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3. Author Correction: A consensus-based transparency checklist.

4. A consensus-based transparency checklist

5. Recommendations and Practical Guidance for performing and reporting validation studies according to the Universal Standard for the validation of blood pressure measuring devices by the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO)

6. Hypothesis, analysis and synthesis, it's all Greek to me

8. A universal standard for the validation of blood pressure measuring devices: Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO) Collaboration Statement

9. Serum uric acid and multiple health outcomes: an umbrella review of evidence from observational studies, clinical trials and Mendelian randomisation studies

10. Registration practices for observational studies on ClinicalTrials.gov indicated low adherence

11. New genetic loci link adipose and insulin biology to body fat distribution.

14. New genetic loci link adipose and insulin biology to body fat distribution

15. Head-to-head randomized trials are mostly industry sponsored and almost always favor the industry sponsor

20. EULAR recommendations for the management of Systemic Lupus Erytematosus (SLE) Report of a Task Force of the European Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT)*

21. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

22. Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

23. Preoperative prediction of long-term survival after coronary artery bypass grafting in patients with low left ventricular ejection fraction

24. Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes

25. UCHL1 is a Parkinson's disease susceptibility gene

27. A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

28. Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

29. Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece

30. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease

31. Lack of replication of thirtheen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

33. Effects of CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles o­n HIV-1 disease progression: An international meta-analysis of individual patient data.

34. Correction of phenotype misclassification based on high-discrimination genetic predictive risk models.

35. Joint European League Against Rheumatism and European Renal Association-European Dialysis and Transplant Association (EULAR/ERA-EDTA) recommendations for the management of adult and paediatric lupus nephritis.

36. Sex-specific differences in effect size estimates at established complex trait loci.

38. What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations.

41. How to use an article about genetic association: C: What are the results and will they help me in caring for my patients?

42. How to use an article about genetic association: B: Are the results of the study valid?

43. Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease.

44. 18F-fluorodeoxyglucose positron emission tomography to evaluate cervical node metastases in patients with head and neck squamous cell carcinoma: a meta-analysis.

45. Genetic effects versus bias for candidate polymorphisms in myocardial infarction: case study and overview of large-scale evidence.

49. Pneumococcal aortitis in the antibiotic era.

50. Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition

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