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Publications

Adaptive Clinical Trial Methods
  • Exact Confidence Bounds Following Adaptive Group Sequential Tests
    “A method for obtaining confidence intervals, point estimates and p-values for the primary effect size parameter at the end of a two-arm group sequential clinical trial in which adaptive changes have been implemented along the way.“
    Werner Brannath, Cyrus R. Mehta and Martin Posch
    Biometrics (publication pending), Blackwell Publishing, 2008
  • Repeated Confidence Intervals for Adaptive Group Sequential Trials
    "Proposing a method for computing conservative confidence intervals for a group sequential test in which an adaptive design change is made one or more times over the course of the trial."
    Cyrus R. Mehta, Peter Bauer, Martin Posch and Werner Brannath
    Statistics in Medicine, a Wiley InterScience publication, 2007

Group Sequential Trial Methods

Exact Inference Methods


Logistic Regression

  • Correspondence: Defibrotide for hepatic VOD in children: exact statistics can help PDF 72KB
    by Dr. R.A. Ammann
    Bone Marrow Transplantation (2004) 34, 277-278
  • A Preliminary Investigation of Maximum Likelihood Logistic Regression versus Exact Logistic Regression PDF: 1,127KB
    by Elizabeth N. King and Thomas P. Ryan
    The American Statistician, August 2002, Vol. 56, No. 3, pp 163-170
    Excerpt: ". . . maximum likelihood can produce very poor, even nonsensical, results under certain conditions."
  • A Modified Score Function Estimator for Multinomial Logistic Regression in Small Samples PDF: 161KB
    by Shelley B. Bull, Carmen Mak, Celiea M.T. Greenwood
    Computational Statistics and Data Analysis, 39 (2002) pp 57-74
  • Efficient Monte Carlo Methods for Conditional Logistic Regression PDF 140KB
    by Cyrus R. Mehta, Nitin R. Patel and Pralay Senchaudhuri
    Journal of the American Statistical Association, March 2000, Vol. 95, No. 449, Theory and Methods, pp 99-108


