| human | Q5 |
| P496 | ORCID iD | 0000-0002-3578-2503 |
| P735 | given name | Marju | Q43466704 |
| Marju | Q43466704 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q51300940 | 1C.07: PRONEUROTENSIN INDEPENDENTLY PREDICTS CARDIOVASCULAR DISEASE. THE MALMÖ PREVENTIVE PROJECT. |
| Q56836084 | 40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 |
| Q57122175 | A Gene Conferring Susceptibility to Type 2 Diabetes in Conjunction With Obesity Is Located on Chromosome 18p11 |
| Q52804042 | A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. |
| Q92082619 | A Health-Conscious Food Pattern Is Associated with Prediabetes and Gut Microbiota in the Malmö Offspring Study |
| Q37050689 | A High Diet Quality Based on Dietary Recommendations Is Not Associated with Lower Incidence of Type 2 Diabetes in the Malmö Diet and Cancer Cohort |
| Q88666762 | A Western dietary pattern is prospectively associated with cardio-metabolic traits and incidence of the metabolic syndrome |
| Q92451898 | A catalog of genetic loci associated with kidney function from analyses of a million individuals |
| Q46118770 | A common variant in PNPLA3, which encodes adiponutrin, is associated with liver fat content in humans |
| Q36988260 | A diabetes-predictive amino acid score and future cardiovascular disease |
| Q91493321 | A favorable lifestyle lowers the risk of coronary artery disease consistently across strata of non-modifiable risk factors in a population-based cohort |
| Q33634188 | A gene score of nine LDL and HDL regulating genes is associated with fluvastatin-induced cholesterol changes in women |
| Q50034788 | A genetic risk score for fasting plasma glucose is independently associated with arterial stiffness: a Mendelian randomization study |
| Q47697202 | A genome wide scan for early onset primary hypertension in Scandinavians |
| Q36016822 | A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study |
| Q35447506 | A male-specific quantitative trait locus on 1p21 controlling human stature |
| Q34145381 | A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses |
| Q50547353 | A non-synonymous variant in SLC30A8 is not associated with type 1 diabetes in the Danish population. |
| Q60956488 | 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 |
| Q78126473 | A paired-sibling analysis of the XbaI polymorphism in the muscle glycogen synthase gene |
| Q81363689 | A polymorphism in the adiponectin gene influences adiponectin expression levels in visceral fat in obese subjects |
| Q51330074 | A population-based study on the prevalence of NASH using scores validated against liver histology. |
| Q43126846 | A prospective study of dietary and supplemental zinc intake and risk of type 2 diabetes depending on genetic variation in SLC30A8. |
| Q33808002 | ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis. |
| Q104509217 | Abdominal Fat and Metabolic Health Markers but Not PNPLA3 Genotype Predicts Liver Fat Accumulation in Response to Excess Intake of Energy and Saturated Fat in Healthy Individuals |
| Q43696026 | Adipocyte size is associated with NAFLD independent of obesity, fat distribution, and PNPLA3 genotype |
| Q44842946 | Adipose tissue is inflamed in NAFLD due to obesity but not in NAFLD due to genetic variation in PNPLA3. |
| Q57303438 | Adiposity and Genetic Factors in Relation to Triglycerides and Triglyceride-Rich Lipoproteins in the Women's Genome Health Study |
| Q57224275 | Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes |
| Q33834492 | An obligatory role for neurotensin in high-fat-diet-induced obesity |
| Q54158424 | Angiotensin converting enzyme (ACE) gene polymorphism in sarcoidosis in relation to associated autoimmune diseases. |
| Q38916878 | Apolipoproteins, lipids and risk of cancer |
| Q44870066 | Association between a polymorphism in the carboxyl ester lipase gene and serum cholesterol profile |
| Q73292433 | Association between a variant in the 11 beta-hydroxysteroid dehydrogenase type 2 gene and primary hypertension |
| Q57271602 | Association between fat intake, physical activity and mortality depending on genetic variation in FTO |
| Q37109483 | Association between glucokinase regulatory protein (GCKR) and apolipoprotein A5 (APOA5) gene polymorphisms and triacylglycerol concentrations in fasting, postprandial, and fenofibrate-treated states |
| Q50125663 | Association between systemic leptin and neurotensin concentration in adult individuals with and without type 2 diabetes mellitus |
| Q90189076 | Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study |
| Q101220339 | Association of Circulating Monocyte Chemoattractant Protein-1 Levels With Cardiovascular Mortality: A Meta-analysis of Population-Based Studies |
