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1. Analysis of singularly perturbed stochastic chemical reaction networks motivated by applications to epigenetic cell memory

3. Identification of proteins associated with type 2 diabetes risk in diverse racial and ethnic populations

5. STEM Outreach to Underresourced Schools: A Model for Inclusive Student Engagement

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

9. Rare variant contribution to the heritability of coronary artery disease

10. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

11. Lower confidence and increased error sensitivity in OCD patients while learning under volatility

12. Evidence for moth pollination in a rhinomyiophilous Erica species from the Cape Floristic Region of South Africa

13. Rare variant contribution to the heritability of coronary artery disease

14. Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height

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

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

19. Determinants of mosaic chromosomal alteration fitness

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

27. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

28. Methanogenic patterns in the gut microbiome are associated with survival in a population of feral horses

29. Mathematical analysis of the limiting behaviors of a chromatin modification circuit

30. Comparison Theorems for Stochastic Chemical Reaction Networks

32. Genetic associations with neural reward responsivity to food cues in children

33. Implementation of Ensemble Predictive Models for Parkinson’s Disease Detection

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

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

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

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

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

43. Determinants of mosaic chromosomal alteration fitness

44. Immunoglobulin G4-related disease presenting with nephrotic syndrome due to minimal change disease: a case report

47. Glucocorticoid Minimization in Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis: An International Survey of Clinicians

48. Post-mortem changes of anisotropic mechanical properties in the porcine brain assessed by MR elastography

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