Bert van den Heuvel

1.3k total citations
19 papers, 703 citations indexed

About

Bert van den Heuvel is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Nephrology. According to data from OpenAlex, Bert van den Heuvel has authored 19 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Pathology and Forensic Medicine and 4 papers in Nephrology. Recurrent topics in Bert van den Heuvel's work include Mitochondrial Function and Pathology (5 papers), ATP Synthase and ATPases Research (4 papers) and Biomedical Research and Pathophysiology (4 papers). Bert van den Heuvel is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), ATP Synthase and ATPases Research (4 papers) and Biomedical Research and Pathophysiology (4 papers). Bert van den Heuvel collaborates with scholars based in Netherlands, Belgium and Germany. Bert van den Heuvel's co-authors include Jan Smeıtınk, Elena Levtchenko, Leo Nijtmans, Rutger O. Vogel, Richard Huijbens, Cristina Ugalde, Noël Knops, Dirk Kuypers, Richard J. Rodenburg and Johan van der Vlag and has published in prestigious journals such as PLoS ONE, Neurology and The American Journal of Human Genetics.

In The Last Decade

Bert van den Heuvel

19 papers receiving 696 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bert van den Heuvel Netherlands 13 380 163 140 88 79 19 703
Davoud Mohtat United States 5 412 1.1× 54 0.3× 25 0.2× 357 4.1× 57 0.7× 6 778
Yoshiharu Muto Japan 15 492 1.3× 28 0.2× 14 0.1× 233 2.6× 53 0.7× 42 917
Reiichi Murakami Japan 15 168 0.4× 11 0.1× 57 0.4× 118 1.3× 17 0.2× 71 599
Rémi Salomon France 9 193 0.5× 19 0.1× 18 0.1× 65 0.7× 30 0.4× 20 467
Madhusudan Venkatareddy United States 12 313 0.8× 18 0.1× 25 0.2× 639 7.3× 67 0.8× 15 838
Gary E. Striker United States 10 253 0.7× 43 0.3× 7 0.1× 211 2.4× 72 0.9× 11 551
Natascha Goemaere Netherlands 12 133 0.3× 10 0.1× 51 0.4× 125 1.4× 35 0.4× 20 698
Jack L. Martin United Kingdom 10 160 0.4× 19 0.1× 19 0.1× 41 0.5× 11 0.1× 21 559
Zhiyu Wang China 8 205 0.5× 20 0.1× 22 0.2× 67 0.8× 12 0.2× 13 410
Giorgia Mandrile Italy 13 584 1.5× 50 0.3× 13 0.1× 49 0.6× 160 2.0× 33 944

Countries citing papers authored by Bert van den Heuvel

Since Specialization
Citations

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

Fields of papers citing papers by Bert van den Heuvel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bert van den Heuvel. 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 Bert van den Heuvel. The network helps show where Bert van den Heuvel may publish in the future.