| Q35965028 | Association of Lipid-Related Genetic Variants with the Incidence of Atrial Fibrillation: The AFGen Consortium |
| Q95926655 | Association of TIM-1 (T-Cell Immunoglobulin and Mucin Domain 1) With Incidence of Stroke |
| Q30303053 | Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis |
| Q30411387 | Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks |
| Q57249783 | Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses |
| Q81052868 | Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes |
| Q43612366 | Beta(2)-adrenergic receptor gene variation and hypertension in subjects with type 2 diabetes |
| Q24622541 | Biological, clinical and population relevance of 95 loci for blood lipids |
| Q64054407 | Biomarkers of blood cadmium and incidence of cardiovascular events in non-smokers: results from a population-based proteomics study |
| Q49807681 | Blood lipid genetic scores, the HMGCR gene and cancer risk: a Mendelian randomization study |
| Q102385002 | Blood pressure and bladder cancer risk in men by use of survival analysis and in interaction with NAT2 genotype, and by Mendelian randomization analysis |
| Q42808906 | CCAAT/enhancer binding protein alpha (C/EBPalpha) in adipose tissue regulates genes in lipid and glucose metabolism and a genetic variation in C/EBPalpha is associated with serum levels of triglycerides |
| Q90920275 | Cardiometabolic Polygenic Risk Scores and Osteoarthritis Outcomes: A Mendelian Randomization Study Using Data From the Malmö Diet and Cancer Study and the UK Biobank |
| Q44253817 | Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene |
| Q57122150 | Characterization of the Annexin I Gene and Evaluation of Its Role in Type 2 Diabetes |
| Q37363218 | Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect |
| Q42456711 | Characterization of the human skeletal muscle glycogen synthase gene (GYS1) promoter |
| Q92760660 | Circulating HER2/ErbB2 Levels Are Associated With Increased Incidence of Diabetes: A Population-Based Cohort Study |
| Q93059472 | Circulating Monocyte Chemoattractant Protein-1 and Risk of Stroke: Meta-Analysis of Population-Based Studies Involving 17 180 Individuals |
| Q94915548 | Circulating protein biomarkers predict incident hypertensive heart failure independently of N-terminal pro-B-type natriuretic peptide levels |
| Q57012027 | Circulating triacylglycerol signatures and insulin sensitivity in NAFLD associated with the E167K variant in TM6SF2 |
| Q36851336 | Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease |
| Q24650362 | Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations |
| Q79143599 | Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individuals |
| Q24598765 | Common variants at 30 loci contribute to polygenic dyslipidemia |
| Q43622538 | Common variants in the beta2-(Gln27Glu) and beta3-(Trp64Arg)--adrenoceptor genes are associated with elevated serum NEFA concentrations and type II diabetes |
| Q88480265 | Commonly consumed beverages associate with different lifestyle and dietary intakes |
| Q95269664 | Comparing Self-Reported Sugar Intake With the Sucrose and Fructose Biomarker From Overnight Urine Samples in Relation to Cardiometabolic Risk Factors |
| Q64117628 | Complement C3 and incident hospitalization due to chronic kidney disease: a population-based cohort study |
| Q50160843 | Connection between BMI related plasma metabolite profile and gut microbiota. |
| Q57271604 | Dairy products and its association with incidence of cardiovascular disease: the Malmö diet and cancer cohort |
| Q37128474 | Defining the spectrum of alleles that contribute to blood lipid concentrations in humans |
| Q56987983 | Diabetes mellitus and risk of prostate cancer in the EuropeanProspectiveInvestigation into Cancer and Nutrition |
| Q36941781 | Diet Quality and Change in Blood Lipids during 16 Years of Follow-up and Their Interaction with Genetic Risk for Dyslipidemia. |
| Q55002836 | Dietary and genetic risk scores and incidence of type 2 diabetes. |
| Q34395592 | Dietary fiber, carbohydrate quality and quantity, and mortality risk of individuals with diabetes mellitus |
| Q40187694 | Dietary starch intake modifies the relation between copy number variation in the salivary amylase gene and BMI. |
| Q90165082 | Dimethylguanidino Valerate: A Lifestyle-Related Metabolite Associated With Future Coronary Artery Disease and Cardiovascular Mortality |
| Q102369495 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals |
| Q40005937 | Do Genetic Factors Modify the Relationship Between Obesity and Hypertriglyceridemia? Findings From the GLACIER and the MDC Studies |
| Q84582796 | Dual metabolic defects are required to produce hypertriglyceridemia in obese subjects |
| Q44272753 | Effects of common polymorphisms in the alpha1A-, alpha2B-, beta1- and beta2-adrenoreceptors on haemodynamic responses to adrenaline |
