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- 2020
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Mark
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
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- Contribution to journal › Article
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Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
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- Contribution to journal › Article
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Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions
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- Contribution to journal › Article
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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
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- Contribution to journal › Article
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A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex
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- Contribution to journal › Article
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Association of Established Blood Pressure Loci With 10-Year Change in Blood Pressure and Their Ability to Predict Incident Hypertension
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- Contribution to journal › Article
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Effect of rare coding variants in the CFI gene on Factor I expression levels
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- Contribution to journal › Article
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Identification of APTX disease-causing mutation in two unrelated Jordanian families with cerebellar ataxia and sensitivity to DNA damaging agents
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- Contribution to journal › Article
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Comprehensive molecular comparison of BRCA1 hypermethylated and BRCA1 mutated triple negative breast cancers
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- Contribution to journal › Article
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Familial risks between Graves disease and Hashimoto thyroiditis and other autoimmune diseases in the population of Sweden
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- Contribution to journal › Article