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- 2018
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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
- 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
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Mark
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
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- Contribution to journal › Article
- 2014
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Mark
Immunochip analysis identifies multiple susceptibility Loci for systemic sclerosis.
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- Contribution to journal › Article
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Mark
Genome-wide Association Study Identifies Five Susceptibility Loci for Follicular Lymphoma outside the HLA Region.
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- Contribution to journal › Article
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Mark
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
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- Contribution to journal › Article
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Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
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- Contribution to journal › Article