J.M.F. Trijbels

505 total citations
7 papers, 413 citations indexed

About

J.M.F. Trijbels is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, J.M.F. Trijbels has authored 7 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Clinical Biochemistry, 4 papers in Molecular Biology and 2 papers in Rheumatology. Recurrent topics in J.M.F. Trijbels's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (2 papers) and ATP Synthase and ATPases Research (2 papers). J.M.F. Trijbels is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (2 papers) and ATP Synthase and ATPases Research (2 papers). J.M.F. Trijbels collaborates with scholars based in Netherlands, Japan and Austria. J.M.F. Trijbels's co-authors include Lambertus P. van den Heuvel, Ralf Triepels, F. Hanefeld, Sylvia Stöckler, Bart Marescau, Henk J. Blom, Albert Tangerman, G. H. J. Boers, J.H. Veerkamp and R. C. A. Sengers and has published in prestigious journals such as Metabolism, Human Mutation and Journal of Bioenergetics and Biomembranes.

In The Last Decade

J.M.F. Trijbels

7 papers receiving 406 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J.M.F. Trijbels Netherlands	6	298	239	60	53	49	7	413
Geoffrey Sherwood Canada	7	326 1.1×	165 0.7×	21 0.3×	14 0.3×	44 0.9×	11	478
A. E. M. Stroomer Netherlands	10	271 0.9×	185 0.8×	19 0.3×	80 1.5×	61 1.2×	13	445
Morten J. Corydon Denmark	7	387 1.3×	365 1.5×	47 0.8×	34 0.6×	101 2.1×	9	489
M. DiRocco Italy	8	353 1.2×	244 1.0×	48 0.8×	64 1.2×	78 1.6×	11	497
L. Kierat Switzerland	13	271 0.9×	266 1.1×	29 0.5×	139 2.6×	99 2.0×	26	496
M.L.P. Brückwilder Netherlands	7	242 0.8×	58 0.2×	109 1.8×	13 0.2×	77 1.6×	9	352
Andrew A.M. Morris United Kingdom	11	701 2.4×	606 2.5×	50 0.8×	70 1.3×	107 2.2×	16	851
Egill Briem Italy	8	437 1.5×	341 1.4×	11 0.2×	75 1.4×	28 0.6×	8	580
J.A.M. Smeitink Netherlands	10	276 0.9×	218 0.9×	17 0.3×	22 0.4×	31 0.6×	17	348
Rebecca Mardach United States	11	193 0.6×	164 0.7×	82 1.4×	53 1.0×	100 2.0×	17	351

Countries citing papers authored by J.M.F. Trijbels

Since Specialization

Citations

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

Fields of papers citing papers by J.M.F. Trijbels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.M.F. Trijbels

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

All Works

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7 of 7 papers shown

1.

Trijbels, J.M.F., et al.. (2000). Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects. Human Mutation. 15(2). 123–134. 237 indexed citations

2.

Stöckler, Sylvia, et al.. (1997). Guanidino compounds in guanidinoacetate methyltransferase deficiency, a new inborn error of creatine synthesis. Metabolism. 46(10). 1189–1193. 80 indexed citations

3.

Huizing, Marjan, et al.. (1996). Importance of mitochondrial transmembrane processes in human mitochondriopathies. Journal of Bioenergetics and Biomembranes. 28(2). 109–114. 18 indexed citations

4.

Sperl, Wolfgang, et al.. (1993). Measurement of Totally Activated Pyruvate Dehydrogenase Complex Activity in Human Muscle: Evaluation of a Useful Assay. PubMed. 47(1). 37–46. 25 indexed citations

5.

Reubsaet, Frans A.G., J.H. Veerkamp, M.L.P. Brückwilder, et al.. (1991). Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1083(3). 305–309. 2 indexed citations

6.

Reubsaet, Frans A.G., J.H. Veerkamp, Hubert Dirven, et al.. (1990). The effect of di(ethylhexyl)phthalate on fatty acid oxidation and carnitine palmitoyltransferase in various rat tissues. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1047(3). 264–270. 24 indexed citations

7.

Blom, Henk J., et al.. (1989). Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemia. Metabolism. 38(6). 577–582. 27 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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