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3. List of Contributors

6. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

10. Acute pharmacodynamic responses to exenatide: Drug-induced increases in insulin secretion and glucose effectiveness

12. Model for Integration of Monogenic Diabetes Diagnosis Into Routine Care: The Personalized Diabetes Medicine Program

13. A Model for Integration of Monogenic Diabetes Diagnosis into Routine Care: The Personalized Diabetes Medicine Program

14. A Model for Integration of Monogenic Diabetes Diagnosis into Routine Care: The Personalized Diabetes Medicine Program

16. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

17. Evaluating the heterogeneous effect of a modifiable risk factor on suicide: The case of vitamin D deficiency

21. Contributors

22. Contributors

23. Surveillance of Depleted Uranium-exposed Gulf War Veterans: More Evidence for Bone Effects

26. Novel BMD loci identified by whole genome sequencing and CRISPR editing in zebrafish: The NHLBI Trans-Omics for Precision Medicine (TOPMED) study

28. Prevalence, control, and treatment of diabetes, hypertension, and high cholesterol in the Amish

30. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

32. Meta‐Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry

33. Disentangling the genetics of lean mass

34. Surveillance results and bone effects in the Gulf War depleted uranium-exposed cohort

37. Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

38. Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

42. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

46. Genetic Variants Associated with Circulating Parathyroid Hormone

47. WRNMutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

50. Correction: Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

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