T. de Koning

448 total citations
6 papers, 225 citations indexed

About

T. de Koning is a scholar working on Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, T. de Koning has authored 6 papers receiving a total of 225 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Clinical Biochemistry, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Physiology. Recurrent topics in T. de Koning's work include Metabolism and Genetic Disorders (5 papers), Amino Acid Enzymes and Metabolism (2 papers) and Diet and metabolism studies (2 papers). T. de Koning is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Amino Acid Enzymes and Metabolism (2 papers) and Diet and metabolism studies (2 papers). T. de Koning collaborates with scholars based in Netherlands, Latvia and United States. T. de Koning's co-authors include Ruud Berger, L. Dorland, Bwee Tien Poll‐The, F. A. Beemer, J. Jaeken, Ron A. Wevers, Leo A. J. Kluijtmans, Jan Smeıtınk, Marjan Huizing and Saskia B. Wortmann and has published in prestigious journals such as The Lancet, Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease.

In The Last Decade

T. de Koning

6 papers receiving 222 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. de Koning Netherlands	6	154	122	79	44	42	6	225
Ardeshir A. Monavari Ireland	7	219 1.4×	203 1.7×	50 0.6×	29 0.7×	50 1.2×	11	294
J.A.M. Smeitink Netherlands	10	218 1.4×	276 2.3×	48 0.6×	31 0.7×	31 0.7×	17	348
Lucy J. Otero United Kingdom	8	180 1.2×	308 2.5×	111 1.4×	49 1.1×	27 0.6×	8	415
Geralyn Creadon‐Swindell United States	6	205 1.3×	203 1.7×	107 1.4×	40 0.9×	37 0.9×	7	297
Cristiana Artiola Italy	9	226 1.5×	143 1.2×	36 0.5×	79 1.8×	39 0.9×	11	315
Jean Larochelle Canada	5	166 1.1×	95 0.8×	92 1.2×	66 1.5×	30 0.7×	7	248
C. Busquets Spain	7	95 0.6×	116 1.0×	27 0.3×	30 0.7×	10 0.2×	11	160
Vladimı́r Bzdúch Slovakia	8	65 0.4×	103 0.8×	41 0.5×	83 1.9×	26 0.6×	28	259
Corinne Gemperle-Britschgi Switzerland	6	62 0.4×	87 0.7×	22 0.3×	22 0.5×	17 0.4×	8	152
Iria Roca Spain	11	165 1.1×	147 1.2×	18 0.2×	109 2.5×	44 1.0×	13	295

Countries citing papers authored by T. de Koning

Since Specialization

Citations

This map shows the geographic impact of T. de Koning'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 T. de Koning with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. de Koning more than expected).

Fields of papers citing papers by T. de Koning

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. de Koning. 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 T. de Koning. The network helps show where T. de Koning may publish in the future.

Co-authorship network of co-authors of T. de Koning

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

All Works

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6 of 6 papers shown

1.

Spronsen, Francjan J. van, M. van Rijn, Marieke Hoeksma, et al.. (2009). Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKU. Journal of Inherited Metabolic Disease. 32(1). 27–31. 31 indexed citations

2.

Wortmann, Saskia B., Richard J. Rodenburg, Marjan Huizing, et al.. (2006). Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation. Molecular Genetics and Metabolism. 88(1). 47–52. 45 indexed citations

3.

Koning, T. de, et al.. (2004). Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency. The Lancet. 364(9452). 2221–2222. 87 indexed citations

4.

Oudshoorn, Johanna H., et al.. (2004). Energy expenditure in patients with propionic and methylmalonic acidaemias. Journal of Inherited Metabolic Disease. 27(1). 111–112. 8 indexed citations

5.

Koning, T. de, Bwee Tien Poll‐The, & J. Jaeken. (1999). Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders. Neuropediatrics. 30(1). 1–4. 27 indexed citations

6.

Koning, T. de, Linda de Vries, Floris Groenendaal, et al.. (1999). Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects. Neuropediatrics. 30(2). 93–95. 27 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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