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Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium
Individual common variants exert weak effects on the risk for autism spectrum disorders
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
A genome-wide scan for common alleles affecting risk for autism
