S. Sacks
Pharmacoepidemiology and Drug Safety · 2004
A researcher in the Science corpus: 1 paper; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom S. Sacks trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- S. Evans (in Statistics and Probability)
Papers from S. Sacks's perspective
Ordered by how strongly the researchers S. Sacks trusts endorse each paper. Same corpus, a different order for every researcher.
- Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reports (Pharmacoepidemiology and Drug Safety)
- A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactions (Pharmacoepidemiology and Drug Safety)
- Statistical aspects of the analysis of data from retrospective studies of disease.
- Empirical bayes screening for multi-item associations (Knowledge Discovery and Data Mining)
- Use of Screening Algorithms and Computer Systems to Efficiently Signal Higher-Than-Expected Combinations of Drugs and Events in the US FDA’s Spontaneous Reports Database (Drug Safety)
- Non‐inferiority trials: design concepts and issues – the encounters of academic consultants in statistics (Statistics in Medicine)
- CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (British medical journal)
- WHO antenatal care randomised trial for the evaluation of a new model of routine antenatal care. (The Lancet)
- Reporting of noninferiority and equivalence randomized trials: an extension of the CONSORT statement. (Journal of the American Medical Association (JAMA))
- Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement (Annals of Internal Medicine)
Their papers
- The reporting odds ratio and its advantages over the proportional reporting ratio (2004) — 1,006 citations