Co-authorship network of co-authors of Bert van den Heuvel

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

All Works

19 of 19 papers shown
1.
Adjobo-Hermans, Merel J.W., Liesbeth T. Wintjes, Bert van den Heuvel, et al.. (2023). SMDT1 variants impair EMRE-mediated mitochondrial calcium uptake in patients with muscle involvement. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1869(8). 166808–166808. 7 indexed citations
2.
Veys, Koenraad, Katharina Hohenfellner, Detlef Böckenhauer, et al.. (2022). Outcome of infantile nephropathic cystinosis depends on early intervention, not genotype: A multicenter sibling cohort study. Journal of Inherited Metabolic Disease. 46(1). 43–54. 12 indexed citations
3.
Vandamme, Timon, Bert van den Heuvel, Jan Van den Brande, et al.. (2019). Should Anti-EGFR Agents Be Used in Right-Sided RAS Wild-type Advanced Colorectal Cancer?. Current Colorectal Cancer Reports. 15(4). 130–134. 1 indexed citations
4.
Elmonem, Mohamed A., Fanny Oliveira Arcolino, Neveen A. Soliman, et al.. (2018). Molecular Basis of Cystinosis: Geographic Distribution, Functional Consequences of Mutations in the <b><i>CTNS</i></b> Gene, and Potential for Repair. ˜The œNephron journals/Nephron journals. 141(2). 133–146. 40 indexed citations
5.
Heuvel, Bert van den, et al.. (2017). 18F-FDG-PET/CT for the detection of disease in patients with head and neck cancer treated with radiotherapy. PLoS ONE. 12(8). e0182350–e0182350. 16 indexed citations
6.
Heuvel, Bert van den, Marc Peeters, Alain Hendlisz, et al.. (2016). Long-acting octreotide as secondary prevention of chemotherapy-induced diarrhea: proof of concept.. PubMed. 3 indexed citations
7.
Volokhina, Elena B., et al.. (2016). Recovery of renal function after long-term dialysis and resolution of cardiomyopathy in a patient with aHUS receiving eculizumab. BMJ Case Reports. 2016. bcr2015213928–bcr2015213928. 10 indexed citations
8.
Mise, Annarita Di, Grazia Tamma, Marianna Ranieri, et al.. (2015). Conditionally immortalized human proximal tubular epithelial cells isolated from the urine of a healthy subject express functional calcium-sensing receptor. American Journal of Physiology-Renal Physiology. 308(11). F1200–F1206. 17 indexed citations
9.
Levtchenko, Elena, et al.. (2015). Platelet abnormalities in nephrotic syndrome. Pediatric Nephrology. 31(8). 1267–1279. 25 indexed citations
10.
Mohamed, Miski, Angel Ashikov, Maïlys Guillard, et al.. (2013). Intellectual disability and bleeding diathesis due to deficient CMP–sialic acid transport. Neurology. 81(7). 681–687. 41 indexed citations
11.
Knops, Noël, Elena Levtchenko, Bert van den Heuvel, & Dirk Kuypers. (2013). From gut to kidney: Transporting and metabolizing calcineurin-inhibitors in solid organ transplantation. International Journal of Pharmaceutics. 452(1-2). 14–35. 62 indexed citations
12.
Besouw, Martine, Jerry A. Schneider, Francesco Emma, et al.. (2012). Copper deficiency in cystinosis patients. Pediatric Nephrology. 27(9). 1634–1635. 2 indexed citations
13.
Joost, Kairit, Richard J. Rodenburg, Andres Piirsoo, et al.. (2010). A Novel Mutation in the SCO2 Gene in a Neonate With Early-Onset Cardioencephalomyopathy. Pediatric Neurology. 42(3). 227–230. 26 indexed citations
14.
Jonckheere, An I., Marije Hogeveen, Leo Nijtmans, et al.. (2009). A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy. BMJ Case Reports. 2009. bcr0720080504–bcr0720080504. 18 indexed citations
15.
Smeıtınk, Jan, Orly Elpeleg, Hana Antonická, et al.. (2006). Distinct Clinical Phenotypes Associated with a Mutation in the Mitochondrial Translation Elongation Factor EFTs. The American Journal of Human Genetics. 79(5). 869–877. 142 indexed citations
16.
Joosten, Simone A., Vanessa van Ham, Leendert A. Trouw, et al.. (2005). Antibody Response Against the Glomerular Basement Membrane Protein Agrin in Patients with Transplant Glomerulopathy. American Journal of Transplantation. 5(2). 383–393. 107 indexed citations
17.
Poinsot, Thierry, et al.. (2005). Large-eddy simulation for the prediction of aerodynamics in IC engines. International Journal of Vehicle Design. 39(4). 368–368. 24 indexed citations
18.
Ugalde, Cristina, Rutger O. Vogel, Richard Huijbens, et al.. (2004). Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. Human Molecular Genetics. 13(20). 2461–2472. 149 indexed citations
19.
Heuvel, Bert van den. (2004). Gene hunting and gene cloning in human OXPHOS deficiency. 2004(Fall). 1 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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