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Your search keyword '"Jørgensen, Torben"' showing total 140 results

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140 results on '"Jørgensen, Torben"'

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1. Cardiac Troponin I and Incident Stroke in European Cohorts: Insights From the BiomarCaRE Project

2. Determinants of social inequalities in stroke incidence across Europe: a collaborative analysis of 126 635 individuals from 48 cohort studies

3. Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

4. Abstract 17668: Heart Failure Epidemiology, Risk Factors and Mortality Risk by Gender in Community Cohorts Across Europe

5. Sex Differences and Similarities in Atrial Fibrillation Epidemiology, Risk Factors, and Mortality in Community Cohorts: Results From the BiomarCaRE Consortium (Biomarker for Cardiovascular Risk Assessment in Europe)

6. Rare and low-frequency coding variants alter human adult height

7. Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota

9. HUMAN GENETICS: Greenlandic Inuit show genetic signatures of diet and climate adaptation

10. Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion

12. Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants1-5

13. FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals

15. Adult height and the risk of cause-specific death and vascular morbidity in 1 million people: individual participant meta-analysis

17. Seasonality of cardiovascular risk factors: an analysis including over 230 000 participants in 15 countries

22. Assessing Risk Prediction Models Using Individual Participant Data From Multiple Studies

27. Richness of human gut microbiome correlates with metabolic markers

28. Population-level changes to promote cardiovascular health

35. No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels

45. Parental origin of sequence variants associated with complex diseases

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