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Assessing thyroid cancer risk using polygenic risk scores
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Genome-wide associations for benign prostatic hyperplasia reveal a genetic corre...
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Genome-wide association identifies seven loci for pelvic organ prolapse in Icela...
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Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation
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Predicted loss and gain of function mutations in ACO1 are associated with erythr...
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Genetic variability in the absorption of dietary sterols affects the risk of cor...
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Association of Chromosome 9p21 with Subsequent Coronary Heart Disease Events: A...
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Subsequent Event Risk in Individuals with Established Coronary Heart Disease: De...
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