F. Trijbels

3.3k total citations · 1 hit paper
40 papers, 2.4k citations indexed

About

F. Trijbels is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, F. Trijbels has authored 40 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 14 papers in Rheumatology. Recurrent topics in F. Trijbels's work include Metabolism and Genetic Disorders (15 papers), Folate and B Vitamins Research (13 papers) and Mitochondrial Function and Pathology (12 papers). F. Trijbels is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Folate and B Vitamins Research (13 papers) and Mitochondrial Function and Pathology (12 papers). F. Trijbels collaborates with scholars based in Netherlands, United States and Germany. F. Trijbels's co-authors include Henk J. Blom, G. H. J. Boers, Godfried D. Vogels, D. G. Franken, Lambertus P. van den Heuvel, T.K.A.B. Eskes, Phyllis Frosst, Edwin C.M. Mariman, Régine P.M. Steegers‐Theunissen and Michelle Heyer and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Neurology.

In The Last Decade

F. Trijbels

40 papers receiving 2.3k 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.

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1995 715 citations F. Trijbels, Lambertus P. van den Heuvel et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Trijbels Netherlands	21	1.4k	836	681	528	340	40	2.4k
Sanjana Dayal United States	27	1.2k 0.9×	845 1.0×	413 0.6×	256 0.5×	188 0.6×	68	3.0k
Qing Wu Canada	23	1.1k 0.8×	660 0.8×	269 0.4×	232 0.4×	457 1.3×	57	1.9k
Zia Fazili United States	22	1.2k 0.8×	406 0.5×	266 0.4×	254 0.5×	326 1.0×	40	2.3k
Isabel Rivera Portugal	19	622 0.4×	768 0.9×	184 0.3×	421 0.8×	244 0.7×	56	1.5k
Viktor Kožich Czechia	36	2.0k 1.4×	1.4k 1.6×	401 0.6×	1.2k 2.2×	415 1.2×	137	3.7k
Farès Namour France	23	722 0.5×	608 0.7×	199 0.3×	171 0.3×	244 0.7×	50	1.7k
D. Stansbie United Kingdom	21	407 0.3×	491 0.6×	331 0.5×	385 0.7×	153 0.5×	45	1.7k
Patricia M. DiBello United States	21	756 0.5×	398 0.5×	225 0.3×	171 0.3×	87 0.3×	44	1.6k
Mindy Zhang United States	21	884 0.6×	476 0.6×	201 0.3×	147 0.3×	279 0.8×	43	2.2k
Rosa‐Maria Guéant‐Rodriguez France	24	968 0.7×	392 0.5×	212 0.3×	152 0.3×	442 1.3×	56	2.0k

Countries citing papers authored by F. Trijbels

Since Specialization

Citations

This map shows the geographic impact of 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 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 F. Trijbels more than expected).

Fields of papers citing papers by F. Trijbels

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of F. Trijbels. A scholar is included among the top collaborators of 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 F. Trijbels. 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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20 of 20 papers shown

Wolf, Nicole I., Andreas Seitz, Inga Harting, et al.. (2003). New Pattern of Brain MRI Lesions in Isolated Complex I Deficiency. Neuropediatrics. 34(3). 156–159. 13 indexed citations

Bree, Angelika de, W. M. Monique Verschuren, Henk J. Blom, et al.. (2001). The homocysteine distribution. Journal of Clinical Epidemiology. 54(5). 462–469. 23 indexed citations

Heil, Sandra G., Karin J.A Lievers, Godfried H.J. Boers, et al.. (2000). Betaine-Homocysteine Methyltransferase (BHMT): Genomic Sequencing and Relevance to Hyperhomocysteinemia and Vascular Disease in Humans. Molecular Genetics and Metabolism. 71(3). 511–519. 62 indexed citations

Loeffen, Jan, Roel Smeets, Jan Smeıtınk, et al.. (1999). The human NADH:ubiquinone oxidoreductase NDUFS5 (15kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I‐deficient patients. Journal of Inherited Metabolic Disease. 22(1). 19–28. 17 indexed citations

