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1. X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements

2. Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization [version 1; peer review: 2 approved]

3. Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

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

5. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

6. Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

7. Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

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

9. The genomics of heart failure: design and rationale of the HERMES consortium

10. Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

11. Quantifying the Excess Risk of Adverse COVID-19 Outcomes in Unvaccinated Individuals With Diabetes Mellitus, Hypertension, Ischaemic Heart Disease or Myocardial Injury: A Meta-Analysis

12. Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium

13. Incorporating sampling weights into robust estimation of Cox proportional hazards regression model, with illustration in the Multi-Ethnic Study of Atherosclerosis

14. Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

15. Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

16. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion

17. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

18. Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

19. Three-Decision Methods: A Sensible Formulation of Significance Tests—and Much Else

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

21. Monogenic and Polygenic Contributions to QTc Prolongation in the Population

23. Bayesian approaches to fixed effects meta-analysis

24. Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

25. Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

26. Blood Pressure and Heart Rate Measures Associated With Increased Risk of Covert Brain Infarction and Worsening Leukoaraiosis in Older Adults

27. Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

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

29. Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

30. Addressing the estimation of standard errors in fixed effects meta-analysis

31. Selecting Shrinkage Parameters for Effect Estimation: The Multi-Ethnic Study of Atherosclerosis

32. Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

33. Taste of a pill: organic cation transporter-3 (OCT3) mediates metformin accumulation and secretion in salivary glands

34. Abstract P378: Risk Factors for Incident Venous Thrombosis and their Associations with Recurrence

35. Abstract P377: Oral Estrogen Hormone Therapy Use after Incident Venous Thrombosis and the Risk of Recurrence

36. beta1- and beta2-adrenergic receptor gene variation, beta-blocker use and risk of myocardial infarction and stroke

37. Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.

38. Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing.

39. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

40. Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.

41. Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

42. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.

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

44. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

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