On the public citation graph
Quantitative and Mechanistic Read Across for Predicting the Skin Sensitization Potential of Alkenes Acting via Michael Addition
0 signed · 136 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jps.2600690938openalex-snapshot
Substituent Constants for Correlation Analysis in Chemistry and Biology.
inferredcites →https://doi.org/10.1002/qsar.19940130106openalex-snapshot
A Classification Model for Allergic Contact Dermatitis
inferredcites →https://doi.org/10.1016/j.bmc.2005.03.011openalex-snapshot
Electrophilicity as a possible descriptor for toxicity prediction
inferredcites →https://doi.org/10.1016/j.tet.2004.06.003openalex-snapshot
Reactivity of the carbon–carbon double bond towards nucleophilic additions. A DFT analysis
inferredcites →https://doi.org/10.1021/jp020715jopenalex-snapshot
Quantitative Characterization of the Local Electrophilicity of Organic Molecules. Understanding the Regioselectivity on Diels−Alder Reactions
inferredcites →https://doi.org/10.1021/tx050075mopenalex-snapshot
Skin Sensitization: Reaction Mechanistic Applicability Domains for Structure−Activity Relationships
inferredcites →https://doi.org/10.1021/tx0601004openalex-snapshot
Mechanistic Applicability Domains for Nonanimal-Based Prediction of Toxicological End Points: General Principles and Application to Reactive Toxicity
inferredcites →https://doi.org/10.1021/tx060102oopenalex-snapshot
Mechanistic Applicability Domains for Non-Animal Based Prediction of Toxicological Endpoints. QSAR Analysis of the Schiff Base Applicability Domain for Skin Sensitization
inferredcites →https://doi.org/10.1021/tx060121yopenalex-snapshot
Electrophilic Chemistry Related to Skin Sensitization. Reaction Mechanistic Applicability Domain Classification for a Published Data Set of 106 Chemicals Tested in the Mouse Local Lymph Node Assay
inferredcites →https://doi.org/10.1021/tx700212uopenalex-snapshot
Verification of the Structural Alerts for Michael Acceptors
inferredcites →https://doi.org/10.1021/tx960104gopenalex-snapshot
Molecular Orbital Parameters as Predictors of Skin Sensitization Potential of Halo- and Pseudohalobenzenes Acting as SNAr Electrophiles
inferredcites →https://doi.org/10.1034/j.1600-0536.2000.042003154.xopenalex-snapshot
Quantitative structure‐activity relationships: sulfonate esters in the local lymph node assay
inferredcites →https://doi.org/10.1034/j.1600-0536.2000.042006344.xopenalex-snapshot
Use of the local lymph node assay for the estimation of relative contact allergenic potency
inferredcites →https://doi.org/10.1034/j.1600-0536.2001.044006331.xopenalex-snapshot
Skin‐sensitization structure‐activity relationships for aldehydes
inferredcites →https://doi.org/10.1034/j.1600-0536.2002.470406.xopenalex-snapshot
Structure–activity relationships for selected fragrance allergens
inferredcites →https://doi.org/10.1080/10517230050121598openalex-snapshot
A NEURAL NETWORK SAR MODEL FOR ALLERGIC CONTACT DERMATITIS
inferredcites →https://doi.org/10.1080/10629360600884371openalex-snapshot
A conceptual framework for predicting the toxicity of reactive chemicals: modeling soft electrophilicity
inferredcites →https://doi.org/10.1080/10629360601054255openalex-snapshot
The role of the European Chemicals Bureau in promoting the regulatory use of (Q)SAR methods
inferredcites →https://doi.org/10.1080/10629360701306118openalex-snapshot
Global (Q)SARs for skin sensitisation–assessment against OECD principles‖
inferredcites →https://doi.org/10.1080/10629369408029901openalex-snapshot
Multivariate Qsar Analysis of a Skin Sensitization Database
inferredcites →https://doi.org/10.1111/j.0105-1873.2004.00322.xopenalex-snapshot
