Exploring Impact of Rare Variation in Systemic Lupus Erythematosus by a Genome Wide Imputation Approach
Author:
Publisher
Frontiers Media SA
Subject
Immunology,Immunology and Allergy
Reference84 articles.
1. The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog);MacArthur;Nucleic Acids Res.,2017
2. Rare variants create synthetic genome-wide associations;Dickson;PLoS Biol.,2010
3. Human genetic variation and its contribution to complex traits;Frazer;Nat Rev Genet.,2009
4. How important are rare variants in common disease?;Saint Pierre;Brief Funct Genomics,2014
5. Rare-variant studies to complement genome-wide association studies;Sazonovs;Annu Rev Genomics Hum Genet.,2018
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