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1. Association of Plasma YKL-40 With MRI, CSF, and Cognitive Markers of Brain Health and Dementia

2. Plasma Proteomic Associations With Incident Ischemic Stroke in Older Adults

3. Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

4. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

5. Abstract WMP101: Plasma Proteomic Determinants Of White Matter Hyperintensities And Covert Brain Infarction In The Cardiovascular Health Study

7. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

8. Association of Serum Neurofilament Light Chain Concentration and MRI Findings in Older Adults

9. Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

10. Twenty-seven-year time trends in dementia incidence in Europe and the United States

11. Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

12. Association of CD14 with incident dementia and markers of brain aging and injury

13. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

14. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

15. ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

16. Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

17. Additional Candidate Genes for Human Atherosclerotic Disease Identified Through Annotation Based on Chromatin Organization

18. Genetic Variants Associated with Circulating Parathyroid Hormone

19. Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis

20. Abstract MP80: Genome-wide Meta-analysis of SNP-by-antihypertensive Treatment Class Effect on Serum Potassium in Cohorts of European and African Ancestry From Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

21. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk

22. White Matter Lesion Progression

23. Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans

24. Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

25. Multiethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

26. Association of Rare Loss-Of-Function Alleles in HAL , Serum Histidine

27. Genetic Overlap Between Diagnostic Subtypes of Ischemic Stroke

28. Abstract 150: Trans-ethnic GWAS of Mri-defined Brain Infarcts: Charge Consortium

29. Genes From a Translational Analysis Support a Multifactorial Nature of White Matter Hyperintensities

30. Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation

31. Strategies to Design and Analyze Targeted Sequencing Data

32. Sequencing of 2 Subclinical Atherosclerosis Candidate Regions in 3669 Individuals

33. Sequencing of SCN5A Identifies Rare and Common Variants Associated With Cardiac Conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

34. Genome-Wide Association Study for Circulating Tissue Plasminogen Activator Levels and Functional Follow-Up Implicates Endothelial STXBP5 and STX2

36. Predicting Stroke Through Genetic Risk Functions

37. Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case–Control and Prospective Cohort Studies

38. Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease

40. Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans

41. Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

42. Association of Variation at the ABO Locus With Circulating Levels of Soluble Intercellular Adhesion Molecule-1, Soluble P-selectin, and Soluble E-selectin

43. A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease

44. Genetic Predictors of Fibrin D-Dimer Levels in Healthy Adults

45. Cerivastatin, genetic variants, and the risk of rhabdomyolysis

46. Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels

47. Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25

48. Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure

49. Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry

50. Genome-Wide Association Studies of MRI-Defined Brain Infarcts

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