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

3. Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

4. A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

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

6. Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study

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

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

9. Clinical and biomarker modifiers of vitamin D treatment response: the Multi-Ethnic Study of Atherosclerosis

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

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

12. Bayesian Approaches to Fixed Effects Meta-Analysis

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

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

15. The multi-ethnic study of atherosclerosis individual response to vitamin D trial: Building a randomized clinical trial into an observational cohort study

16. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

17. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

18. Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium

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

20. 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

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

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

23. Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

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

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

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

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

28. Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging

29. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

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

31. Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

32. Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

33. 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

34. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

35. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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

37. Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

38. Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

39. Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

40. Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

41. General Framework for Meta‐Analysis of Haplotype Association Tests

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

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

44. Model-robust regression and a Bayesian 'sandwich' estimator

45. Common Variation in Fatty Acid Genes and Resuscitation From Sudden Cardiac Arrest

47. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

48. KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference

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

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