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Nigel Stallard

Medical and Pharmaceutical Statistics Research Unit

University of Reading

U.K

[email]@reading.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Medical and Pharmaceutical Statistics Research Unit, University of Reading, U.K. 1998 - 2004

References

  1. Statistical evaluation of an acute dermal toxicity test using the dermal fixed dose procedure. Stallard, N., Whitehead, A., Indans, I. Hum. Exp. Toxicol (2004) [Pubmed]
  2. Including a time-of-year effect in the analysis of a matched case-control study. Stallard, N., Tombs, L. Stat. Med (2004) [Pubmed]
  3. A statistical evaluation of the fixed dose procedure. Stallard, N., Whitehead, A. Altern. Lab. Anim (2004) [Pubmed]
  4. Sequential designs for phase III clinical trials incorporating treatment selection. Stallard, N., Todd, S. Stat. Med (2003) [Pubmed]
  5. Decision-theoretic designs for phase II clinical trials allowing for competing studies. Stallard, N. Biometrics (2003) [Pubmed]
  6. Statistical evaluation of the fixed concentration procedure for acute inhalation toxicity assessment. Stallard, N., Whitehead, A., Indans, I. Hum. Exp. Toxicol (2003) [Pubmed]
  7. Statistical evaluation of the revised fixed-dose procedure. Stalla, N., Whitehead, A., Ridgway, P. Hum. Exp. Toxicol (2002) [Pubmed]
  8. Stopping rules for phase II studies. Stallard, N., Whitehead, J., Todd, S., Whitehead, A. Br. J. Clin. Pharmacol (2001) [Pubmed]
  9. Decision-theoretic designs for pre-phase II screening trials in oncology. Stallard, N., Thall, P.F. Biometrics (2001) [Pubmed]
  10. Exact sequential tests for single samples of discrete responses using spending functions. Stallard, N., Todd, S. Stat. Med (2000) [Pubmed]
  11. Decision theoretic designs for phase II clinical trials with multiple outcomes. Stallard, N., Thall, P.F., Whitehead, J. Biometrics (1999) [Pubmed]
  12. Sample size determination for phase II clinical trials based on Bayesian decision theory. Stallard, N. Biometrics (1998) [Pubmed]
 
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