Further evaluation of quantitative structure–activity relationship models for the prediction of the skin sensitization potency of selected fragrance allergens
inferredcites →https://doi.org/10.1201/9780203642627openalex-snapshot
Predicting Chemical Toxicity and Fate
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470686263.ch15openalex-snapshot
(Q)SAR Models of Adverse Responses: Acute Systemic Toxicity
inferred← citeshttps://doi.org/10.1002/9780470921920.edm139openalex-snapshot
QSAR and Molecular Modeling Approaches for Prediction of Drug Metabolism
inferred← citeshttps://doi.org/10.1002/9781119650034.ch18openalex-snapshot
In Silico Modeling as a Tool to Predict and Characterize Plant Toxicity
inferred← citeshttps://doi.org/10.1002/hlca.201400340openalex-snapshot
Boyd Group Electronegativity Influence on the Parr Global Electrophilicity of Vilsmeier Reagent‐Derived Imidates: New Insights toward Improving Mitsunobu Chemistry
inferred← citeshttps://doi.org/10.1002/jat.4395openalex-snapshot
Assessment of commercial polymers with and without reactive groups using amino acid derivative reactivity assay based on both molar concentration approach and gravimetric approach
inferred← citeshttps://doi.org/10.1002/minf.201000011openalex-snapshot
Are Mechanistic and Statistical QSAR Approaches Really Different? MLR Studies on 158 Cycloalkyl‐Pyranones
inferred← citeshttps://doi.org/10.1002/minf.201800121openalex-snapshot
Filling Data Gaps by Read‐across: A Mini Review on its Application, Developments and Challenges
inferred← citeshttps://doi.org/10.1002/qsar.200960011openalex-snapshot
Formation of Structural Categories to Allow for Read‐Across for Teratogenicity
inferred← citeshttps://doi.org/10.1002/wcms.1240openalex-snapshot
In silico toxicology: computational methods for the prediction of chemical toxicity
inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_11openalex-snapshot
Prediction of Harmful Human Health Effects of Chemicals from Structure
inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_2openalex-snapshot
The Use of Quantum Mechanics Derived Descriptors in Computational Toxicology
inferred← citeshttps://doi.org/10.1007/978-1-4020-9783-6_7openalex-snapshot
Chemical Category Formation and Read-Across for the Prediction of Toxicity
inferred← citeshttps://doi.org/10.1007/978-3-031-33871-7_9openalex-snapshot
Read-Across and RASAR Tools from the DTC Laboratory
inferred← citeshttps://doi.org/10.1007/978-3-031-52057-0_3openalex-snapshot
Quantitative Read-Across (q-RA) and Quantitative Read-Across Structure–Activity Relationships (q-RASAR)—Genesis and Model Development
inferred← citeshttps://doi.org/10.1007/s00204-014-1277-8openalex-snapshot
Proposal of an in silico profiler for categorisation of repeat dose toxicity data of hair dyes
inferred← citeshttps://doi.org/10.1007/s00204-014-1421-5openalex-snapshot
SEURAT: Safety Evaluation Ultimately Replacing Animal Testing—Recommendations for future research in the field of predictive toxicology
inferred← citeshttps://doi.org/10.1007/s10260-025-00794-0openalex-snapshot
From animal testing to in Silico models: a systematic review and practical guide to cosmetic assessment
inferred← citeshttps://doi.org/10.1007/s12195-011-0189-4openalex-snapshot
Perspectives on Non-Animal Alternatives for Assessing Sensitization Potential in Allergic Contact Dermatitis
inferred← citeshttps://doi.org/10.1007/s43188-025-00283-2openalex-snapshot
Regulatory frameworks for fragrance safety in cosmetics: a global overview
inferred← citeshttps://doi.org/10.1016/j.chemolab.2022.104613openalex-snapshot
Quantitative predictions from chemical read-across and their confidence measures
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2008.06.052openalex-snapshot
