Peter Almgren (Former)
1 – 199 of 199
- show: 250
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2021
-
Mark
Methodological considerations for identifying multiple plasma proteins associated with all-cause mortality in a population-based prospective cohort
(
- Contribution to journal › Article
-
Mark
The genomics of heart failure : design and rationale of the HERMES consortium
(
- Contribution to journal › Article
-
Mark
Amino acids predict prognosis in patients with acute dyspnea
(
- Contribution to journal › Article
- 2020
-
Mark
Plasma kidney injury molecule-1 (p-KIM-1) levels and deterioration of kidney function over 16 years
2020) In Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 35(2). p.265-273(
- Contribution to journal › Article
-
Mark
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
(
- Contribution to journal › Article
-
Mark
Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality : a prospective study
(
- Contribution to journal › Article
-
Mark
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
(
- Contribution to journal › Article
- 2019
-
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
(
- Contribution to journal › Article
-
Mark
A genetic risk score for hypertension is associated with risk of thoracic aortic aneurysm
(
- Contribution to journal › Article
-
Mark
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
(
- Contribution to journal › Article
-
Mark
Commonly consumed beverages associate with different lifestyle and dietary intakes
(
- Contribution to journal › Article
-
Mark
Polygenetic risk for coronary artery disease increases hospitalization burden and mortality
(
- Contribution to journal › Article
-
Mark
Dimethylguanidino Valerate : A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality
(
- Contribution to journal › Article
-
Mark
Subsequent Event Risk in Individuals With Established Coronary Heart Disease
(
- Contribution to journal › Article
-
Mark
A catalog of genetic loci associated with kidney function from analyses of a million individuals
(
- Contribution to journal › Article
-
Mark
Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus
(
- Contribution to journal › Article
- 2018
-
Mark
Novel subgroups of adult-onset diabetes and their association with outcomes : A data-driven cluster analysis of six variables
(
- Contribution to journal › Article
-
Mark
N1-methylnicotinamide is a signalling molecule produced in skeletal muscle coordinating energy metabolism
(
- Contribution to journal › Article
-
Mark
Incident diabetes mellitus may explain the association between sleep duration and incident coronary heart disease
(
- Contribution to journal › Article
-
Mark
Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study
(
- Contribution to journal › Article
-
Mark
SNPs related to vitamin D and breast cancer risk : A case-control study
(
- Contribution to journal › Article
-
Mark
Dietary and genetic risk scores and incidence of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
A genome-wide association study of IgM antibody against phosphorylcholine : Shared genetics and phenotypic relationship to chronic lymphocytic leukemia
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- Contribution to journal › Article
-
Mark
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(
- Contribution to journal › Article
-
Mark
Association between genetic risk variants and glucose intolerance during pregnancy in north Indian women
(
- Contribution to journal › Article
-
Mark
Plasma levels of the proprotein convertase furin and incidence of diabetes and mortality
(
- Contribution to journal › Article
-
Mark
Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence
(
- Contribution to journal › Article
-
Mark
Multi-ethnic genome-wide association study for atrial fibrillation
(
- Contribution to journal › Article
-
Mark
First trimester enterovirus IgM and beta cell autoantibodies in mothers to children affected by type 1 diabetes autoimmunity before 7 years of age
(
- Contribution to journal › Article
-
Mark
Plasma concentration of Caspase-8 is associated with short sleep duration and the risk of incident diabetes mellitus
(
- Contribution to journal › Article
-
Mark
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
(
- Contribution to journal › Article
-
Mark
Genome-wide analysis yields new loci associating with aortic valve stenosis
(
- Contribution to journal › Article
-
Mark
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
(
- Contribution to journal › Article
-
Mark
Connection between BMI-Related Plasma Metabolite Profile and Gut Microbiota
(
- Contribution to journal › Article
- 2017
-
Mark
Plasma stem cell factor levels are associated with risk of cardiovascular disease and death
(
- Contribution to journal › Article
-
Mark
Insulin secretion and action in North Indian women during pregnancy
(
- Contribution to journal › Article
-
Mark
Elevated Markers of Death Receptor-Activated Apoptosis are Associated with Increased Risk for Development of Diabetes and Cardiovascular Disease
(
- Contribution to journal › Article
-
Mark
Genetic determinants of circulating GIP and GLP-1 concentrations
(
- Contribution to journal › Article
-
Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
(
- Contribution to journal › Article
-
Mark
Utilization of genetic data can improve the prediction of type 2 diabetes incidence in a Swedish cohort
(
- Contribution to journal › Article
-
Mark
ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis
(
- Contribution to journal › Article
-
Mark
Fasting levels of growth hormone are associated with carotid intima media thickness but are not affected by fluvastatin treatment
(
- Contribution to journal › Article
-
Mark
Genetic Risk Prediction of Atrial Fibrillation
(
- Contribution to journal › Article
-
Mark
Genetic determinants of growth hormone and GH-related phenotypes
(
- Contribution to journal › Article
-
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
-
Mark
High Level of Fasting Plasma Proenkephalin-A Predicts Deterioration of Kidney Function and Incidence of CKD
(
- Contribution to journal › Article
-
Mark
Parent-of-origin effects on gene expression in trios with type 2 diabetic offspring
2017)(
- Contribution to conference › Poster
- 2016
-
Mark
Risk factor exposure in individuals free from cardiovascular disease differs according to age at first myocardial infarction.
