Statistics in Medicine

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  Publication Venue For

  • Targeted maximum likelihood estimation of causal effects with interference: A simulation study..  41:4554-4577. 2022
  • Constrained randomization and statistical inference for multi-arm parallel cluster randomized controlled trials..  41:1862-1883. 2022
  • Bayesian variable selection for understanding mixtures in environmental exposures..  40:4850-4871. 2021
  • Propensity score weighting for causal subgroup analysis..  40:4294-4309. 2021
  • Propensity score weighting for covariate adjustment in randomized clinical trials..  40:842-858. 2021
  • Simultaneous record linkage and causal inference with propensity score subclassification..  37:3533-3546. 2018
  • Identifying optimal dosage regimes under safety constraints: An application to long term opioid treatment of chronic pain..  37:1407-1418. 2018
  • Sample size determination for jointly testing a cause-specific hazard and the all-cause hazard in the presence of competing risks..  37:1389-1401. 2018
  • Accommodating the ecological fallacy in disease mapping in the absence of individual exposures..  36:4930-4942. 2017
  • Bayesian multinomial probit modeling of daily windows of susceptibility for maternal PM2.5 exposure and congenital heart defects..  35:2786-2801. 2016
  • Multiple imputation for harmonizing longitudinal non-commensurate measures in individual participant data meta-analysis..  34:3399-3414. 2015
  • A marginalized zero-inflated Poisson regression model with overall exposure effects..  33:5151-5165. 2014
  • Imputation of confidential data sets with spatial locations using disease mapping models..  33:1928-1945. 2014
  • Correction to How to interpret a small increase in AUC with an additional risk prediction marker: Decision analysis comes through [Statist. Med. (2015) 33, 22, 3946-3959] DOI: 10.1002/sim.6195.  34:900. 2014
  • A latent factor linear mixed model for high-dimensional longitudinal data analysis..  32:4229-4239. 2013
  • Propensity score weighting with multilevel data..  32:3373-3387. 2013
  • Phase II clinical trials with time-to-event endpoints: Optimal two-stage designs with one-sample log-rank test 2013
  • A spatio-temporal absorbing state model for disease and syndromic surveillance..  31:2123-2136. 2012
  • Sensitivity analysis for unmeasured confounding in principal stratification settings with binary variables..  31:949-962. 2012
  • Correction: Evaluation metrics for biostatistical and epidemiological collaborations.  31:600. 2012
  • Authors' reply.  31:96-97. 2012
  • A min-max combination of biomarkers to improve diagnostic accuracy.  30:3266. 2011
  • The end of the beginning: A commentary on 'Evaluation metrics for biostatistical and epidemiological collaborations': A rejoinder.  30:2783-2784. 2011
  • Hierarchical spatial modeling of uncertainty in air pollution and birth weight study..  30:2187-2198. 2011
  • Estimating propensity scores with missing covariate data using general location mixture models..  30:627-641. 2011
  • Comparative effectiveness research: Policy context, methods development and research infrastructure..  29:1963-1976. 2010
  • Joint Bayesian analysis of birthweight and censored gestational age using finite mixture models..  29:1710-1723. 2010
  • A bivariate survival model with compound Poisson frailty..  29:275-283. 2010
  • A robust method for comparing two treatments in a confirmatory clinical trial via multivariate time-to-event methods that jointly incorporate information from longitudinal and time-to-event data..  29:75-85. 2010
  • Response to ‘Net reclassification improvement and decision theory’ by Vickers et al ..  28:526-528. 2009
  • Semiparametric Bayesian modeling of random genetic effects in family-based association studies..  28:113-139. 2009
  • 'Smooth' inference for survival functions with arbitrarily censored data..  27:5421-5439. 2008
  • Empirical estimation of life expectancy from large clinical trials: use of left-truncated, right-censored survival analysis methodology..  27:5525-5555. 2008
  • Covariate adjustment for two-sample treatment comparisons in randomized clinical trials: a principled yet flexible approach..  27:4658-4677. 2008
