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2. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

5. Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

6. Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

7. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

8. Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network

10. Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets

11. Returning integrated genomic risk and clinical recommendations: The eMERGE study

15. Abstract 15706: Common- and Rare-Variant Genetic Architecture of Heart Failure Across the Allele Frequency Spectrum

16. Abstract 13711: Clonal Hematopoiesis Driven by TET2 and ASXL1 but Not DNMT3A is Associated With Interleukin 6 Levels, Cardiac Biomarkers, Cardiac Remodeling, and Risk of Atrial Fibrillation

18. Multiancestral polygenic risk score for pediatric asthma

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

21. Genome-wide polygenic score to predict chronic kidney disease across ancestries

23. Neptune: an environment for the delivery of genomic medicine

24. Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions

25. Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

26. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

27. Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

29. Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk

30. Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

32. Abstract 10822: Familial Hypercholesterolemia in the EMERGE Network: 1-Year Outcomes After Return of Results

33. Atrial Fibrillation and Clonal Hematopoiesis in TET2 and ASXL1

34. Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network

35. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

36. Facilitating phenotype transfer using a common data model

38. Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases

41. Super and Nonresponders to Catheter Ablation for Atrial Fibrillation: A Quality-of-Life Assessment Using Patient Reported Outcomes

43. Abstract 15209: LPA Variants Are Associated With Aortic Valve Stenosis, Heart Failure and Chronic Kidney Disease

44. Abstract 14663: High Rate of Arrhythmia Diagnoses Following Return of Pathogenic/likely Pathogenic Variants in an Unselected Population

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

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

47. Returning integrated genomic risk and clinical recommendations: The eMERGE study

48. Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results

49. Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia

50. S-22-4: GENOME WIDE ASSOCIATION STUDY OF FIBROMUSCULAR DYSPLASIA REVEALS MECHANISTIC LINKS WITH BLOOD PRESSURE REGULATION AND OTHER VASCULAR DISEASES

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