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Type 1 diabetes genome-wide association analysis with imputation identifies five new risk regions

https://doi.org/10.1101/120022

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Unstable diabetes in a patient receiving anti-TNF- for rheumatoid arthritis

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Genotype Imputation

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TNF-α and IFN-γ gene variation and genetic susceptibility to type 1 diabetes and its microangiopathic complications

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Evaluation of polygenic risk scores to differentiate between type 1 and type 2 diabetes

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Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow‐Up Studies

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Multi-tissue multi-omics integration reveals tissue-specific pathways, gene networks and drug candidates for type 1 diabetes

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Genetics of type 1 diabetes

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Identification of loci where DNA methylation potentially mediates genetic risk of type 1 diabetes

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The role of endoplasmic reticulum aminopeptidases in type 1 diabetes mellitus

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Discovery of new myositis genetic associations through leveraging other immune-mediated diseases

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Comparison of methods for transcriptome imputation through application to two common complex diseases

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An integrated multi-omics approach identifies the landscape of interferon-α-mediated responses of human pancreatic beta cells

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Genetics of diabetes mellitus and diabetes complications

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The impact of proinflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes

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Approaches and advances in the genetic causes of autoimmune disease and their implications

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RápidoPGS: a rapid polygenic score calculator for summary GWAS data without a test dataset

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Functional genomics in autoimmune diseases

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Enhanced genetic analysis of type 1 diabetes by selecting variants on both effect size and significance, and by integration with autoimmune thyroid disease

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Causal associations between type 1 diabetes and COVID-19 infection and prognosis: a two-sample Mendelian randomization study

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Childhood adiposity and risk of type 1 diabetes: A Mendelian randomization study

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Polimorfismo (cag) del gen atxn2 como factor de riesgo relacionado con diabetes mellitus tipo 2

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La dérive génétique : un outil pour identifier de nouveaux facteurs impliqués dans la pathogénie des maladies complexes tel le diabète auto-immune de la souris non obèse diabétique

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