Found: 7
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Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 1, p. 122, doi. 10.1093/hmg/ddp473
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- Publication type:
- Article
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry.
- Published in:
- 2012
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- Publication type:
- Letter
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
- Published in:
- Nature Genetics, 2011, v. 43, n. 12, p. 1193, doi. 10.1038/ng.998
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- Publication type:
- Article
Corrigendum: Multiple common variants for celiac disease influencing immune gene expression.
- Published in:
- 2010
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- Publication type:
- Correction notice
Multiple common variants for celiac disease influencing immune gene expression.
- Published in:
- Nature Genetics, 2010, v. 42, n. 4, p. 295, doi. 10.1038/ng.543
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- Publication type:
- Article
New susceptibility genes for ulcerative colitis.
- Published in:
- Nature Genetics, 2008, v. 40, n. 6, p. 686, doi. 10.1038/ng0608-686
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- Publication type:
- Article
A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 1, p. 1, doi. 10.1371/journal.pgen.1001283
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- Publication type:
- Article