| Q50059701 | Elevated Markers of Death Receptor-Activated Apoptosis are Associated with Increased Risk for Development of Diabetes and Cardiovascular Disease. |
| Q40042355 | Eosinophil Cationic Protein, Carotid Plaque, and Incidence of Stroke |
| Q91043737 | Ergothioneine is associated with reduced mortality and decreased risk of cardiovascular disease |
| Q42390043 | Erratum to: The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levels |
| Q57336880 | Erratum: Corrigendum: Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans |
| Q53140618 | Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. |
| Q48185853 | Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls |
| Q102202543 | Estimated salt intake and risk of atrial fibrillation in a prospective community-based cohort |
| Q103835897 | Evidence for a protective role of placental growth factor in cardiovascular disease |
| Q39786100 | Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes |
| Q30276497 | Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits |
| Q37727765 | Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia |
| Q57401681 | Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes |
| Q74671814 | Expression of naturally occurring variants in the muscle glycogen synthase gene |
| Q57823148 | FADD (Fas-Associated Protein With Death Domain), Caspase-3, and Caspase-8 and Incidence of Ischemic Stroke |
| Q35797073 | 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 |
| Q35000921 | Fat and carbohydrate intake modify the association between genetic variation in the FTO genotype and obesity. |
| Q88945733 | Food patterns in relation to weight change and incidence of type 2 diabetes, coronary events and stroke in the Malmö Diet and Cancer cohort |
| Q41127370 | Food sources of fat may clarify the inconsistent role of dietary fat intake for incidence of type 2 diabetes. |
| Q24633183 | From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus |
| Q34916970 | Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry |
| Q92803566 | Genetic Predisposition for Renal Dysfunction and Incidence of CKD in the Malmö Diet and Cancer Study |
| Q37682697 | Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease |
| Q57271598 | 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 Malmö Diet and Cancer Cohort |
| Q52837850 | Genetic determinants of circulating GIP and GLP-1 concentrations. |
| Q33748692 | Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study |
| Q55272361 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. |
| Q21563435 | Genetic prediction of future type 2 diabetes |
| Q37142066 | Genetic susceptibility to dyslipidemia and incidence of cardiovascular disease depending on a diet quality index in the Malmö Diet and Cancer cohort. |
| Q37300015 | Genetic susceptibility to obesity and diet intakes: association and interaction analyses in the Malmö Diet and Cancer Study |
| Q74316947 | Genetic variants of thiazide-sensitive NaCl-cotransporter in Gitelman's syndrome and primary hypertension |
| Q34036583 | Genetic variation in FADS1 has little effect on the association between dietary PUFA intake and cardiovascular disease. |
| Q47379175 | Genetic variation in PNPLA3 (adiponutrin) confers sensitivity to weight loss-induced decrease in liver fat in humans |
| Q51364415 | Genetic variation in PNPLA3 but not APOC3 influences liver fat in non-alcoholic fatty liver disease. |
| Q35053168 | Genetic variation in SULF2 is associated with postprandial clearance of triglyceride-rich remnant particles and triglyceride levels in healthy subjects |
| Q51431569 | Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohorts. |
| Q36763818 | Genetic variation in the fat mass and obesity-associated gene (FTO) in association with food preferences in healthy adults |
| Q28771769 | Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus |
| Q38610278 | Genetics of coronary heart disease: towards causal mechanisms, novel drug targets and more personalized prevention. |
| Q99591622 | Genome-Wide Polygenic Score, Clinical Risk Factors, and Long-Term Trajectories of Coronary Artery Disease |
| Q64983356 | Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. |
| Q113815800 | Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention |
| Q29547214 | Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels |
| Q29614414 | Genome-wide association study identifies eight loci associated with blood pressure |
| Q61480149 | Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank |
| Q56342134 | Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium |
| Q100694636 | Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals |
| Q51296688 | Glucose-Dependent Insulinotropic Polypeptide Stimulates Osteopontin Expression in the Vasculature via Endothelin-1 and CREB. |