(
- Contribution to journal › Article
-
Mark
Apo-lipoproteins, lipids and risk of cancer.
(
- Contribution to journal › Article
-
Mark
Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.
(
- Contribution to journal › Article
-
Mark
Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes
(
- Contribution to journal › Article
-
Mark
N-terminal prosomatostatin as a risk marker for cardiovascular disease and diabetes in a general population
(
- Contribution to journal › Article
-
Mark
Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1/TaqIA on insulin sensitivity
(
- Contribution to journal › Article
-
Mark
Increased Melatonin Signaling Is a Risk Factor for Type 2 Diabetes
(
- Contribution to journal › Article
-
Mark
A Comparison of Rule-based Analysis with Regression Methods in Understanding the Risk Factors for Study Withdrawal in a Pediatric Study
(
- Contribution to journal › Article
-
Mark
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
DNA methylation of loci within ABCG1 and PHOSPHO1 in blood DNA is associated with future type 2 diabetes risk
(
- Contribution to journal › Article
-
Mark
Exome array analysis of ischaemic stroke : results from a southern Swedish study
(
- Contribution to journal › Article
-
Mark
Postprandial Levels of Branch Chained and Aromatic Amino Acids Associate with Fasting Glycaemia
(
- Contribution to journal › Article
- 2015
-
Mark
Cystatin C Is Not Causally Related to Coronary Artery Disease.
(
- Contribution to journal › Article
-
Mark
Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth Hormone.
(
- Contribution to journal › Article
-
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
-
Mark
Stable Peptide of the Endogenous Opioid Enkephalin Precursor and Breast Cancer Risk.
(
- Contribution to journal › Article
-
Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
-
Mark
Prevalence and Risk Factors of Gestational Diabetes in Punjab, North India - Results from a Population Screening Program.
(
- Contribution to journal › Article
-
Mark
The growth hormone receptor exon 3 deleted/full-length polymorphism is associated with central adiposity in the general population.
(
- Contribution to journal › Article
-
Mark
Duffy antigen receptor genetic variant and the association with Interleukin 8 levels.
(
- Contribution to journal › Article
-
Mark
Less pronounced response to exercise in healthy relatives to type 2 diabetics compared to controls.
(
- Contribution to journal › Article
-
Mark
GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb.
(
- Contribution to journal › Article
-
Mark
Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts
(
- Contribution to journal › Article
-
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
-
Mark
SNPS in FGF5 and ZNF652 show parent-of-origin specific effects on blood pressure in families from the Botnia study
2015)(
- Contribution to conference › Abstract
- 2014
-
Mark
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease.
(
- Contribution to journal › Article
-
Mark
Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.
(
- Contribution to journal › Article
-
Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
-
Mark
A Central Role for GRB10 in Regulation of Islet Function in Man.
(
- Contribution to journal › Article
-
Mark
Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.
(
- Contribution to journal › Article
-
Mark
Fasting levels of high-sensitivity growth hormone predict cardiovascular morbidity and mortality: the malmö diet and cancer study.
(
- Contribution to journal › Article
-
Mark
Altered DNA methylation and differential expression of genes influencing metabolism and inflammation in adipose tissue from subjects with type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö Diet and Cancer.
(
- Contribution to journal › Article
-
Mark
Cystatin C identifies cardiovascular risk better than creatinine-based estimates of glomerular filtration in middle-aged individuals without a history of cardiovascular disease.
(
- Contribution to journal › Article
- 2013
-
Mark
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
(
- Contribution to journal › Article
-
Mark
Plasma lipid composition and risk of developing cardiovascular disease.
(
- Contribution to journal › Article
-
Mark
Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets.
(
- Contribution to journal › Article
-
Mark
Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction.
(
- Contribution to journal › Article
-
Mark
Maternal transmission of variants in the THADA gene to offspring with type 2 diabetes
2013)(
- Contribution to conference › Poster
- 2012
-
Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmo Diet and cancer study
(
- Contribution to journal › Article
-
Mark
Secreted frizzled-related protein 4 reduces insulin secretion and is overexpressed in type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Prediction of Blood Pressure Changes Over Time and Incidence of Hypertension by a Genetic Risk Score in Swedes.