Classification of chemicals according to mechanism of aquatic toxicity: An evaluation of the implementation of the Verhaar scheme in Toxtree
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2009.04.010openalex-snapshot
Modeling photoinduced toxicity of PAHs based on DFT-calculated descriptors
inferred← citeshttps://doi.org/10.1016/j.comtox.2019.100117openalex-snapshot
Development of a fragment-based in silico profiler for SN2 thiol reactivity and its application in predicting toxicity of chemicals towards Tetrahymena pyriformis
inferred← citeshttps://doi.org/10.1016/j.comtox.2022.100220openalex-snapshot
A strategy to define applicability domains for read-across
inferred← citeshttps://doi.org/10.1016/j.crtox.2024.100183openalex-snapshot
Low-cost quantum mechanical descriptors for data efficient skin sensitization QSAR models
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120036openalex-snapshot
Mechanism-based QSAR and molecular simulation reveal the toxicity of marine disinfection byproducts to Vibrio fischeri
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2026.100338openalex-snapshot
Recent advances in computational modelling, artificial intelligence, and in silico strategies for predicting adverse effects in skincare safety: A critical review
inferred← citeshttps://doi.org/10.1016/j.neuro.2020.04.009openalex-snapshot
Application of the hard and soft, acids and bases (HSAB) theory as a method to predict cumulative neurotoxicity
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.10.308openalex-snapshot
Development of thresholds of excess toxicity for environmental species and their application to identification of modes of acute toxic action
inferred← citeshttps://doi.org/10.1016/j.snb.2013.12.001openalex-snapshot
(E)-2-(Benzo[d]thiazol-2-yl)-3-heteroarylacrylonitriles as efficient Michael acceptors for cysteine: Real application in biological imaging
inferred← citeshttps://doi.org/10.1016/j.taap.2012.03.018openalex-snapshot
VirtualToxLab — A platform for estimating the toxic potential of drugs, chemicals and natural products
inferred← citeshttps://doi.org/10.1016/j.tox.2013.11.009openalex-snapshot
Pyridoxylamine reactivity kinetics as an amine based nucleophile for screening electrophilic dermal sensitizers
inferred← citeshttps://doi.org/10.1016/j.toxlet.2014.09.004openalex-snapshot
OpenVirtualToxLab—A platform for generating and exchanging in silico toxicity data
inferred← citeshttps://doi.org/10.1016/j.toxlet.2016.04.013openalex-snapshot
Molecular mechanisms of endocrine and metabolic disruption: An in silico study on antitrypanosomal natural products and some derivatives
inferred← citeshttps://doi.org/10.1016/j.toxlet.2021.05.011openalex-snapshot
Theoretical modeling of structure-toxicity relationship of cyanides
inferred← citeshttps://doi.org/10.1016/j.watres.2009.05.002openalex-snapshot
Dechlorination of chloroacetanilide herbicides by plant growth regulator sodium bisulfite
inferred← citeshttps://doi.org/10.1016/j.yrtph.2009.09.006openalex-snapshot
A framework for using structural, reactivity, metabolic and physicochemical similarity to evaluate the suitability of analogs for SAR-based toxicological assessments
inferred← citeshttps://doi.org/10.1016/j.yrtph.2013.08.018openalex-snapshot
Establishing the level of safety concern for chemicals in food without the need for toxicity testing
inferred← citeshttps://doi.org/10.1016/j.yrtph.2015.03.001openalex-snapshot
Principles for identification of High Potency Category Chemicals for which the Dermal Sensitisation Threshold (DST) approach should not be applied
inferred← citeshttps://doi.org/10.1016/j.yrtph.2016.07.018openalex-snapshot
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?
