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24-h ambulatory blood pressure is linked to chromosome 18q21-22 and genetic variation of NEDD4L associates with cross-sectional and longitudinal blood pressure in Swedes

scientific article published on 21 June 2006

A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes

artículo científico publicado en 2018

A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity

article

A Variant Upstream of the CDH13 Adiponectin Receptor Gene and Metabolic Syndrome in Swedes

article

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A central role for GRB10 in regulation of islet function in man.

artículo científico publicado en 2014

A common variant upstream of the PAX6 gene influences islet function in man.

artículo científico publicado en 2011

A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study

artículo científico publicado en 2010

A functional variant of the NEDD4L gene is associated with beneficial treatment response with β-blockers and diuretics in hypertensive patients

scientific article published on 01 February 2011

A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women

artículo científico publicado en 2009

A genetic risk score for hypertension is associated with risk of thoracic aortic aneurysm

artículo científico publicado en 2019

A genome wide scan for early onset primary hypertension in Scandinavians

artículo científico publicado en 2003

A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia

artículo científico publicado en 2018

A male-specific quantitative trait locus on 1p21 controlling human stature

artículo científico publicado en 2005

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

artículo científico publicado en 2003

A myocardial infarction genetic risk score is associated with markers of carotid atherosclerosis

artículo científico publicado en 2011

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

article

A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene

artículo científico publicado en 1999

A variation in 3' UTR of hPTP1B increases specific gene expression and associates with insulin resistance

scientific article published on 06 February 2002

ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis.

artículo científico publicado en 2017

Age influences DNA methylation and gene expression of COX7A1 in human skeletal muscle

article

Altered DNA methylation and differential expression of genes influencing metabolism and inflammation in adipose tissue from subjects with type 2 diabetes

artículo científico publicado en 2014

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

artículo científico publicado en 2017

An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA.

artículo científico publicado en 2009

Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth Hormone

artículo científico publicado en 2015

Apolipoproteins, lipids and risk of cancer

artículo científico publicado en 2016

Assessment of conventional cardiovascular risk factors and multiple biomarkers for the prediction of incident heart failure and atrial fibrillation

artículo científico publicado en 2010

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

artículo científico publicado en 2010

Association between adducin-1 G460W variant and blood pressure in Swedes is dependent on interaction with body mass index and gender

artículo científico publicado en 2007

Association between genetic risk variants and glucose intolerance during pregnancy in north Indian women

Association between the human glycoprotein PC-1 gene and elevated glucose and insulin levels in a paired-sibling analysis

artículo científico publicado en 2000

Association of Chromosome 9p21 With Subsequent Coronary Heart Disease Events

artículo científico publicado en 2019

Association of common variation in the HNF1alpha gene region with risk of type 2 diabetes

scientific article published on 01 August 2005

Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis

artículo científico publicado en 2014

Association of the E23K polymorphism in the KCNJ11 gene with gestational diabetes mellitus

scientific article published on 17 November 2005

Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes

artículo científico publicado en 2004

Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes

article

Association testing of the protein tyrosine phosphatase 1B gene (PTPN1) with type 2 diabetes in 7,883 people

artículo científico publicado en 2005

Association testing of variants in the hepatocyte nuclear factor 4alpha gene with risk of type 2 diabetes in 7,883 people

artículo científico publicado en 2005

Authors' Reply

article published 28 February 2006

Blood-based biomarkers of age-associated epigenetic changes in human islets associate with insulin secretion and diabetes

artículo científico publicado en 2016

Cardiovascular consequences of a polygenetic component of blood pressure in an urban-based longitudinal study: the Malmö diet and cancer

artículo científico publicado en 2014

Cardiovascular morbidity and mortality associated with the metabolic syndrome

artículo científico publicado en 2001

Characterization of the Annexin I Gene and Evaluation of Its Role in Type 2 Diabetes

article

Chromosome 2q12, the ADRA2B I/D polymorphism and metabolic syndrome

artículo científico publicado en 2009

Chromosome 9p21 genetic variation explains 13% of cardiovascular disease incidence but does not improve risk prediction

artículo científico publicado en 2013

Chronic complications in patients with slowly progressing autoimmune type 1 diabetes (LADA).

