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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
Not available
S-EPMC5595282
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biostudies-literature
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Expectant Management vs Medication for Patent Ductus Arteriosus in Preterm Infants: The PDA Randomized Clinical Trial.
Not available
S-EPMC12690482
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biostudies-literature
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Whole-genome sequence-based analysis of thyroid function.
Not available
S-EPMC4366514
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biostudies-literature
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Behavioral Deficits at 18-22 Months of Age Are Associated with Early Cerebellar Injury and Cognitive and Language Performance in Children Born Extremely Preterm.
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S-EPMC6394414
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biostudies-literature
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Exome-wide association study of plasma lipids in >300,000 individuals.
Not available
S-EPMC5709146
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biostudies-literature
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A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease.
Not available
S-EPMC5219001
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biostudies-literature
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The UK10K project identifies rare variants in health and disease.
Not available
S-EPMC4773891
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biostudies-literature
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Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Not available
S-EPMC5409098
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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel.
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S-EPMC4579394
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biostudies-literature
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The neurophysiological brain-fingerprint of Parkinson's disease.
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S-EPMC11253223
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