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Identification and description of the uncertainty, variability, bias and influence in quantitative structure-activity relationships (QSARs) for toxicity prediction

Regulatory toxicology and pharmacology, 2019-08, Vol.106, p.90-104

2019

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Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology

Chemical reviews, 2011-04, Vol.111 (4), p.2562-2596

2011

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Clustering a Chemical Inventory for Safety Assessment of Fragrance Ingredients: Identifying Read-Across Analogs to Address Data Gaps

Chemical research in toxicology, 2020-07, Vol.33 (7), p.1709-1718

2020

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Equations for estimating binary mixture toxicity: 3-methyl-2-butanone with a series of electrophiles

PloS one, 2024-07, Vol.19 (7), p.e0306382

2024

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Integrated approach to testing and assessment for predicting rodent genotoxic carcinogenicity

Journal of applied toxicology, 2016-12, Vol.36 (12), p.1536-1550

2016

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Uncertainty in the results from oral repeated dose toxicity tests: Impact on regulatory classifications

Regulatory toxicology and pharmacology, 2024-01, Vol.146, p.105541-105541, Article 105541

2024

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Lessons learned from read-across case studies for repeated-dose toxicity

Regulatory toxicology and pharmacology, 2017-08, Vol.88, p.185-191

2017

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Estimating uncertainty in LLNA EC3 data and its impact on regulatory classifications

Regulatory toxicology and pharmacology, 2023-03, Vol.139, p.105357-105357, Article 105357

2023

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Automated read-across workflow for predicting acute oral toxicity: I. The decision scheme in the QSAR toolbox

Regulatory toxicology and pharmacology, 2021-10, Vol.125, p.105015, Article 105015

2021

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An End Point-Specific Framework for Read-Across Analog Selection for Human Health Effects

Chemical research in toxicology, 2022-12, Vol.35 (12), p.2324-2334

2022

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Determination of “fitness-for-purpose” of quantitative structure-activity relationship (QSAR) models to predict (eco-)toxicological endpoints for regulatory use

Regulatory toxicology and pharmacology, 2021-07, Vol.123, p.104956-104956, Article 104956

2021

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Chemical applicability domain of the Local Lymph Node Assay (LLNA) for skin sensitisation potency. Part 3. Apparent discrepancies between LLNA and GPMT sensitisation potential: False positives or differences in sensitivity?

Regulatory toxicology and pharmacology, 2016-10, Vol.80, p.260-267

2016

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Skin Sensitization QMM for HRIPT NOEL Data: Aldehyde Schiff-Base Domain

Chemical research in toxicology, 2017-06, Vol.30 (6), p.1309-1316

2017

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Development of a Decision Tree for Mitochondrial Dysfunction: Uncoupling of Oxidative Phosphorylation

Chemical research in toxicology, 2018-08, Vol.31 (8), p.814-820

2018

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The implementation of RAAF in the OECD QSAR Toolbox

Regulatory toxicology and pharmacology, 2019-07, Vol.105, p.51-61

2019

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The Adverse Outcome Pathway for Skin Sensitisation: Moving Closer to Replacing Animal Testing

Alternatives to laboratory animals, 2016-10, Vol.44 (5), p.453-460

2016

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Building up a QSAR model for toxicity toward Tetrahymena pyriformis by the Monte Carlo method: A case of benzene derivatives

Environmental toxicology and pharmacology, 2016-03, Vol.42, p.135-145

2016

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A practical guidance for Cramer class determination

Regulatory toxicology and pharmacology, 2015-12, Vol.73 (3), p.971-984

2015

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Kinetic-Based Reactivity for Michael Acceptors: Structural Activity Relationships and Its Relationship to Excess Acute Fish Toxicity

Bulletin of environmental contamination and toxicology, 2016-12, Vol.97 (6), p.752-756

2016

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Mechanistic relationship between biodegradation and bioaccumulation. Practical outcomes

Regulatory toxicology and pharmacology, 2019-10, Vol.107, p.104411, Article 104411

2019

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Validation of the performance of TIMES genotoxicity models with EFSA pesticide data

Mutagenesis, 2019-03, Vol.34 (1), p.83-90

2019

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Current status of methods for defining the applicability domain of (Quantitative) structure-activity relationships : The report and recommendations of ECVAM workshop 52

Alternatives to laboratory animals, 2005-04, Vol.33 (2), p.155-173

2005

Volltextzugriff (PDF)

Gilman D. Veith (1944-2013) - A dedication

SAR and QSAR in environmental research, 2014, Vol.25 (4), p.249-251

Schultz, Terry W.

2014

Volltextzugriff (PDF)

Development of a Fragment-Based in Silico Profiler for Michael Addition Thiol Reactivity

Chemical research in toxicology, 2016-06, Vol.29 (6), p.1073-1081

2016

Volltextzugriff (PDF)

Current status of methods for defining the applicability domain of (quantitative) structure-activity relationships

Alternatives to laboratory animals, 2005, Vol.33 (2), p.155-173

2005

Volltextzugriff (PDF)

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Identification and description of the uncertainty, variability, bias and influence in quantitative structure-activity relationships (QSARs) for toxicity prediction

Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology

Clustering a Chemical Inventory for Safety Assessment of Fragrance Ingredients: Identifying Read-Across Analogs to Address Data Gaps

Equations for estimating binary mixture toxicity: 3-methyl-2-butanone with a series of electrophiles

Integrated approach to testing and assessment for predicting rodent genotoxic carcinogenicity

Uncertainty in the results from oral repeated dose toxicity tests: Impact on regulatory classifications

Lessons learned from read-across case studies for repeated-dose toxicity

Estimating uncertainty in LLNA EC3 data and its impact on regulatory classifications

Automated read-across workflow for predicting acute oral toxicity: I. The decision scheme in the QSAR toolbox

An End Point-Specific Framework for Read-Across Analog Selection for Human Health Effects

Determination of “fitness-for-purpose” of quantitative structure-activity relationship (QSAR) models to predict (eco-)toxicological endpoints for regulatory use

Chemical applicability domain of the Local Lymph Node Assay (LLNA) for skin sensitisation potency. Part 3. Apparent discrepancies between LLNA and GPMT sensitisation potential: False positives or differences in sensitivity?

Skin Sensitization QMM for HRIPT NOEL Data: Aldehyde Schiff-Base Domain

Development of a Decision Tree for Mitochondrial Dysfunction: Uncoupling of Oxidative Phosphorylation

The implementation of RAAF in the OECD QSAR Toolbox

The Adverse Outcome Pathway for Skin Sensitisation: Moving Closer to Replacing Animal Testing

Building up a QSAR model for toxicity toward Tetrahymena pyriformis by the Monte Carlo method: A case of benzene derivatives

A practical guidance for Cramer class determination

Kinetic-Based Reactivity for Michael Acceptors: Structural Activity Relationships and Its Relationship to Excess Acute Fish Toxicity

Mechanistic relationship between biodegradation and bioaccumulation. Practical outcomes

Validation of the performance of TIMES genotoxicity models with EFSA pesticide data

Current status of methods for defining the applicability domain of (Quantitative) structure-activity relationships : The report and recommendations of ECVAM workshop 52

Gilman D. Veith (1944-2013) - A dedication

Development of a Fragment-Based in Silico Profiler for Michael Addition Thiol Reactivity

Current status of methods for defining the applicability domain of (quantitative) structure-activity relationships

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