artículo científico publicado en 1999

Clinical risk factors, DNA variants, and the development of type 2 diabetes

artículo científico publicado en 2008

Common Variants in the ENPP1 Gene Are Not Reproducibly Associated With Diabetes or Obesity

article

Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease

artículo científico publicado en 2014

Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals

artículo científico publicado en 2006

Common variants in HNF-1 alpha and risk of type 2 diabetes

artículo científico publicado en 2006

Common variants in MODY genes increase the risk of gestational diabetes mellitus

artículo científico publicado en 2006

Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetes

artículo científico publicado en 2008

Commonly consumed beverages associate with different lifestyle and dietary intakes

scientific article published on 26 April 2018

Connection between BMI related plasma metabolite profile and gut microbiota.

artículo científico publicado en 2018

Contribution of Known and Unknown Susceptibility Genes to Early-Onset Diabetes in Scandinavia: Evidence for Heterogeneity

article

Contribution of insulin-stimulated glucose uptake and basal hepatic insulin sensitivity to surrogate measures of insulin sensitivity

artículo científico publicado en 2004

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

artículo científico publicado en 2009

Cystatin C Is Not Causally Related to Coronary Artery Disease

artículo científico publicado en 2015

Cystatin C identifies cardiovascular risk better than creatinine-based estimates of glomerular filtration in middle-aged individuals without a history of cardiovascular disease.

artículo científico publicado en 2013

DNA methylation of loci within ABCG1 and PHOSPHO1 in blood DNA is associated with future type 2 diabetes risk

artículo científico publicado en 2016

Determinants of kidney function in Swedish families: role of heritable factors

artículo científico publicado en 2008

Diabetes-associated HLA genotypes affect birthweight in the general population

artículo científico publicado en 2005

Dietary and genetic risk scores and incidence of type 2 diabetes.

artículo científico publicado en 2018

Dimethylguanidino Valerate: A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality

artículo científico publicado en 2019

Dipping and variability of blood pressure and heart rate at night are heritable traits

artículo científico publicado en 2005

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

Duffy antigen receptor genetic variant and the association with Interleukin 8 levels

artículo científico publicado en 2015

Elevated Markers of Death Receptor-Activated Apoptosis are Associated with Increased Risk for Development of Diabetes and Cardiovascular Disease.

artículo científico publicado en 2017

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

artículo científico publicado en 2017

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2011

Evaluation of Common Variants in the Six Known Maturity-Onset Diabetes of the Young (MODY) Genes for Association With Type 2 Diabetes

article

Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes

artículo científico publicado en 2016

Exome array analysis of ischaemic stroke: results from a southern Swedish study

artículo científico publicado en 2016

Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

article

Fasting levels of growth hormone are associated with carotid intima media thickness but are not affected by fluvastatin treatment

artículo científico publicado en 2017

Fasting levels of high-sensitivity growth hormone predict cardiovascular morbidity and mortality: the Malmö Diet and Cancer study

artículo científico publicado en 2014

First trimester enterovirus IgM and beta cell autoantibodies in mothers to children affected by type 1 diabetes autoimmunity before 7 years of age.

artículo científico publicado en 2018

GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb

artículo científico publicado en 2015

Genetic Risk Prediction of Atrial Fibrillation

artículo científico publicado en 2016

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic and epigenetic factors are associated with expression of respiratory chain component NDUFB6 in human skeletal muscle

artículo científico publicado en 2007

Genetic and nongenetic regulation of CAPN10 mRNA expression in skeletal muscle

artículo científico publicado en 2005

Genetic determinants of circulating GIP and GLP-1 concentrations

artículo científico publicado en 2017

Genetic determinants of growth hormone and GH-related phenotypes

artículo científico publicado en 2017

Genetic evidence of assortative mating in humans

article

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Genetic polymorphisms for estimating risk of atrial fibrillation in the general population: a prospective study

artículo científico publicado en 2012

Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis

scientific article published on 27 July 2012

Genetic prediction of future type 2 diabetes

artículo científico publicado en 2005

Genetic prediction of postpartum diabetes in women with gestational diabetes mellitus

artículo científico publicado en 2012

Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs

artículo científico publicado en 2009

Genome-wide analysis yields new loci associating with aortic valve stenosis

artículo científico publicado en 2018

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

artículo científico publicado en 2007

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

scientific article published on 09 January 2020

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

artículo científico publicado en 2011

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

artículo científico publicado en 2009

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study

artículo científico publicado en 2002

Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality: a prospective study

scientific article published on 23 January 2020

Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes

artículo científico publicado en 2005

Haplotype structure and genotype-phenotype correlations of the sulfonylurea receptor and the islet ATP-sensitive potassium channel gene region

artículo científico publicado en 2004

Haplotype structures and large-scale association testing of the 5' AMP-activated protein kinase genes PRKAA2, PRKAB1, and PRKAB2 [corrected] with type 2 diabetes

artículo científico publicado en 2006

Heritability and familiality of type 2 diabetes and related quantitative traits in the Botnia Study

article by Peter Almgren et al published 9 August 2011 in Diabetologia

Heritability of ambulatory and office blood pressure phenotypes in Swedish families

artículo científico publicado en 2004

High Level of Fasting Plasma Proenkephalin-A Predicts Deterioration of Kidney Function and Incidence of CKD.

