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1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.

2. Identifying therapeutic targets for cancer among 2074 circulating proteins and risk of nine cancers

4. Genome-wide characterization of circulating metabolic biomarkers

5. Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.

6. South Asian medical cohorts reveal strong founder effects and high rates of homozygosity

7. Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease

8. Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.

9. Misexpression of inactive genes in whole blood is associated with nearby rare structural variants

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

11. A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology

13. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

14. A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease

15. Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer’s disease

16. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

17. An atlas of genetic scores to predict multi-omic traits

18. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program

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

20. South Asian Patient Population Genetics Reveal Strong Founder Effects and High Rates of Homozygosity – New Resources for Precision Medicine

21. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

22. Identifying and visualising multimorbidity and comorbidity patterns in patients in the English National Health Service: a population-based study

23. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

25. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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

28. Insights into the genetic architecture of haematological traits from deep phenotyping and whole-genome sequencing for two Mediterranean isolated populations

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

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

32. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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

34. Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

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

36. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

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

38. A nutritional biomarker score of the Mediterranean diet and incident type 2 diabetes: Integrated analysis of data from the MedLey randomised controlled trial and the EPIC-InterAct case-cohort study

40. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

41. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

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

43. Markers of imminent myocardial infarction

44. Dietary amino acids and risk of stroke subtypes : a prospective analysis of 356,000 participants in seven European countries

45. Dietary intake of plant- and animal-derived protein and incident cardiovascular diseases: the pan-European EPIC-CVD case–cohort study

46. Dietary amino acids and risk of stroke subtypes: a prospective analysis of 356,000 participants in seven European countries

47. Dietary intake of plant- and animal-derived protein and incident cardiovascular diseases:the pan-European EPIC-CVD case–cohort study

48. Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19

49. Development and validation of a universal blood donor genotyping platform: a multinational prospective study

50. Proteome-wide association study and functional validation identify novel protein markers for pancreatic ductal adenocarcinoma

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