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The Use of Multiplicity Corrections, Order Statistics and Generalized Family-Wise Statistics with Application to Genome-Wide StudiesGenome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathwaysA large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genesSeqHBase: a big data toolset for family based sequencing data analysisA missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data.Selecting tagging SNPs for association studies using power calculations from genotype data.Mining Retrospective Data for Virtual Prospective Drug Repurposing: L-DOPA and Age-related Macular DegenerationA candidate gene approach identifies the TRAF1/C5 region as a risk factor for rheumatoid arthritisNeither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's diseaseA large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.Pro-inflammatory immune responses are associated with clinical signs and symptoms of human anaplasmosis.Genome-wide association scan in psoriasis: new insights into chronic inflammatory disease.Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.Genetic-based prediction of disease traits: prediction is very difficult, especially about the futureFurther genetic evidence for three psoriasis-risk genes: ADAM33, CDKAL1, and PTPN22.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisIdentification of two gene variants associated with risk of advanced fibrosis in patients with chronic hepatitis C.The inflammatory disease-associated variants in IL12B and IL23R are not associated with rheumatoid arthritisUse of an electronic medical record to create the marshfield clinic twin/multiple birth cohortChanges in Gut and Plasma Microbiome following Exercise Challenge in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS).Phenome-wide association studies (PheWASs) for functional variantsReflections on the Field of Human Genetics: A Call for Increased Disease Genetics TheoryDifferential Lipid Response to Statins Is Associated With Variants in the BUD13-APOA5 Gene Region.Multiple Loci within the major histocompatibility complex confer risk of psoriasis.The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem.Cell line donor genotype and its influence on experimental phenotype: Toll-like receptor SNPs and potential variability in innate immunity.Complex host genetic susceptibility to Staphylococcus aureus infections.Validation of a metabolite panel for early diagnosis of type 2 diabetes.Genetic and Functional Associations with Decreased Anti-inflammatory Tumor Necrosis Factor Alpha Induced Protein 3 in Macrophages from Subjects with Axial Spondyloarthritis.Genetic evidence of PTPN22 effects on chronic lymphocytic leukemia.A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.The Impact of Diagnostic Code Misclassification on Optimizing the Experimental Design of Genetic Association Studies.Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study.Association between IL13 polymorphisms and psoriatic arthritis is modified by smoking.Pairwise linkage disequilibrium under disease modelsVariants in the 5q31 cytokine gene cluster are associated with psoriasisMeta-analysis evidence of a differential risk of the FCRL3 -169T-->C polymorphism in white and East Asian rheumatoid arthritis patientsDetailed genetic characterization of the interleukin-23 receptor in psoriasisA probabilistic approach to large-scale association scans: a semi-Bayesian method to detect disease-predisposing alleles
P50
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P50
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Steven J. Schrodi
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