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- 2022
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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
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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
- 2021
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Mark
Elevated circulating follistatin associates with an increased risk of type 2 diabetes
(
- 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
(
- Contribution to journal › Article
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Mark
Circulating protein biomarkers predict incident hypertensive heart failure independently of N-terminal pro-B-type natriuretic peptide levels
(
- Contribution to journal › Article
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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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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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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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Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
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- Contribution to journal › Article
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Mark
The associations of self-rated health with cardiovascular risk proteins : A proteomics approach
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- Contribution to journal › Article
- 2018
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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
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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
(
- 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
ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis
(
- 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
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- Contribution to journal › Article
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Mark
Genetic determinants of circulating GIP and GLP-1 concentrations
(
- Contribution to journal › Article
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Mark
Exome-wide association study of plasma lipids in >300,000 individuals
(
- Contribution to journal › Article
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Mark
Soluble Urokinase-type Plasminogen Activator Receptor (suPAR) and Impaired Kidney Function in the Population-based Malmö Diet and Cancer Study
(
- 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.
(
- Contribution to journal › Article
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Mark
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
(
- Contribution to journal › Article
- 2015
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Mark
Intakes of omega-3 polyunsaturated fatty acids and blood pressure change over time: Possible interaction with genes involved in 20-HETE and EETs metabolism.
(
- Contribution to journal › Article
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Mark
Stable Peptide of the Endogenous Opioid Enkephalin Precursor and Breast Cancer Risk.
(
- Contribution to journal › Article
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Mark
Gene×dietary pattern interactions in obesity: analysis of up to 68,317 adults of European ancestry.
(
- Contribution to journal › Article
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Mark
Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age.
2015) In International Journal of Obesity(
- Contribution to journal › Article
- 2014
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Mark
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
(
- Contribution to journal › Article
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Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
(
- Contribution to journal › Article
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Mark
FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals.
(
- Contribution to journal › Article
- 2013
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Mark
Network-based Analysis of Genome Wide Association Data Provides Novel Candidate Genes for Lipid and Lipoprotein Traits
(
- Contribution to journal › Article
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Mark
Adipose tissue is inflamed in NAFLD due to obesity but not in NAFLD due to genetic variation in PNPLA3
(
- Contribution to journal › Article
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Mark
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
(
- 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.
(
- Contribution to journal › Article
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Mark
Role of TCF7L2 risk variant and dietary fibre intake on incident type 2 diabetes.
(
- Contribution to journal › Article
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Mark
Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality.
(
- Contribution to journal › Article
- 2011
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Mark
Pleiotropic Effects of GIP on Islet Function Involve Osteopontin
(
- 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
The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol
(
- Contribution to journal › Article
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Mark
Testing for an Unusual Distribution of Rare Variants
(
- Contribution to journal › Article
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Mark
Association between fat intake, physical activity and mortality depending on genetic variation in FTO.
(
- Contribution to journal › Article
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Mark
Dairy products and its association with incidence of cardiovascular disease: the Malmö diet and cancer cohort.
(
- 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
Testing for an unusual distribution of rare variation
(
- Contribution to journal › Published meeting abstract
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Mark
Interpretation of genome wide association data for lipoprotein traits using systems biology approach
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.323-323(
- Contribution to journal › Published meeting abstract
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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
Niemann-Pick C1 Modulates Hepatic Triglyceride Metabolism and Its Genetic Variation Contributes to Serum Triglyceride Levels
(
- Contribution to journal › Article
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Mark
High intake of fermented milk is associated with decreased risk of type 2 diabetes and better insulin sensitivity
2010) 46th Annual Meeting of the European-Association-for-the- Study-of-Diabetes (EASD) In Diabetologia 53(Suppl. 1). p.358-358(
- Contribution to journal › Published meeting abstract
-
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
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
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
(
- 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
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
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
-
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
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
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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
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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
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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
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Mark
Fat and carbohydrate intake modify the association between genetic variation in the FTO genotype and obesity.
(
- Contribution to journal › Article
- 2008
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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
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Mark
Cholesterol gene polymorphisms and cardiovascular events - Reply
(
- Contribution to journal › Letter
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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
Defining the spectrum of alleles that contribute to blood lipid concentrations in humans
(
- Contribution to journal › Scientific review
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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
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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
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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
The search for putative unifying genetic factors for components of the metabolic syndrome.
(
- Contribution to journal › Article
-
Mark
New insights into impaired muscle glycogen synthesis.
(
- Contribution to journal › Letter
- 2007
-
Mark
The variable clinical phenotype of liver glycogen synthase deficiency
(
- 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
-
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
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Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- Contribution to journal › Article
- 2006
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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
-
Mark
A polymorphism in the adiponectin gene influences adiponectin expression levels in visceral fat in obese subjects
(
- 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
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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
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Mark
Characterization of the human skeletal muscle glycogen synthase gene (GYS1) promoter.
(
- Contribution to journal › Article
-
Mark
Association between a polymorphism in the carboxyl ester lipase gene and serum cholesterol profile
(
- 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
- 2003
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Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
-
Mark
Effects of common polymorphisms in the alpha(1A)-, alpha(2B)-, beta(1)- and beta(2)-adrenoreceptors on haemodynamic responses to adrenaline
(
- Contribution to journal › Article
-
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
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Mark
Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: Report of three new mutations
(
- Contribution to journal › Article