| Q74320465 | Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations |
| Q57802372 | Growth differentiation factor 15 is positively associated with incidence of diabetes mellitus: the Malmö Diet and Cancer-Cardiovascular Cohort |
| Q100496892 | Gut microbiota composition in relation to intake of added sugar, sugar-sweetened beverages and artificially sweetened beverages in the Malmö Offspring Study |
| Q96290990 | Height, body mass index, and prostate cancer risk and mortality by way of detection and cancer risk category |
| Q40656900 | High Level of Fasting Plasma Proenkephalin-A Predicts Deterioration of Kidney Function and Incidence of CKD. |
| Q64241987 | High Levels of Soluble Lectinlike Oxidized Low-Density Lipoprotein Receptor-1 Are Associated With Carotid Plaque Inflammation and Increased Risk of Ischemic Stroke |
| Q92655552 | High Plasma sRAGE (Soluble Receptor for Advanced Glycation End Products) Is Associated With Slower Carotid Intima-Media Thickness Progression and Lower Risk for First-Time Coronary Events and Mortality |
| Q57271599 | High disaccharide intake associates with atherogenic lipoprotein profile |
| Q44517811 | High intakes of protein and processed meat associate with increased incidence of type 2 diabetes. |
| Q37729192 | Higher Levels of Serum Zonulin May Rather Be Associated with Increased Risk of Obesity and Hyperlipidemia, Than with Gastrointestinal Symptoms or Disease Manifestations |
| Q92756608 | Human PNPLA3-I148M variant increases hepatic retention of polyunsaturated fatty acids |
| Q90245088 | Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease |
| Q100689511 | Identification of Inflammatory and Disease-Associated Plasma Proteins that Associate with Intake of Added Sugar and Sugar-Sweetened Beverages and Their Role in Type 2 Diabetes Risk |
| Q87409473 | Impaired fibrous repair: a possible contributor to atherosclerotic plaque vulnerability in patients with type II diabetes |
| Q40318581 | Impaired hepatic lipid synthesis from polyunsaturated fatty acids in TM6SF2 E167K variant carriers with NAFLD. |
| Q63348335 | Increased Plasma Proneurotensin Levels Identify NAFLD in Adults With and Without Type 2 Diabetes |
| Q57457458 | Increased vascular endothelial growth factor D is associated with atrial fibrillation and ischaemic stroke |
| Q35958484 | Intake levels of dietary long-chain PUFAs modify the association between genetic variation in FADS and LDL-C. |
| Q40281476 | Intakes of omega-3 polyunsaturated fatty acids and blood pressure change over time: Possible interaction with genes involved in 20-HETE and EETs metabolism |
| Q40949611 | Integrator of Stress Responses Calmodulin Binding Transcription Activator 1 (Camta1) Regulates miR-212/miR-132 Expression and Insulin Secretion |
| Q38864204 | Interaction between rs10830963 polymorphism in MTNR1B and lifestyle intervention on occurrence of gestational diabetes |
| Q73176529 | Interaction between the Asn291Ser variant of the LPL gene and insulin resistance on dyslipidaemia in high risk individuals for Type 2 diabetes mellitus |
| Q34351920 | Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies |
| Q36579238 | Inverse relationship between a genetic risk score of 31 BMI loci and weight change before and after reaching middle age |
| Q37409448 | Ion mobility analysis of lipoprotein subfractions identifies three independent axes of cardiovascular risk |
| Q36692469 | Isolation and Characterization of the Human Muscle Glycogen Synthase Gene |
| Q71215659 | Lack of association between the Gly40Ser polymorphism in the glucagon receptor gene and NIDDM in Finland |
| Q30252611 | Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. |
| Q91938289 | Lifestyle and cancer incidence and mortality risk depending on family history of cancer in two prospective cohorts |
| Q45210179 | Lifestyle factors and mortality risk in individuals with diabetes mellitus: are the associations different from those in individuals without diabetes? |
| Q50456990 | Liver fat content and hepatic insulin sensitivity in overweight patients with type 1 diabetes. |
| Q30408720 | Loss-of-function mutations in APOC3, triglycerides, and coronary disease |
| Q96021626 | MARC1 variant rs2642438 increases hepatic phosphatidylcholines and decreases severity of non-alcoholic fatty liver disease in humans |
| Q98620582 | Magnitude of rise in proneurotensin is related to amount of triglyceride appearance in blood after standardized oral intake of both saturated and unsaturated fat |
| Q35916172 | Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes |
| Q94557211 | Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthood |
| Q37610893 | Meta-analysis of gene-level tests for rare variant association |
