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Common risk alleles for inflammatory diseases are targets of recent positive selection. American journal of human genetics, 2013/04/04, Volume 92, Issue 4, p.517-29, (2013)
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Chromatin marks identify critical cell types for fine mapping complex trait variants. Nature genetics, 2013/02/01, Volume 45, Issue 2, p.124-30, (2013)
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Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron, 2013/01/23, Volume 77, Issue 2, p.235-42, (2013)
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Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis. American journal of human genetics, 2013/01/10, Volume 92, Issue 1, p.15-27, (2013)
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Autoimmunity: insights from human genomics. Current opinion in immunology, 2012/10/01, Volume 24, Issue 5, p.513-5, (2012)
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Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nature genetics, 2012/03/25, (2012)
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Use of a Multiethnic Approach to Identify Rheumatoid- Arthritis-Susceptibility Loci, 1p36 and 17q12. American journal of human genetics, 2012/03/09, Volume 90, Issue 3, p.524-532, (2012)
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Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis. Nature genetics, 2012/01/29, Volume 44, Issue 3, p.291-6, (2012)
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A rare penetrant mutation in CFH confers high risk of age-related macular degeneration. Nature genetics, 2011/10/23, Volume 43, Issue 12, p.1232-6, (2011)
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Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. PLoS genetics, 2011/01/13, Volume 7, Issue 1, p.e1001273, (2011)
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Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records. American journal of human genetics, 2011/01/07, Volume 88, Issue 1, p.57-69, (2011)
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature genetics, 2010/11/01, Volume 42, Issue 11, p.937-48, (2010)
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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS genetics, 2010/09/09, Volume 6, Issue 9, (2010)
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nature genetics, 2010/07/01, Volume 42, Issue 7, p.579-89, (2010)
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The landscape of somatic copy-number alteration across human cancers. Nature, 2010/02/18, Volume 463, Issue 7283, p.899-905, (2010)
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Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS genetics, 2009/06/01, Volume 5, Issue 6, p.e1000534, (2009)
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Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nature genetics, 2008/10/01, Volume 40, Issue 10, p.1216-23, (2008)
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