L. Bruinvis

1.3k total citations
33 papers, 1.0k citations indexed

About

L. Bruinvis is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, L. Bruinvis has authored 33 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Clinical Biochemistry, 20 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in L. Bruinvis's work include Metabolism and Genetic Disorders (27 papers), Metabolomics and Mass Spectrometry Studies (8 papers) and Diet and metabolism studies (8 papers). L. Bruinvis is often cited by papers focused on Metabolism and Genetic Disorders (27 papers), Metabolomics and Mass Spectrometry Studies (8 papers) and Diet and metabolism studies (8 papers). L. Bruinvis collaborates with scholars based in Netherlands, United States and Switzerland. L. Bruinvis's co-authors include D. Ketting, S.K. Wadman, M. Durán, Hildegard Przyrembel, H. J. Bremer, Kathrin Becker, L. Dorland, U. Wendel, Colin van der Heiden and J.P. Kamerling and has published in prestigious journals such as Clinical Chemistry, The Journal of Pediatrics and Clinica Chimica Acta.

In The Last Decade

L. Bruinvis

33 papers receiving 997 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L. Bruinvis Netherlands 17 746 707 214 123 112 33 1.0k
H.J. ten Brink Netherlands 22 729 1.0× 732 1.0× 220 1.0× 172 1.4× 109 1.0× 43 1.3k
Harbhajan S. Paul United States 18 438 0.6× 386 0.5× 287 1.3× 159 1.3× 241 2.2× 36 830
BD Ross United Kingdom 4 182 0.2× 345 0.5× 226 1.1× 118 1.0× 107 1.0× 5 899
Dirk Kohlmüller Germany 13 515 0.7× 540 0.8× 206 1.0× 76 0.6× 34 0.3× 22 1.0k
Lois M. Walker United States 9 130 0.2× 341 0.5× 230 1.1× 197 1.6× 136 1.2× 13 873
Carole Hall United States 14 294 0.4× 471 0.7× 175 0.8× 50 0.4× 84 0.8× 18 674
Nancy J. Hutson United States 16 188 0.3× 554 0.8× 316 1.5× 232 1.9× 295 2.6× 18 1.2k
KIMIYOSHI OHNO Japan 16 170 0.2× 380 0.5× 82 0.4× 372 3.0× 80 0.7× 25 774
Luc J. Debeer Belgium 17 536 0.7× 899 1.3× 394 1.8× 291 2.4× 84 0.8× 27 1.3k
Bernice Friedmann United States 19 150 0.2× 446 0.6× 259 1.2× 134 1.1× 115 1.0× 22 924

Countries citing papers authored by L. Bruinvis

Since Specialization
Citations

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

Fields of papers citing papers by L. Bruinvis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Bruinvis

