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333 results on '"Chang, Kyong-Mi"'

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1. Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

2. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

3. Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis

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

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

7. A roadmap for serum biomarkers for hepatitis B virus: current status and future outlook

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

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

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

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

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

15. The power of genetic diversity in genome-wide association studies of lipids

17. Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19

19. Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes

20. Association of the transthyretin variant V122I with polyneuropathy among individuals of African ancestry

22. Association Between Severe Serum Alanine Aminotransferase Flares and Hepatitis B e Antigen Seroconversion and HBV DNA Decrease in Untreated Patients With Chronic HBV Infection

23. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

24. Gender Differences in Demographic and Health Characteristics of the Million Veteran Program Cohort

27. Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease

28. Genome-wide association study of peripheral artery disease in the Million Veteran Program

29. Abstract 16710: CYP2C19 Polymorphisms and Clinical Outcomes Following Percutaneous Coronary Intervention (PCI) in the Million Veterans Program (MVP)

31. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program

36. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

37. Author Correction : The power of genetic diversity in genome-wide association studies of lipids

38. Association of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program

39. Risk of Hepatocellular Carcinoma After Spontaneous Clearance of Hepatitis C Virus and in Noncirrhosis Chronic Hepatitis C Patients With Sustained Virological Response: A Systematic Review.

40. Early Outcomes of SARS-CoV-2 Infection in a Multisite Prospective Cohort of Inpatient Veterans.

41. Characteristics of Adults in the Hepatitis B Research Network in North America Reflect Their Country of Origin and Hepatitis B Virus Genotype

42. A research agenda for curing chronic hepatitis B virus infection

43. Research priorities for the discovery of a cure for chronic hepatitis B: Report of a workshop

46. Prevalence of hepatitis B antiviral drug resistance variants in North American patients with chronic hepatitis B not receiving antiviral treatment

47. Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait

48. Genome-wide association study and replication of liver enzyme loci

50. Innate Lymphoid Cells Promote Anatomical Containment of Lymphoid-Resident Commensal Bacteria

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