Martijn J. de Groot

612 total citations
14 papers, 450 citations indexed

About

Martijn J. de Groot is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Martijn J. de Groot has authored 14 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 5 papers in Biochemistry. Recurrent topics in Martijn J. de Groot's work include Metabolism and Genetic Disorders (9 papers), Amino Acid Enzymes and Metabolism (5 papers) and Metabolomics and Mass Spectrometry Studies (3 papers). Martijn J. de Groot is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Amino Acid Enzymes and Metabolism (5 papers) and Metabolomics and Mass Spectrometry Studies (3 papers). Martijn J. de Groot collaborates with scholars based in Netherlands, United Kingdom and India. Martijn J. de Groot's co-authors include Francjan J. van Spronsen, Marieke Hoeksma, Dirk‐Jan Reijngoud, Nenad Blau, Margreet van Rijn, Will A. Coumans, Riemer H. J. A. Slart, Ger J. Vusse, Anne M. J. Paans and Danique van Vliet and has published in prestigious journals such as Circulation Research, The American Journal of Human Genetics and Journal of Cerebral Blood Flow & Metabolism.

In The Last Decade

Martijn J. de Groot

14 papers receiving 444 citations

Peers

Martijn J. de Groot

PHYSI

BIOCH

RHEUM

Pascale Delonlay France

H. R. Scholte Netherlands

Marina A. Schwab Germany

Norma Spécola Argentina

Marina Morath Germany

W. Ruitenbeek Netherlands

Hildgund Schmidt Germany

Danijela Petković Ramadža Croatia

Viruna Neergheen United Kingdom

F. G�ttler Denmark

Pascale Delonlay France

Martijn J. de Groot

255 ×0.7

304 ×1.2

100 ×0.6

PHYSI

73 ×0.8

BIOCH

33 ×0.6

RHEUM

Citations per year, relative to Martijn J. de Groot Martijn J. de Groot (= 1×) peers Pascale Delonlay

Countries citing papers authored by Martijn J. de Groot

Since Specialization

Citations

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

Fields of papers citing papers by Martijn J. de Groot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martijn J. de Groot. 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 Martijn J. de Groot. The network helps show where Martijn J. de Groot may publish in the future.

Co-authorship network of co-authors of Martijn J. de Groot

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

All Works

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14 of 14 papers shown

Gerritsen, Karin G. F., et al.. (2025). Kidney Cysts in Autosomal Dominant Polycystic Kidney Disease and Alport Syndrome: Two Familial Cases Illustrating Diagnostic Challenges. American Journal of Kidney Diseases. 86(4). 570–574. 1 indexed citations

Yoon, Jihoon G., Seungbok Lee, Soo Yeon Kim, et al.. (2024). De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder. The American Journal of Human Genetics. 111(8). 1588–1604. 1 indexed citations

Dijkhuizen, Trijnie, Martijn J. de Groot, Sheela Nampoothiri, et al.. (2018). Increased Recurrence Risk in Phelan-McDermid (22q13.3 Deletion) Syndrome: the Importance of FISH Demonstrated by a Case Series of Five Families. 2(4). 1–14. 2 indexed citations

Bruinenberg, Vibeke M., Danique van Vliet, Martijn J. de Groot, et al.. (2016). The Behavioral Consequence of Phenylketonuria in Mice Depends on the Genetic Background. Frontiers in Behavioral Neuroscience. 10. 233–233. 22 indexed citations

Vliet, Danique van, Terry G. J. Derks, Margreet van Rijn, et al.. (2014). Single amino acid supplementation in aminoacidopathies: a systematic review. Orphanet Journal of Rare Diseases. 9(1). 7–7. 25 indexed citations

Vliet, Danique van, Rianne Jahja, Martijn J. de Groot, et al.. (2014). BH4 treatment in BH4-responsive PKU patients: preliminary data on blood prolactin concentrations suggest increased cerebral dopamine concentrations. Molecular Genetics and Metabolism. 114(1). 29–33. 15 indexed citations

Groot, Martijn J. de, Paul E. Sijens, Dirk‐Jan Reijngoud, Anne M. J. Paans, & Francjan J. van Spronsen. (2014). Phenylketonuria: Brain Phenylalanine Concentrations Relate Inversely to Cerebral Protein Synthesis. Journal of Cerebral Blood Flow & Metabolism. 35(2). 200–205. 17 indexed citations

Groot, Martijn J. de, Marieke Hoeksma, Dirk‐Jan Reijngoud, et al.. (2013). Phenylketonuria: reduced tyrosine brain influx relates to reduced cerebral protein synthesis. Orphanet Journal of Rare Diseases. 8(1). 133–133. 35 indexed citations

Groot, Martijn J. de, Marieke Hoeksma, Margreet van Rijn, Riemer H. J. A. Slart, & Francjan J. van Spronsen. (2012). Relationships between lumbar bone mineral density and biochemical parameters in phenylketonuria patients. Molecular Genetics and Metabolism. 105(4). 566–570. 45 indexed citations

10.

Spronsen, Francjan J. van, Martijn J. de Groot, Marieke Hoeksma, Dirk‐Jan Reijngoud, & Margreet van Rijn. (2010). Large neutral amino acids in the treatment of PKU: from theory to practice. Journal of Inherited Metabolic Disease. 33(6). 671–676. 61 indexed citations

11.

Groot, Martijn J. de, et al.. (2010). Metabolic investigations prevent liver transplantation in two young children with citrullinemia type I. Journal of Inherited Metabolic Disease. 33(S3). 413–416. 17 indexed citations

12.

Groot, Martijn J. de, Marieke Hoeksma, Nenad Blau, Dirk‐Jan Reijngoud, & Francjan J. van Spronsen. (2009). Pathogenesis of cognitive dysfunction in phenylketonuria: Review of hypotheses☆. Molecular Genetics and Metabolism. 99. S86–S89. 164 indexed citations

13.

Groot, Martijn J. de, Will A. Coumans, P. H. M. Willemsen, & Ger J. Vusse. (1993). Substrate-induced changes in the lipid content of ischemic and reperfused myocardium. Its relation to hemodynamic recovery.. Circulation Research. 72(1). 176–186. 22 indexed citations

14.

Bilsen, Marc van, et al.. (1989). Degradation of adenine nucleotides in ischemic and reperfused rat heart. American Journal of Physiology-Heart and Circulatory Physiology. 257(1). H47–H54. 23 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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