| Q101155742 | Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline |
| Q56361973 | Multi-ethnic genome-wide association study for atrial fibrillation |
| Q34467062 | Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension |
| Q24320564 | Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0 |
| Q30657033 | Network-based analysis of genome wide association data provides novel candidate genes for lipid and lipoprotein traits |
| Q53691985 | Neurotensin Is a Lipid-Induced Gastrointestinal Peptide Associated with Visceral Adipose Tissue Inflammation in Obesity. |
| Q33317352 | New insights into impaired muscle glycogen synthesis |
| Q43057859 | Niemann-Pick C1 modulates hepatic triglyceride metabolism and its genetic variation contributes to serum triglyceride levels |
| Q42460607 | No relationship between identified variants in the uncoupling protein 2 gene and energy expenditure |
| Q40467411 | Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults. |
| Q34221038 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals |
| Q38345643 | Novel mutations and a mutational hotspot in the MODY3 gene |
| Q51023062 | Obesity/insulin resistance rather than liver fat increases coagulation factor activities and expression in humans. |
| Q92337211 | Overeating Saturated Fat Promotes Fatty Liver and Ceramides Compared With Polyunsaturated Fat: A Randomized Trial |
| Q42460893 | Parallel manifestation of insulin resistance and beta cell decompensation is compatible with a common defect in Type 2 diabetes |
| Q63408528 | Patatin-like phospholipase domain-containing 3 (PNPLA3) I148M (rs738409) affects hepatic VLDL secretion in humans and in vitro |
| Q90842255 | Periodontal disease is associated with carotid plaque area: the Malmö Offspring Dental Study (MODS) |
| Q92666157 | Phenotypic and genotypic differences between Indian and Scandinavian women with gestational diabetes mellitus |
| Q34070466 | Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children |
| Q29615729 | Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study |
| Q50058192 | Plasma concentration of Caspase-8 is associated with short sleep duration and the risk of incident diabetes mellitus |
| Q37147707 | Plasma copeptin and the risk of diabetes mellitus |
| Q90981202 | Plasma kidney injury molecule-1 (p-KIM-1) levels and deterioration of kidney function over 16 years |
| Q57142040 | Plasma levels of the proprotein convertase furin and incidence of diabetes and mortality |
| Q51350524 | Plasma proneurotensin and incidence of diabetes, cardiovascular disease, breast cancer, and mortality. |
| Q47902774 | Plasma stem cell factor levels are associated with risk of cardiovascular disease and death. |
| Q35180057 | Pleiotropic effects of GIP on islet function involve osteopontin |
| Q89010113 | Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence |
| Q71006970 | Polymorphism at the rad gene is not associated with NIDDM in Finns |
| Q34122336 | Polymorphism in the Calpain 10 gene influences glucose metabolism in human fat cells |
| Q33267324 | Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality |
| Q73296776 | Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and diabetes project |
| Q74180003 | Polymorphism in the beta(1)-adrenergic receptor gene and hypertension |
| Q46691746 | Polymorphisms associated with cholesterol and risk of cardiovascular events |
| Q46262135 | Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population |
| Q50781857 | Prediction of non-alcoholic fatty liver disease and liver fat using metabolic and genetic factors. |
| Q45711780 | Predictors of Liver Fat and Stiffness in Non-Alcoholic Fatty Liver Disease (NAFLD) - an 11-Year Prospective Study. |
| Q79088021 | Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals |
| Q51245206 | Proneurotensin predicts cardiovascular disease in an elderly population. |
| Q92184278 | Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis |
| Q104470519 | Reduced oxidized LDL in T2D plaques is associated with a greater statin usage but not with future cardiovascular events |
| Q57303741 | Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes |
| Q52327404 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. |
| Q88658044 | Risk of bladder cancer by disease severity in relation to metabolic factors and smoking: A prospective pooled cohort study of 800,000 men and women |
| Q54941960 | Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes: A Mendelian Randomization Study. |
| Q36208149 | Role of TCF7L2 risk variant and dietary fibre intake on incident type 2 diabetes |
| Q38315411 | Role of the Gly460Trp polymorphism of the alpha-adducin gene in primary hypertension in Scandinavians |
