Stephan Schaller

Thorlabs (Germany) — Germany

Computer Science · Physical Sciences

12h-index622citations73works2.22yr avg
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Research Topics

Computational Drug Discovery Methods(14), Pharmacogenetics and Drug Metabolism(11), Statistical Methods in Clinical Trials(7), Effects and risks of endocrine disrupting chemicals(6), Diabetes Management and Research(5)

Publications73 total

Open Systems Pharmacology Community Conference ( <scp>OSP</scp> ‐ <scp>CC</scp> ) Proceedings 2025
CPT Pharmacometrics & Systems Pharmacology·2026Open Access
Integration of in vitro and in silico approaches enables prediction of drug-induced liver injury
Archives of Toxicology·2026Open Access
A Physiologically Based Pharmacokinetic Framework for Predicting Drug Exposure in the Female Reproductive Tract
2026Open Access
Reducing Animal Use in Toxicological Research through Open-Source Individualized (PB)PK/QST Modeling: A Case Study with Phenobarbital in Dogs
2026Open Access
A pipeline for generating large virtual dog populations to predict preclinical drug-induced liver injury
2026Open Access
Correction: Susilo et al. Whole-Body Physiologically Based Pharmacokinetic Modeling Framework for Tissue Target Engagement of CD3 Bispecific Antibodies. Pharmaceutics 2025, 17, 500
Pharmaceutics·2025Open Access
Transversal Learning in Regulatory application of Complex Mechanistic models in Risk Assessment. Thyroid Disruptors and what we learn from Drug Development
Zenodo (CERN European Organization for Nuclear Research)·2025Open Access
Transversal Learning in Regulatory application of Complex Mechanistic models in Risk Assessment. Thyroid Disruptors and what we learn from Drug Development
Zenodo (CERN European Organization for Nuclear Research)·2025Open Access
High-throughput PBK modelling for dermal exposure: a pragmatic approach to predict systemic pharmacokinetics
2025Open Access
Integration of <i>In Vitro</i> and <i>In Silico</i> Approaches Enables Prediction of Drug-Induced Liver Injury
2025Open Access
Comparison of physiologically based pharmacokinetic modeling platforms for developmental neurotoxicity in vitro to in vivo extrapolation
Toxicological Sciences·2025Open Access
From simulation to application: enhancing preclinical evaluation of dissolvable microarray patches through PBPK modelling
Drug Delivery and Translational Research·2025Open Access
CEC03-05 Integrated PBPK/QST modeling to inform the safety assessmentpractical hands-on examples across multiple disease areas
Toxicology Letters·2025
P18-107 Reducing Animal Use in Toxicological Research through Open-Source Individualized (PB)PK/QST Modeling: A Case Study with Phenobarbital in Dogs
Toxicology Letters·2025Open Access
Potential systemic availability classification of chemicals for safety assessment
Environment International·2025· 1 citedOpen Access
Modernizing Preclinical Drug Development: The Role of New Approach Methodologies
ACS Pharmacology & Translational Science·2025· 12 cited
Whole-Body Physiologically Based Pharmacokinetic Modeling Framework for Tissue Target Engagement of CD3 Bispecific Antibodies
Pharmaceutics·2025· 1 citedOpen Access
Harnessing Open‐Source Solutions: Insights From the First Open Systems Pharmacology (<scp>OSP</scp>) Community Conference
CPT Pharmacometrics & Systems Pharmacology·2025Open Access
Potential Systemic Availability Classification of Chemicals for Safety Assessment
2025Open Access
Digital twin-enhanced three-organ microphysiological system for studying drug pharmacokinetics in pregnant women
Frontiers in Pharmacology·2025· 12 citedOpen Access
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Frequent Co-authors

Lars Kuepfer(10), Alicia Paini(9), Pavel Balazki(8), Jörg Lippert(7), Thomas Eißing(7), Vanessa Baier(7), René Geci(6), Markus Ebeling(6), David Heckmann(6), Colin G. Scanes(5), Audrey J. Bone(5), Thomas G. Preuß(5), Rolf Burghaus(4), Andreas Schuppert(4), Johannes Witt(4), Christian Maaß(4), Thorsten Lehr(3), Donato Teutonico(3), Stefan Willmann(3), Thomas R. Pieber(3)