Ron A. Wevers

29.4k total citations · 1 hit paper
490 papers, 17.3k citations indexed

About

Ron A. Wevers is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Ron A. Wevers has authored 490 papers receiving a total of 17.3k indexed citations (citations by other indexed papers that have themselves been cited), including 281 papers in Molecular Biology, 137 papers in Clinical Biochemistry and 112 papers in Physiology. Recurrent topics in Ron A. Wevers's work include Metabolism and Genetic Disorders (137 papers), Lysosomal Storage Disorders Research (61 papers) and Glycosylation and Glycoproteins Research (59 papers). Ron A. Wevers is often cited by papers focused on Metabolism and Genetic Disorders (137 papers), Lysosomal Storage Disorders Research (61 papers) and Glycosylation and Glycoproteins Research (59 papers). Ron A. Wevers collaborates with scholars based in Netherlands, United States and Germany. Ron A. Wevers's co-authors include Udo F. H. Engelke, Baziel G.M. van Engelen, Éva Morava, Willy N. J. M. Colier, Mireille C. P. Van Beekvelt, Jan Smeıtınk, Dirk J. Lefeber, Ben J. H. M. Poorthuis, F.J.M. Gabreëls and J.G.N. de Jong and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of the American Chemical Society.

In The Last Decade

Ron A. Wevers

480 papers receiving 16.9k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The frequency of lysosomal storage diseases in The Netherlands

1999 522 citations Ron A. Wevers et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Ron A. Wevers	8.3k	3.9k	3.0k	2.2k	2.1k	490	17.3k
Vadivel Ganapathy	17.4k 2.1×	3.9k 1.0×	3.4k 1.2×	2.1k 1.0×	1.2k 0.6×	505	33.9k
Yau‐Huei Wei	13.3k 1.6×	2.7k 0.7×	3.1k 1.1×	1.5k 0.7×	719 0.3×	448	23.1k
Jan Smeıtınk	15.7k 1.9×	2.5k 0.6×	7.0k 2.4×	1.3k 0.6×	2.0k 1.0×	348	22.3k
Matthias A. Hediger	14.8k 1.8×	2.9k 0.8×	1.6k 0.5×	3.0k 1.4×	731 0.4×	256	33.5k
Hiroyuki Arai	15.2k 1.8×	6.6k 1.7×	828 0.3×	2.5k 1.2×	501 0.2×	489	29.2k
Toshiro Fujita	13.8k 1.7×	4.4k 1.1×	1.1k 0.4×	4.8k 2.2×	1.8k 0.9×	706	38.5k
Hiroshi Yamamoto	9.2k 1.1×	1.5k 0.4×	5.1k 1.7×	3.2k 1.5×	326 0.2×	710	24.1k
Salvatore DiMauro	23.0k 2.8×	3.2k 0.8×	12.6k 4.3×	1.2k 0.6×	3.1k 1.5×	408	29.6k
Yoshikatsu Kanai	13.3k 1.6×	1.7k 0.4×	3.8k 1.3×	1.7k 0.8×	641 0.3×	324	27.9k
Raymond C. Harris	8.6k 1.0×	2.5k 0.7×	859 0.3×	2.3k 1.1×	431 0.2×	334	22.5k

Countries citing papers authored by Ron A. Wevers

Since Specialization

Citations

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

Fields of papers citing papers by Ron A. Wevers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ron A. Wevers. 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 Ron A. Wevers. The network helps show where Ron A. Wevers may publish in the future.

Co-authorship network of co-authors of Ron A. Wevers

This figure shows the co-authorship network connecting the top 25 collaborators of Ron A. Wevers. A scholar is included among the top collaborators of Ron A. Wevers 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 Ron A. Wevers. Ron A. Wevers 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

Engelke, Udo F. H., Ruud L. E. G. Aspers, Jona Merx, et al.. (2025). Semi-Targeted Nuclear Magnetic Resonance Metabolomics via Parahydrogen-Induced Hyperpolarization for Enhanced Sensitivity to Metabolic Composition. Journal of the American Chemical Society. 147(36). 33185–33192.

Karnebeek, Clara D.M. van, Valérie Gailus‐Durner, Udo F. H. Engelke, et al.. (2025). New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse. Brain Communications. 7(6). fcaf397–fcaf397. 1 indexed citations

Glendorf, Tine, Antonius E. van Herwaarden, Hanka Venselaar, et al.. (2024). A rare homozygous INS variant causes adult-onset diabetes. BMJ Open Diabetes Research & Care. 12(6). e004418–e004418.

