R. J. A. Wanders - Concepedia

Author

R. J. A. Wanders

Also Known As

R J A Wanders, R J Wanders, R. J A Wanders, R. J. A. (a) Wanders, R. J. A. Wanders, R. J.A. Wanders, R.J.A. Wanders, Ronald J A Wanders, Ronald J.A. Wanders

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

University of Amsterdam Utrecht University Amsterdam UMC Location University of Amsterdam Ghent University Wilhelmina Children's Hospital

About

R. J. A. Wanders is an author at University of Amsterdam specializing in medicine, metabolism, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	26	1.6K
2	Biochemistry	15	19	947
3	Health Sciences	6	6	333
4	Natural Sciences	5	5	353
5	Allergy	1	1	32

R. J. A. Wanders

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome Sander M. Houten, Wietse Kuis, Marinus Duran, Nature Genetics Cause Hyperimmunoglobulinaemia DPeriodic Fever SyndromeAutoimmune DiseaseDisease MechanismImmunodeficiencies	1999	520
Defective peroxisomal catabolism of branched fatty acyl coenzyme A in mice lacking the sterol carrier protein-2/sterol carrier protein-x gene function U. Seedorf, M. Raabe, Peter Ellinghaus, Genes & Development	1998	261
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein Lodewijk IJlst, R. J. A. Wanders, S. Ushikubo, Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism Mitochondrial BiogenesisBiochemistryMitochondrial FunctionMajor Disease-causing MutationMetabolic Disease	1994	158
Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder R. J. A. Wanders, Herbert Schumacher, J. Heikoop, Journal of Inherited Metabolic Disease Mendelian DisorderBiochemistryGenetic DisorderGeneticsMetabolic Disease	1992	130
Plasmalogens participate in very-long-chain fatty acid-induced pathology Pedro Brites, P. A. W. Mooyer, L. el Mrabet, Brain Lipid PeroxidationPathologyCell DeathOxidative StressObesity	2008	110
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease. A. W. Schram, Anneke Strijland, Takashi Hashimoto, Proceedings of the National Academy of Sciences Acyl-coa OxidaseLipid PeroxidationMolecular BiologyRedox BiologyOxidative Stress	1986	106
Molecular basis of hepatic carnitine palmitoyltransferase I deficiency. Lodewijk IJlst, Hanna Mandel, W. Oostheim, Journal of Clinical Investigation GeneticsMolecular BiologyHepatic Carnitine PalmitoyltransferaseMolecular GeneticsMetabolic Syndrome	1998	94
Sterol Carrier Protein X (SCPx) Is a Peroxisomal Branched-Chain β-Ketothiolase Specifically Reacting with 3-Oxo-pristanoyl-CoA: A New, Unique Role for SCPx in Branched-Chain Fatty Acid Metabolism in Peroxisomes R. J. A. Wanders, Simone Denis, Fred S. Wouters, Biochemical and Biophysical Research Communications Lipid SynthesisBiochemistryUnique RoleMetabolismSteroid Metabolism	1997	89
Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: A peroxisomal entity amenable to plasmapheresis F. A. Beemer, Marc Espeel, R. A. M. G. Donckerwocke, Journal of Inherited Metabolic Disease Regenerative MedicineDeficient Plasmalogen SynthesisBone DiseaseDevelopmental BiologyHealth Sciences	1992	55
Enoyl-CoA Hydratase Deficiency: Identification of a New Type of D-Bifunctional Protein Deficiency E.G. van Grunsven, Petra A.W. Mooijer, Patrick Aubourg, Human Molecular Genetics	1999	52

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