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

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

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

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

7. Rare genetic variants explain missing heritability in smoking.

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

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

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

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

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

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

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

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

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

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

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

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

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

21. Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

22. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

23. Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.

24. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

25. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

26. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

27. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

28. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

29. Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

30. Genome-wide association study identifies 48 common genetic variants associated with handedness

31. Inherited causes of clonal haematopoiesis in 97,691 whole genomes

32. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.

33. Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

34. Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education

35. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.

36. Integrating Genetic and Transcriptomic Data to Identify Genes Underlying Obesity Risk Loci

37. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry

38. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

39. A Genome-Wide Association Study Identifies Blood Disorder–Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos

40. Genetic analyses of diverse populations improves discovery for complex traits.

41. Disentangling the genetics of lean mass.

42. Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.

43. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

44. Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.

45. PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

46. The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

47. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

48. Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

49. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

50. Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

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