Houthuijs, Kas J., Rianne E. van Outersterp, Jonathan Martens, et al.. (2024). A spectroscopic test suggests that fragment ion structure annotations in MS/MS libraries are frequently incorrect. Communications Chemistry. 7(1). 30–30. 17 indexed citations

Vaz, Frédéric M., Jan B. van Klinken, Henk van Lenthe, et al.. (2024). Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1869(2). 159447–159447. 3 indexed citations

Jans, Judith, Vassiliki Konstantopoulou, René G. Feichtinger, et al.. (2023). PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening. Metabolites. 13(11). 1141–1141. 1 indexed citations

Outersterp, Rianne E. van, Jona Merx, Udo F. H. Engelke, et al.. (2023). Distinguishing Oligosaccharide Isomers Using Far-Infrared Ion Spectroscopy: Identification of Biomarkers for Inborn Errors of Metabolism. Analytical Chemistry. 95(26). 9787–9796. 3 indexed citations

Paperna, Tamar, Mario García‐Domínguez, Eric S. Shinwell, et al.. (2023). Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia. Journal of Medical Genetics. 60(11). 1133–1141. 6 indexed citations

Engelke, Udo F. H., Jean‐Baptiste Roullet, Sanne Broekman, et al.. (2023). Succinic semialdehyde dehydrogenase deficiency in mice and in humans: An untargeted metabolomics perspective. Journal of Inherited Metabolic Disease. 47(3). 417–430. 3 indexed citations

10.

Rumund, Anouke van, Lukas Pavelka, Rianne A.J. Esselink, et al.. (2021). Peripheral decarboxylase inhibitors paradoxically induce aromatic L-amino acid decarboxylase. npj Parkinson s Disease. 7(1). 29–29. 16 indexed citations

11.

Outersterp, Rianne E. van, Sam J. Moons, Udo F. H. Engelke, et al.. (2021). Amadori rearrangement products as potential biomarkers for inborn errors of amino-acid metabolism. Communications Biology. 4(1). 367–367. 23 indexed citations

12.

Outersterp, Rianne E. van, Udo F. H. Engelke, Jona Merx, et al.. (2021). Metabolite Identification Using Infrared Ion Spectroscopy─Novel Biomarkers for Pyridoxine-Dependent Epilepsy. Analytical Chemistry. 93(46). 15340–15348. 23 indexed citations

13.

Tinnevelt, Gerjen H., Udo F. H. Engelke, Ron A. Wevers, et al.. (2020). Variable Selection in Untargeted Metabolomics and the Danger of Sparsity. Metabolites. 10(11). 470–470. 5 indexed citations

14.

Dewulf, Joseph P., Elsa Wiame, Imen Dorboz, et al.. (2019). SLC13A3 variants cause acute reversible leukoencephalopathy and α‐ketoglutarate accumulation. Annals of Neurology. 85(3). 385–395. 19 indexed citations

15.

Martens, Jonathan, Giel Berden, Rianne E. van Outersterp, et al.. (2017). Molecular identification in metabolomics using infrared ion spectroscopy. Scientific Reports. 7(1). 59 indexed citations

16.

Rao, Jyotsna U., Udo F. H. Engelke, Richard J. Rodenburg, et al.. (2013). Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma. Clinical Cancer Research. 19(14). 3787–3795. 44 indexed citations

17.

Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2008). Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa. Medizinische Genetik. 20(1).

18.

Groenen, Pascal M.W., Petronella G.M. Peer, Ron A. Wevers, et al.. (2003). Maternal myo-inositol, glucose, and zinc status is associated with the risk of offspring with spina bifida. American Journal of Obstetrics and Gynecology. 189(6). 1713–1719. 81 indexed citations

19.

Moolenaar, Sytske H., Udo F. H. Engelke, Manfred Spraul, et al.. (2001). β‐Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine. Magnetic Resonance in Medicine. 46(5). 1014–1017. 43 indexed citations

20.

Wevers, Ron A., J.F. de Rijk-van Andel, Chad A. Brautigam, et al.. (1999). A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC). Journal of Inherited Metabolic Disease. 22(4). 364–373. 38 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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