Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants
Author:
Funder
European Commission Seventh Framework Programme for Research and Technological Development Health
Ministerio de Economía y Competitividad
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference107 articles.
1. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019;Buniello;Nucleic Acids Res.,2019
2. A haplotype map of the human genome;Olivier;Physiol. Genomics,2003
3. Evidence for substantial fine-scale variation in recombination rates across the human genome;Crawford;Nat. Genet.,2004
4. High-resolution haplotype structure in the human genome;Daly;Nat. Genet.,2001
5. A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence;Dawson;Genome Res.,2001
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