Anton F. H. Stalenhoef

Author

Also Known As

A F H Stalenhoef, A F Stalenhoef, A STALENHOEF, A Stalenhoef, A. F. H Stalenhoef, A. F. H. STALENHOEF, A. F. H. Stalenhoef, A. F. STALENHOEF, A. F. Stalenhoef, A. F.H. Stalenhoef

399

Publications

26.4K

Citations

H-Index

151

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Amsterdam UMC Location University of Amsterdam University of Amsterdam University Medical Center Utrecht

About

Anton F. H. Stalenhoef is an author at Radboud University Nijmegen specializing in medicine, atherosclerosis, and cardiovascular disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	96	6.6K
2	Public Health	24	33	1.8K
3	Health Sciences	21	27	2.4K
4	Allergy	3	3	150
5	Natural Sciences	2	2	44

Anton F. H. Stalenhoef

190

Publications

15.3K

Citations

H-Index

Page 1

	Year	Citations
Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society Marina Cuchel, Éric Bruckert, Henry N. Ginsberg, European Heart Journal	2014	1K
Enhanced susceptibility to in vitro oxidation of the dense low density lipoprotein subfraction in healthy subjects. Jacqueline de Graaf, Heidi L.M. Hak-Lemmers, M.P.C. Hectors, Arteriosclerosis and Thrombosis A Journal of Vascular Biology Healthy SubjectsLipid PeroxidationEnhanced SusceptibilityOxidative ModificationRedox Biology	1991	718
Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: report of the thirty‐person/ten‐country panel Philip J. Barter, Christie M. Ballantyne, Rafael Carmena, Journal of Internal Medicine	2006	470
Efficacy and Safety of a Novel Cholesteryl Ester Transfer Protein Inhibitor, JTT-705, in Humans Greetje J. de Grooth, Jan Albert Kuivenhoven, Anton F. H. Stalenhoef, Circulation	2002	451
Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype–phenotype relationship, and clinical outcome Barbara Sjouke, D. Meeike Kusters, Iris Kindt, European Heart Journal	2014	434
Deficiency of interleukin-18 in mice leads to hyperphagia, obesity and insulin resistance Mihai G. Netea, Leo A. B. Joosten, Eli C. Lewis, Nature Medicine ObesityMetabolic SyndromeInflammationInsulin ResistanceMetabolic Disorder	2006	415
Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively Kangmo Lu, Mi-Hye Lee, E. Starr Hazard, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsPathologyMolecular Genetics	2001	353
Improved Measurement of Low-Density-Lipoprotein Susceptibility to Copper-Induced Oxidation: Application of a Short Procedure for Isolating Low-Density Lipoprotein Henne A. Kleinveld, Heidi L.M. Hak-Lemmers, Anton F. H. Stalenhoef, Clinical Chemistry Low-density LipoproteinLipid PeroxidationRedox BiologyOxidative StressBioanalysis	1992	349
Relationship between stearoyl-CoA desaturase activity and plasma triglycerides in human and mouse hypertriglyceridemia Alan Attie, Ronald M. Krauss, Mark P. Gray-Keller, Journal of Lipid Research	2002	344
Engagement of fatty acids with toll‐like receptor 2 drives interleukin‐1β production via the ASC/caspase 1 pathway in monosodium urate monohydrate crystal–induced gouty arthritis Leo A. B. Joosten, Mihai G. Netea, Eleni Mylona, Arthritis & Rheumatism	2010	324

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