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- 2022
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Mark
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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Mark
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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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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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
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Mark
Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
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- Contribution to journal › Article
- 2018
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Mark
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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Mark
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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Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
- 2017
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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
Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD
(
- 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
(
- 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
(
- 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
- 2013
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Mark
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
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- Contribution to journal › Article
- 2012
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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
- 2011
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Mark
Pleiotropic Effects of GIP on Islet Function Involve Osteopontin
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- Contribution to journal › Article
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Mark
FTO, Type 2 Diabetes, and Weight Gain Throughout Adult Life A Meta-Analysis of 41,504 Subjects From the Scandinavian HUNT, MDC, and MPP Studies
(
- Contribution to journal › Article
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Mark
Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk: A Meta-Analysis of 218,166 Adults and 19,268 Children
(
- Contribution to journal › Article
- 2010
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Mark
Genome wide association analysis for free fatty acid levels in DGI
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.322-322(
- Contribution to journal › Published meeting abstract
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
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Mark
Plasma copeptin and the risk of diabetes mellitus.
(
- Contribution to journal › Article
- 2009
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Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
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- Contribution to journal › Article
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Mark
A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans
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- Contribution to journal › Article
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Mark
Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohorts
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- Contribution to journal › Article
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Mark
Genome-wide association study identifies eight loci associated with blood pressure
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- Contribution to journal › Article
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Mark
Prediction of Non-Alcoholic Fatty Liver Disease and Liver Fat Using Metabolic and Genetic Factors
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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
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Mark
Is there a unifying genetic factor predisposing to the metabolic syndrome?
2008) 44th EASD Annual Meeting of the European Association for the Study of Diabetes In Diabetologia 51(S1). p.32-33(
- Contribution to journal › Published meeting abstract
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Mark
C/EBP{alpha} in adipose tissue regulates genes in lipid and glucose metabolism and a genetic variation in C/EBP{alpha} is associated with serum levels of triglycerides.
(
- Contribution to journal › Article
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Mark
New insights into impaired muscle glycogen synthesis.
(
- Contribution to journal › Letter
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Mark
The search for putative unifying genetic factors for components of the metabolic syndrome.
(
- Contribution to journal › Article
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Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- Contribution to journal › Article
- 2007
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Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
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Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article
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Mark
Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
(
- Contribution to journal › Article
- 2006
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Mark
A polymorphism in the adiponectin gene influences adiponectin expression levels in visceral fat in obese subjects
(
- Contribution to journal › Article
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Mark
Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses
(
- Contribution to journal › Article
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Mark
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
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Mark
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals
(
- Contribution to journal › Article
- 2005
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Mark
Genetic prediction of future type 2 diabetes
(
- Contribution to journal › Article
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Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
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- Contribution to journal › Article
- 2004
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Mark
Characterization of the human skeletal muscle glycogen synthase gene (GYS1) promoter.
(
- Contribution to journal › Article
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Mark
Parallel manifestation of insulin resistance and beta cell decompensation is compatible with a common defect in Type 2 diabetes.
(
- Contribution to journal › Article
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Mark
Association between a polymorphism in the carboxyl ester lipase gene and serum cholesterol profile
(
- Contribution to journal › Article
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Mark
Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes
(
- Contribution to journal › Article
- 2003
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
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Mark
The insertion/deletion variation in the alpha2B-adrenoceptor does not seem to modify the risk for acute myocardial infarction, but may modify the risk for hypertension in sib-pairs from families with type 2 diabetes
(
- Contribution to journal › Article
- 2002
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Mark
Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.
(
- Contribution to journal › Article
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Mark
Polymorphism in the Calpain 10 gene influences glucose metabolism in human fat cells
(
- Contribution to journal › Article
-
Mark
Variants in the calpain-10 gene predispose to insulin resistance and elevated free fatty acid levels.
(
- Contribution to journal › Article
- 2001
-
Mark
Common variants in the beta2-(Gln27Glu) and beta3-(Trp64Arg)--adrenoceptor genes are associated with elevated serum NEFA concentrations and type II diabetes
(
- Contribution to journal › Article
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Mark
Beta(2)-adrenergic receptor gene variation and hypertension in subjects with type 2 diabetes
(
- Contribution to journal › Article
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Mark
The ACE gene I/D polymorphism is associated with higher mortality in men with hypertension and type 2 diabetes
(
- Contribution to journal › Article
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Mark
Characterization of the annexin I gene and evaluation of its role in type 2 diabetes
(
- Contribution to journal › Article
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Mark
The dysmetabolic syndrome
(
- Contribution to journal › Article
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Mark
Polymorphism in the beta(1)-adrenergic receptor gene and hypertension
(
- Contribution to journal › Article
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Mark
A gene conferring susceptibility to type 2 diabetes in conjunction with obesity is located on chromosome 18p11
(
- Contribution to journal › Article
- 2000
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Mark
Association between a variant in the 11 beta-hydroxysteroid dehydrogenase type 2 gene and primary hypertension
(
- Contribution to journal › Article
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Mark
Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians
(
- Contribution to journal › Article
-
Mark
Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension
(
- Contribution to journal › Article
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Mark
Interaction between the Asn291Ser variant of the LPL gene and insulin resistance on dyslipidaemia in high risk individuals for Type 2 diabetes mellitus
(
- Contribution to journal › Article
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Mark
Angiotensin converting enzyme (ACE) gene polymorphism in sarcoidosis in relation to associated autoimmune diseases
(
- Contribution to journal › Article
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Mark
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
(
- Contribution to journal › Article
-
Mark
The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of stroke
(
- Contribution to journal › Article
- 1999
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Mark
A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene
(
- Contribution to journal › Article
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Mark
Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and diabetes project
(
- Contribution to journal › Article
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Mark
Expression of naturally occurring variants in the muscle glycogen synthase gene
(
- Contribution to journal › Article