2012) In Hypertension(
- Contribution to journal › Article
-
Mark
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases
(
- Contribution to journal › Article
-
Mark
Reduced Insulin Exocytosis in Human Pancreatic β-cells With Gene Variants Linked to Type 2 Diabetes.
(
- Contribution to journal › Article
-
Mark
Genetic Polymorphisms for Estimating Risk of Atrial Fibrillation in the General Population: A Prospective Study
(
- Contribution to journal › Letter
-
Mark
Genetic prediction of postpartum diabetes in women with gestational diabetes mellitus
(
- Contribution to journal › Article
-
Mark
Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.
2012) In Journal of Internal Medicine(
- Contribution to journal › Article
-
Mark
The Triglyceride Content in Skeletal Muscle Is Associated with Hepatic But Not Peripheral Insulin Resistance in Elderly Twins.
2012) In The Journal of clinical endocrinology and metabolism(
- Contribution to journal › Article
-
Mark
A common variant upstream of the PAX6 gene influences islet function in man.
(
- Contribution to journal › Article
-
Mark
Vasoactive Peptides with Angiogenesis-Regulating Activity Predict Cancer Risk in Males.
2012) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 21(3). p.513-522(
- Contribution to journal › Article
-
Mark
Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality.
(
- Contribution to journal › Article
-
Mark
Impact of an Exercise Intervention on DNA Methylation in Skeletal Muscle From First-Degree Relatives of Patients With Type 2 Diabetes.
2012) In Diabetes(
- Contribution to journal › Article
-
Mark
Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.
(
- Contribution to journal › Article
-
Mark
A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis.
(
- Contribution to journal › Article
-
Mark
The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
(
- Contribution to journal › Article
- 2011
-
Mark
Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes
(
- Contribution to journal › Article
-
Mark
A functional variant of the NEDD4L gene is associated with beneficial treatment response with β-blockers and diuretics in hypertensive patients.
(
- Contribution to journal › Article
-
Mark
Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes.
2011) In Nutrition Metabolism and Cardiovascular Diseases(
- Contribution to journal › Article
-
Mark
Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study.
(
- Contribution to journal › Article
-
Mark
A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes.
(
- Contribution to journal › Article
-
Mark
Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes.
(
- Contribution to journal › Article
- 2010
-
Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
(
- Contribution to journal › Article
-
Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
-
Mark
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
(
- Contribution to journal › Article
-
Mark
Hundreds of variants clustered in genomic loci and biological pathways affect human height
(
- Contribution to journal › Article
-
Mark
NordicDB: a Nordic pool and portal for genome-wide control data
(
- Contribution to journal › Article
-
Mark
The common functional polymorphism -50G>T of the CYP2J2 gene is not associated with ischemic coronary and cerebrovascular events in an urban-based sample of Swedes.
(
- Contribution to journal › Article
-
Mark
Prediction of postpartum diabetes in women with gestational diabetes mellitus
(
- Contribution to journal › Article
-
Mark
A gene score of nine LDL and HDL regulating genes is associated with fluvastatin induced cholesterol changes in women.
(
- Contribution to journal › Article
-
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
-
Mark
A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study
(
- Contribution to journal › Article
-
Mark
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
(
- Contribution to journal › Article
-
Mark
Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes.
(
- Contribution to journal › Article
-
Mark
Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation.
(
- Contribution to journal › Article
-
Mark
An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA.
(
- Contribution to journal › Article
-
Mark
The Association of Mitochondrial Content with Prevalent and Incident Type 2 Diabetes.
(
- Contribution to journal › Article
-
Mark
Plasma copeptin and the risk of diabetes mellitus.
(
- Contribution to journal › Article
- 2009
-
Mark
Homozygosity for the EPHX2 K55R Polymorphism Increases the Long-Term Risk of Ischemic Stroke in Men: A Study in Swedes
2009) 10th Annual Conference on Arteriosclerosis, Thrombosis and Vascular Biology In Arteriosclerosis, Thrombosis, and Vascular Biology 29(7). p.23-24(
- Contribution to journal › Published meeting abstract
-
Mark
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs
(
- Contribution to journal › Article
-
Mark
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
(
- Contribution to journal › Article
-
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
-
Mark
Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome.
(
- Contribution to journal › Article
-
Mark
Novel and conventional biomarkers for prediction of incident cardiovascular events in the community.
(
- Contribution to journal › Article
- 2008
-
Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
(
- Contribution to journal › Article
-
Mark
Interaction Between Renal Function and Microalbuminuria for Cardiovascular Risk in Hypertension The Nordic Diltiazem Study
(
- Contribution to journal › Article
-
Mark
Functional polymorphism of the NEDD4L gene strongly influences cardiovascular outcome in hypertensive patients treated with beta-blockers and diuretics
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.143-144(
- Contribution to journal › Published meeting abstract
-
Mark
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
(
- Contribution to journal › Article
-
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
Determinants of kidney function in Swedish families. Role of heritable factors
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.131-131(
- Contribution to journal › Published meeting abstract
-
Mark
Determinants of kidney function in Swedish families: role of heritable factors.
