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Effect of rivastigmine as an adjunct to usual care with haloperidol on duration of delirium and mortality in critically ill patients: a multicentre, double-blind, placebo-controlled randomised trial

The Lancet (British edition), 2010-11, Vol.376 (9755), p.1829-1837

2010

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Recommendations for the design of small population clinical trials

Orphanet journal of rare diseases, 2018-11, Vol.13 (1), p.195-195, Article 195

2018

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Sequential designs with small samples: Evaluation and recommendations for normal responses

Statistical methods in medical research, 2018-04, Vol.27 (4), p.1115-1127

2018

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Reporting of covariate selection and balance assessment in propensity score analysis is suboptimal: a systematic review

Journal of clinical epidemiology, 2015-02, Vol.68 (2), p.122-131

2015

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Why was this transfusion given? Identifying clinical indications for blood transfusion in health care data

Clinical epidemiology, 2018-01, Vol.10, p.353-362

2018

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Dealing With Missing Outcome Data in Randomized Trials and Observational Studies

American journal of epidemiology, 2012-02, Vol.175 (3), p.210-217

2012

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Meta-analyses triggered by previous (false-)significant findings: problems and solutions

Systematic reviews, 2015-04, Vol.4 (1), p.57-57, Article 57

2015

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Challenges of defining a non-inferiority margin: a case study of non-inferiority randomized controlled trials of oral anti-thrombolytic agents for prophylaxis of venous thromboembolic events after orthopedic surgery

Trials, 2011-12, Vol.12 (S1), p.A32-A32, Article A32

2011

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Possible data-generating models of longitudinal continuous outcomes and intercurrent events to investigate estimands

Statistics in biopharmaceutical research, 2024-06, p.1-25

2024

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Methods to control for unmeasured confounding in pharmacoepidemiology: an overview

International journal of clinical pharmacy, 2016-06, Vol.38 (3), p.714-723

2016

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Exploring interaction effects in small samples increases rates of false-positive and false-negative findings: results from a systematic review and simulation study

Journal of clinical epidemiology, 2014-07, Vol.67 (7), p.821-829

2014

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Rapid response to methylphenidate as an add-on therapy to mirtazapine in the treatment of major depressive disorder in terminally ill cancer patients: A four-week, randomized, double-blinded, placebo-controlled study

European neuropsychopharmacology, 2014-04, Vol.24 (4), p.491-498

2014

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Selecting a classification function for class prediction with gene expression data

Bioinformatics, 2016-06, Vol.32 (12), p.1814-1822

2016

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Justification of exclusion criteria was underreported in a review of cardiovascular trials

Journal of clinical epidemiology, 2014-06, Vol.67 (6), p.635-644

2014

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Level of evidence for promising subgroup findings in an overall non-significant trial

Statistical methods in medical research, 2016-10, Vol.25 (5), p.2193-2213

2016

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Comparing HAMD17 and HAMD subscales on their ability to differentiate active treatment from placebo in randomized controlled trials

Journal of affective disorders, 2013-03, Vol.145 (3), p.363-369

2013

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Estimates of subgroup treatment effects in overall nonsignificant trials: To what extent should we believe in them?

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2017-07, Vol.16 (4), p.280-295

2017

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Effects of recruitment strategies and demographic factors on inclusion in a large scale vaccination trial in adults 65 years and older

Vaccine, 2014-05, Vol.32 (25), p.2989-2994

2014

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The effect of renal denervation added to standard pharmacologic treatment versus standard pharmacologic treatment alone in patients with resistant hypertension: Rationale and design of the SYMPATHY trial

The American heart journal, 2014-03, Vol.167 (3), p.308-314.e3

2014

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Improving clinical trial efficiency by biomarker-guided patient selection

Trials, 2014-04, Vol.15 (1), p.103-103, Article 103

2014

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Joint modeling of endpoints can be used to answer various research questions in randomized clinical trials

Journal of clinical epidemiology, 2022-07, Vol.147, p.32-39

2022

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An Analytical Approach to Assess the Predictive Value of Biomarkers in Phase II Decision Making

Journal of biopharmaceutical statistics, 2013-09, Vol.23 (5), p.1106-1123

2013

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Pharmacogenetics in randomized controlled trials: considerations for trial design

Pharmacogenomics, 2011-10, Vol.12 (10), p.1485-1492

2011

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Level of evidence for promising subgroup findings: The case of trends and multiple subgroups

Statistics in medicine, 2019-06, Vol.38 (14), p.2561-2572

2019

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Potential of adaptive clinical trial designs in pharmacogenetic research

Pharmacogenomics, 2012-04, Vol.13 (5), p.571-578

2012

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Effect of rivastigmine as an adjunct to usual care with haloperidol on duration of delirium and mortality in critically ill patients: a multicentre, double-blind, placebo-controlled randomised trial

Recommendations for the design of small population clinical trials

Sequential designs with small samples: Evaluation and recommendations for normal responses

Reporting of covariate selection and balance assessment in propensity score analysis is suboptimal: a systematic review

Why was this transfusion given? Identifying clinical indications for blood transfusion in health care data

Dealing With Missing Outcome Data in Randomized Trials and Observational Studies

Meta-analyses triggered by previous (false-)significant findings: problems and solutions

Challenges of defining a non-inferiority margin: a case study of non-inferiority randomized controlled trials of oral anti-thrombolytic agents for prophylaxis of venous thromboembolic events after orthopedic surgery

Possible data-generating models of longitudinal continuous outcomes and intercurrent events to investigate estimands

Methods to control for unmeasured confounding in pharmacoepidemiology: an overview

Exploring interaction effects in small samples increases rates of false-positive and false-negative findings: results from a systematic review and simulation study

Rapid response to methylphenidate as an add-on therapy to mirtazapine in the treatment of major depressive disorder in terminally ill cancer patients: A four-week, randomized, double-blinded, placebo-controlled study

Selecting a classification function for class prediction with gene expression data

Justification of exclusion criteria was underreported in a review of cardiovascular trials

Level of evidence for promising subgroup findings in an overall non-significant trial

Comparing HAMD17 and HAMD subscales on their ability to differentiate active treatment from placebo in randomized controlled trials

Estimates of subgroup treatment effects in overall nonsignificant trials: To what extent should we believe in them?

Effects of recruitment strategies and demographic factors on inclusion in a large scale vaccination trial in adults 65 years and older

The effect of renal denervation added to standard pharmacologic treatment versus standard pharmacologic treatment alone in patients with resistant hypertension: Rationale and design of the SYMPATHY trial

Improving clinical trial efficiency by biomarker-guided patient selection

Joint modeling of endpoints can be used to answer various research questions in randomized clinical trials

An Analytical Approach to Assess the Predictive Value of Biomarkers in Phase II Decision Making

Pharmacogenetics in randomized controlled trials: considerations for trial design

Level of evidence for promising subgroup findings: The case of trends and multiple subgroups

Potential of adaptive clinical trial designs in pharmacogenetic research

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