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1. Stroke genetics informs drug discovery and risk prediction across ancestries

2. Kidney omics in hypertension: from statistical associations to biological mechanisms and clinical applications

3. Stroke genetics informs drug discovery and risk prediction across ancestries (vol 611, pg 115, 2022)

4. Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

5. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

6. The Polygenic and Monogenic Basis of Blood Traits and Diseases

7. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

8. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (vol 50, pg 524, 2018)

9. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

10. Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke

11. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (vol 50, pg 1412, 2018)

12. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 26, 2018)

13. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017)

14. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

15. New blood pressure associated loci identified in meta-analyses of 475,000 individuals

16. Rare and low-frequency coding variants alter human adult height

17. Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

18. Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

20. Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21. Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

22. Bayesian refinement of association signals for 14 loci in 3 common diseases

23. Confirmation of novel type 1 diabetes risk loci in families.

24. Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes.

25. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

26. Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

27. Confirmation of novel type 1 diabetes risk loci in families

28. Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

29. De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.

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

31. Profiling the genome and proteome of metabolic dysfunction-associated steatotic liver disease identifies potential therapeutic targets.

32. Plasma proteomic associations with genetics and health in the UK Biobank.

33. Hepatocyte mARC1 promotes fatty liver disease.

34. Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries.

35. Rare and common genetic determinants of metabolic individuality and their effects on human health.

36. Stroke genetics informs drug discovery and risk prediction across ancestries.

37. Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke.

38. Kidney omics in hypertension: from statistical associations to biological mechanisms and clinical applications.

39. Associations of genetically predicted IL-6 signaling with cardiovascular disease risk across population subgroups.

41. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.

42. Leveraging human genetic data to investigate the cardiometabolic effects of glucose-dependent insulinotropic polypeptide signalling.

43. Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.

44. Genetic Evidence for Repurposing of GLP1R (Glucagon-Like Peptide-1 Receptor) Agonists to Prevent Heart Failure.

45. An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank.

46. Mendelian randomization for studying the effects of perturbing drug targets.

47. A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.

48. A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits.

49. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.

50. Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.

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