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1. Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

2. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

4. Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores

5. Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

6. Determinants of mosaic chromosomal alteration fitness

7. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

8. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

9. Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

12. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants

13. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

14. Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine

15. Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts

17. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

18. Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

19. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

21. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

22. Impact of individual and environmental factors on dietary or lifestyle interventions to prevent type 2 diabetes development: a systematic review

23. Genetic insights into resting heart rate and its role in cardiovascular disease

24. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

25. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes

26. Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

29. Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry

30. Rare genetic variants explain missing heritability in smoking

31. A saturated map of common genetic variants associated with human height

32. Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

33. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

34. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

35. Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

36. Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

37. Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations

38. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

39. A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

40. Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts

41. Rare coding variants in RCN3 are associated with blood pressure

42. Whole genome sequence analysis of blood lipid levels in >66,000 individuals

43. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

44. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

45. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

46. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

47. Genomics and phenomics of body mass index reveals a complex disease network

48. Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

49. MagicalRsq-X:A cross-cohort transferable genotype imputation quality metric

50. An integrative framework to prioritize genes in more than 500 loci associated with body mass index

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