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1. Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

2. Retraction Note: Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

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

4. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

6. Data challenges for international health emergencies: lessons learned from ten international COVID-19 driver projects

8. Correction: Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

9. Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

10. Changes in preterm birth and stillbirth during COVID-19 lockdowns in 26 countries

11. The impact of the COVID-19 pandemic on cardiovascular disease prevention and management

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

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

15. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

16. A genome‐wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

17. RETRACTED ARTICLE: Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

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

19. Discovery of novel heart rate-associated loci using the Exome Chip

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

30. Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

31. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.

35. Towards a standardised cross-sectoral data access agreement template for research: a core set of principles for data access within trusted research environments

37. Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

38. Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

40. Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

41. Cancer incidence and mortality in 23 000 patients with type 1 diabetes in the UK: Long‐term follow‐up

42. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

43. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

44. Definitions of eHealth

45. Development and evaluation of rapid data-enabled access to routine clinical information to enhance early recruitment to the national clinical platform trial of COVID-19 community treatments

47. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

48. Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

49. The genetic architecture of type 2 diabetes

50. Shared Genetic Aetiology between Cognitive Ability and Cardiovascular Disease Risk Factors: Generation Scotland's Scottish Family Health Study

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