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- 2010
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Mark
Genetic susceptibility for obesity increases the risk of type 2 diabetes and is modified by macronutrient intakes
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.50-50(
- Contribution to journal › Published meeting abstract
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Mark
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
(
- Contribution to journal › Article
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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
Does macronutrient intake or physical activity level interact with genetic risk for increased fasting glucose?
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.313-313(
- Contribution to journal › Published meeting abstract
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Mark
A gene score of nine LDL and HDL regulating genes is associated with fluvastatin induced cholesterol changes in women.
(
- Contribution to journal › Article
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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
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
(
- 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
Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states
(
- 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
(
- Contribution to journal › Article
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Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
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Mark
Prediction of Non-Alcoholic Fatty Liver Disease and Liver Fat Using Metabolic and Genetic Factors
(
- 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
(
- Contribution to journal › Article
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Mark
The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver
(
- Contribution to journal › Article
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Mark
Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population
(
- Contribution to journal › Article
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Mark
Association between fat intake, physical activity and mortality depending on genetiv variation in FTO
2009) 45th Annual Meeting of the European-Association-for-the-Study-of-Diabetes In Diabetologia 52(Suppl 1). p.104-104(
- Contribution to journal › Published meeting abstract
-
Mark
Functional characterisation of the glucokinase regulatory protein gene variant P446L shows diminished regulation by fructose-6 phosphate resulting in increased glucokinase activity
2009) 45th Annual Meeting of the European-Association-for-the-Study-of-Diabetes In Diabetologia 52(Suppl 1). p.237-237(
- Contribution to journal › Published meeting abstract
-
Mark
ION Mobility Analysis Of Lipoprotein Subfractions Suggests Three Independent Mechanisms Of Cardiovascular Risk
(
- Contribution to journal › Published meeting abstract
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Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
-
Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies 3 Independent Axes of Cardiovascular Risk
2009) Joint Nutrition, Physical Activity and Metabolism Conference/49th Cardiovascular Disease Epidemiology and Prevention, 2009 In Circulation 119(10). p.282-283(
- Contribution to journal › Published meeting abstract
-
Mark
Fat and carbohydrate intake modify the association between genetic variation in the FTO genotype and obesity.
(
- Contribution to journal › Article
-
Mark
Ion Mobility Analysis of Lipoprotein Subfractions Identifies Three Independent Axes of Cardiovascular Risk.
(
- Contribution to journal › Article
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Mark
The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.
(
- Contribution to journal › Article
- 2008
-
Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
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Mark
Using the mouse model to confirm genes identified by genomewide association studies for the complex trait HDL cholesterol
2008) Arteriosclerosis, Thrombosis, and Vascular Biology Annual Conference 2008Back In Arteriosclerosis, Thrombosis, and Vascular Biology 28(6). p.36-36(
- Contribution to journal › Published meeting abstract
-
Mark
Defining the spectrum of alleles that contribute to blood lipid concentrations in humans
(
- Contribution to journal › Scientific review
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Mark
Cholesterol gene polymorphisms and cardiovascular events - Reply
(
- Contribution to journal › Letter
-
Mark
A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population
(
- Contribution to journal › Article
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Mark
Polymorphism associated with cholesterol and risk of cardiovascular events
(
- 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
-
Mark
The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of cardiovascular risk factors and coronary events in patients with hypertension
2008) 18th Scientific Meeting of the European-Society-of-Hypertension/22nd Scientific Meeting of the International-Society-of-Hypertension In Journal of Hypertension 26(Suppl. 1). p.141-142(
- Contribution to journal › Published meeting abstract
-
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
-
Mark
Association between an estrogen receptor alpha polymorphism (ERA : rs2234693) and the metabolic syndrome and cardiovascular and cerebrovascular morbidity and mortality
2008) 18th Scientific Meeting of the European-Society-of-Hypertension/22nd Scientific Meeting of the International-Society-of-Hypertension In Journal of Hypertension 26(Suppl. 1). p.341-341(
- Contribution to journal › Published meeting abstract
-
Mark
New insights into impaired muscle glycogen synthesis.
(
- Contribution to journal › Letter
-
Mark
The search for putative unifying genetic factors for components of the metabolic syndrome.
(
- Contribution to journal › Article
- 2007
-
Mark
The variable clinical phenotype of liver glycogen synthase deficiency
(
- Contribution to journal › Article
-
Mark
Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
(
- Contribution to journal › Article
-
Mark
A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study
(
- Contribution to journal › Article
-
Mark
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
- 2006
-
Mark
A polymorphism in the adiponectin gene influences adiponectin expression levels in visceral fat in obese subjects
(
- Contribution to journal › Article
-
Mark
Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses
(
- Contribution to journal › Article
-
Mark
Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality.
(
- Contribution to journal › Article
-
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
-
Mark
Genetic prediction of future type 2 diabetes
(
- Contribution to journal › Article
-
Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
(
- Contribution to journal › Article
- 2004
-
Mark
Association between a polymorphism in the carboxyl ester lipase gene and serum cholesterol profile
(
- Contribution to journal › Article
-
Mark
Characterization of the human skeletal muscle glycogen synthase gene (GYS1) promoter.
(
- Contribution to journal › Article
-
Mark
Parallel manifestation of insulin resistance and beta cell decompensation is compatible with a common defect in Type 2 diabetes.
(
- Contribution to journal › Article
-
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