J. Shao

发表

Sample Size Calculations In Clinical Research

S. Chow, Hansheng Wang, J. Shao, 2007 .

On the Difference between the Classical and Inverse Methods of Calibration

S. Chow, J. Shao, 1990 .

Reproducibility probability in clinical trials

S. Chow, J. Shao, 2002, Statistics in medicine.

Statistical inference for cancer trials with treatment switching

S. Chow, J. Shao, Mark Chang, 2005, Statistics in medicine.

Sample Size Calculations in Clinical Research, Second Edition

Shein-Chung Chow, Jun Shao, S. Chow, 2003 .

Dose–Response Studies

S. Chow, Hansheng Wang, J. Shao, 2007 .

A new procedure for the estimation of variance components

S. Chow, J. Shao, 1988 .

Constructing Release Targets for Drug Products: A Bayesian Decision Theory Approach

S. Chow, J. Shao, 1991 .

STATISTICAL TESTS FOR POPULATION BIOEQUIVALENCE

S. Chow, Hansheng Wang, J. Shao, 2003 .

Group Sequential Methods

Shein-Chung Chow, Jun Shao, Hansheng Wang, 2007 .

Dose–Response Studies

Shein-Chung Chow, Jun Shao, Yuliya Lokhnygina, 2007 .

DRUG SHELF-LIFE ESTIMATION

Shein-Chung Chow, Jun Shao, S. Chow, 2001 .

An Alternative Approach for the Assessment of Bioequivalence Between Two Formulations of a Drug

S. Chow, J. Shao, 2007 .

Individual bioequivalence testing under 2×3 designs

S. Chow, Hansheng Wang, J. Shao, 2002, Statistics in medicine.

Sample Size Calculation in Other Areas

Shein-Chung Chow, Jun Shao, Yuliya Lokhnygina, 2003 .

Assessing Bioequivalence Using Genomic Data

S. Chow, J. Shao, Li Li, 2004, Journal of biopharmaceutical statistics.

Comparing Time-to-Event Data

Shein-Chung Chow, Jun Shao, Hansheng Wang, 2007 .

ON THE ASSESSMENT OF SIMILARITY FOR DISSOLUTION PROFILES OF TWO DRUG PRODUCTS

S. Chow, J. Shao, 2002, Journal of biopharmaceutical statistics.

Stability analysis for drugs with multiple active ingredients

S. Chow, J. Shao, 2007, Statistics in Medicine.

Analysis of clinical data with breached blindness

S. Chow, J. Shao, 2004, Statistics in medicine.

Inference for Clinical Trials with Some Protocol Amendments

Shein-Chung Chow, Jun Shao, S. Chow, 2005, Journal of biopharmaceutical statistics.

On non‐inferiority margin and statistical tests in active control trials

Shein-Chung Chow, Jun Shao, S. Chow, 2006, Statistics in medicine.

TEST FOR TREATMENT EFFECT BASED ON BINARY DATA WITH RANDOM SAMPLE SIZES

S. Chow, J. Shao, 1990 .

Test for batch-to-batch variation in stability analysis.

J Shao, S C Chow, S. Chow, 1989, Statistics in medicine.

A note on statistical methods for assessing therapeutic equivalence.

S. Chow, J. Shao, 2002, Controlled clinical trials.

Two-stage sampling in pharmaceutical applications.

J Shao, S C Chow, S. Chow, 1993, Statistics in medicine.

Statistics in Drug Research: Methodologies and Recent Developments

S. Chow, J. Shao, 2002 .

A NOTE ON SAMPLE SIZE CALCULATION FOR MEAN COMPARISONS BASED ON NONCENTRAL t-STATISTICS

Shein-Chung Chow, Jun Shao, S. Chow, 2002, Journal of biopharmaceutical statistics.

The bootstrap procedure in individual bioequivalence.

S C Chow, J Shao, B Wang, 2000, Statistics in medicine.

On statistical analysis for placebo-challenging designs in clinical trials.

S. Chow, J. Shao, H. Ho, 2000, Statistics in medicine.

Statistical methods for two-sequence three-period cross-over designs with incomplete data.

J Shao, S C Chow, S. Chow, 1997, Statistics in medicine.

In vitro bioequivalence testing

S. Chow, Hansheng Wang, J. Shao, 2003, Statistics in medicine.

ASSESSING SENSITIVITY AND SIMILARITY IN BRIDGING STUDIES

Shein-Chung Chow, Jun Shao, S. Chow, 2002, Journal of biopharmaceutical statistics.

Statistical Inference in Stability Analysis

Shein-Chung Chow, Jun Shao, S. Chow, 1994 .

Variable screening in predicting clinical outcome with high-dimensional microarrays

Shein-Chung Chow, Jun Shao, S. Chow, 2007 .

Stability Analysis with Discrete Responses

S. Chow, J. Shao, 2003, Journal of biopharmaceutical statistics.