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- 2018
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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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Functional investigations of HNF1A identify rare variants as risk factors for type 2 diabetes in the general population
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- Contribution to journal › Article
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Variation in maturity-onset diabetes of the young genes influence response to interventions for diabetes prevention
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- Contribution to journal › Article
- 2016
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Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
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- Contribution to journal › Article
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A reference panel of 64,976 haplotypes for genotype imputation
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- Contribution to journal › Article
- 2015
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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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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
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- Contribution to journal › Article
- 2014
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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
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Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
2014) In Proceedings of the National Academy of Sciences of the United States of America 111(36). p.32-13127(
- 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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Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes.
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- Contribution to journal › Article
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Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
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- Contribution to journal › Article
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Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
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- Contribution to journal › Article
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Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
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- Contribution to journal › Article
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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
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
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- Contribution to journal › Article
- 2013
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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
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- Contribution to journal › Article
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Mark
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
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- Contribution to journal › Article
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Large-scale association analysis identifies new risk loci for coronary artery disease
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- Contribution to journal › Article
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Common variants associated with plasma triglycerides and risk for coronary artery disease
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- Contribution to journal › Article