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1. AIPatient: Simulating Patients with EHRs and LLM Powered Agentic Workflow

2. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

3. A scoping review of using Large Language Models (LLMs) to investigate Electronic Health Records (EHRs)

4. Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

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

6. Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers

7. Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

8. Rare coding variants in RCN3 are associated with blood pressure

10. Design and pilot results from the Million Veteran Program Return Of Actionable Results (MVP-ROAR) Study

12. Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

13. Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits

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

16. Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential

17. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

18. A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

19. Broad clinical manifestations of polygenic risk for coronary artery disease in the Women’s Health Initiative

20. Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program

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

22. Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes

23. Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

24. Epigenome-wide association study of diet quality in the Women's Health Initiative and TwinsUK cohort.

25. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

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

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

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

32. Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

33. Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

34. An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis

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

36. Integration of rare expression outlier-associated variants improves polygenic risk prediction

37. A translational genomics approach identifies IL10RB as the top candidate gene target for COVID-19 susceptibility

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

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

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

42. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study

43. Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study

44. DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.

46. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

47. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

48. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

49. Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

50. An epigenetic clock analysis of race/ethnicity, sex, and coronary heart disease

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