  • A distribution-free test of constant mean in linear mixed effects models..  27:3833-3846. 2008
  • Estimation of propensity scores using generalized additive models..  27:3805-3816. 2008
  • Sample size calculation for the weighted rank statistics with paired survival data..  27:3350-3365. 2008
  • Joint modeling of sensitivity and specificity..  27:1745-1761. 2008
  • Age-specific prevalence and years of healthy life in a system with three health states..  27:1371-1386. 2008
  • Randomized phase II trials with a prospective control..  27:568-583. 2008
  • Comments on 'Integrated discrimination and net reclassification improvements - Practical advice'.  27:207-212. 2008
  • Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond..  27:157-172. 2008
  • Relative quantification based on logistic models for individual polymerase chain reactions..  26:5596-5611. 2007
  • Morphometric analysis for early detection of changes in cellular structure in a toxicological experiment..  26:5253-5266. 2007
  • A correlated frailty model with long-term survivors for estimating the heritability of breast cancer..  26:3722-3734. 2007
  • Analysis on binary responses with ordered covariates and missing data..  26:3443-3458. 2007
  • Bayesian methods for searching for optimal rules for timing intercourse to achieve pregnancy..  26:1920-1936. 2007
  • Stability analysis for drugs with multiple active ingredients..  26:1512-1517. 2007
  • Bivariate random effect model using skew-normal distribution with application to HIV-RNA..  26:1255-1267. 2007
  • Choice of time scale and its effect on significance of predictors in longitudinal studies..  26:1343-1359. 2007
  • Performance assessment for radiologists interpreting screening mammography..  26:1532-1551. 2007
  • Inference for case-control studies when exposure status is both informatively missing and misclassified..  25:4065-4080. 2006
  • Bayesian semi-parametric ROC analysis..  25:3905-3928. 2006
  • Estimating measures of diagnostic accuracy when some covariate information is missing..  25:2981-2993. 2006
  • Interval estimation for treatment effects using propensity score matching..  25:2230-2256. 2006
  • Author's reply [4].  25:1437-1438. 2006
  • On non-inferiority margin and statistical tests in active control trials..  25:1101-1113. 2006
  • Rank tests for clustered survival data when dependent subunits are randomized..  25:361-373. 2006
  • Examining accuracy of screening mammography using an event order model..  25:267-283. 2006
  • Assay validation for left-censored data..  24:3347-3360. 2005
  • A multiple testing procedure to associate gene expression levels with survival..  24:3077-3088. 2005
  • Sample size for a two-group comparison of repeated binary measurements using GEE..  24:2583-2596. 2005
  • Statistical inference for cancer trials with treatment switching..  24:1783-1790. 2005
  • Assessing intra, inter and total agreement with replicated readings..  24:1371-1384. 2005
  • A practical approach for comparing means of two groups without equal variance assumption: H. Wang and S. Chow, Statistics in Medicine 2002; 21:3137-3151..  24:817-818. 2005
  • Analysis of clinical data with breached blindness: by Shein-Chung Chow and Jun Shao Statistics in Medicine 2004; 23:1185-1193..  24:819-821. 2005
  • Stratification and weighting via the propensity score in estimation of causal treatment effects: a comparative study..  23:2937-2960. 2004
  • Strength of accumulating evidence and data monitoring committee decision making..  23:2659-2672. 2004
  • Overall C as a measure of discrimination in survival analysis: model specific population value and confidence interval estimation..  23:2109-2123. 2004
  • Sample size determination for comparing several survival curves with unequal allocations..  23:1793-1815. 2004
  • Should statisticians reporting to data monitoring committees be independent of the trial sponsor and leadership?.  23:1503-1505. 2004
  • Analysis of clinical data with breached blindness..  23:1185-1193. 2004
  • On the estimation of the binomial probability in multistage clinical trials..  23:881-896. 2004
  • Admissible two-stage designs for phase II cancer clinical trials..  23:561-569. 2004
