Maaike C. de Vries

2.0k total citations
41 papers, 1.2k citations indexed

About

Maaike C. de Vries is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Maaike C. de Vries has authored 41 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Clinical Biochemistry, 30 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in Maaike C. de Vries's work include Metabolism and Genetic Disorders (34 papers), Mitochondrial Function and Pathology (28 papers) and Diet and metabolism studies (13 papers). Maaike C. de Vries is often cited by papers focused on Metabolism and Genetic Disorders (34 papers), Mitochondrial Function and Pathology (28 papers) and Diet and metabolism studies (13 papers). Maaike C. de Vries collaborates with scholars based in Netherlands, Germany and United States. Maaike C. de Vries's co-authors include Richard J. Rodenburg, Éva Morava, Jan Smeıtınk, Mirian C. H. Janssen, Lambertus P. van den Heuvel, Frans A. Hol, Marije Hogeveen, Annet M. Bosch, M. Estela Rubio‐Gozalbo and Francjan J. van Spronsen and has published in prestigious journals such as Brain, Neurology and Pediatric Research.

In The Last Decade

Maaike C. de Vries

41 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maaike C. de Vries Netherlands 19 923 827 321 155 122 41 1.2k
A. A. M. Morris United Kingdom 17 613 0.7× 529 0.6× 254 0.8× 126 0.8× 115 0.9× 27 1.0k
Carla Carducci Italy 17 948 1.0× 818 1.0× 216 0.7× 173 1.1× 84 0.7× 47 1.5k
C. Jakobs Netherlands 17 680 0.7× 621 0.8× 223 0.7× 84 0.5× 116 1.0× 39 1.1k
Irina Anselm United States 16 810 0.9× 477 0.6× 122 0.4× 303 2.0× 98 0.8× 29 1.2k
F. Sedel France 18 384 0.4× 365 0.4× 682 2.1× 94 0.6× 69 0.6× 35 1.3k
Rafael Borba Rosa Brazil 17 491 0.5× 448 0.5× 160 0.5× 41 0.3× 18 0.1× 21 807
Raffaele Maletta Italy 18 589 0.6× 206 0.2× 564 1.8× 133 0.9× 34 0.3× 53 1.3k
Hiroko Iwamoto Japan 11 383 0.4× 268 0.3× 141 0.4× 109 0.7× 120 1.0× 33 652
K. Bartholomé Germany 16 441 0.5× 636 0.8× 181 0.6× 102 0.7× 108 0.9× 27 931
Manuela Grazina Portugal 15 443 0.5× 164 0.2× 91 0.3× 232 1.5× 40 0.3× 45 847

Countries citing papers authored by Maaike C. de Vries

Since Specialization
Citations

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

Fields of papers citing papers by Maaike C. de Vries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maaike C. de Vries

This figure shows the co-authorship network connecting the top 25 collaborators of Maaike C. de Vries. A scholar is included among the top collaborators of Maaike C. de Vries 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 Maaike C. de Vries. Maaike C. de Vries 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.
Zimmermann, Franz, et al.. (2024). Vaccine safety in children with genetically confirmed mitochondrial disease. Immunology Letters. 271. 106946–106946. 1 indexed citations
2.
Cate, Floris E.A. Udink ten, Sacha Ferdinandusse, Simone Denis, et al.. (2022). Neonatal Long-Chain 3-Ketoacyl-CoA Thiolase deficiency: Clinical-biochemical phenotype, sodium-D,L-3-hydroxybutyrate treatment experience and cardiac evaluation using speckle echocardiography. Molecular Genetics and Metabolism Reports. 31. 100873–100873. 3 indexed citations
3.
Strijker, Marin, Laura A. Tseng, Curtis R. Coughlin, et al.. (2021). Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study. European Journal of Paediatric Neurology. 33. 112–120. 10 indexed citations
4.
Vries, Maaike C. de, David A. Brown, Mitchell E. Allen, et al.. (2020). Safety of drug use in patients with a primary mitochondrial disease: An international Delphi‐based consensus. Journal of Inherited Metabolic Disease. 43(4). 800–818. 40 indexed citations
5.
Molema, Femke, Hanneke A. Haijes, Mirian C. H. Janssen, et al.. (2020). High protein prescription in methylmalonic and propionic acidemia patients and its negative association with long-term outcome. Clinical Nutrition. 40(5). 3622–3630. 9 indexed citations
6.
Conte, Federica, Éva Morava, Nurulamin Abu Bakar, et al.. (2020). Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots. Molecular Genetics and Metabolism. 131(1-2). 135–146. 19 indexed citations
7.
Ferdinandusse, Sacha, Gert J. Geurtsen, Carla E. M. Hollak, et al.. (2020). Deep phenotyping classical galactosemia: clinical outcomes and biochemical markers. Brain Communications. 2(1). fcaa006–fcaa006. 27 indexed citations
8.
Schrantee, Anouk, Matthan W.A. Caan, Carla E. M. Hollak, et al.. (2020). Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcome. Molecular Genetics and Metabolism. 131(4). 370–379. 9 indexed citations
9.
Fuchs, Sabine A., Imre F. Schene, Peter G. J. Nikkels, et al.. (2018). Aminoacyl-tRNA synthetase deficiencies in search of common themes. Genetics in Medicine. 21(2). 319–330. 68 indexed citations
10.
Wegberg, Annemiek M. J. van, et al.. (2018). Anthropomorphic measurements and nutritional biomarkers after 5 years of BH 4 treatment in phenylketonuria patients. Molecular Genetics and Metabolism. 124(4). 238–242. 6 indexed citations
11.
Jahja, Rianne, Francjan J. van Spronsen, Leo de Sonneville, et al.. (2017). Long-Term Follow-Up of Cognition and Mental Health in Adult Phenylketonuria: A PKU-COBESO Study. Behavior Genetics. 47(5). 486–497. 47 indexed citations
12.
Jahja, Rianne, Stephan C. J. Huijbregts, Leo de Sonneville, et al.. (2017). Cognitive profile and mental health in adult phenylketonuria: A PKU-COBESO study.. Neuropsychology. 31(4). 437–447. 55 indexed citations
13.
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
14.
Jahja, Rianne, Francjan J. van Spronsen, Leo de Sonneville, et al.. (2014). Is BRIEF a useful instrument in day to day care of patients with phenylketonuria?. Molecular Genetics and Metabolism. 114(3). 425–430. 7 indexed citations
15.
Jahja, Rianne, Stephan C. J. Huijbregts, Leo de Sonneville, et al.. (2013). Mental health and social functioning in early treated Phenylketonuria: The PKU-COBESO study. Molecular Genetics and Metabolism. 110. S57–S61. 34 indexed citations
16.
Jonckheere, An I., G. Herma Renkema, Lambert P. van den Heuvel, et al.. (2013). A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy. Brain. 136(5). 1544–1554. 73 indexed citations
17.
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
18.
Morava, Éva, Thatjana Gardeitchik, Tamás Kozicz, et al.. (2010). Depressive behaviour in children diagnosed with a mitochondrial disorder. Mitochondrion. 10(5). 528–533. 68 indexed citations
19.
Verhagen, Eduard, et al.. (2007). [Hopeless and unbearable suffering and deliberate ending of life of newborn infants].. PubMed. 151(26). 1474–7. 3 indexed citations
20.
Semmekrot, B. A., et al.. (2004). [Optimal breastfeeding to prevent hyperbilirubinaemia in healthy, term newborns].. PubMed. 148(41). 2016–9. 17 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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