R. J. A. Wanders

3.5k total citations · 1 hit paper
65 papers, 2.7k citations indexed

About

R. J. A. Wanders is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, R. J. A. Wanders has authored 65 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 44 papers in Clinical Biochemistry and 15 papers in Physiology. Recurrent topics in R. J. A. Wanders's work include Metabolism and Genetic Disorders (44 papers), Peroxisome Proliferator-Activated Receptors (27 papers) and Mitochondrial Function and Pathology (14 papers). R. J. A. Wanders is often cited by papers focused on Metabolism and Genetic Disorders (44 papers), Peroxisome Proliferator-Activated Receptors (27 papers) and Mitochondrial Function and Pathology (14 papers). R. J. A. Wanders collaborates with scholars based in Netherlands, United States and Germany. R. J. A. Wanders's co-authors include J. M. Tager, Albert K. Groen, Roelof van der Meer, Hans V. Westerhoff, Johanna Assies, P. G. Barth, R. B. H. Schutgens, Björn M. van Geel, Bernadette S. Jakobs and Lodewijk IJlst and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The Journal of Cell Biology.

In The Last Decade

R. J. A. Wanders

65 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Quantification of the contribution of various steps to the control of mitochondrial respiration.

1982 525 citations R. J. A. Wanders, J. M. Tager et al. profile →

Peers

Countries citing papers authored by R. J. A. Wanders

Since Specialization

Citations

This map shows the geographic impact of R. J. A. Wanders's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by R. J. A. Wanders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. J. A. Wanders more than expected).

Fields of papers citing papers by R. J. A. Wanders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R. J. A. Wanders. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by R. J. A. Wanders. The network helps show where R. J. A. Wanders may publish in the future.

