Kees Schoonderwoerd

1.5k total citations
41 papers, 1.0k citations indexed

About

Kees Schoonderwoerd is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Kees Schoonderwoerd has authored 41 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 9 papers in Biochemistry. Recurrent topics in Kees Schoonderwoerd's work include Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (11 papers) and Lipid metabolism and biosynthesis (8 papers). Kees Schoonderwoerd is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (11 papers) and Lipid metabolism and biosynthesis (8 papers). Kees Schoonderwoerd collaborates with scholars based in Netherlands, United States and Germany. Kees Schoonderwoerd's co-authors include Hans Jansen, I.F.M. de Coo, Hubert J.M. Smeets, H. Stam, Willem C. Hülsmann, W.C. Hülsmann, Wim J. Sluiter, Alexandra T.M. Hendrickx, Mike Gerards and B.J.C. van den Bosch and has published in prestigious journals such as Blood, Circulation Research and Brain.

In The Last Decade

Kees Schoonderwoerd

41 papers receiving 981 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kees Schoonderwoerd Netherlands 20 558 305 202 159 129 41 1.0k
Naotaka Sekiguchi Japan 10 250 0.4× 164 0.5× 113 0.6× 285 1.8× 36 0.3× 22 803
P. H. M. Willemsen Netherlands 19 907 1.6× 104 0.3× 514 2.5× 431 2.7× 116 0.9× 25 1.3k
Brett O. Schönekess Canada 10 724 1.3× 163 0.5× 685 3.4× 347 2.2× 65 0.5× 14 1.3k
Masahiro Okouchi Japan 15 331 0.6× 94 0.3× 92 0.5× 167 1.1× 50 0.4× 20 883
Susanna Petrosyan United States 7 921 1.7× 125 0.4× 102 0.5× 328 2.1× 67 0.5× 11 1.3k
Irena Duka United States 10 304 0.5× 93 0.3× 245 1.2× 89 0.6× 28 0.2× 12 994
Jodil Willems Netherlands 15 855 1.5× 60 0.2× 361 1.8× 411 2.6× 81 0.6× 19 1.2k
Vera Schultz United States 18 629 1.1× 75 0.2× 122 0.6× 250 1.6× 47 0.4× 22 1.0k
Katharina Völker Germany 14 370 0.7× 54 0.2× 258 1.3× 127 0.8× 105 0.8× 32 726
Rosa Bretón‐Romero United States 16 429 0.8× 49 0.2× 184 0.9× 252 1.6× 81 0.6× 22 875

Countries citing papers authored by Kees Schoonderwoerd

Since Specialization
Citations

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

Fields of papers citing papers by Kees Schoonderwoerd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kees Schoonderwoerd