  • Growth velocity assessment in paediatric AIDS: smoothing, penalized quantile regression and the definition of growth failure..  23:509-526. 2004
  • The heritability of cause-specific mortality: a correlated gamma-frailty model applied to mortality due to respiratory diseases in Danish twins born 1870-1930..  22:3873-3887. 2003
  • ROC methodology within a monitoring framework..  22:3473-3488. 2003
  • A global sensitivity analysis of performance of a medical diagnostic test when verification bias is present..  22:2711-2721. 2003
  • Evaluating medical diagnostic tests at the subunit level in the presence of verification bias..  22:2161-2176. 2003
  • Power calculations for large multi-arm placebo-controlled studies of dichotomous outcomes..  22:1943-1954. 2003
  • Estimating correlation by using a general linear mixed model: evaluation of the relationship between the concentration of HIV-1 RNA in blood and semen..  22:1457-1464. 2003
  • Sample size estimation for GEE method for comparing slopes in repeated measurements data..  22:1305-1315. 2003
  • Missing data in the 2 x 2 table: patterns and likelihood-based analysis for cross-sectional studies with supplemental sampling..  22:517-534. 2003
  • A parametric model for long-term follow-up data from phase III breast cancer clinical trials..  22:339-352. 2003
  • In vitro bioequivalence testing..  22:55-68. 2003
  • A practical approach for comparing means of two groups without equal variance assumption..  21:3137-3151. 2002
  • The ebb and flow of the NHS waiting list: how do recruitment and admission affect event-based measures of the length of 'time-to-admission'?.  21:2991-3009. 2002
  • Industry perspectives on ICH guidelines..  21:2949-2957. 2002
  • A multistate model for the genetic analysis of the ageing process..  21:2511-2526. 2002
  • Reproducibility probability in clinical trials..  21:1727-1742. 2002
  • Individual bioequivalence testing under 2x3 designs..  21:629-648. 2002
  • The impact of the international guideline entitled Statistical Principles for Clinical Trials (ICH E9)..  20:2549-2560. 2001
  • Using observational data to estimate prognosis: an example using a coronary artery disease registry..  20:2505-2532. 2001
  • Evaluation of an adjusted chi-square statistic as applied to observational studies involving clustered binary data..  20:2149-2161. 2001
  • Sample size calculations for clustered binary data..  20:1971-1982. 2001
  • Two-phase shelf-life estimation..  20:1239-1248. 2001
  • Bayesian analyses of longitudinal binary data using Markov regression models of unknown order..  20:755-770. 2001
  • Tests for 2 x K contingency tables with clustered ordered categorical data..  20:785-794. 2001
  • Assessing human fertility using several markers of ovulation..  20:965-978. 2001
  • Detecting treatment-by-centre interaction in multi-centre clinical trials..  20:193-213. 2001
  • Strategic use of statistical thinking in drug development..  19:3211-3217. 2000
  • Preface. Bioequilavence measures..  19:2719. 2000
  • The bootstrap procedure in individual bioequivalence..  19:2741-2754. 2000
  • First steps in analysing NHS waiting times: avoiding the 'stationary and closed population' fallacy..  19:2037-2051. 2000
  • Modelling covariance structure in the analysis of repeated measures data..  19:1793-1819. 2000
  • On statistical analysis for placebo-challenging designs in clinical trials..  19:1029-1037. 2000
  • Comparison of diagnostic markers with repeated measurements: a non-parametric ROC curve approach..  19:511-523. 2000
  • Prognostic models based on literature and individual patient data in logistic regression analysis..  19:141-160. 2000
  • Accounting for unreported and missing intercourse in human fertility studies.  19:665-679. 2000
  • The role of biostatistics in the prevention, detection and treatment of fraud in clinical trials..  18:3435-3451. 1999
  • Evaluating the exposure and disease relationship with adjustment for different types of exposure misclassification: a regression approach..  18:2795-2808. 1999
  • Testing proportionality in the proportional odds model fitted with GEE..  18:1419-1433. 1999
  • A regression model for multivariate random length data..  18:199-211. 1999