artículo científico publicado en 2016

High levels of nonesterified fatty acids are associated with increased familial risk of cardiovascular disease

artículo científico publicado en 2000

High-density haplotype structure and association testing of the insulin-degrading enzyme (IDE) gene with type 2 diabetes in 4,206 people

artículo científico publicado en 2006

Homozygosity for the EPHX2 K55R polymorphism increases the long-term risk of ischemic stroke in men: a study in Swedes

artículo científico publicado en 2010

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of CpG-SNPs associated with type 2 diabetes and differential DNA methylation in human pancreatic islets

artículo científico publicado en 2013

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

artículo científico publicado en 2013

Impact of an exercise intervention on DNA methylation in skeletal muscle from first-degree relatives of patients with type 2 diabetes

artículo científico publicado en 2012

Impact of the peroxisome proliferator activated receptor-gamma coactivator-1beta (PGC-1beta) Ala203Pro polymorphism on in vivo metabolism, PGC-1beta expression and fibre type composition in human skeletal muscle

scientific article published on 20 June 2007

Incident diabetes mellitus may explain the association between sleep duration and incident coronary heart disease.

artículo científico publicado en 2017

Increased Melatonin Signaling Is a Risk Factor for Type 2 Diabetes

artículo científico publicado en 2016

Insulin secretion and action in North Indian women during pregnancy.

artículo científico publicado en 2017

Insulin secretion and insulin sensitivity in relation to glucose tolerance: lessons from the Botnia Study

artículo científico publicado en 2000

Intakes of omega-3 polyunsaturated fatty acids and blood pressure change over time: Possible interaction with genes involved in 20-HETE and EETs metabolism

artículo científico publicado en 2015

Interaction between renal function and microalbuminuria for cardiovascular risk in hypertension: the nordic diltiazem study

artículo científico publicado en 2008

Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1/TaqIA on insulin sensitivity

artículo científico publicado en 2016

Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age

artículo científico publicado en 2015

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Less pronounced response to exercise in healthy relatives to type 2 diabetic subjects compared with controls

artículo científico publicado en 2015

Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes

artículo científico publicado en 2007

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

artículo científico publicado en 2010

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

artículo científico publicado en 2008

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

artículo científico publicado en 2020

Modelling of OGTT curve identifies 1 h plasma glucose level as a strong predictor of incident type 2 diabetes: results from two prospective cohorts

artículo científico publicado en 2014

Molecular correlates for maximal oxygen uptake and type 1 fibers

artículo científico publicado en 2008

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2018

Multiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twins

artículo científico publicado en 2004

N-Terminal Prosomatostatin as a Risk Marker for Cardiovascular Disease and Diabetes in a General Population

artículo científico publicado en 2016

N1-methylnicotinamide is a signalling molecule produced in skeletal muscle coordinating energy metabolism.

artículo científico publicado en 2018

NordicDB: a Nordic pool and portal for genome-wide control data

artículo científico publicado en 2010

Novel and conventional biomarkers for prediction of incident cardiovascular events in the community

artículo científico publicado en 2009

Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables

artículo científico publicado en 2018

Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium

artículo científico publicado en 2012

P128 Identification de nouveaux polymorphismes génétiques associés au risque de diabète de type 2 chez les obèses et non obèses européens

Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms

artículo científico publicado en 2012

Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus

scientific article published on 29 April 2019

Plasma concentration of Caspase-8 is associated with short sleep duration and the risk of incident diabetes mellitus

artículo científico publicado en 2018

Plasma copeptin and the risk of diabetes mellitus

artículo científico publicado en 2010

Plasma kidney injury molecule-1 (p-KIM-1) levels and deterioration of kidney function over 16 years

artículo científico publicado en 2020

Plasma levels of the proprotein convertase furin and incidence of diabetes and mortality

artículo científico publicado en 2018

Plasma lipid composition and risk of developing cardiovascular disease

artículo científico publicado en 2013

Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality

artículo científico publicado en 2012

Plasma stem cell factor levels are associated with risk of cardiovascular disease and death.