Epidemiology Related

  • Mauritsen, R.H. (1984). “Logistic RegressionWith Random Effects.” Unpublished Ph.D. thesis, Department of Biostatistics, University ofWashington.
  • McCullagh, P. and Nelder, J. A. (1989). “Generalized Linear Models.” Chapman and Hall.
  • Mehta, C.R., Patel, N.R., and Gray, R. (1986). “Computing an Exact Confidence Interval for the Common Odds Ratio in Several 2×2 Contingency Tables.” Journal of the American Statistical Association 80:969–973.
  • Moolgavkar, S.H. and Venzon, D.J. (1987). “Confidence Regions in Curved Exponential Families: Application to Matched Case-control and Survival Studies with General Relative Risk Functions.” Ann. Stat. 15(346):359.
  • Morgan, B. J. T. (1992). “Analysis of Quantal Response Data.” Chapman and Hall.
  • Nelder, J.A. and Mead, R. (1965). “A Simplex Method for Function Minimization.” Computer J. 7:308–313.
  • Ochi,Y. (1983). “The Correlated Probit Regression of Binary Responses with Extra-binomial Variability.” Ph.D. thesis. Department of Biostatistics, University of Washington.
  • Ochi,Y. and Prentice, R.L. (1983). “Regression Methods for Count Data with Extra-binomial Variation.” Pp. 127–139 in Atomic Bomb Survivor Data: Utilization and Analysis, edited by R. Prentice and D. Thompson. Philadelphia: SIAM.
  • Paul, S.R. (1982). “Analysis of Proportions of Affected Foetuses in Teratological Experiments.” Biometrics 38:361–370.
  • Pendergast, J., Gange, S. J., Newton, M. A., Linstrom, M. J., Palta, M., and Fisher, M. R. (1996). “A Survey of Methods for Analyzing Clustered Binary Response Data.” International Statistical Review 64:89–118.
  • Pierce, D.A. (1976). “A Random Effects Model for Matched Pairs of Binomial Data.” Tech. report no. 55, Dept. of Statistics, Oregon State University.
  • Pierce, D.A. and Sands, B.R. (1975). “Extra-Bernoulli Variation in Binary Data.” Tech. report no. 46, Dept. of Statistics, Oregon State University.
  • Pregibon, D. (1981). “Logistic Regression Diagnostics.” Ann. of Stat. 9(4):705–724
  • Prentice, R.L. (1986). “Correlated Binary Regression Using an Extended Beta-Binomial Distribution, with Discussion of Correlation Included by Covariate Measurement Error.” Journal of the American Statistical Association 81:321–327.
  • Prentice, R.L. and Mason, M.W. (1986). “On the Application of Linear Relative Risk Regression Models.” Biometrics 42:109–120.
  • Press,W.H., et al. (1992). Numerical Recipes in FORTRAN. Cambridge University Press.
  • Segreti, A.C. and Munson, A.E. (1981). “Estimation of the Median Lethal Dose when Responses within a Litter are Correlated.” Biometrics 37:153–156.
  • Self, S.G. and Liang, K. (1987). “Asymptotic Properties of Maximum Likelihood Estimator and Likelihood Ratio Tests under Nonstandard Conditions.” Journal of the American Statistical Association 82:605–610.
  • Self, S.G. and Mauritsen, R.H. (1992). “Power Calculations for Likelihood Ratio Tests in Generalized Linear Models.” Biometrics 48:31–39.
  • Shano, D.F. and Phua, K.H. (1976). “Algorithm 500, Minimization of Unconstrained Multivariate Functions [E4].” ACM Trans. on Math. Software 2(1):87–94.
  • Shapiro, S., Sloan, D., et al. (1979) “Oral-Contraceptive Use in Relation to Myocardial Infarction.” Lancet, April 7, 1979, 743–746.
  • Skellam, J.G. (1948). “A Probability Distribution Derived from the Binomial Distribution by Regarding the Probability of Success as Variable between the Sets of Trials.” J. Royal Statis. Soc. B 10(2):257–265.
  • Southward, M.G. and Van Ryzin, J. (1972). “Estimating the Mean of a Random Binomial Parameter.” Proc. of the Sixth Berkeley Symposium on Math. Stat. and Prob. 4:249–263.
  • Stiratelli, R., Laird, N. andWare, J. H. (1984). “Random Effects Models for Serial Observations with Dichotomous Response.” Biometrics 40:961–971.
  • Storer, B.E. and Crowley, J. (1985). “A Diagnostic for Cox Regression and General Conditional Likelihoods.” Journal of the American Statistical Association 80:139–147.
  • Storer, B.E.,Wacholder, S. and Breslow, N.E. (1983). “Maximum Likelihood Fitting of General Risk Models to Stratified Data.” Applied Statistics 32:172–181.
  • Tarone, R.E. (1979). “Testing the Goodness of Fit of the Binomial Distribution.”
    Biometrika 66(3):585–590.
  • Thomas, D.C. (1981). “General Relative Risk Functions for Survival Time and Matched Case-control Analysis.” Biometrics 37:673–686.
  • Van Ryzin, J. (1975). “Estimating the Mean of a Random Binomial Parameter with Trial Size Random.” Sankhya 37(1):10–27.
  • Væth, M. (1985). “On the Use ofWald’s Test in Exponential Families.” Int’l. Stat. Rev. 53(2):199–214.
  • Wacholder, S. (1986). “Binomial Regression in GLIM: Estimating Risk Ratios and Risk Differences.” Am. J. Epi. 123(1):174–184.
  • Weil, C.S. (1970). “Selection of the Valid Number of Sampling Units and a Consideration of their Combination in Toxicological Studies Involving Reproduction, Teratogenesis or Carcinogenesis.” Fd. Cosmet. Toxicol. 8:177–182.
  • Wichmann, B.A. and Hill, I.D. (1982). “An efficient and portable pseudo-random number generator.” Applied Statistics 31, 188-190.
  • Williams, D. (1975). “The Analysis of Binary Responses from Toxicological Experiments Involving Reproduction and Teratogenicity.” Biometrics 31:949–952.


Toxicity Related

  • Catalano PJ, and Ryan LM (1992). Bivariate latent variable models for clustered discrete and continuous outcomes. Journal of the American Statistical Association, 87:651-658.
  • Catalano PJ, Scharfstein DO, Ryan LM, Kimmel CA, and Kimmel GL (1993). Statistical model for fetal death, fetal weight, and malformation in developmental toxicity studies. Teratology, 47:281-290.
  • Catalano PJ, Scharfstein DO, Ryan LM (1994). Modeling fetal death and malformation in developmental toxicity. Risk Analysis, 14:611-619.
  • Catalano PJ (1997). Bivariate modelling of clustered continuous and ordered categorical outcomes. Statistics in Medicine, 16: 883-900.
  • Crump KS(1984), A new method for determining allowable daily intakes. Fundamental and Applied Toxicology, 4:854-871.
  • Crump KS (1995). Use of the benchmark dose approach in health risk assessment, Risk Assessment Forum, US EPA.
  • Kimmel CA, Gaylor DW (1988). Issues in Qualitative and Quantitative Risk Analysis for Developmental Toxicology. Risk Analysis, 8:15-20.
  • Ryan LM (1992). Quantitative risk assessment for developmental toxicity. Biometrics, 48:163-174.