(
- Contribution to journal › Article
-
Mark
Functional variation of the NEDD4L gene predicts ischemic stroke
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.134-134(
- Contribution to journal › Published meeting abstract
-
Mark
Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The V433M Variant of the CYP4F2 Is Associated With Ischemic Stroke in Male Swedes Beyond Its Effect on Blood Pressure.
(
- Contribution to journal › Article
-
Mark
Clinical risk factors, DNA variants, and the development of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscle.
(
- Contribution to journal › Article
-
Mark
Molecular correlates for maximal oxygen uptake (VO2max) and type 1 fibers.
(
- Contribution to journal › Article
-
Mark
The Environmental Determinants of Diabetes in the Young (TEDDY) Study
(
- Contribution to journal › Article
- 2007
-
Mark
Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion
(
- Contribution to journal › Article
-
Mark
Impact of the peroxisome proliferator activated receptor-gamma coactivator-1 beta (PGC-1 beta) Ala203Pro polymorphism on in vivo metabolism, PGC-1 beta expression and fibre type composition in human skeletal muscle
(
- Contribution to journal › Article
-
Mark
Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender.
(
- Contribution to journal › Article
-
Mark
The environmental determinants of diabetes in the young (TEDDY) study: Study design
(
- Contribution to journal › Article
-
Mark
Variants in the FFAR1 Gene Are Associated with Beta Cell Function
(
- Contribution to journal › Article
-
Mark
Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle
(
- Contribution to journal › Article
-
Mark
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
(
- 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
Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes
(
- Contribution to journal › Article
-
Mark
The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes.
(
- Contribution to journal › Article
-
Mark
Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
(
- Contribution to journal › Article
- 2006
-
Mark
Authors' reply.
(
- Contribution to journal › Letter
-
Mark
Common variants in HNF-1 alpha and risk of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Common variants in MODY genes increase the risk of gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Haplotype structures and large-scale association testing of the 5 ' AMP-activated protein kinase genes PRK4A2, PRKAB1, and PRK4B1 with type 2 diabetes
(
- 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 variants in the ENPP1 gene are not reproducibly associated with diabetes or obesity
(
- 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
-
Mark
24-hour Ambulatory Blood Pressure is Linked to Chromosome 18q21-22 and Genetic Variation of NEDD4L Associates with Cross-Sectional and Longitudinal Blood Pressure in Swedes.
(
- Contribution to journal › Article
-
Mark
The Kruppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people
(
- Contribution to journal › Article
-
Mark
High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people
(
- Contribution to journal › Article
- 2005
-
Mark
Association of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Diabetes-associated HLA genotypes affect birthweight in the general population.
(
- Contribution to journal › Article
-
Mark
Dipping and variability of blood pressure and heart rate at night are heritable traits.
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Genetic prediction of future type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
(
- Contribution to journal › Article
-
Mark
Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
Association of common variation in the HNF1 alpha gene region with risk of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people
(
- Contribution to journal › Article
-
Mark
Genetic and Nongenetic Regulation of CAPN10 mRNA Expression in Skeletal Muscle.
(
- Contribution to journal › Article
-
Mark
Association testing of variants in the hepatocyte nuclear factor 4 alpha gene with risk of type 2 diabetes in 7,883 people
(
- Contribution to journal › Article
-
Mark
A male-specific quantitative trait locus on 1p21 controlling human stature
(
- Contribution to journal › Article
- 2004
-
Mark
Contribution of insulin-stimulated glucose uptake and basal hepatic insulin sensitivity to surrogate measures of insulin sensitivity.
(
- Contribution to journal › Article
-
Mark
The FOXC2 C-512T Polymorphism Is Associated with Obesity and Dyslipidemia.
(
- 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
-
Mark
Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins.
(
- Contribution to journal › Article
-
Mark
Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region.
(
- Contribution to journal › Article
-
Mark
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- Contribution to journal › Article
- 2003
-
Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
-
Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
-
Mark
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity.
(
- Contribution to journal › Article
- 2002
-
Mark
A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
(
- Contribution to journal › Article
-
Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
- 2001
-
Mark
The metabolic syndrome influences the risk of chronic complications in patients with type II diabetes
(
- Contribution to journal › Article
-
Mark
Characterization of the annexin I gene and evaluation of its role in type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Cardiovascular morbidity and mortality associated with the metabolic syndrome
(
- Contribution to journal › Article
-
Mark
Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes
(
- Contribution to journal › Article
- 2000
-
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
-
Mark
A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene
(
- Contribution to journal › Article