C Boelen

611 total citations
18 papers, 455 citations indexed

About

C Boelen is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Boelen has authored 18 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Boelen's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (9 papers) and Neonatal Health and Biochemistry (3 papers). C Boelen is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (9 papers) and Neonatal Health and Biochemistry (3 papers). C Boelen collaborates with scholars based in Netherlands, United States and Switzerland. C Boelen's co-authors include H. D. Bakker, J Kastelein, Harry R. Büller, Björn E. Groenemeijer, A. van den Ende, Annet M. Bosch, H.C. Knipscheer, D.E. van Diermen, Francjan J. van Spronsen and M. Estela Rubio‐Gozalbo and has published in prestigious journals such as Academic Medicine, Atherosclerosis and Pediatric Research.

In The Last Decade

C Boelen

16 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C Boelen Netherlands 11 197 190 108 85 75 18 455
Corinne De Laet Belgium 14 321 1.6× 185 1.0× 60 0.6× 154 1.8× 44 0.6× 26 631
Carla Cuthbert United States 13 249 1.3× 161 0.8× 39 0.4× 56 0.7× 61 0.8× 24 529
Jason D’Amore United States 8 67 0.3× 166 0.9× 59 0.5× 25 0.3× 23 0.3× 24 536
Evelina Maines Italy 10 64 0.3× 67 0.4× 42 0.4× 75 0.9× 17 0.2× 53 325
Raúl Calzada‐León Mexico 10 21 0.1× 139 0.7× 108 1.0× 24 0.3× 51 0.7× 25 399
Joycelyn Atchison United States 14 22 0.1× 73 0.4× 92 0.9× 46 0.5× 58 0.8× 22 429
Shubha Srinivasan Australia 13 18 0.1× 136 0.7× 116 1.1× 139 1.6× 265 3.5× 31 631
Dennis O. Mook‐Kanamori Netherlands 13 16 0.1× 73 0.4× 53 0.5× 88 1.0× 133 1.8× 28 438
Trine Tangeraas Norway 13 138 0.7× 167 0.9× 70 0.6× 41 0.5× 47 0.6× 33 543
Wei Gu China 12 22 0.1× 68 0.4× 57 0.5× 27 0.3× 18 0.2× 36 351

Countries citing papers authored by C Boelen

Since Specialization
Citations

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

Fields of papers citing papers by C Boelen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Boelen

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

All Works

18 of 18 papers shown
1.
Hofstede, Floris C., Annet M. Bosch, M. Estela Rubio‐Gozalbo, et al.. (2016). The neonatal tetrahydrobiopterin loading test in phenylketonuria: what is the predictive value?. Orphanet Journal of Rare Diseases. 11(1). 10–10. 10 indexed citations
2.
Demirdas, Serwet, Heleen Maurice‐Stam, C Boelen, et al.. (2013). Evaluation of quality of life in PKU before and after introducing tetrahydrobiopterin (BH4); a prospective multi-center cohort study. Molecular Genetics and Metabolism. 110. S49–S56. 32 indexed citations
3.
Rijn, Margreet van, Floris C. Hofstede, Annet M. Bosch, et al.. (2013). Tetrahydrobiopterin responsiveness in phenylketonuria: prediction with the 48-hour loading test and genotype. Orphanet Journal of Rare Diseases. 8(1). 103–103. 31 indexed citations
4.
Boelen, C, Berthil H.C.M.T. Prinsen, Lodewijk IJlst, et al.. (2012). Necrotizing Enterocolitis and Respiratory Distress Syndrome as First Clinical Presentation of Mitochondrial Trifunctional Protein Deficiency. JIMD Reports. 7. 1–6. 9 indexed citations
5.
Hoedt, Amber E. ten, Heleen Maurice‐Stam, C Boelen, et al.. (2011). Parenting a child with phenylketonuria or galactosemia: implications for health‐related quality of life. Journal of Inherited Metabolic Disease. 34(2). 391–398. 59 indexed citations
6.
Hoedt, Amber E. ten, Carla E. M. Hollak, C Boelen, et al.. (2011). "MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial. Orphanet Journal of Rare Diseases. 6(1). 48–48. 15 indexed citations
7.
Hofstede, Floris C., Annet M. Bosch, Carla E. M. Hollak, et al.. (2011). The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: Evaluation of protocol and influence of baseline phenylalanine concentration. Molecular Genetics and Metabolism. 104. S60–S63. 13 indexed citations
8.
Lopriore, Enrico, et al.. (2009). Neonatal carnitine palmitoyltransferase II deficiency: failure of treatment despite prolonged survival: Table 1. BMJ Case Reports. 2009. bcr0220091550–bcr0220091550. 4 indexed citations
9.
Morava, Éva, R. C. A. Sengers, H. ter Laak, et al.. (2004). Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defective oxidative phosphorylation in two siblings with Sengers-like syndrome. European Journal of Pediatrics. 163(8). 467–471. 29 indexed citations
10.
Heuvel, Lambert P.W.J. van den, Roel Smeets, Daniela Skladal, et al.. (2003). Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex I. Journal of Inherited Metabolic Disease. 26(8). 813–815. 60 indexed citations
11.
Grafakou, Olga, Frans A. Hol, Karl Otfried Schwab, et al.. (2003). Exercise intolerance, muscle pain and lactic acidaemia associated with a 7497G>A mutation in the tRNASer(UCN) gene. Journal of Inherited Metabolic Disease. 26(6). 593–600. 18 indexed citations
12.
Boelen, C, et al.. (2001). [Trends in the prevalence of caries in Dutch children].. PubMed. 108(12). 487–91. 4 indexed citations
13.
Boelen, C, et al.. (2000). Influenza-A-pneumonie. Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank. 144(41).
14.
Boelen, C, et al.. (2000). Asking the world experts in family medicine. Suggestions for the Hokkaido Centre for Family Medicine.. PubMed. 3–10. 2 indexed citations
15.
Boelen, C, et al.. (2000). [Influenza A pneumonia].. PubMed. 144(41). 1937–41.
16.
Knipscheer, H.C., C Boelen, J Kastelein, et al.. (1996). Short-Term Efficacy and Safety of Pravastatin in 72 Children with Familial Hypercholesterolemia. Pediatric Research. 39(5). 867–871. 124 indexed citations
17.
Boelen, C. (1995). Prospects for change in medical education in the twenty-first century. Academic Medicine. 70(7). S21–8. 43 indexed citations
18.
Knipscheer, H.C., et al.. (1994). Short-term safety, tolerance and efficacy of pravastatin in 72 children with FH. Atherosclerosis. 109(1-2). 256–257. 2 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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2026