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1. Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis

2. Hypertension genetics past, present and future applications

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3. The Histone Deacetylase 9 Stroke-Risk Variant Promotes Apoptosis and Inflammation in a Human iPSC-Derived Smooth Muscle Cells Model

4. Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure

5. Genetically predicted levels of the human plasma proteome and risk of stroke: a Mendelian Randomization study

6. Genetically predicted levels of the human plasma proteome and risk of stroke: a Mendelian Randomization study

7. Do Cerebral Small Vessel Disease and Multiple Sclerosis Share Common Mechanisms of White Matter Injury?

8. Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease: A Mendelian Randomization Study

9. The BS variant of C4 protects against age-related loss of white matter microstructural integrity

10. Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

11. Protein Engineering on Human Recombinant Follistatin: Enhancing Pharmacokinetic Characteristics for Therapeutic Application

12. Should Family Be Permitted in a Trauma Bay?

13. Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes

14. Type 2 diabetes, glucose, insulin, BMI, and ischemic stroke subtypes

15. An Examination of Polygenic Score Risk Prediction in Individuals With First-Episode Psychosis

16. The role of haematological traits in risk of ischaemic stroke and its subtypes

17. Influence of Genetic Variation in PDE3A on Endothelial Function and Stroke

18. Association of common genetic variants with brain microbleeds

19. Influence of Genetic Variation in

20. Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

21. Homocysteine and small vessel stroke: A mendelian randomization analysis

22. Abstract 20: Cross-Phenotype Meta-Analysis of Intracerebral Hemorrhageand Small Vessel Ischemic Stroke Identifies Two Novel Genetic Loci at 2q33 and 13q34

23. Encephalopathy in a Large Cohort of British Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients

24. HYPERTENSIVE PATIENTS WITH GREATER GENETIC RISK RESPOND LESS EFFECTIVELY TO TREATMENT AND ARE MORE LIKELY TO BE TREATMENT RESISTANT

25. Comprehensive Discovery and Quantitation of Protein Heterogeneity via LC-MS/MS Peptide Mapping for Clone Selection of a Therapeutic Protein

26. Correction: Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

27. How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study

29. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

30. Genetic and Inflammatory Biomarkers Classify Small Intestine Inflammation in Asymptomatic First-degree Relatives of Patients With Crohn’s Disease

31. Circulating Vitamin K₁ Levels in Relation to Ischemic Stroke and Its Subtypes: A Mendelian Randomization Study

32. Genome-wide association meta-analysis of functional outcome after ischemic stroke

33. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

34. Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke

36. Genetically-Predicted Adult Height and Alzheimer's Disease

37. Homogeneous case subgroups increase power in genetic association studies

38. Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12

39. Genetic risk of Spontaneous intracerebral hemorrhage: Systematic review and future directions

40. 17q25 Locus Is Associated With White Matter Hyperintensity Volume in Ischemic Stroke, But Not With Lacunar Stroke Status

41. Using Phenotypic Heterogeneity to Increase the Power of Genome-Wide Association Studies: Application to Age at Onset of Ischaemic Stroke Subphenotypes

42. Pharmacogenetic testing through the direct-to-consumer genetic testing company 23andMe

43. COL4A2 is associated with lacunar ischemic stroke and deep ICH

44. Atrial Fibrillation Genetic Risk and Ischemic Stroke Mechanisms

45. ukbtools: An R package to manage and query UK Biobank data

46. GISCOME - Genetics of Ischaemic Stroke Functional Outcome network: A protocol for an international multicentre genetic association study

47. New insights into mechanisms of small vessel disease stroke from genetics

48. Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study

49. Genetic discovery in multi-ethnic populations

50. 070 Rheumatoid Arthritis Risk and Prognostic Factors Identified in European and Asian Populations are also Relevant in African Ancestry Individuals: The Genra Study