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- 2024
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Mark
A genomic mutational constraint map using variation in 76,156 human genomes
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- Contribution to journal › Article
- 2023
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Mark
Genetic insights into resting heart rate and its role in cardiovascular disease
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- Contribution to journal › Article
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Mark
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
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- Contribution to journal › Article
- 2022
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Mark
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
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- Contribution to journal › Article
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Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
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- Contribution to journal › Article
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Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
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- Contribution to journal › Article
- 2021
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Mark
Adult-onset type 1 diabetic patients with less severe clinical manifestation have less risk DR-DQ genotypes than childhood-onset patients
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- Contribution to journal › Article
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Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
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- Contribution to journal › Article
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Mark
The trans-ancestral genomic architecture of glycemic traits
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- Contribution to journal › Article
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Mark
Novel Reclassification of Adult Diabetes Is Useful to Distinguish Stages of β-Cell Function Linked to the Risk of Vascular Complications : The DOLCE Study From Northern Ukraine
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- Contribution to journal › Article
- 2019
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Mark
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
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- Contribution to journal › Article
- 2018
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Mark
Predictors of responses to clinic-based childhood obesity care
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- Contribution to journal › Article
- 2017
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
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- Contribution to journal › Article
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Mark
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
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- Contribution to journal › Article
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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- Contribution to journal › Article
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Mark
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
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- Contribution to journal › Article
- 2016
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Mark
The genetic architecture of type 2 diabetes
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- Contribution to journal › Article
- 2014
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Mark
Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes
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- Contribution to journal › Article
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Mark
Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes
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- Contribution to journal › Article
- 2013
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Mark
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
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- Contribution to journal › Article
- 2012
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Mark
SNP in the genome-wide association study hotspot on chromosome 9p21 confers susceptibility to diabetic nephropathy in type 1 diabetes
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- Contribution to journal › Article
- 2010
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Mark
Analysis of TBC1D4 in patients with severe insulin resistance
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- Contribution to journal › Letter
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Mark
Genetic association analysis of LARS2 with type 2 diabetes
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- Contribution to journal › Article
- 2009
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Mark
The T allele of rs7903146 TCF7L2 is associated with impaired insulinotropic action of incretin hormones, reduced 24 h profiles of plasma insulin and glucagon, and increased hepatic glucose production in young healthy men
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- Contribution to journal › Article
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Mark
Functional Variant Disrupts Insulin Induction of USF1 Mechanism for USF1-Associated Dyslipidemias
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- Contribution to journal › Article
- 2008
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Mark
A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population
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- Contribution to journal › Article
- 2007
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Mark
Genetics of gestational diabetes mellitus.
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- Contribution to journal › Scientific review
- 2002
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Mark
Plasma ProANP(1-30) reflects salt sensitivity in subjects with heredity for hypertension
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- Contribution to journal › Article
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Mark
The genetic abnormality in the beta cell determines the response to an oral glucose load
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- Contribution to journal › Article