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Byron Jones
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Cited by
Year
Design and analysis of cross-over trials
B Jones, MG Kenward
Chapman and Hall/CRC, 2003
21982003
Trials to assess equivalence: the importance of rigorous methods
B Jones, P Jarvis, JA Lewis, AF Ebbutt
Bmj 313 (7048), 36-39, 1996
11681996
Guidelines for controlled trials of drugs in migraine
International Headache Society Clinical Trials Subcommittee, ...
Cephalalgia 20 (9), 765-786, 2000
7532000
Statistical inference
PH Garthwaite, IT Jolliffe, B Jones
OUP Oxford, 2002
3962002
Bioequivalence and statistics in clinical pharmacology
SD Patterson, B Jones
Chapman and Hall/CRC, 2017
2022017
Exchange and interchange procedures to search for optimal designs
B Jones, JA Eccleston
Journal of the Royal Statistical Society Series B: Statistical Methodology …, 1980
971980
The analysis of data from 2× 2 cross‐over trials with baseline measurements
MG Kenward, B Jones
Statistics in Medicine 6 (8), 911-926, 1987
901987
A log‐linear model for binary cross‐over data
MG Kenward, B Jones
Journal of the Royal Statistical Society: Series C (Applied Statistics) 36 …, 1987
731987
Statistical approaches for conducting network meta‐analysis in drug development
B Jones, J Roger, PW Lane, A Lawton, C Fletcher, JC Cappelleri, H Tate, ...
Pharmaceutical Statistics 10 (6), 523-531, 2011
702011
The design of multicentre trials
V Fedorov, B Jones
Statistical Methods in Medical Research 14 (3), 205-248, 2005
702005
Modelling binary data from a three‐period cross‐over trial
B Jones, MG Kenward
Statistics in Medicine 6 (5), 555-564, 1987
701987
Equireplicate balanced block designs with unequal block sizes
SC Gupta, B Jones
Biometrika 70 (2), 433-440, 1983
671983
Modelling and design of cross‐over trials
B Jones, AN Donev
Statistics in Medicine 15 (13), 1435-1446, 1996
591996
A comparison of various estimators of a treatment difference for a multi‐centre clinical trial
B Jones, D Teather, J Wang, JA Lewis
Statistics in medicine 17 (15‐16), 1767-1777, 1998
571998
Alternative approaches to the analysis of binary and categorical repeated measurements
MG Kenward, B Jones
Journal of Biopharmaceutical Statistics 2 (2), 137-170, 1992
561992
Kullback–Leibler divergence for evaluating bioequivalence
V Dragalin, V Fedorov, S Patterson, B Jones
Statistics in medicine 22 (6), 913-930, 2003
532003
The case for cross‐over trials in phase III
B Jones, JA Lewis
Statistics in Medicine 14 (9), 1025-1038, 1995
481995
Efficient repeated measurements designs with equal and unequal period sizes
I Iqbal, B Jones
Journal of statistical planning and inference 42 (1-2), 79-88, 1994
471994
An algorithm for deriving optimal block designs
B Jones
Technometrics 18 (4), 451-458, 1976
461976
Batch‐to‐batch pharmacokinetic variability confounds current bioequivalence regulations: a dry powder inhaler randomized clinical trial
E Burmeister Getz, KJ Carroll, B Jones, LZ Benet
Clinical Pharmacology & Therapeutics 100 (3), 223-231, 2016
452016
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