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- 2016
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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
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
Immunochip analysis identifies multiple susceptibility Loci for systemic sclerosis.
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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
A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
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- Contribution to journal › Article
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Mark
Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci.
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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
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Mark
Meta-Analysis of Genome-Wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage.
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- Contribution to journal › Article
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Mark
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland
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- Contribution to journal › Article
- 2013
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Mark
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
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- Contribution to journal › Article