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- 2022
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The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease : evidence from cross-sectional, longitudinal and Mendelian randomisation analyses
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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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Elevated circulating follistatin associates with an increased risk of type 2 diabetes
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- Contribution to journal › Article
- 2020
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Mark
Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease
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- Contribution to journal › Article
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Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality : a prospective study
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- Contribution to journal › Article
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Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
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- Contribution to journal › Article
- 2019
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Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
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- Contribution to journal › Article
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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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Novel subgroups of adult-onset diabetes and their association with outcomes : A data-driven cluster analysis of six variables
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- Contribution to journal › Article
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A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
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- Contribution to journal › Article
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Association between genetic risk variants and glucose intolerance during pregnancy in north Indian women
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- Contribution to journal › Article
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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
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
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- Contribution to journal › Article
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Mark
N1-methylnicotinamide is a signalling molecule produced in skeletal muscle coordinating energy metabolism
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- Contribution to journal › Article
- 2017
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Mark
Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD
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- Contribution to journal › Article
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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
Genetic determinants of circulating GIP and GLP-1 concentrations
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- Contribution to journal › Article
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Mark
Exome-wide association study of plasma lipids in >300,000 individuals
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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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Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls
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- Contribution to journal › Article
- 2016
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Mark
Glucose-Dependent Insulinotropic Polypeptide (GIP) Stimulates Osteopontin Expression in the Vasculature via Endothelin-1 and CREB.
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- Contribution to journal › Article
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Mark
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
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- Contribution to journal › Article
- 2012
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Mark
A systems genetics approach identifies genes and pathways for type 2 diabetes in human islets.
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- Contribution to journal › Article
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Mark
Genetic Variation in the Glucose-Dependent Insulinotropic Polypeptide Receptor Modifies the Association between Carbohydrate and Fat Intake and Risk of Type 2 Diabetes in the Malmo Diet and Cancer Cohort.
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- Contribution to journal › Article
- 2007
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Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
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- Contribution to journal › Article
- 2004
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Parallel manifestation of insulin resistance and beta cell decompensation is compatible with a common defect in Type 2 diabetes.
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- Contribution to journal › Article
- 2003
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
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- Contribution to journal › Article
- 2002
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Mark
Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.
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- Contribution to journal › Article