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- 2020
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Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
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- Contribution to journal › Article
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Mark
BMD-Related Genetic Risk Scores Predict Site-Specific Fractures as Well as Trabecular and Cortical Bone Microstructure
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- Contribution to journal › Article
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Mark
The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias
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- Contribution to journal › Letter
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Mark
Mortality risks associated with sibling heart failure
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- Contribution to journal › Article
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Mark
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
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- Contribution to journal › Article
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Mark
Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant
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- Contribution to journal › Article
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Mark
An integrative phenotype–genotype approach using phenotypic characteristics from the UAE national diabetes study identifies HSD17B12 as a candidate gene for obesity and type 2 diabetes
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- Contribution to journal › Article
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Mark
Evaluating drug targets through human loss-of-function genetic variation
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- Contribution to journal › Article
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Mark
Transcript expression-aware annotation improves rare variant interpretation
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- Contribution to journal › Article
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Mark
A structural variation reference for medical and population genetics
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- Contribution to journal › Article