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1. The genetic landscape of neuro-related proteins in human plasma

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. Genome-wide characterization of circulating metabolic biomarkers

5. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

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

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

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

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

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

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

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

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

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

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

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

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

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

22. The common VTE-protective G haplotype of F5 increases factor V-short, TFPI function, and risk of bleeding

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44. Genetic Associations of Circulating Cardiovascular Proteins With Gestational Hypertension and Preeclampsia

45. Association of plasma biomarkers of fruit and vegetable intake with incident type 2 diabetes : InterAct case-cohort study in eight European countries

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

48. Polygenic basis and biomedical consequences of telomere length variation

49. 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

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