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1. Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

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

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

4. Determinants of mosaic chromosomal alteration fitness.

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

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

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

8. Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

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

11. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.

12. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

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

17. Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes.

18. The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

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

21. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program.

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

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

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

25. Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.

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

27. Rare genetic variants explain missing heritability in smoking.

28. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

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

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

32. TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

33. Monogenic and Polygenic Contributions to QTc Prolongation in the Population.

35. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

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

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

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

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

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

42. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

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

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

45. Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

46. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

47. The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.

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

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

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

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