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- 2019
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Mark
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
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- Contribution to journal › Article
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Mark
Loss of ZnT8 function protects against diabetes by enhanced insulin secretion
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- Contribution to journal › Article
- 2018
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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
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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Mark
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
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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.
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- Contribution to journal › Article
- 2014
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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
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Mark
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
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes.
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- Contribution to journal › Article
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Mark
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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Mark
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
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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
- 2013
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Mark
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