M. E. J. den Boer

785 total citations
7 papers, 564 citations indexed

About

M. E. J. den Boer is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, M. E. J. den Boer has authored 7 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Clinical Biochemistry, 4 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in M. E. J. den Boer's work include Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Peroxisome Proliferator-Activated Receptors (3 papers). M. E. J. den Boer is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (4 papers) and Peroxisome Proliferator-Activated Receptors (3 papers). M. E. J. den Boer collaborates with scholars based in Netherlands, United Kingdom and Italy. M. E. J. den Boer's co-authors include Frits A. Wijburg, Ronald J. A. Wanders, Lodewijk IJlst, A. H. van Gennip, P. Vreken, H. S. A. Heymans, Andrew A. M. Morris, Hans R. Waterham, Jos P.N. Ruiter and Carlo Dionisi‐Vici and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Pediatric Research.

In The Last Decade

M. E. J. den Boer

7 papers receiving 553 citations

Peers

M. E. J. den Boer
Keow Giak Sim Australia
Mohamed A. Nada United States
Dennis Bartholomew United States
A. Briddon United Kingdom
S. K. Hall United Kingdom
P. J. Lee United Kingdom
Barry Lewis Australia
A. Green United Kingdom
Keow Giak Sim Australia
M. E. J. den Boer
Citations per year, relative to M. E. J. den Boer M. E. J. den Boer (= 1×) peers Keow Giak Sim

Countries citing papers authored by M. E. J. den Boer

Since Specialization
Citations

This map shows the geographic impact of M. E. J. den Boer'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 M. E. J. den Boer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. E. J. den Boer more than expected).

Fields of papers citing papers by M. E. J. den Boer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. E. J. den Boer. 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 M. E. J. den Boer. The network helps show where M. E. J. den Boer may publish in the future.

Co-authorship network of co-authors of M. E. J. den Boer

This figure shows the co-authorship network connecting the top 25 collaborators of M. E. J. den Boer. A scholar is included among the top collaborators of M. E. J. den Boer 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 M. E. J. den Boer. M. E. J. den Boer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
1.
Boer, M. E. J. den, Frits A. Wijburg, Michel Vekemans, et al.. (2005). Long-Chain Fatty Acid Oxidation during Early Human Development. Pediatric Research. 57(6). 755–759. 70 indexed citations
2.
Boer, M. E. J. den, et al.. (2003). Mitochondrial trifunctional protein deficiency: A severe fatty acid oxidation disorder with cardiac and neurologic involvement. The Journal of Pediatrics. 142(6). 684–689. 60 indexed citations
3.
Boer, M. E. J. den. (2003). Mitochondrial trifunctional protein in disease and development. 1 indexed citations
4.
Boer, M. E. J. den, Jos P.N. Ruiter, Ronald J. A. Wanders, et al.. (2003). High activity of fatty acid oxidation enzymes in human placenta: Implications for fetal‐maternal disease. Journal of Inherited Metabolic Disease. 26(4). 385–392. 50 indexed citations
5.
Boer, M. E. J. den, Ronald J. A. Wanders, Andrew A. M. Morris, et al.. (2002). Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency: Clinical Presentation and Follow-Up of 50 Patients. PEDIATRICS. 109(1). 99–104. 129 indexed citations
6.
Boer, M. E. J. den, Lodewijk IJlst, Frits A. Wijburg, et al.. (2000). Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low. Pediatric Research. 48(2). 151–154. 44 indexed citations
7.
Wanders, Ronald J. A., P. Vreken, M. E. J. den Boer, et al.. (1999). Disorders of mitochondrial fatty acyl‐CoA β‐oxidation. Journal of Inherited Metabolic Disease. 22(4). 442–487. 210 indexed citations

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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