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Progress towards identifying inflammatory bowel disease susceptibility genes. Novartis Foundation symposium, 2011/12/08, Volume 263, p.3-11; discussion 11-6, 211-8, (2011)
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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease. Nature genetics, 2011/10/09, Volume 43, Issue 11, p.1066-73, (2011)
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LRRK2 is involved in the IFN-gamma response and host response to pathogens. Journal of immunology (Baltimore, Md. : 1950), 2010/11/01, Volume 185, Issue 9, p.5577-85, (2010)
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Autoimmune diseases: insights from genome-wide association studies. Human molecular genetics, 2008/10/15, Volume 17, Issue R2, p.R116-21, (2008)
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Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Nature genetics, 2008/09/01, Volume 40, Issue 9, p.1059-61, (2008)
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Risk alleles for multiple sclerosis identified by a genomewide study. The New England journal of medicine, 2007/08/30, Volume 357, Issue 9, p.851-62, (2007)
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A second major histocompatibility complex susceptibility locus for multiple sclerosis. Annals of neurology, 2007/03/01, Volume 61, Issue 3, p.228-36, (2007)
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A functional candidate screen for coeliac disease genes. European journal of human genetics : EJHG, 2006/11/01, Volume 14, Issue 11, p.1215-22, (2006)
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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nature genetics, 2006/10/01, Volume 38, Issue 10, p.1166-72, (2006)
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Haplotype-based association analysis of 56 functional candidate genes in the IBD6 locus on chromosome 19. European journal of human genetics : EJHG, 2006/06/01, Volume 14, Issue 6, p.780-90, (2006)
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Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4. American journal of human genetics, 2005/12/01, Volume 77, Issue 6, p.1044-60, (2005)
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The promise and perils of interpreting genetic associations in Crohn's disease. Gut, 2005/10/01, Volume 54, Issue 10, p.1354-7, (2005)
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A high-density screen for linkage in multiple sclerosis. American journal of human genetics, 2005/09/01, Volume 77, Issue 3, p.454-67, (2005)
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Association of DLG5 R30Q variant with inflammatory bowel disease. European journal of human genetics : EJHG, 2005/07/01, Volume 13, Issue 7, p.835-9, (2005)
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Paths to understanding the genetic basis of autoimmune disease. Nature, 2005/06/02, Volume 435, Issue 7042, p.584-9, (2005)
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A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms. American journal of human genetics, 2005/04/01, Volume 76, Issue 4, p.634-46, (2005)
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Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci. American journal of medical genetics. Part A, 2004/11/01, Volume 130A, Issue 4, p.345-50, (2004)
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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping. Human molecular genetics, 2004/09/01, Volume 13, Issue 17, p.1943-9, (2004)
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