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- Publications
- Influence
The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials
- J. P. Higgins, D. Altman, +7 authors J. Sterne
- Medicine
- BMJ : British Medical Journal
- 18 October 2011
Flaws in the design, conduct, analysis, and reporting of randomised trials can cause the effect of an intervention to be underestimated or overestimated. The Cochrane Collaboration’s tool for… Expand
The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration
- A. Liberati, D. Altman, +7 authors D. Moher
- Psychology, Medicine
- PLoS medicine
- 1 July 2009
Alessandro Liberati and colleagues present an Explanation and Elaboration of the PRISMA Statement, updated guidelines for the reporting of systematic reviews and meta-analyses.
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration
- A. Liberati, D. Altman, +7 authors D. Moher
- Medicine
- BMJ : British Medical Journal
- 21 July 2009
Systematic reviews and meta-analyses are essential to summarise evidence relating to efficacy and safety of healthcare interventions accurately and reliably. The clarity and transparency of these… Expand
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration.
- A. Liberati, D. Altman, +7 authors D. Moher
- Medicine
- Journal of clinical epidemiology
- 1 October 2009
Systematic reviews and meta-analyses are essential to summarize evidence relating to efficacy and safety of health care interventions accurately and reliably. The clarity and transparency of these… Expand
The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.
- E. von Elm, D. Altman, M. Egger, S. Pocock, P. Gøtzsche, J. Vandenbroucke
- Medicine
- Preventive medicine
- 1 November 2007
Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalisability. The… Expand
CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials.
- D. Moher, S. Hopewell, +6 authors D. Altman
- Medicine
- International journal of surgery
- 2012
Overwhelming evidence shows the quality of reporting of randomised controlled trials (RCTs) is not optimal. Without transparent reporting, readers cannot judge the reliability and validity of trial… Expand
The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.
- E. von Elm, D. Altman, M. Egger, S. Pocock, P. Gøtzsche, J. Vandenbroucke
- Medicine
- Bulletin of the World Health Organization
- 1 November 2007
Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalizability. The… Expand
CONSORT 2010 Explanation and Elaboration: Updated guidelines for reporting parallel group randomised trials.
- D. Moher, S. Hopewell, +6 authors D. Altman
- Medicine
- Journal of clinical epidemiology
- 2010
Overwhelming evidence shows the quality of reporting of randomised controlled trials (RCTs) is not optimal. Without transparent reporting, readers cannot judge the reliability and validity of trial… Expand
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration
- J. Vandenbroucke, E. von Elm, +6 authors M. Egger
- Medicine
- PLoS medicine
- 1 October 2007
Much medical research is observational. The reporting of observational studies is often of insufficient quality. Poor reporting hampers the assessment of the strengths and weaknesses of a study and… Expand
SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials
- A. Chan, J. Tetzlaff, +10 authors D. Moher
- Medicine
- BMJ
- 9 January 2013
High quality protocols facilitate proper conduct, reporting, and external review of clinical trials. However, the completeness of trial protocols is often inadequate. To help improve the content and… Expand