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2. Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

3. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

6. GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification

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

8. General and abdominal adiposity and hypertension in eight world regions: a pooled analysis of 837 population-based studies with 7·5 million participants

9. An LGR6 frameshift variant abrogates receptor expression on select leukocyte subsets and is associated with viral infections

11. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

13. Genetic insights into resting heart rate and its role in cardiovascular disease

14. Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure

16. Predicted Deleterious Variants in Cardiomyopathy Genes Prognosticate Mortality and Composite Outcomes in the UK Biobank

17. The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction

18. Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

21. Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

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

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

26. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

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

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

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

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

33. Diagnostic and prognostic value of ECG-predicted hypertension-mediated left ventricular hypertrophy using machine learning

34. Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure

35. Frequency, Penetrance, and Variable Expressivity of Dilated Cardiomyopathy–Associated Putative Pathogenic Gene Variants in UK Biobank Participants

36. Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease

37. A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

39. Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

42. NMR metabolomic modeling of age and lifespan: A multicohort analysis.

43. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

44. Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

46. SMIM1 absence is associated with reduced energy expenditure and excess weight

47. Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals

48. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

49. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.

50. Genome-Wide Interaction Analysis with DASH Diet Score Identified Novel Loci for Systolic Blood Pressure

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