Sawcer, Stephen
Wijmenga, Cisca
Parkes, Miles
Cucca, Francesco
Franke, Andre
Deloukas, Panos
Rich, Stephen S.
Todd, John A.
van Heel, David A.
Brown, Matthew A.
Title Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
Formatted title
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
Journal name Nature Genetics   Check publisher's open access policy
ISSN 1061-4036
1546-1718
Publication date 2012-01
Year available 2011
Sub-type Letter to editor, brief commentary or brief communication
DOI 10.1038/ng.1037
Volume 44
Issue 1
Start page 3
End page 5
Total pages 3
Place of publication New York, NY, United States
Publisher Nature Publishing Group
Collection year 2013
Language eng
Keyword Celiac-Disease
Q-Index Code CX
Q-Index Status Confirmed Code
Institutional Status UQ
Additional Notes Correspondence, Published online 27 December 2011

Document type: Journal Article
Sub-type: Letter to editor, brief commentary or brief communication
Collections: Non HERDC
UQ Diamantina Institute Publications
 
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Created: Mon, 15 Apr 2013, 12:11:03 EST by Kylie Hengst on behalf of UQ Diamantina Institute