W. Ruitenbeek

6.1k total citations · 1 hit paper
118 papers, 4.8k citations indexed

About

W. Ruitenbeek is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, W. Ruitenbeek has authored 118 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 85 papers in Clinical Biochemistry and 17 papers in Physiology. Recurrent topics in W. Ruitenbeek's work include Metabolism and Genetic Disorders (85 papers), Mitochondrial Function and Pathology (76 papers) and ATP Synthase and ATPases Research (24 papers). W. Ruitenbeek is often cited by papers focused on Metabolism and Genetic Disorders (85 papers), Mitochondrial Function and Pathology (76 papers) and ATP Synthase and ATPases Research (24 papers). W. Ruitenbeek collaborates with scholars based in Netherlands, Germany and United States. W. Ruitenbeek's co-authors include R. C. A. Sengers, J. M. F. Trijbels, A.J.M. Janssen, F.J.M. Gabreëls, J. M. W. van den Ouweland, J. A. Maassen, H.H.P.J. Lemkes, J. J. P. van de Kamp, Lodewijk A. Sandkuijl and Johan Fischer and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

W. Ruitenbeek

117 papers receiving 4.6k 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.

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1992 839 citations W. Ruitenbeek et al. profile →

Peers

W. Ruitenbeek

PHYSI

CMN

R. C. A. Sengers Netherlands

H.R. Scholte Netherlands

Angela Maria Serena Lezza Italy

Stephan Zierz Germany

Flemming Wibrand Denmark

Frank N. Gellerich Germany

Marisol Corral‐Debrinski France

Linsey Stiles United States

Stefano Di Donato Italy

Jean Bastin France

R. C. A. Sengers Netherlands

W. Ruitenbeek

3.3k ×0.9

1.8k ×0.8

543 ×0.8

PHYSI

362 ×0.9

CMN

270 ×0.7

Citations per year, relative to W. Ruitenbeek W. Ruitenbeek (= 1×) peers R. C. A. Sengers

Countries citing papers authored by W. Ruitenbeek

Since Specialization

Citations

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

Fields of papers citing papers by W. Ruitenbeek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W. Ruitenbeek

This figure shows the co-authorship network connecting the top 25 collaborators of W. Ruitenbeek. A scholar is included among the top collaborators of W. Ruitenbeek 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 W. Ruitenbeek. W. Ruitenbeek 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

Boer, Nanne K.H. de, Luc J. J. Derijks, W. Ruitenbeek, et al.. (2007). Extended Thiopurine Metabolite Assessment During 6‐Thioguanine Therapy for Immunomodulation in Crohn's Disease. The Journal of Clinical Pharmacology. 47(2). 187–191. 13 indexed citations

Ruitenbeek, W., et al.. (2006). Excitatory amino acid release and electrocortical brain activity after hypoxemia in near-term lambs. Brain and Development. 28(6). 380–388. 6 indexed citations

Smeıtınk, Jan, B. A. Semmekrot, H.R. Scholte, et al.. (1999). Treatment and molecular analysis of neonatal carnitine palmitoyltransferase II deficiency.. Pediatric Research. 2 indexed citations

Messina, Angela, Marta Oliva, Marjan Huizing, et al.. (1999). Mapping of the Human Voltage-Dependent Anion Channel Isoforms 1 and 2 Reconsidered. Biochemical and Biophysical Research Communications. 255(3). 707–710. 20 indexed citations

Barth, P. G., Ronald J. A. Wanders, W. Ruitenbeek, et al.. (1998). Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families. Neuromuscular Disorders. 8(5). 296–304. 11 indexed citations

Heuvel, Lambert van den, W. Ruitenbeek, Roel Smeets, et al.. (1998). Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit. The American Journal of Human Genetics. 62(2). 262–268. 224 indexed citations

Huizing, Marjan, W. Ruitenbeek, Lambert P. van den Heuvel, et al.. (1998). Human Mitochondrial Transmembrane Metabolite Carriers: Tissue Distribution and Its Implication for Mitochondrial Disorders. Journal of Bioenergetics and Biomembranes. 30(3). 277–284. 72 indexed citations

Steeghs, Karen, A. Heerschap, A. de Haan, et al.. (1997). Use of gene targeting for compromising energy homeostasis in neuro-muscular tissues: The role of sarcomeric mitochondrial creatine kinase. Journal of Neuroscience Methods. 71(1). 29–41. 44 indexed citations

Domburg, Peter Henricus Maria Franciscus van, A.A.W.M. Gabreëls‐Festen, F.J.M. Gabreëls, et al.. (1996). Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status. Brain. 119(3). 997–1010. 25 indexed citations

10.

Nijtmans, Leo, P. G. Barth, Carsten R. Lincke, et al.. (1995). Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1270(2-3). 193–201. 16 indexed citations

11.

Duncan, David B., Karl Herholz, Harald Kugel, et al.. (1995). Positron emission tomography and magnetic resonance spectroscopy of cerebral glycolysis in children with congenital lactic acidosis. Annals of Neurology. 37(3). 351–358. 26 indexed citations

12.

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

13.

Krägeloh‐Mann, Ingeborg, Wolfgang Grodd, M. Schöning, et al.. (1993). PROTON SPECTROSCOPY IN FIVE PATIENTS WITH LEIGH'S DISEASE AND MITOCHONDRIAL ENZYME DEFICIENCY. Developmental Medicine & Child Neurology. 35(9). 769–776. 34 indexed citations

14.

Engelen, Baziel G.M. van, et al.. (1993). A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome. Annals of Neurology. 34(3). 410–412. 205 indexed citations

15.

Sperl, Wolfgang, J. M. F. Trijbels, W. Ruitenbeek, et al.. (1992). Postnatal Development of Pyruvate Oxidation in Quadriceps Muscle of the Rat. Neonatology. 61(3). 188–200. 5 indexed citations

16.

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

17.

Bosman, G.J.C.G.M., et al.. (1992). No evidence for reduced thrombocyte cytochrome oxidase activity in Alzheimer's disease. Neurology. 42(6). 1246–1246. 25 indexed citations

18.

Sperl, Wolfgang, J. M. F. Trijbels, W. Ruitenbeek, et al.. (1992). Enzyme Activities of the Mitochondrial Energy Generating System in Skeletal Muscle Tissue of Preterm and Fullterm Neonates. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 29(6). 638–645. 20 indexed citations

19.

Obermaier–Kusser, B., et al.. (1991). Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA^Leu(UUR)]. FEBS Letters. 286(1-2). 67–70. 28 indexed citations

20.

Korenke, Georg Christoph, Herman Bentlage, W. Ruitenbeek, et al.. (1990). Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies. European Journal of Pediatrics. 150(2). 104–108. 25 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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