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

All Works

20 of 20 papers shown
1.
Durán, M., L. Bruinvis, D. Ketting, & L. Dorland. (1993). Diagnosis of mitochondrial fatty acid oxidation defects.. PubMed. 28(1). 19–25. 4 indexed citations
2.
Dorland, L., D. Ketting, L. Bruinvis, & M. Durán. (1991). Medium‐ and long‐chain 3‐hydroxymonocarboxylic acids: Analysis by gas chromatography combined with mass spectrometry. Biomedical Chromatography. 5(4). 161–164. 12 indexed citations
3.
Durán, M., Ronald J. A. Wanders, L. Dorland, et al.. (1991). 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment. European Journal of Pediatrics. 150(3). 190–195. 64 indexed citations
4.
Klerk, J. B. C. de, M. Durán, L. Dorland, et al.. (1988). A patient with mevalonic aciduria presenting with hepatosplenomegaly, congenital anaemia, thrombocytopenia and leukocytosis. Journal of Inherited Metabolic Disease. 11(S2). 233–236. 16 indexed citations
5.
Durán, M., D. Ketting, L. Bruinvis, et al.. (1987). Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolism. Clinica Chimica Acta. 165(2-3). 197–204. 14 indexed citations
6.
Durán, M., F. A. Beemer, L. Bruinvis, D. Ketting, & S.K. Wadman. (1987). D-Glyceric Acidemia: An Inborn Error Associated with Fructose Metabolism. Pediatric Research. 21(5). 502–506. 21 indexed citations
7.
Durán, M., L. Bruinvis, & S.K. Wadman. (1986). Quantitative gas chromatographic determination of urinary hydantoin-5-propionic acid in patients with disorders of folate/vitamin B12 metabolism. Journal of Chromatography B Biomedical Sciences and Applications. 381(2). 401–405. 2 indexed citations
8.
Durán, Marinus, Grant Mitchell, Johannis B.C. de Klerk, et al.. (1985). Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids. The Journal of Pediatrics. 107(3). 397–404. 44 indexed citations
9.
Durán, M., J. B. C. de Klerk, S.K. Wadman, L. Bruinvis, & D. Ketting. (1984). The differential diagnosis of dicarboxylic aciduria. Journal of Inherited Metabolic Disease. 7(S1). 48–51. 30 indexed citations
10.
Dorland, L., M. Durán, S.K. Wadman, et al.. (1983). Isovalerylglucuronide, a new urinary metabolite in isovaleric acidemia. Identification problems due to rearrangement reactions. Clinica Chimica Acta. 134(1-2). 77–83. 16 indexed citations
11.
Durán, M., Frans J. Walther, L. Bruinvis, & S.K. Wadman. (1983). The urinary excretion of ethylmalonic acid: What level requires further attention?. Biochemical Medicine. 29(2). 171–175. 15 indexed citations
12.
13.
Durán, M., et al.. (1982). Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism. The Journal of Pediatrics. 101(4). 551–554. 48 indexed citations
14.
Kamerling, J.P., M. Durán, L. Bruinvis, et al.. (1982). The absolute configuration of urinary 5-hydroxyhexanoic acid — a product of fatty acid (ω-1)-oxidation — in patients with non-ketotic dicarboxylic aciduria. Clinica Chimica Acta. 125(3). 247–254. 7 indexed citations
15.
Kamerling, J.P., M. Durán, Gerrit J. Gerwig, et al.. (1981). Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas—liquid chromatography. Journal of Chromatography B Biomedical Sciences and Applications. 222(2). 276–283. 29 indexed citations
16.
Przyrembel, Hildegard, H. J. Bremer, M. Durán, et al.. (1979). Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels. European Journal of Pediatrics. 130(1). 1–14. 14 indexed citations
17.
Durán, M., et al.. (1979). Two sistes with isovaleric acidaemia, multiple attacks of ketoacidosis and normal development. European Journal of Pediatrics. 131(3). 205–211. 13 indexed citations
18.
Durán, M., L. Bruinvis, D. Ketting, & S.K. Wadman. (1978). Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia. Journal of Inherited Metabolic Disease. 1(3). 105–107. 10 indexed citations
19.
Bruinvis, L., D. Ketting, P.K. De Bree, et al.. (1977). Hereditary Mitochondrial Myopathy with Lactic Acidemia, A DeToni-Fanconi-Debr?? Syndrome, and a Defective Respiratory Chain in Voluntary Striated Muscles. Pediatric Research. 11(10). 1088–1088. 139 indexed citations
20.
Wadman, S.K., M. Durán, D. Ketting, et al.. (1976). D-Glyceric acidemia in a patient with chronic metabolic acedosis. Clinica Chimica Acta. 71(3). 477–484. 37 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by H.J. ten Brink Breakdown of academic impact, for papers by Harbhajan S. Paul Breakdown of academic impact, for papers by BD Ross Breakdown of academic impact, for papers by Dirk Kohlmüller Breakdown of academic impact, for papers by Lois M. Walker Breakdown of academic impact, for papers by Carole Hall Breakdown of academic impact, for papers by Nancy J. Hutson Breakdown of academic impact, for papers by KIMIYOSHI OHNO Breakdown of academic impact, for papers by Luc J. Debeer Breakdown of academic impact, for papers by Bernice Friedmann
Rankless by CCL
2026