Genetic and Genomic Medicine
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A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifiesANXA1as a susceptibility locus for persistent wheezing
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Common genetic variations in telomere length genes and lung cancer
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Reserpine maintains photoreceptor survival in retinal ciliopathy by resolving proteostasis imbalance and ciliogenesis defects
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Recessive pathogenic variants inMCATcause combined oxidative phosphorylation deficiency
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Associations of genetic and infectious risk factors with coronary heart disease
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Evaluating the effect of metabolic traits on oral and oropharyngeal cancer risk using Mendelian randomization
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Regulatoryde novomutations underlying intellectual disability
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Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study
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A Progeroid Syndrome Caused by RAF1 deficiency Underscores the importance of RTK signaling for Human Development
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The missing link between genetic association and regulatory function
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