Maaike C. de Vries

2.0k citations

41 papers · 1.2k indexed · h-index 19

Molecular Biology top 10%
Clinical Biochemistry top 0.2%
Physiology top 10%
Genetics
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Richard J. Rodenburg Jan Smeıtınk Éva Morava Mirian C. H. Janssen Lambertus P. van den Heuvel Marije Hogeveen Frans A. Hol Annet M. Bosch
Topics: Metabolism and Genetic Disorders (34 papers)Mitochondrial Function and Pathology (28 papers)Diet and metabolism studies (13 papers)
Cited by: Clinical Biochemistry Biological Psychiatry Molecular Biology
Journals: Brain Neurology Pediatric Research
Partner nations: Netherlands Germany United States

In The Last Decade

Maaike C. de Vries

41 papers receiving 1.2k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Vaccine safety in children with genetically confirmed mitochondrial disease 2024 ·Immunology Letters ·(unknown),Franz Zimmermann,(unknown),Maaike C. de Vries,Lonneke de Boer,Mirian C. H. Janssen,(unknown),Saskia B. Wortmann	1
2	Neonatal Long-Chain 3-Ketoacyl-CoA Thiolase deficiency: Clinical-biochemical phenotype, sodium-D,L-3-hydroxybutyrate treatment experience and cardiac evaluation using speckle echocardiography 2022 ·Molecular Genetics and Metabolism Reports ·(unknown),(unknown),Floris E.A. Udink ten Cate,Sacha Ferdinandusse,Simone Denis,Sabine A. Fuchs,(unknown),Rosa Geurtzen,Annemiek M. J. van Wegberg,Marleen C.D.G. Huigen,Leo A. J. Kluijtmans,Ronald J. A. Wanders,Terry G. J. Derks,Lonneke de Boer,Riekelt H. Houtkooper,Maaike C. de Vries,Clara D.M. van Karnebeek	3
3	Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study 2021 ·European Journal of Paediatric Neurology ·Marin Strijker,Laura A. Tseng,(unknown),(unknown),(unknown),Curtis R. Coughlin,(unknown),Francjan J. van Spronsen,Monique Williams,Maaike C. de Vries,Henriëtte E. Westerlaan,Levinus A. Bok,Clara D.M. van Karnebeek,Roelineke J. Lunsing	10
4	Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots 2020 ·Molecular Genetics and Metabolism ·Federica Conte,Éva Morava,Nurulamin Abu Bakar,Saskia B. Wortmann,(unknown),Stephanie Grünewald,Ellen Crushell,Lihadh Al‐Gazali,Maaike C. de Vries,(unknown),Jozef Hertecant,(unknown),David Kronn,Annette Feigenbaum,Ralph Fingerhut,Sunnie Wong,Monique van Scherpenzeel,Nicol C. Voermans,Dirk J. Lefeber	19
5	Safety of drug use in patients with a primary mitochondrial disease: An international Delphi‐based consensus 2020 ·Journal of Inherited Metabolic Disease ·Maaike C. de Vries,David A. Brown,Mitchell E. Allen,Laurence A. Bindoff,Gráinne S. Gorman,Amel Karaa,(unknown),Costanza Lamperti,Robert McFarland,Yi Shiau Ng,Mar O’Callaghan,Robert D. S. Pitceathly,Shamima Rahman,Frans G. M. Rüssel,Kristin N. Varhaug,Tom J.J. Schirris,Michelangelo Mancuso	40
6	High protein prescription in methylmalonic and propionic acidemia patients and its negative association with long-term outcome 2020 ·Clinical Nutrition ·Femke Molema,Hanneke A. Haijes,Mirian C. H. Janssen,Annet M. Bosch,F. J. van Spronsen,Mark Mulder,Nanda M. Verhoeven‐Duif,Judith Jans,Ans T. van der Ploeg,Margreet A. E. M. Wagenmakers,M. Estela Rubio‐Gozalbo,Martijn C.G.J. Brouwers,Maaike C. de Vries,Sabine A. Fuchs,Janneke G. Langendonk,Dimitris Rizopoulos,Peter M. van Hasselt,Monique Williams	9
7	Does the 48-hour BH4 loading test miss responsive PKU patients? 2019 ·Molecular Genetics and Metabolism ·Annemiek M. J. van Wegberg,(unknown),Esther van Dam,Maaike C. de Vries,Mirian C. H. Janssen,M. Rebecca Heiner‐Fokkema,Francjan J. van Spronsen	7
8	Aminoacyl-tRNA synthetase deficiencies in search of common themes 2018 ·Genetics in Medicine ·Sabine A. Fuchs,Imre F. Schene,(unknown),(unknown),Peter G. J. Nikkels,Koen L.I. van Gassen,Suzanne W. J. Terheggen-Lagro,Saskia N. van der Crabben,Sanne E. Hoeks,Laetitia E.M. Niers,Nicole I. Wolf,Maaike C. de Vries,David A. Koolen,Roderick H.J. Houwen,Margot F. Mulder,Peter M. van Hasselt	68
9	The impact of metabolic control and tetrahydrobiopterin treatment on health related quality of life of patients with early-treated phenylketonuria: A PKU-COBESO study 2018 ·Molecular Genetics and Metabolism ·Stephan C. J. Huijbregts,Annet M. Bosch,(unknown),Rianne Jahja,Martijn C.G.J. Brouwers,Leo de Sonneville,Maaike C. de Vries,Floris C. Hofstede,Carla E. M. Hollak,Mirian C. H. Janssen,Janneke G. Langendonk,M. Estela Rubio‐Gozalbo,Jaap J. van der Meere,Ans T. van der Ploeg,Francjan J. van Spronsen	20