artículo científico publicado en 2017

Polygenetic risk for coronary artery disease increases hospitalization burden and mortality

artículo científico publicado en 2019

Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence

artículo científico publicado en 2018

Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality

artículo científico publicado en 2006

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

artículo científico publicado en 2007

Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes

artículo científico publicado en 2001

Postprandial Levels of Branch Chained and Aromatic Amino Acids Associate with Fasting Glycaemia

artículo científico publicado en 2016

Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants

Prediction of blood pressure changes over time and incidence of hypertension by a genetic risk score in Swedes

artículo científico publicado en 2012

Prediction of postpartum diabetes in women with gestational diabetes mellitus

artículo científico publicado en 2009

Predictors of and longitudinal changes in insulin sensitivity and secretion preceding onset of type 2 diabetes

artículo científico publicado en 2005

Prevalence and risk factors of gestational diabetes in Punjab, North India: results from a population screening program

artículo científico publicado en 2015

Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals

artículo científico publicado en 2003

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

artículo científico publicado en 2019

Reduced insulin exocytosis in human pancreatic β-cells with gene variants linked to type 2 diabetes

artículo científico publicado en 2012

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

artículo científico publicado en 2018

Risk factor exposure in individuals free from cardiovascular disease differs according to age at first myocardial infarction

artículo científico publicado en 2016

SNPs related to vitamin D and breast cancer risk: a case-control study

artículo científico publicado en 2018

Secreted frizzled-related protein 4 reduces insulin secretion and is overexpressed in type 2 diabetes

artículo científico publicado en 2012

Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women: results from two cohort studies in Swedes

artículo científico publicado en 2011

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

artículo científico publicado en 2009

Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21.

scientific article published on 22 January 2014

Soluble Urokinase-type Plasminogen Activator Receptor (suPAR) and Impaired Kidney Function in the Population-based Malmö Diet and Cancer Study

artículo científico publicado en 2017

Stable Peptide of the Endogenous Opioid Enkephalin Precursor and Breast Cancer Risk

artículo científico publicado en 2015

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

artículo científico publicado en 2012

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure

artículo científico publicado en 2008

Subsequent Event Risk in Individuals With Established Coronary Heart Disease

artículo científico publicado en 2019

The FOXC2 C-512T polymorphism is associated with obesity and dyslipidemia.

artículo científico publicado en 2004

The GH receptor exon 3 deleted/full-length polymorphism is associated with central adiposity in the general population

artículo científico publicado en 2014

The Krüppel-like factor 11 (KLF11) Q62R polymorphism is not associated with type 2 diabetes in 8,676 people

artículo científico publicado en 2006

The Renalase Asp37Glu polymorphism is not associated with hypertension and cardiovascular events in an urban-based prospective cohort: the Malmö Diet and cancer study

artículo científico publicado en 2012

The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of stroke

artículo científico publicado en 2000

The V433M variant of the CYP4F2 is associated with ischemic stroke in male Swedes beyond its effect on blood pressure

artículo científico publicado en 2008

The association of mitochondrial content with prevalent and incident type 2 diabetes.

artículo científico publicado en 2010

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

artículo científico publicado en 2010

The functional variant V433M of the CYP4F2 and the metabolic syndrome in Swedes

artículo científico publicado en 2012

The functional variant of the CLC-Kb channel T481S is not associated with blood pressure or hypertension in Swedes

artículo científico publicado en 2007

The metabolic syndrome influences the risk of chronic complications in patients with type II diabetes

artículo científico publicado en 2001

The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension

artículo científico publicado en 2009

The triglyceride content in skeletal muscle is associated with hepatic but not peripheral insulin resistance in elderly twins

artículo científico publicado en 2012

Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study

artículo científico publicado en 2017

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Utilization of genetic data can improve the prediction of type 2 diabetes incidence in a Swedish cohort

artículo científico publicado en 2017

Vanin-1 T26I polymorphism, hypertension and cardiovascular events in two large urban-based prospective studies in Swedes

artículo científico publicado en 2011

Variants in the FFAR1 gene are associated with beta cell function

artículo científico publicado en 2007

Variation in GYS1 interacts with exercise and gender to predict cardiovascular mortality

artículo científico publicado en 2007

Vasoactive peptides with angiogenesis-regulating activity predict cancer risk in males

artículo científico publicado en 2012

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

artículo

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