Found: 29
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Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics.
- Published in:
- Human Genomics, 2004, v. 1, n. 2, p. 98, doi. 10.1186/1479-7364-1-2-98
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- Article
A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples.
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- BMC Genomics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2164-15-274
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- Article
Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.
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- Human Molecular Genetics, 2015, v. 24, n. 6, p. 1774, doi. 10.1093/hmg/ddu581
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- Article
Seven newly identified loci for autoimmune thyroid disease.
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- Human Molecular Genetics, 2012, v. 21, n. 23, p. 5202
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- Article
Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.
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- Human Molecular Genetics, 2012, v. 21, n. 2, p. 322, doi. 10.1093/hmg/ddr468
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- Article
Widespread seasonal gene expression reveals annual differences in human immunity and physiology.
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- Nature Communications, 2015, v. 6, n. 5, p. 7000, doi. 10.1038/ncomms8000
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- Article
Genetic feature engineering enables characterisation of shared risk factors in immune-mediated diseases.
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- Genome Medicine, 2020, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13073-020-00797-4
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- Article
A Type I Interferon Transcriptional Signature Precedes Autoimmunity in Children Genetically at Risk for Type 1 Diabetes.
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- Diabetes, 2014, v. 63, n. 7, p. 2538, doi. 10.2337/db13-1777
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- Article
Inherited Variation in Vitamin D Genes Is Associated With Predisposition to Autoimmune Disease Type 1 Diabetes.
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- Diabetes, 2011, v. 60, n. 5, p. 1624, doi. 10.2337/db10-1656
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T1DBase: New Developments in a Type 1 Diabetes Community Website.
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- Diabetes, 2007, v. 56, p. A643
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- Article
Resolving mechanisms of immune‐mediated disease in primary CD4 T cells.
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- EMBO Molecular Medicine, 2020, v. 12, n. 5, p. 1, doi. 10.15252/emmm.202012112
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- Article
Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
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- Nature Genetics, 2015, v. 47, n. 8, p. 962, doi. 10.1038/ng0815-962c
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- Article
Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.
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- Nature Genetics, 2015, v. 47, n. 7, p. 839, doi. 10.1038/ng.3330
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- Article
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
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- Nature Genetics, 2015, v. 47, n. 4, p. 381, doi. 10.1038/ng.3245
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- Article
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource.
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- Nature Genetics, 2009, v. 41, n. 9, p. 1011, doi. 10.1038/ng.434
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- Article
A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region.
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- Nature Genetics, 2006, v. 38, n. 6, p. 617, doi. 10.1038/ng1800
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- Article
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
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- PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005272
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- Article
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
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- PLoS Genetics, 2015, v. 11, n. 5, p. 1, doi. 10.1371/journal.pgen.1005272
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- Article
Epigenetic analysis of regulatory T cells using multiplex bisulfite sequencing.
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- European Journal of Immunology, 2015, v. 45, n. 11, p. 3200, doi. 10.1002/eji.201545646
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- Article
Chromosome contacts in activated T cells identify autoimmune disease candidate genes.
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- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1285-0
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- Article
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
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- Nature, 2013, v. 498, n. 7453, p. 232, doi. 10.1038/nature12170
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- Article
T1DBase: update 2011, organization and presentation of large-scale data sets for type 1 diabetes research.
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- Nucleic Acids Research, 2011, v. 39, n. suppl_1, p. D997, doi. 10.1093/nar/gkq912
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- Article
VSEAMS: a pipeline for variant set enrichment analysis using summary GWAS data identifies IKZF3, BATF and ESRRA as key transcription factors in type 1 diabetes.
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- Bioinformatics, 2014, v. 30, n. 23, p. 3342, doi. 10.1093/bioinformatics/btu571
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- Article
T1DBase: integration and presentation of complex data for type 1 diabetes research.
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- Nucleic Acids Research, 2007, v. 35, p. d742, doi. 10.1093/nar/gkl933
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- Article
T1DBase, a community web-based resource for type 1 diabetes research.
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- Nucleic Acids Research, 2005, v. 33, n. suppl 1, p. d544
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- Article
Fine mapping chromatin contacts in capture Hi-C data.
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- BMC Genomics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12864-018-5314-5
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- Article
A Method for Gene-Based Pathway Analysis Using Genomewide Association Study Summary Statistics Reveals Nine New Type 1 Diabetes Associations.
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- Genetic Epidemiology, 2014, v. 38, n. 8, p. 661, doi. 10.1002/gepi.21853
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- Article
Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases.
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- Human Molecular Genetics, 2015, v. 24, n. 12, p. 3305, doi. 10.1093/hmg/ddv077
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- Article
Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetes.
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- BMC Genetics, 2006, v. 7, p. 22, doi. 10.1186/1471-2156-7-22
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- Article