10	Anthropomorphic measurements and nutritional biomarkers after 5 years of BH 4 treatment in phenylketonuria patients 2018 ·Molecular Genetics and Metabolism ·(unknown),Annemiek M. J. van Wegberg,Esther van Dam,Maaike C. de Vries,Mirian C. H. Janssen,Francjan J. van Spronsen	6
11	Cognitive profile and mental health in adult phenylketonuria: A PKU-COBESO study. 2017 ·Neuropsychology ·Rianne Jahja,Stephan C. J. Huijbregts,Leo de Sonneville,Jaap J. van der Meere,(unknown),Annet M. Bosch,Carla E. M. Hollak,M. Estela Rubio‐Gozalbo,Martijn C.G.J. Brouwers,Floris C. Hofstede,Maaike C. de Vries,Mirian C. H. Janssen,Ans T. van der Ploeg,Janneke G. Langendonk,Francjan J. van Spronsen	55
12	Long-Term Follow-Up of Cognition and Mental Health in Adult Phenylketonuria: A PKU-COBESO Study 2017 ·Behavior Genetics ·Rianne Jahja,Francjan J. van Spronsen,Leo de Sonneville,Jaap J. van der Meere,Annet M. Bosch,Carla E. M. Hollak,M. Estela Rubio‐Gozalbo,Martijn C.G.J. Brouwers,Floris C. Hofstede,Maaike C. de Vries,Mirian C. H. Janssen,Ans T. van der Ploeg,Janneke G. Langendonk,Stephan C. J. Huijbregts	47
13	The neonatal tetrahydrobiopterin loading test in phenylketonuria: what is the predictive value? 2016 ·Orphanet Journal of Rare Diseases ·(unknown),Floris C. Hofstede,Annet M. Bosch,M. Estela Rubio‐Gozalbo,Maaike C. de Vries,C Boelen,Margreet van Rijn,Francjan J. van Spronsen	10
14	Is BRIEF a useful instrument in day to day care of patients with phenylketonuria? 2014 ·Molecular Genetics and Metabolism ·(unknown),Rianne Jahja,Francjan J. van Spronsen,Leo de Sonneville,Jaap J. van der Meere,Annet M. Bosch,Carla E. M. Hollak,M. Estela Rubio‐Gozalbo,Martijn C.G.J. Brouwers,Floris C. Hofstede,Maaike C. de Vries,Mirian C. H. Janssen,Ans T. van der Ploeg,Janneke G. Langendonk,Stephan C. J. Huijbregts	7
15	A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy 2013 ·Brain ·An I. Jonckheere,G. Herma Renkema,(unknown),Lambert P. van den Heuvel,Alexander Hoischen,Christian Gilissen,Sander B. Nabuurs,Martijn A. Huynen,Maaike C. de Vries,Jan Smeıtınk,Richard J. Rodenburg	73
16	Mental health and social functioning in early treated Phenylketonuria: The PKU-COBESO study 2013 ·Molecular Genetics and Metabolism ·Rianne Jahja,Stephan C. J. Huijbregts,Leo de Sonneville,Jaap J. van der Meere,Annet M. Bosch,Carla E. M. Hollak,M. Estela Rubio‐Gozalbo,Martijn C.G.J. Brouwers,Floris C. Hofstede,Maaike C. de Vries,Mirian C. H. Janssen,(unknown),Janneke G. Langendonk,Francjan J. van Spronsen	34
17	Developing outcome measures for pediatric mitochondrial disorders: Which complaints and limitations are most burdensome to patients and their parents? 2012 ·Mitochondrion ·Saskia Koene,Saskia B. Wortmann,Maaike C. de Vries,An I. Jonckheere,Éva Morava,Imelda J. M. de Groot,Jan Smeıtınk	32
18	The 48-hour tetrahydrobiopterin loading test in patients with phenylketonuria: Evaluation of protocol and influence of baseline phenylalanine concentration 2011 ·Molecular Genetics and Metabolism ·(unknown),(unknown),Floris C. Hofstede,(unknown),Annet M. Bosch,(unknown),Carla E. M. Hollak,C. Jonkers,M. Estela Rubio‐Gozalbo,(unknown),Maaike C. de Vries,(unknown),Mirian C. H. Janssen,(unknown),C Boelen,(unknown),M. Rebecca Heiner‐Fokkema,Marjon van Rijn,F. J. van Spronsen	13
19	Depressive behaviour in children diagnosed with a mitochondrial disorder 2010 ·Mitochondrion ·Éva Morava,Thatjana Gardeitchik,Tamás Kozicz,Lonneke de Boer,Saskia Koene,Maaike C. de Vries,Robert McFarland,(unknown),Richard J. Rodenburg,C.M. Verhaak	68
20	[Optimal breastfeeding to prevent hyperbilirubinaemia in healthy, term newborns]. 2004 ·PubMed ·B. A. Semmekrot,Maaike C. de Vries,G. P. J. M. Gerrits,(unknown)	17

About Maaike C. de Vries

Maaike C. de Vries is a scholar working on Clinical Biochemistry, Biochemistry and Physiology, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (34 papers), Mitochondrial Function and Pathology (28 papers) and Diet and metabolism studies (13 papers). The work is most often cited by research in Clinical Biochemistry (827 citations), Biological Psychiatry (40 citations) and Molecular Biology (923 citations). Maaike C. de Vries has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Richard J. Rodenburg, Jan Smeıtınk, Éva Morava, Mirian C. H. Janssen, Lambertus P. van den Heuvel, Marije Hogeveen, Frans A. Hol, Annet M. Bosch, M. Estela Rubio‐Gozalbo and Francjan J. van Spronsen. Their work appears in journals such as Brain, Neurology and Pediatric Research.

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