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131 results on '"Loos, Ruth"'

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

2. Determinants of mosaic chromosomal alteration fitness

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

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

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

8. PFAS Exposures and the Human Metabolome: A Systematic Review of Epidemiological Studies

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

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

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

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

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

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

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

18. Rare genetic variants explain missing heritability in smoking

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

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

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

23. Composite trait Mendelian randomization reveals distinct metabolic and lifestyle consequences of differences in body shape

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

27. Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities

28. Author Correction: The genomics of childhood eating behaviours

29. Implementing genomic screening in diverse populations

30. The genomics of childhood eating behaviours

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

34. Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

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

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

38. The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

39. Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics

41. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

42. Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

43. Associations of autozygosity with a broad range of human phenotypes

44. Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

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

46. Mendelian randomisation analyses find pulmonary factors mediate the effect of height on coronary artery disease

47. Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity

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

49. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

50. Complex patterns of direct and indirect association between the transcription Factor-7 like 2 gene, body mass index and type 2 diabetes diagnosis in adulthood in the Hispanic Community Health Study/Study of Latinos

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