Steven Verhaegen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Steven Verhaegen has a total of 60 co-authors. Here are the top co-authors by number of shared publications:
- Erik Ropstad
Department of Production Animal Clinical Sciences, Norwegian University of Life Sciences, P.O. Box 5003, NO-1432, Ås, Norway
7 shared publications - Karin Elisabeth Zimmer
Department of Preclinical Sciences and Pathology, Norwegian University of Life Sciences, P.O. Box 5003, NO-1432 Ås, Norway
4 shared publications - Ajay Yadav
Department of Production Animal Clinical Sciences, Norwegian University of Life Sciences, P.O. Box 369 Sentrum, NO-0102, Oslo, Norway; Section for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, P.O. Box 1068, Blindern, NO-0316, Oslo, Norway
3 shared publications - Hanne Friis Berntsen
Department of Production Animal Clinical Sciences, Norwegian University of Life Sciences, P.O. Box 369 Sentrum, NO-0102, Oslo, Norway; National Institute of Occupational Health, P.O. Box 5330 Majorstuen, NO-0304, Oslo, Norway
3 shared publications - Lisa Connolly
Institute for Global Food Security, School of Biological Sciences, Queen’s University Belfast, Belfast, UK
3 shared publications - Ragnhild Elisabeth Paulsen
Section for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, Faculty of Mathematics and Natural Sciences, University of Oslo, Oslo, Norway
3 shared publications
Latest Publications
- Open Access
- 22 September 2026
- Published by Springer Nature in Exposure and Health
- Vol. 18 (5) , 68
Evaluation of Hepatotoxicity in the Human In Vitro HepG2 Model After Exposure to Ten Individual UV Filters, and Six Sunscreen Products After Ex Vivo Pig Skin Permeation
- 22 September 2026
- Published by Springer Nature in Exposure and Health
- Vol. 18 (5) , 68
Open AccessEvaluation of Hepatotoxicity in the Human In Vitro HepG2 Model After Exposure to Ten Individual UV Filters, and Six Sunscreen Products After Ex Vivo Pig Skin Permeation
- Open Access
- 27 June 2022
- Published by Elsevier in Environment International
- Vol. 166, 107379
Exposure to a human relevant mixture of persistent organic pollutants or to perfluorooctane sulfonic acid alone dysregulates the developing cerebellum of chicken embryo
- 27 June 2022
- Published by Elsevier in Environment International
- Vol. 166, 107379
Open AccessExposure to a human relevant mixture of persistent organic pollutants or to perfluorooctane sulfonic acid alone dysregulates the developing cerebellum of chicken embryo
- Open Access
- 1 January 2022
- Published by Elsevier in NeuroToxicology
- Vol. 88, 79-87
Peripherally administered persistent organic pollutants distribute to the brain of developing chicken embryo in concentrations relevant for human exposure
- 1 January 2022
- Published by Elsevier in NeuroToxicology
- Vol. 88, 79-87
Open AccessPeripherally administered persistent organic pollutants distribute to the brain of developing chicken embryo in concentrations relevant for human exposure
- Open Access
- 10 May 2021
- Published by Springer Nature in Exposure and Health
- Vol. 13 (3) , 465-475
Effects of Defined Mixtures of Persistent Organic Pollutants (POPs) on Pre-lethal Cytotoxicity in the Human A-498 Kidney Cell Line In Vitro
A total mixture of 29 persistent organic pollutants (POPs) modelled from Scandinavian blood concentrations was used to expose human A-498 kidney cells for 24 h over a concentration range spanning below to above blood level (1/10x, 1x, 50x, 100x, 500x). Its constituent submixtures (PFAA, Br, Cl) and co-mixtures (PFAA + Br, PFAA + Cl, Br + Cl) were also tested. Valinomycin (12 µM) was used as a cytotoxic comparative compound. Cell number (CN), nuclear area (NA), nuclear intensity (NI), mitochondrial membrane potential (MMP), and mitochondrial mass (MM) were assessed using high content analysis (HCA). Only the co-mixtures (PFAA + Cl, PFAA + Br) at 50x and 50x, 500x decreased CN, respectively. NI was increased by the total mixture at 500x and Cl mixture at all concentrations tested. MMP was increased by the total mixture at 100x and 500x, PFAA at 1x, Br + Cl and PFAA + Cl at 100x and 500x, respectively. MM was decreased by the total mixture at 500x. In contrast, valinomycin decreased CN and surviving cells showed a decrease in MMP and an increase in MM. In conclusion, POP exposure altered mitochondrial metabolism and induced cell death via an alternative mechanism to valinomycin. Only specific combinations of individual chemical classes, but not the total mixture, affected cell number.
