Herman Bentlage

594 total citations
17 papers, 479 citations indexed

About

Herman Bentlage is a scholar working on Molecular Biology, Clinical Biochemistry and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Herman Bentlage has authored 17 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 2 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Herman Bentlage's work include Mitochondrial Function and Pathology (15 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (8 papers). Herman Bentlage is often cited by papers focused on Mitochondrial Function and Pathology (15 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (8 papers). Herman Bentlage collaborates with scholars based in Netherlands, Germany and United States. Herman Bentlage's co-authors include Giuseppe Attardi, Hermann Schägger, U. Wendel, W. Ruitenbeek, R. C. A. Sengers, J. M. F. Trijbels, I.F.M. de Coo, H. J. ter Laak, Kathy Pfeiffer and W. Ruitenbeek and has published in prestigious journals such as Neurology, Annals of Neurology and Methods in enzymology on CD-ROM/Methods in enzymology.

In The Last Decade

Herman Bentlage

17 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Herman Bentlage Netherlands 12 404 242 47 27 27 17 479
Barbara S. Miles United States 10 357 0.9× 304 1.3× 50 1.1× 17 0.6× 62 2.3× 12 462
J. P. Colombo Switzerland 11 116 0.3× 121 0.5× 30 0.6× 29 1.1× 43 1.6× 19 271
Christa Bräutigam Germany 8 206 0.5× 190 0.8× 21 0.4× 91 3.4× 36 1.3× 8 357
Akiko Ichinohe Japan 10 200 0.5× 162 0.7× 11 0.2× 29 1.1× 47 1.7× 17 396
F. Lermé France 8 556 1.4× 136 0.6× 12 0.3× 36 1.3× 60 2.2× 15 644
Katharina Lackner Austria 9 301 0.7× 57 0.2× 36 0.8× 16 0.6× 57 2.1× 12 369
Edward Kmiotek United States 12 271 0.7× 150 0.6× 29 0.6× 40 1.5× 94 3.5× 14 461
Yvonne Wohlfarter Austria 6 236 0.6× 61 0.3× 18 0.4× 14 0.5× 82 3.0× 8 327
J Bozal Spain 10 238 0.6× 63 0.3× 14 0.3× 48 1.8× 30 1.1× 66 432
Domenico Marzulli Italy 16 351 0.9× 56 0.2× 16 0.3× 54 2.0× 71 2.6× 30 505

Countries citing papers authored by Herman Bentlage

Since Specialization
Citations

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

Fields of papers citing papers by Herman Bentlage

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Herman Bentlage

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

All Works

17 of 17 papers shown
1.
Bentlage, Herman, et al.. (2024). The Industrial Application Potential of Sugar Beet Pulp Derived Monosaccharides d‐Galacturonic Acid and l‐Arabinose.. ChemBioChem. 25(24). e202400521–e202400521. 4 indexed citations
2.
Outersterp, Rianne E. van, Sam J. Moons, Udo F. H. Engelke, et al.. (2021). Amadori rearrangement products as potential biomarkers for inborn errors of amino-acid metabolism. Communications Biology. 4(1). 367–367. 23 indexed citations
3.
Martens, Jonathan, Giel Berden, Herman Bentlage, et al.. (2018). Unraveling the unknown areas of the human metabolome: the role of infrared ion spectroscopy. Journal of Inherited Metabolic Disease. 41(3). 367–377. 44 indexed citations
4.
Dionisi‐Vici, Carlo, W. Ruitenbeek, G. Fariello, et al.. (1997). New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency. Annals of Neurology. 42(4). 661–665. 10 indexed citations
5.
Wendel, U., Herman Bentlage, Jan Smeıtınk, et al.. (1997). Clinical heterogeneity in respiratory chain complex III deficiency in childhood. Journal of the Neurological Sciences. 149(1). 111–117. 53 indexed citations
6.
Rubio‐Gozalbo, M. Estela, W. Ruitenbeek, Herman Bentlage, et al.. (1997). Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV. European Journal of Pediatrics. 156(12). 931–934. 3 indexed citations
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Bentlage, Herman & Anne Chomyn. (1996). [20] Immunoprecipitation of human mitochondrial translation products with peptide-specific antibodies. Methods in enzymology on CD-ROM/Methods in enzymology. 264. 218–228. 1 indexed citations
10.
11.
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
12.
Wendel, U., W. Ruitenbeek, Herman Bentlage, R. C. A. Sengers, & J. M. F. Trijbels. (1995). Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain. European Journal of Pediatrics. 154(11). 915–918. 8 indexed citations
13.
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
14.
Bentlage, Herman, I.F.M. de Coo, H. ter Laak, et al.. (1995). Human Diseases with Defects in Oxidative Phosphorylation. European Journal of Biochemistry. 227(3). 909–915. 35 indexed citations
15.
Vries, Daniëlle de, et al.. (1994). Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation. Journal of the Neurological Sciences. 124(1). 77–82. 43 indexed citations
16.
Sperl, Wolfgang, W. Ruitenbeek, R. C. A. Sengers, et al.. (1992). Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies. European Journal of Pediatrics. 151(3). 192–195. 16 indexed citations
17.
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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