Biased under-reporting of research reflects biased under-submission more than biased editorial rejection [v1; ref status: indexed, http://f1000r.es/ViIqTX]

by Iain Chalmers, Kay Dickersin
Published 2013-01-01

Differences in reporting of analyses in internal company documents versus published trial reports: comparisons in industry-sponsored trials in off-label uses of gabapentin.

by S Swaroop Vedula, Tianjing Li, Kay Dickersin
Published 2013-01-01

Design, Analysis, and Reporting of Crossover Trials for Inclusion in a Meta-Analysis.

by Tianjing Li, Tsung Yu, Barbara S Hawkins, Kay Dickersin
Published 2015-01-01

Outcomes in Cochrane systematic reviews addressing four common eye conditions: an evaluation of completeness and comparability.

by Ian J Saldanha, Kay Dickersin, Xue Wang, Tianjing Li
Published 2014-01-01

Using ClinicalTrials.gov to supplement information in ophthalmology conference abstracts about trial outcomes: a comparison study.

by Roberta W Scherer, Lynn Huynh, Ann-Margret Ervin, Kay Dickersin
Published 2015-01-01

Can we depend on investigators to identify and register randomized controlled trials?

by Roberta W Scherer, Pamela C Sieving, Ann-Margret Ervin, Kay Dickersin
Published 2012-01-01

Caveat emptor: the combined effects of multiplicity and selective reporting

by Tianjing Li, Evan Mayo-Wilson, Nicole Fusco, Hwanhee Hong, Kay Dickersin
Published 2018-09-01

Principios del registro internacional de protocolos y resultados de ensayos clínicos a base de intervenciones de salud en seres humanos: Declaración de Ottawa (parte 1)

by Karmela Krleza-Jeric, An-Wen Chan, Kay Dickersin, Ida Sim, Jeremy Grimshaw, Christian Gluud
Published 2006-06-01

Opportunities for selective reporting of harms in randomized clinical trials: Selection criteria for non-systematic adverse events

by Evan Mayo-Wilson, Nicole Fusco, Hwanhee Hong, Tianjing Li, Joseph K. Canner, Kay Dickersin
Published 2019-09-01

Outcome choice and definition in systematic reviews leads to few eligible studies included in meta-analyses: a case study

by Ian J. Saldanha, Kristina B. Lindsley, Sarah Money, Hannah J. Kimmel, Bryant T. Smith, Kay Dickersin
Published 2020-02-01

Development, implementation and evaluation of an online course on evidence-based healthcare for consumers

by Genie Han, Musa Mayer, Joseph Canner, Kristina Lindsley, Reva Datar, Jimmy Le, Annette Bar-Cohen, Janice Bowie, Kay Dickersin
Published 2020-10-01

Comparative effectiveness research: challenges for medical journals.

by Harold C Sox, Mark Helfand, Jeremy Grimshaw, Kay Dickersin, PLoS Medicine Editors, David Tovey, J André Knottnerus, Peter Tugwell
Published 2010-04-01

Who has used internal company documents for biomedical and public health research and where did they find them?

by L Susan Wieland, Lainie Rutkow, S Swaroop Vedula, Christopher N Kaufmann, Lori M Rosman, Claire Twose, Nirosha Mahendraratnam, Kay Dickersin
Published 2014-01-01

Methods to identify and prioritize patient-centered outcomes for use in comparative effectiveness research

by Evan Mayo-Wilson, Asieh Golozar, Terrie Cowley, Nicole Fusco, Gillian Gresham, Jennifer Haythornthwaite, Elizabeth Tolbert, Jennifer L. Payne, Lori Rosman, Susan Hutfless, Joseph K. Canner, Kay Dickersin
Published 2018-06-01

Evaluating Data Abstraction Assistant, a novel software application for data abstraction during systematic reviews: protocol for a randomized controlled trial

by Ian J. Saldanha, Christopher H. Schmid, Joseph Lau, Kay Dickersin, Jesse A. Berlin, Jens Jap, Bryant T. Smith, Simona Carini, Wiley Chan, Berry De Bruijn, Byron C. Wallace, Susan M. Hutfless, Ida Sim, M. Hassan Murad, Sandra A. Walsh, Elizabeth J. Whamond, Tianjing Li
Published 2016-11-01

Correction to: Integrating multiple data sources (MUDS) for meta-analysis to improve patient-centered outcomes research: a protocol

by Evan Mayo-Wilson, Susan Hutfless, Tianjing Li, Gillian Gresham, Nicole Fusco, Jeffrey Ehmsen, James Heyward, Swaroop Vedula, Diana Lock, Jennifer Haythornthwaite, Jennifer L. Payne, Theresa Cowley, Elizabeth Tolbert, Lori Rosman, Claire Twose, Elizabeth A. Stuart, Hwanhee Hong, Peter Doshi, Catalina Suarez-Cuervo, Sonal Singh, Kay Dickersin
Published 2018-03-01

SPIRIT 2013 Statement: defining standard protocol items for clinical trials

by An-Wen Chan, Jennifer M. Tetzlaff, Douglas G. Altman, Andreas Laupacis, Peter C. Gøtzsche, Karmela Krleža-Jerić, Asbjørn Hrobjartsson, Howard Mann, Kay Dickersin, Jesse A. Berlin, Caroline J. Dore, Wendy R. Parulekar, William S.M. Summerskill, Trish Groves, Kenneth F. Schulz, Harold C. Sox, Frank W. Rockhold, Drummond Rennie, David Moher