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- 2020
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Mark
Global Public Perceptions of Genomic Data Sharing : What Shapes the Willingness to Donate DNA and Health Data?
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- Contribution to journal › Article
- 2019
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Mark
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes
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- Contribution to journal › Article
- 2018
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Mark
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
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- Contribution to journal › Article
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Mark
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
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- Contribution to journal › Article
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Mark
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
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- Contribution to journal › Article
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Mark
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
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- Contribution to journal › Article
- 2017
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Mark
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays
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- Contribution to journal › Article
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Mark
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis
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- Contribution to journal › Article
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Mark
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
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- Contribution to journal › Article
- 2016
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Mark
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
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- Contribution to journal › Article