| Q58121796 | Saturated Fat Is More Metabolically Harmful for the Human Liver Than Unsaturated Fat or Simple Sugars |
| Q92570030 | Selenoprotein-P Deficiency Predicts Cardiovascular Disease and Death |
| Q95307664 | Self-reported bowel symptoms are associated with differences in overall gut microbiota composition and enrichment of Blautia in a population-based cohort |
| Q47138654 | Sequence data and association statistics from 12,940 type 2 diabetes cases and controls |
| Q37142098 | Several type 2 diabetes-associated variants in genes annotated to WNT signaling interact with dietary fiber in relation to incidence of type 2 diabetes |
| Q57271595 | Sex-specific interactions between the IRS1 polymorphism and intakes of carbohydrates and fat on incident type 2 diabetes |
| Q24643492 | Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans |
| Q37505203 | Smoking modifies the associated increased risk of future cardiovascular disease by genetic variation on chromosome 9p21. |
| Q37716096 | Soluble Urokinase-type Plasminogen Activator Receptor (suPAR) and Impaired Kidney Function in the Population-based Malmö Diet and Cancer Study |
| Q38779976 | Sphingolipids Contribute to Human Atherosclerotic Plaque Inflammation |
| Q38985242 | Stable Peptide of the Endogenous Opioid Enkephalin Precursor and Breast Cancer Risk |
| Q93103980 | Subclinical atherosclerosis and its progression are modulated by PLIN2 through a feed-forward loop between LXR and autophagy |
| Q37202422 | Sugar-sweetened beverage consumption and genetic predisposition to obesity in 2 Swedish cohorts |
| Q45071780 | Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis |
| Q37648324 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease |
| Q51320229 | TCF7L2 type 2 diabetes risk variant, lifestyle factors, and incidence of prostate cancer. |
| Q33847792 | Testing for an unusual distribution of rare variants |
| Q39465645 | The IRS1 rs2943641 variant and risk of future cancer among morbidly obese individuals |
| Q54539620 | The MBOAT7 variant rs641738 alters hepatic phosphatidylinositols and increases severity of non-alcoholic fatty liver disease in humans. |
| Q102320786 | The Malmö Offspring Study (MOS): design, methods and first results |
| Q42096203 | The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver |
| Q37669834 | The PNPLA3 Ile148Met interacts with overweight and dietary intakes on fasting triglyceride levels |
| Q100673196 | The PNPLA3-I148M variant confers an antiatherogenic lipid profile in insulin-resistant patients |
| Q94585121 | The PNPLA3-I148M variant increases polyunsaturated triglycerides in human adipose tissue |
| Q33914336 | The T 54 allele of the intestinal fatty acid-binding protein 2 is associated with a parental history of stroke |
| Q35513040 | The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants |
| Q91935862 | The associations of self-rated health with cardiovascular risk proteins: a proteomics approach |
| Q35092297 | The chromosome 9p21 variant interacts with vegetable and wine intake to influence the risk of cardiovascular disease: a population based cohort study |
| Q34328284 | The dysmetabolic syndrome |
| Q29583824 | The genetic architecture of type 2 diabetes |
| Q33653853 | The gut microbiome as a target for prevention and treatment of hyperglycaemia in type 2 diabetes: from current human evidence to future possibilities |
| Q97522027 | The gut microbiota-related metabolite phenylacetylglutamine associates with increased risk of incident coronary artery disease |
| Q24802084 | 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 |
| Q34955848 | The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol |
| Q46084946 | The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension |
| Q92940171 | The plasma protein profile and cardiovascular risk differ between intima-media thickness of the common carotid artery and the bulb: A meta-analysis and a longitudinal evaluation |
| Q100502041 | The proteoglycan mimecan is associated with carotid plaque vulnerability and increased risk of future cardiovascular death |
| Q57420178 | The putative role of the hormone-sensitive lipase gene in the pathogenesis of Type II diabetes mellitus and abdominal obesity |
| Q28681102 | The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis |
| Q40036840 | The search for putative unifying genetic factors for components of the metabolic syndrome |
| Q46702053 | The variable clinical phenotype of liver glycogen synthase deficiency |
| Q34631381 | Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis |
| Q38800651 | Transcriptional regulation of the miR-212/miR-132 cluster in insulin-secreting β-cells by cAMP-regulated transcriptional co-activator 1 and salt-inducible kinases |
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