Search

Your search keyword '"Chang, Kyong-Mi"' showing total 555 results

Search Constraints

Start Over You searched for: Author "Chang, Kyong-Mi" Remove constraint Author: "Chang, Kyong-Mi" Publication Year Range Last 50 years Remove constraint Publication Year Range: Last 50 years
555 results on '"Chang, Kyong-Mi"'

Search Results

1. Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver disease.

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

3. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

4. Characteristics of Older Patients With Immunotolerant Chronic Hepatitis B Virus Infection

5. A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality

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

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

8. Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits

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

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

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

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

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

16. Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies

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

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

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

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

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

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

26. Virus-associated Inflammation Imprints an Inflammatory Profile on Long-lived Monocyte-derived Macrophages in the Human Liver

27. Improved Survival Among all Interferon-α-Treated Patients in HCV-002, a Veterans Affairs Hepatitis C Cohort of 2211 Patients, Despite Increased Cirrhosis Among Nonresponders

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

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

31. 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

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

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

36. CXCL12 regulates coronary artery dominance in diverse populations and links development to disease

37. A Missense Variant in Human Perilipin 2 (Plin2 Ser251pro) Reduces Hepatic Steatosis In Mice

38. Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin.

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. Dissecting the Genetic Architecture of Intracranial Aneurysms

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

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

43. A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization

44. Abstract 560: Genetics Of Physical Activity And Risk Of Cardiovascular Disease

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

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

Catalog

Books, media, physical & digital resources