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2. Genetic risk factors for COVID-19 and influenza are largely distinct

5. Clinical correlates of CT imaging-derived phenotypes among lean and overweight patients with hepatic steatosis

6. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

9. Facilitating return of actionable genetic research results from a biobank repository: Participant uptake and utilization of digital interventions

10. Prior vaccination promotes early activation of memory T cells and enhances immune responses during SARS-CoV-2 breakthrough infection

13. mTORCI controls murine postprandial hepatic glycogen synthesis via Ppp1r3b

14. Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

15. Germline Exome Sequencing for Men with Testicular Germ Cell Tumor Reveals Coding Defects in Chromosomal Segregation and Protein-targeting Genes

16. Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation

17. Progression of Coronary Artery Calcification and Risk of Clinical Events in CKD: The Chronic Renal Insufficiency Cohort Study

20. A missense variant in human perilipin 2 (PLIN2 Ser251Pro) reduces hepatic steatosis in mice

22. Large-scale identification of undiagnosed hepatic steatosis using natural language processing

24. Rare genetic variants explain missing heritability in smoking

25. A saturated map of common genetic variants associated with human height

26. Abstract 18244: A Multi-Ancestry GWAS of Calcific Aortic Stenosis Among 2.7 Million Individuals

29. Targeting the coronavirus nucleocapsid protein through GSK-3 inhibition

30. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

31. Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries

32. Whole-genome sequencing reveals host factors underlying critical COVID-19

33. High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease

34. A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

36. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

37. Guidance for the diagnosis and treatment of hypolipidemia disorders

38. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

40. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

41. Association of Inherited Mutations in DNA Repair Genes with Localized Prostate Cancer

42. Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

44. Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes

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

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

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

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