inferred← citeshttps://doi.org/10.1016/j.yrtph.2018.11.002openalex-snapshot
Molecular fingerprint-derived similarity measures for toxicological read-across: Recommendations for optimal use
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.2c00224openalex-snapshot
Computer-Aided Discovery and Redesign for Respiratory Sensitization: A Tiered Mechanistic Model to Deliver Robust Performance Across a Diverse Chemical Space
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.4c00244openalex-snapshot
Estimation of the Skin Sensitization Potential of Chemicals of the Acyl Domain Using DFT-Based Calculations
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.4c00289openalex-snapshot
Capturing Differential Quality of Experimental Evidence in a Predictive Quantum-Mechanical Model for Respiratory Sensitization
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.6b00341openalex-snapshot
A History of the Molecular Initiating Event
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.6b00361openalex-snapshot
Validation of a Fragment-Based Profiler for Thiol Reactivity for the Prediction of Toxicity: Skin Sensitization and Tetrahymena pyriformis
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.9b00518openalex-snapshot
Clustering a Chemical Inventory for Safety Assessment of Fragrance Ingredients: Identifying Read-Across Analogs to Address Data Gaps
inferred← citeshttps://doi.org/10.1021/acs.est.5b05918openalex-snapshot
Adverse Outcome Pathway (AOP) Informed Modeling of Aquatic Toxicology: QSARs, Read-Across, and Interspecies Verification of Modes of Action
inferred← citeshttps://doi.org/10.1021/acs.jcim.8b00130openalex-snapshot
Using Transition State Modeling To Predict Mutagenicity for Michael Acceptors
inferred← citeshttps://doi.org/10.1021/acs.jcim.9b00316openalex-snapshot
A Fast Ab Initio Predictor Tool for Covalent Reactivity Estimation of Acrylamides
inferred← citeshttps://doi.org/10.1021/acs.jctc.7b00764openalex-snapshot
Automated Transition State Search and Its Application to Diverse Types of Organic Reactions
inferred← citeshttps://doi.org/10.1021/cr078014bopenalex-snapshot
Update 1 of: Electrophilicity Index
inferred← citeshttps://doi.org/10.1021/cr100098nopenalex-snapshot
Measurement and Estimation of Electrophilic Reactivity for Predictive Toxicology
inferred← citeshttps://doi.org/10.1021/cr100149popenalex-snapshot
Update 2 of: Electrophilicity Index
inferred← citeshttps://doi.org/10.1021/tx100172xopenalex-snapshot
Prediction of Michael-Type Acceptor Reactivity toward Glutathione
inferred← citeshttps://doi.org/10.1021/tx100218hopenalex-snapshot
Mechanistic Category Formation for the Prediction of Respiratory Sensitization
inferred← citeshttps://doi.org/10.1021/tx100420wopenalex-snapshot
Chemistry-Based Risk Assessment for Skin Sensitization: Quantitative Mechanistic Modeling for the SNAr Domain
inferred← citeshttps://doi.org/10.1021/tx2003257openalex-snapshot
Application of the Hard and Soft, Acids and Bases (HSAB) Theory to Toxicant–Target Interactions
inferred← citeshttps://doi.org/10.1021/tx300417zopenalex-snapshot
Substituent Effects on the Reactivity of Benzoquinone Derivatives with Thiols
inferred← citeshttps://doi.org/10.1021/tx4000655openalex-snapshot
Predicting Skin Sensitization Potency for Michael Acceptors in the LLNA Using Quantum Mechanics Calculations
inferred← citeshttps://doi.org/10.1021/tx400110fopenalex-snapshot
Integrative Chemical–Biological Read-Across Approach for Chemical Hazard Classification
inferred← citeshttps://doi.org/10.1021/tx8002438openalex-snapshot
Formation of Categories from Structure−Activity Relationships To Allow Read-Across for Risk Assessment: Toxicity of α,β-Unsaturated Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/tx800431xopenalex-snapshot
High Throughput Kinetic Profiling Approach for Covalent Binding to Peptides: Application to Skin Sensitization Potency of Michael Acceptor Electrophiles
inferred← citeshttps://doi.org/10.1021/tx9001463openalex-snapshot
Electrophilic Reaction Chemistry of Low Molecular Weight Respiratory Sensitizers