- 10 May 2021
- Published by Springer Nature in Exposure and Health
- Vol. 13 (3) , 465-475
Open AccessEffects of Defined Mixtures of Persistent Organic Pollutants (POPs) on Pre-lethal Cytotoxicity in the Human A-498 Kidney Cell Line In Vitro
A total mixture of 29 persistent organic pollutants (POPs) modelled from Scandinavian blood concentrations was used to expose human A-498 kidney cells for 24 h over a concentration range spanning below to above blood level (1/10x, 1x, 50x, 100x, 500x). Its constituent submixtures (PFAA, Br, Cl) and co-mixtures (PFAA + Br, PFAA + Cl, Br + Cl) were also tested. Valinomycin (12 µM) was used as a cytotoxic comparative compound. Cell number (CN), nuclear area (NA), nuclear intensity (NI), mitochondrial membrane potential (MMP), and mitochondrial mass (MM) were assessed using high content analysis (HCA). Only the co-mixtures (PFAA + Cl, PFAA + Br) at 50x and 50x, 500x decreased CN, respectively. NI was increased by the total mixture at 500x and Cl mixture at all concentrations tested. MMP was increased by the total mixture at 100x and 500x, PFAA at 1x, Br + Cl and PFAA + Cl at 100x and 500x, respectively. MM was decreased by the total mixture at 500x. In contrast, valinomycin decreased CN and surviving cells showed a decrease in MMP and an increase in MM. In conclusion, POP exposure altered mitochondrial metabolism and induced cell death via an alternative mechanism to valinomycin. Only specific combinations of individual chemical classes, but not the total mixture, affected cell number.
- Open Access
- 1 March 2021
- Published by Elsevier in Reproductive Toxicology
- Vol. 100, 109-119
A human relevant mixture of persistent organic pollutants (POPs) and perfluorooctane sulfonic acid (PFOS) differentially affect glutamate induced excitotoxic responses in chicken cerebellum granule neurons (CGNs) in vitro
- 1 March 2021
- Published by Elsevier in Reproductive Toxicology
- Vol. 100, 109-119
Open AccessA human relevant mixture of persistent organic pollutants (POPs) and perfluorooctane sulfonic acid (PFOS) differentially affect glutamate induced excitotoxic responses in chicken cerebellum granule neurons (CGNs) in vitro
- Open Access
- 1 March 2019
- Published by Elsevier in Chemosphere
- Vol. 218, 328-339
Effects of defined mixtures of POPs and endocrine disruptors on the steroid metabolome of the human H295R adrenocortical cell line
- 1 March 2019
- Published by Elsevier in Chemosphere
- Vol. 218, 328-339
Open AccessEffects of defined mixtures of POPs and endocrine disruptors on the steroid metabolome of the human H295R adrenocortical cell line
- 1 October 2018
- Published by Elsevier in Toxicology in Vitro
- Vol. 52, 332-341
LC-MS/MS based profiling and dynamic modelling of the steroidogenesis pathway in adrenocarcinoma H295R cells
- 1 October 2018
- Published by Elsevier in Toxicology in Vitro
- Vol. 52, 332-341
LC-MS/MS based profiling and dynamic modelling of the steroidogenesis pathway in adrenocarcinoma H295R cells
- 1 November 2015
- Published by Elsevier in Reproductive Toxicology
- Vol. 57, 130-139
Steroidogenic differential effects in neonatal porcine Leydig cells exposed to persistent organic pollutants derived from cod liver oil
- 1 November 2015
- Published by Elsevier in Reproductive Toxicology
- Vol. 57, 130-139
Steroidogenic differential effects in neonatal porcine Leydig cells exposed to persistent organic pollutants derived from cod liver oil
- 1 April 2015
- Published by Elsevier in Toxicology in Vitro
- Vol. 29 (3) , 575-581
Biotransformation of zearalenone and zearalenols to their major glucuronide metabolites reduces estrogenic activity
- 1 April 2015
- Published by Elsevier in Toxicology in Vitro
- Vol. 29 (3) , 575-581
Biotransformation of zearalenone and zearalenols to their major glucuronide metabolites reduces estrogenic activity
- 1 January 1994
- Published by Springer Nature
- Vol. 355, 183-187
Analysis of HIV Infections in Human Macrophage-Like Cell Lines
- 1 January 1994
- Published by Springer Nature
- Vol. 355, 183-187
Analysis of HIV Infections in Human Macrophage-Like Cell Lines