This figure shows the co-authorship network connecting the top 25 collaborators of Kees Schoonderwoerd. A scholar is included among the top collaborators of Kees Schoonderwoerd 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 Kees Schoonderwoerd. Kees Schoonderwoerd 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.
Gavrilov, Dimitar, et al.. (2019). Clinical, biochemical and molecular characteristics of malonyl-CoA decarboxylase deficiency and long-term follow-up of nine patients. Molecular Genetics and Metabolism. 128(1-2). 113–121. 6 indexed citations
2.
Kamps, Rick, Radek Szklarczyk, Tom E. J. Theunissen, et al.. (2018). Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease. European Journal of Human Genetics. 26(4). 537–551. 22 indexed citations
3.
Theunissen, Tom E. J., Rick Kamps, Alexandra T.M. Hendrickx, et al.. (2018). Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause. Frontiers in Genetics. 9. 400–400. 62 indexed citations
4.
Theunissen, Tom E. J., Suzanne C.E.H. Sallevelt, Debby M.E.I. Hellebrekers, et al.. (2017). Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome Sequencing. The Journal of Pediatrics. 182. 371–374.e2. 6 indexed citations
5.
Theunissen, Tom E. J., Mike Gerards, Debby M.E.I. Hellebrekers, et al.. (2017). Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect. Frontiers in Molecular Neuroscience. 10. 336–336. 7 indexed citations
6.
Verma, Jyotsna, Divya C. Thomas, Kwang‐Jen Hsiao, et al.. (2015). Inherited metabolic disorders: Quality management for laboratory diagnosis. Clinica Chimica Acta. 447. 1–7. 7 indexed citations
7.
Gerards, Mike, Rick Kamps, Bart de Koning, et al.. (2013). Exome sequencing reveals a novel Moroccan founder mutation inSLC19A3as a new cause of early-childhood fatal Leigh syndrome. Brain. 136(3). 882–890. 69 indexed citations
8.
Westermann, C.M., L. Dorland, O. P. van Diggelen, et al.. (2011). Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD. Molecular Genetics and Metabolism. 104(3). 273–278. 15 indexed citations
9.
Bijvelds, Marcel J. C., Alex L. Nigg, Kees Schoonderwoerd, et al.. (2007). Cholesterol Depletion and Genistein as Tools to Promote F508delCFTR Retention at the Plasma Membrane. Cellular Physiology and Biochemistry. 20(5). 473–482. 15 indexed citations
10.
Spruijt, Liesbeth, Hubert Smeets, Alexandra T.M. Hendrickx, et al.. (2007). A MELAS-Associated ND1 Mutation Causing Leber Hereditary Optic Neuropathy and Spastic Dystonia. Archives of Neurology. 64(6). 890–890. 41 indexed citations
11.
Liem, David, Olivier C. Manintveld, Kees Schoonderwoerd, et al.. (2007). Ischemic preconditioning modulates mitochondrial respiration, irrespective of the employed signal transduction pathway. Translational research. 151(1). 17–26. 23 indexed citations
12.
Blok, Marinus J., Liesbeth Spruijt, I.F.M. de Coo, et al.. (2007). Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. Journal of Medical Genetics. 44(4). e74–e74. 49 indexed citations
13.
Schoonderwoerd, Kees, et al.. (2006). Regulation of the cell swelling‐activated chloride conductance by cholesterol‐rich membrane domains. Acta Physiologica. 187(1-2). 295–303. 15 indexed citations
14.
Coo, I.F.M. de, Osama Soliman, Folkert J. ten Cate, et al.. (2006). Cardiac Involvement in Adults With m.3243A>G MELAS Gene Mutation. The American Journal of Cardiology. 99(2). 264–269. 56 indexed citations
15.
Jacobs, L.J.A.M., I.F.M. de Coo, Jeroen G. Nijland, et al.. (2004). Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation. Molecular Human Reproduction. 11(3). 223–228. 31 indexed citations
16.
McFalls, Edward O., David Liem, Kees Schoonderwoerd, et al.. (2003). Mitochondrial function: the heart of myocardial preservation. Journal of Laboratory and Clinical Medicine. 142(3). 141–148. 21 indexed citations
17.
Schoonderwoerd, Kees & H. Stam. (1992). Lipid metabolism of myocardial endothelial cells. Molecular and Cellular Biochemistry. 116(1-2). 171–179. 9 indexed citations
18.
Schoonderwoerd, Kees, et al.. (1989). Enhanced lipolysis of myocardial triglycerides during low-flow ischemia and anoxia in the isolated rat heart. Basic Research in Cardiology. 84(2). 165–173. 29 indexed citations
19.
Stam, H., Kees Schoonderwoerd, & W.C. Hülsmann. (1987). Synthesis, storage and degradation of myocardial triglycerides. Steinkopff eBooks. 82 Suppl 1. 19–28. 17 indexed citations
20.
Schoonderwoerd, Kees, et al.. (1987). Stimulation of myocardial neutral triglyceride lipase activity by adenosine-3’:5’-monophosphate: involvement of glycogenolysis. Steinkopff eBooks. 82 Suppl 1. 29–35. 8 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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