inferred← citeshttps://doi.org/10.1021/tx9003648openalex-snapshot
Experimental Reactivity Parameters for Toxicity Modeling: Application to the Acute Aquatic Toxicity of SN2 Electrophiles to Tetrahymena pyriformis
inferred← citeshttps://doi.org/10.1039/9781849731744-00030openalex-snapshot
Approaches for Grouping Chemicals into Categories
inferred← citeshttps://doi.org/10.1039/9781849732093-00193openalex-snapshot
The Use of Frontier Molecular Orbital Calculations in Predictive Reactive Toxicology
inferred← citeshttps://doi.org/10.1039/9781849732093-00346openalex-snapshot
Adverse Outcome Pathways: A Way of Linking Chemical Structure to In Vivo Toxicological Hazards
inferred← citeshttps://doi.org/10.1039/9781849732093-00446openalex-snapshot
Biological Read-Across: Mechanistically-Based Species–Species and Endpoint–Endpoint Extrapolations
inferred← citeshttps://doi.org/10.1039/9781849734400-00001openalex-snapshot
An Introduction to Chemical Grouping, Categories and Read-Across to Predict Toxicity
inferred← citeshttps://doi.org/10.1039/9781849734400-00030openalex-snapshot
Approaches for Grouping Chemicals into Categories
inferred← citeshttps://doi.org/10.1039/b802832jopenalex-snapshot
Electrophilicity index within a conceptual DFT framework
inferred← citeshttps://doi.org/10.1039/d3em00322aopenalex-snapshot
Read-across-based intelligent learning: development of a global q-RASAR model for the efficient quantitative predictions of skin sensitization potential of diverse organic chemicals
inferred← citeshttps://doi.org/10.1039/d3me00077jopenalex-snapshot
Theoretical insights into the compatibility of template-monomer-crosslinker-solvent for cortisol molecularly imprinted polymer pre-polymerization
inferred← citeshttps://doi.org/10.1039/d4em00173gopenalex-snapshot
ARKA: a framework of dimensionality reduction for machine-learning classification modeling, risk assessment, and data gap-filling of sparse environmental toxicity data
inferred← citeshttps://doi.org/10.1080/10408444.2018.1528207openalex-snapshot
Computational approaches for skin sensitization prediction
inferred← citeshttps://doi.org/10.1080/10629360802348985openalex-snapshot
Identification of mechanisms of toxic action for skin sensitisation using a SMARTS pattern based approach
inferred← citeshttps://doi.org/10.1080/1062936x.2011.604100openalex-snapshot
Repeatability analysis of theTetrahymena pyriformispopulation growth impairment assay
inferred← citeshttps://doi.org/10.1080/1062936x.2013.792874openalex-snapshot
Experimental verification, and domain definition, of structural alerts for protein binding: epoxides, lactones, nitroso, nitros, aldehydes and ketones
inferred← citeshttps://doi.org/10.1080/1062936x.2013.820793openalex-snapshot
Experimental verification of structural alerts for the protein binding of cyclic compounds acting as Michael acceptors
inferred← citeshttps://doi.org/10.1088/0957-4484/26/1/015701openalex-snapshot
Novel approach for efficient predictions properties of large pool of nanomaterials based on limited set of species: nano-read-across
inferred← citeshttps://doi.org/10.1093/toxsci/kfx196openalex-snapshot
The Impact of Novel Assessment Methodologies in Toxicology on Green Chemistry and Chemical Alternatives
inferred← citeshttps://doi.org/10.1111/j.1600-0536.2008.01473.xopenalex-snapshot
Read‐across to rank skin sensitization potential: subcategories for the Michael acceptor domain
inferred← citeshttps://doi.org/10.1111/j.1600-0536.2011.01899.xopenalex-snapshot
Clinical and experimental studies of octocrylene's allergenic potency
inferred← citeshttps://doi.org/10.1177/026119290903700506openalex-snapshot
In Silico Toxicology in Drug Discovery — Concepts Based on Three-dimensional Models
inferred← citeshttps://doi.org/10.1177/026119290903700512openalex-snapshot
The use of Mechanisms and Modes of Toxic Action in Integrated Testing Strategies: The Report and Recommendations of a Workshop held as part of the European Union OSIRIS Integrated Project
inferred← citeshttps://doi.org/10.1177/026119291103900206openalex-snapshot
