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1. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions.

3. General and abdominal adiposity and hypertension in eight world regions: a pooled analysis of 837 population-based studies with 7·5 million participants

4. Atherosclerotic Plaque Epigenetic Age Acceleration Predicts a Poor Prognosis and Is Associated With Endothelial-to-Mesenchymal Transition in Humans

5. Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults

6. Estimating dose-response relationships for vitamin D with coronary heart disease, stroke, and all-cause mortality: observational and Mendelian randomisation analyses

7. Genetic insights into biological mechanisms governing human ovarian ageing

8. Stroke genetics informs drug discovery and risk prediction across ancestries

10. Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk

14. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

15. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.

17. Simplification of a registry-based algorithm for ejection fraction prediction in heart failure patients: Applicability in cardiology centres of the Netherlands.

18. The Diagnostic Value of ECG Characteristics for Vasospastic and Microvascular Angina: A Systematic Review.

19. The YOUth study: Rationale, design, and study procedures

20. Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses

21. Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length

22. Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries

24. ANOCA patients with and without coronary vasomotor dysfunction present with limited electrocardiographic remodeling

25. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

26. The Diagnostic Value of ECG Characteristics for Vasospastic and Microvascular Angina: A Systematic Review

30. HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

31. Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations

32. Enhancement of the Binding Energy of Charged Excitons in Disordered Quantum Wires

33. Loci influencing blood pressure identified using a cardiovascular gene-centric array

34. A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation

35. Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations

36. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

37. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

38. Pre-diagnosis insulin-like growth factor-I and risk of epithelial invasive ovarian cancer by histological subtypes : A collaborative re-analysis from the Ovarian Cancer Cohort Consortium

43. Age at Menopause and the Risk of Stroke: Observational and Mendelian Randomization Analysis in 204 244 Postmenopausal Women

44. Genome-wide association study identifies eight loci associated with blood pressure

45. Interaction between genes and macronutrient intake on the risk of developing type 2 diabetes: systematic review and findings from European Prospective Investigation into Cancer (EPIC)-InterAct

46. DNA methylome analysis identifies accelerated epigenetic ageing associated with postmenopausal breast cancer susceptibility

47. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

48. Discovery of common and rare genetic risk variants for colorectal cancer

49. Epigenome-wide association study of adiposity and future risk of obesity-related diseases

50. Interplay between genetic predisposition, macronutrient intake and type 2 diabetes incidence: analysis within EPIC-InterAct across eight European countries

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