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

2. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

3. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

4. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

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

6. Identification of a functional FADS1 3′UTR variant associated with erythrocyte n-6 polyunsaturated fatty acids levels

7. Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults

8. Worldwide trends in blood pressure from 1975 to 2015: a pooled analysis of 1479 population-based measurement studies with 19·1 million participants

10. Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

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

26. HEART DISEASE: Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

29. Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors

30. Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

31. Genetic studies of body mass index yield new insights for obesity biology

32. New genetic loci link adipose and insulin biology to body fat distribution

35. Influence of cholesteryl ester transfer protein, peroxisome proliferator–activated receptor α, apolipoprotein E, and apolipoprotein A-I polymorphisms on high-density lipoprotein cholesterol, apolipoprotein A-I, lipoprotein A-I, and lipoprotein A-I:A-II concentrations: the Prospective Epidemiological Study of Myocardial Infarction study

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

41. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

44. National trends in total cholesterol obscure heterogeneous changes in HDL and non-HDL cholesterol and total-to-HDL cholesterol ratio : a pooled analysis of 458 population-based studies in Asian and Western countries

46. Risk factors for coronary heart disease in patients treated for human immunodeficiency virus infection compared with the general population

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