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Are polygenic risk scores for systolic blood pressure and LDL-cholesterol associated with treatment effectiveness, and clinical outcomes among those on treatment?
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Assessment of the causal relevance of ECG parameters for risk of atrial fibrillation: A mendelian randomisation study.
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Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.
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Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families.
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Effects of smoking status, history and intensity on heart rate variability in the general population: The CHRIS study.
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Myopia in Chinese families shows linkage to 10q26.13.
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Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.
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Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.
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Genetic Variants Associated with Circulating Parathyroid Hormone.
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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
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Height-reducing variants and selection for short stature in Sardinia.
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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.
Li Q. et al, (2015), Hum Genet, 134, 131 - 146
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium
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Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world.
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Modulation of genetic associations with serum urate levels by body-mass-index in humans.
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