  • Combining classification trees using MLE.  18:727-740. 1999
  • The effects of measurement error in response variables and tests of association of explanatory variables in change models..  17:2597-2606. 1998
  • Comparing risk-adjustment methods for provider profiling..  16:2645-2664. 1997
  • Testing homogeneity of intra-run variance parameters in immunoassay..  16:1765-1776. 1997
  • Bayesian inference in two-phase prevalence studies..  16:1121-1133. 1997
  • Statistical methods for two-sequence three-period cross-over designs with incomplete data..  16:1031-1039. 1997
  • The impact of patient compliance on drug concentration profile in multiple doses..  15:659-669. 1996
  • Multivariable prognostic models: issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors..  15:361-387. 1996
  • A statistic for comparing two correlated markers which are prognostic for time to an event..  14:2217-2225. 1995
  • The restricted cubic spline as baseline hazard in the proportional hazards model with step function time-dependent covariables..  14:2119-2129. 1995
  • Non-parametric estimation for the difference or ratio of median failure times for paired observations..  14:275-281. 1995
  • Stopping a clinical trial early: frequentist and Bayesian approaches applied to a CALGB trial in non-small-cell lung cancer..  13:1313-1327. 1994
  • The case against independent monitoring committees..  13:1411-1414. 1994
  • Assays for recombinant proteins: a problem in non-linear calibration..  13:1165-1179. 1994
  • Two-stage sampling in pharmaceutical applications..  12:1999-2008. 1993
  • A survey of monitoring practices in cancer clinical trials..  12:435-450. 1993
  • Data monitoring and interim analyses in the pharmaceutical industry: ethical and logistical considerations..  12:471-479. 1993
  • DATA MONITORING AND INTERIM ANALYSES IN THE PHARMACEUTICAL-INDUSTRY - ETHICAL AND LOGISTICAL CONSIDERATIONS - MONITORING OF CLINICAL-TRIALS AND INTERIM ANALYSES FROM A DRUG SPONSORS POINT-OF-VIEW - DISCUSSION.  12:493-495. 1993
  • Discussion: Stephen George, a survey of monitoring practices in cancer clinical trials: Stephanie Green and John Crowley, data monitoring committees for Southwest Oncology Group clinical trials.  12:457-459. 1993
  • Analysing the relationship between change in a risk factor and risk of disease..  11:783-797. 1992
  • Test for batch-to-batch variation in stability analysis..  11:269-270. 1992
  • Correction: Outlier detection in bioavailability/bioequivalence studies (Statistics in Medicine (1990) 9 (549-558)).  11:425. 1992
  • On the estimation of total variability in assay validation..  10:1543-1553. 1991
  • Analyses of black and white differentials in the age trajectory of mortality in two closed cohort studies..  10:1043-1059. 1991
  • Methods for the analysis and assessment of clinical databases: the clinician's perspective..  10:617-628. 1991
  • Outlier detection in bioavailability/bioequivalence studies..  9:549-558. 1990
  • Test for batch-to-batch variation in stability analysis..  8:883-890. 1989
  • Commentary. Response to Dr Halperin on ‘models of the interaction of mortality and the evolution of risk factor distribution: A general stochastic process formulation’.  7:293-295. 1988
  • Estimating hidden morbidity via its effect on mortality and disability..  7:325-336. 1988
  • Models of the interaction of mortality and the evolution of risk factor distribution: a general stochastic process formulation..  7:239-256. 1988
  • The bootstrap and identification of prognostic factors via Cox's proportional hazards regression model..  4:39-46. 1985
  • Regression modelling strategies for improved prognostic prediction..  3:143-152. 1984
  • Tying clinical research to patient care by use of an observational database..  3:375-387. 1984
  • Strategies for analysing ecological health data: models of the biological risk of individuals..  1:163-181. 1982
  • Discussion: Frank W Rockhold and G Enas, data monitoring and interim analyses in the pharmaceutical industry: Ethical and logistical considerations: George W Williams et al, monitoring of clinical trials and interim analyses from a drug sponsor's point of view 1993