Loeffen, Jan, Roel Smeets, Jan Smeıtınk, et al.. (1998). The X‐chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: Tissue expression and mutation detection. Journal of Inherited Metabolic Disease. 21(3). 210–215. 16 indexed citations

Kluijtmans, Leo A. J., et al.. (1997). A Common 844INS68 Insertion Variant in the Cystathionine β-Synthase Gene. Biochemical and Molecular Medicine. 62(1). 23–25. 59 indexed citations

Franken, D. G., Henk J. Blom, G. H. J. Boers, et al.. (1996). Thiamine (vitamin B1) supplementation does not reduces fasting blood homocysteine concentration in most homozygotes for homocystinuria. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1317(2). 101–104. 11 indexed citations

Franken, D. G., Godfried H.J. Boers, Henk J. Blom, et al.. (1996). Prevalence of familial mild hyperhomocysteinemia. Atherosclerosis. 125(1). 71–80. 21 indexed citations

Kluijtmans, Leo A. J., G. H. J. Boers, W.O. Renier, et al.. (1996). Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.. Journal of Clinical Investigation. 98(2). 285–289. 81 indexed citations

10.

Bentlage, Herman, A.J.M. Janssen, Anne Chomyn, et al.. (1995). Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1234(1). 63–73. 17 indexed citations

11.

Trijbels, F., Lambertus P. van den Heuvel, Henk J. Blom, et al.. (1995). Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. The Lancet. 346(8982). 1070–1071. 715 indexed citations breakdown →

12.

Bentlage, Herman, I.F.M. de Coo, H. ter Laak, et al.. (1995). Human Diseases with Defects in Oxidative Phosphorylation. 1. Decreased Amounts of Assembled Oxidative Phosphorylation Complexes in Mitochondrial Encephalomyopathies. European Journal of Biochemistry. 227(3). 909–915. 33 indexed citations

13.

Smeıtınk, Jan, Ron A. Wevers, W. Ruitenbeek, et al.. (1992). A Method for Quantitative Measurement of Mitochondrial Creatine Kinase in Human Skeletal Muscle. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 29(2). 196–201. 20 indexed citations

14.

Smeıtınk, Jan, W. Ruitenbeek, R. C. A. Sengers, et al.. (1992). Maturation of Mitochondrial and other Isoenzymes of Creatine Kinase in Skeletal Muscle of Preterm Born Infants. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 29(3). 302–306. 14 indexed citations

15.

Smeıtınk, Jan, et al.. (1992). Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria. Journal of Inherited Metabolic Disease. 17(1). 67–73. 1 indexed citations

16.

Smeıtınk, Jan, A. M. Stadhouders, R. C. A. Sengers, et al.. (1992). Mitochondrial creatine kinase containing crystals, creatine content and mitochondrial creatine kinase activity in chronic progressive external ophthalmoplegia. Neuromuscular Disorders. 2(1). 35–40. 16 indexed citations

17.

Abreu, Ronney A. De, et al.. (1988). Reference values for nucleosides and nucleobases in cerebrospinal fluid of children.. Clinical Chemistry. 34(7). 1439–1442. 9 indexed citations

18.

Ruitenbeek, W., et al.. (1986). 149 ESTIMATION OF PYRUVATE DEHYDROGENASE (E1) ACTIVITY IN HUMAN SKELETAL MUSCLE. Pediatric Research. 20(10). 1059–1059. 8 indexed citations

19.

Trijbels, F., R. C. A. Sengers, A.J.M. Janssen, et al.. (1983). A patient with lactic acidaemia and cytochrome oxidase deficiency. Journal of Inherited Metabolic Disease. 6(S2). 127–128. 23 indexed citations

20.

Willems, Hans L., et al.. (1978). Determination of pyruvate oxidation rate and citric acid cycle activity in intact human leukocytes and fibroblasts.. Clinical Chemistry. 24(2). 200–203. 40 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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