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

2. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction

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

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

6. Genome-wide characterization of circulating metabolic biomarkers

7. Markers of imminent myocardial infarction

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

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

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

11. Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries

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

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

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

15. Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

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

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

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

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

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

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

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

24. Estimating dose-response relationships for vitamin D with coronary heart disease, stroke, and all-cause mortality: observational and Mendelian randomisation analyses

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

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

28. Author Correction: Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets

29. Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

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

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

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

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

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

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

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

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

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

42. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases

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

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

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

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

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

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

49. Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke

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

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