Co-authorship network of co-authors of R. J. A. Wanders

This figure shows the co-authorship network connecting the top 25 collaborators of R. J. A. Wanders. A scholar is included among the top collaborators of R. J. A. Wanders based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with R. J. A. Wanders. R. J. A. Wanders is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Equine acquired multiple acyl-CoA dehydrogenase deficiency (MADD) in 14 horses associated with ingestion of Maple leaves (Acer pseudoplatanus) covered with European tar spot (Rhytisma acerinum) 2010 ·Molecular Genetics and Metabolism ·J.H. van der Kolk, Inge D. Wijnberg, C.M. Westermann, L. Dorland, Monique G.M. de Sain–van der Velden, (unknown), M. Durán, J. Dijkstra, J J van der Lugt, R. J. A. Wanders, E. Gruys	21
2	In vivo and in vitro studies on the interaction of valproic acid and metabolites with the leucine oxidative metabolism 2007 ·Journal of Inherited Metabolic Disease ·(unknown), Jos P.N. Ruiter, Lodewijk IJlst, C. C. P. Aires, Luísa Diogo, Patrice Garcia, Isabel Tavares de Almeida, (unknown), Jerry Vockley, R. J. A. Wanders, M. F. B. Silva	1
3	Differential inhibitory effect of long-chain acyl-CoA esters on succinate and glutamate transport into rat liver mitochondria and its possible implications for long-chain fatty acid oxidation defects 2005 ·Molecular Genetics and Metabolism ·Fátima V. Ventura, (unknown), Lodewijk IJlst, Isabel Tavares de Almeida, R. J. A. Wanders	31
4	A new case of succinyl‐CoA:acetoacetate transferase deficiency: Favourable course despite very low residual activity 2001 ·Journal of Inherited Metabolic Disease ·Ivo Barić, (unknown), Ksenija Fumić, (unknown), (unknown), Jos P.N. Ruiter, R. J. A. Wanders	10
5	Carbohydrate-deficient glycoprotein syndrome type 1a: A variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances 2000 ·The Journal of Pediatrics ·C. Heleen van Ommen, (unknown), P. G. Barth, P. Vreken, R. J. A. Wanders, (unknown)	25
6	Muscular carnitine palmitoyltransferase II deficiency in infancy 2000 ·Pediatric Neurology ·Haggit Hurvitz, Aharon Klar, Isabelle Korn‐Lubetzki, R. J. A. Wanders, Orly Elpeleg	17
7	Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil" 1999 ·Journal of Neurology Neurosurgery & Psychiatry ·Björn M. van Geel, Johanna Assies, E.B. Haverkort, J.H.T.M. Koelman, B Verbeeten, R. J. A. Wanders, P. G. Barth	80
8	Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: Mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata 1998 ·Journal of Inherited Metabolic Disease ·R. J. A. Wanders, G. J. Romeijn	15
9	Clinical approach to inherited peroxisomal disorders: A series of 27 patients 1998 ·Annals of Neurology ·Matthias R. Baumgartner, Bwee Tien Poll‐The, Nanda M. Verhoeven, C. Jakobs, Marc Espeel, Frank Roels, Daniel Rabier, Thierry Levade, Marie-Odile Rolland, Maria Carmen Martínez, R. J. A. Wanders, Jean Marie Saudubray	41
10	X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy 1997 ·Journal of Neurology Neurosurgery & Psychiatry ·Björn M. van Geel, Johanna Assies, R. J. A. Wanders, P. G. Barth	106
11	Fatty Acid β-Oxidation in Peroxisomes and Mitochondria: The First, Unequivocal Evidence for the Involvement of Carnitine in Shuttling Propionyl-CoA from Peroxisomes to Mitochondria 1995 ·Biochemical and Biophysical Research Communications ·Bernadette S. Jakobs, R. J. A. Wanders	79
12	Delay in diagnosis of X-linked adrenoleukodystrophy 1993 ·Clinical Neurology and Neurosurgery ·Björn M. van Geel, Johanna Assies, E.B. Haverkort, P. G. Barth, R. J. A. Wanders, R. B. H. Schutgens, A. Keyser, Casper P. Zwetsloot	15
13	First report of prenatal diagnosis of long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency in a pregnancy at risk 1993 ·Prenatal Diagnosis ·Celia Pérez‐Cerdá, B. Merinero, Antonio Moreno Jiménez, María J. García, (unknown), (unknown), R. J. A. Wanders, Magdalena Ugarte	9
14	Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme. 1990 ·Journal of Clinical Investigation ·J. Heikoop, C W van Roermund, Wilhelm W. Just, Rob Ofman, R. B. H. Schutgens, H. S. A. Heymans, R. J. A. Wanders, J. M. Tager	50
15	Peroxisomal β-oxidation defect with detectable peroxisomes: A case with neonatal onset and progressive course 1990 ·European Journal of Pediatrics ·P. G. Barth, R. J. A. Wanders, R. B. H. Schutgens, E. M. Bleeker‐Wagemakers, (unknown)	17
16	Human liver l-alanine — glyoxylate aminotransferase: Characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method 1990 ·Clinica Chimica Acta ·R. J. A. Wanders, (unknown), Carlo W.T. van Roermund, R. B. H. Schutgens, (unknown), Suzanne Jurriaans, Joseph M. Tager	18
17	Direct demonstration that the deficient oxidation of very long chain fatty acids in X-linked adrenoleukodystrophy is due to an impaired ability of peroxisomes to activate very long chain fatty acids 1988 ·Biochemical and Biophysical Research Communications ·R. J. A. Wanders, Carlo W.T. van Roermund, M.J.A. van Wijland, R. B. H. Schutgens, H. van den Bosch, A. W. Schram, J. M. Tager	131
18	X-Linked adrenoleukodystrophy: Defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters 1987 ·Clinica Chimica Acta ·R. J. A. Wanders, (unknown), M.J.A. van Wijland, (unknown), (unknown), R. B. H. Schutgens, Elisabeth M. Brouwer-Kelder, A. W. Schram, J. M. Tager, H. van den Bosch, Casper G. Schalkwijk	48
19	Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome 1987 ·Clinica Chimica Acta ·R. J. A. Wanders, Carlo W.T. van Roermund, Ronald Westra, R. B. H. Schutgens, (unknown), J. M. Tager, L.A.H. Monnens, (unknown), L. Govaerts, Hildegard Przyrembel, Eric D. Wolff, W. Blom, J. G. M. Huijmans, (unknown)	27
20	Infantile Refsum disease: an inherited peroxisomal disorder 1987 ·European Journal of Pediatrics ·Bwee Tien Poll‐The, J. M. Saudubray, H. Ogier, (unknown), J Scotto, L.A.H. Monnens, L. Govaerts, Frank Roels, Alfons Cornelis, R. B. H. Schutgens, R. J. A. Wanders, A. W. Schram, J. M. Tager	98

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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