The Use of a Chemistry-based Profiler for Covalent DNA Binding in the Development of Chemical Categories for Read-across for Genotoxicity
inferred← citeshttps://doi.org/10.1177/026119291404200606openalex-snapshot
Development of an In Silico Profiler for Respiratory Sensitisation
inferred← citeshttps://doi.org/10.1177/1091581820944395openalex-snapshot
Evaluating Skin Sensitization Via Soft and Hard Multivariate Modeling
inferred← citeshttps://doi.org/10.1186/2050-6511-15-76openalex-snapshot
Modeling skin sensitization potential of mechanistically hard-to-be-classified aniline and phenol compounds with quantum mechanistic properties
inferred← citeshttps://doi.org/10.1271/bbb.90731openalex-snapshot
Electrophiles in Foods: The Current Status of Isothiocyanates and Their Chemical Biology
inferred← citeshttps://doi.org/10.1289/ehp3614openalex-snapshot
Nonanimal Models for Acute Toxicity Evaluations: Applying Data-Driven Profiling and Read-Across
inferred← citeshttps://doi.org/10.14573/altex.1601251openalex-snapshot
Toward Good Read-Across Practice (GRAP) guidance
inferred← citeshttps://doi.org/10.14573/altex.2011.1.045openalex-snapshot
Formation of mechanistic categories and local models to facilitate the prediction of toxicity
inferred← citeshttps://doi.org/10.14573/altex.2011.2.131openalex-snapshot
A critique of the EC’s expert (draft) reports on the status of alternatives for cosmetics testing to meet the 2013 deadline
inferred← citeshttps://doi.org/10.1517/17425255.2011.629186openalex-snapshot
A review of the use ofin silicomethods to predict the chemistry of molecular initiating events related to drug toxicity
inferred← citeshttps://doi.org/10.15760/etd.1406openalex-snapshot
Substituent Effects on Reactivity and Allergenicity of Benzoquinone
inferred← citeshttps://doi.org/10.17615/wb20-z498openalex-snapshot
Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles
inferred← citeshttps://doi.org/10.2174/157488612804096614openalex-snapshot
In Silico Assessment of Adverse Effects of a Large Set of 6-Fluoroquinolones Obtained from a Study of Tuberculosis Chemotherapy
inferred← citeshttps://doi.org/10.2174/1574886311207040313openalex-snapshot
In Silico Assessment of Adverse Effects of a Large Set of 6-Fluoroquinolones Obtained from a Study of Tuberculosis Chemotherapy
inferred← citeshttps://doi.org/10.21767/2471-3082.100034openalex-snapshot
Relationships between the Reduced Glutathione (GSH) Reactivity of Dental Methacrylates, Michael-reaction Acceptors and their 13C-NMR Chemical Shift of -Carbons
inferred← citeshttps://doi.org/10.24377/ljmu.t.00009686openalex-snapshot
The Development of a Fragment-Based in silico Profiler for the Prediction of Thiol Reactivity and Toxicity
inferred← citeshttps://doi.org/10.3109/10408440903524262openalex-snapshot
Non-animal sensitization testing: State-of-the-art
inferred← citeshttps://doi.org/10.3109/10408444.2010.494175openalex-snapshot
A review of the electrophilic reaction chemistry involved in covalent DNA binding
inferred← citeshttps://doi.org/10.3109/10408444.2010.532768openalex-snapshot
Methyl methacrylate and respiratory sensitization: A Critical review
inferred← citeshttps://doi.org/10.3109/10408444.2011.598141openalex-snapshot
A review of the electrophilic reaction chemistry involved in covalent protein binding relevant to toxicity
inferred← citeshttps://doi.org/10.3390/ijms160511659openalex-snapshot
Acute Toxicity-Supported Chronic Toxicity Prediction: A k-Nearest Neighbor Coupled Read-Across Strategy
inferred← citeshttps://doi.org/10.3390/ijms19103015openalex-snapshot
QSAR and Classification Study on Prediction of Acute Oral Toxicity of N-Nitroso Compounds
inferred← citeshttps://doi.org/10.4103/ijp.ijp_304_17openalex-snapshot
A big data approach with artificial neural network and molecular similarity for chemical data mining and endocrine disruption prediction
inferred← citeshttps://doi.org/10.4156/jdcta.vol4.issue2.13openalex-snapshot
Classification of Skin Sensitizers on the Basis of Their Effective Concentration 3 Values by Using Adaptive Boosting Method
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.