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- 2022
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Mark
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults
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- Contribution to journal › Article
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Mark
Germline Mutations in CIDEB and Protection against Liver Disease
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- Contribution to journal › Article
- 2021
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Mark
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
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- Contribution to journal › Article
- 2018
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Mark
Genome-wide analysis yields new loci associating with aortic valve stenosis
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- Contribution to journal › Article
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
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- Contribution to journal › Article
- 2017
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Mark
Rare and low-frequency coding variants alter human adult height
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- Contribution to journal › Article
- 2016
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Mark
A reference panel of 64,976 haplotypes for genotype imputation
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- Contribution to journal › Article
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Mark
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
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- Contribution to journal › Article
- 2015
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Mark
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
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- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article