Rudy N. Van Coster

1.6k total citations
18 papers, 723 citations indexed

About

Rudy N. Van Coster is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Rudy N. Van Coster has authored 18 papers receiving a total of 723 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 4 papers in Clinical Biochemistry. Recurrent topics in Rudy N. Van Coster's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Rudy N. Van Coster is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Rudy N. Van Coster collaborates with scholars based in Belgium, United States and Germany. Rudy N. Van Coster's co-authors include J M De Smet, Keijo Mattila, Karin Thelen, Juha Laakso, Dieter Lütjohann, Hannu Päivä, Terho Lehtimäki, Boél De Paepe, Wilhelm Breuer and Ernst Bause and has published in prestigious journals such as Neurology, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Rudy N. Van Coster

18 papers receiving 701 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rudy N. Van Coster Belgium	13	434	151	111	109	98	18	723
A.J. Aarsman Netherlands	16	614 1.4×	128 0.8×	151 1.4×	169 1.6×	32 0.3×	22	1.0k
Bernice H. Wong Singapore	14	713 1.6×	109 0.7×	62 0.6×	79 0.7×	25 0.3×	21	1.1k
Stanley J. Wertheimer United States	12	449 1.0×	72 0.5×	43 0.4×	99 0.9×	33 0.3×	19	888
Marcella Marcellini Italy	15	405 0.9×	73 0.5×	33 0.3×	66 0.6×	192 2.0×	16	905
L.W. Estes United States	7	219 0.5×	265 1.8×	117 1.1×	46 0.4×	44 0.4×	9	563
Akira Kamei Japan	18	399 0.9×	231 1.5×	81 0.7×	118 1.1×	11 0.1×	89	923
Thomas Schlüter Germany	18	298 0.7×	102 0.7×	130 1.2×	64 0.6×	27 0.3×	28	786
Voraratt Champattanachai Thailand	17	826 1.9×	63 0.4×	96 0.9×	75 0.7×	299 3.1×	37	1.1k
P. Kölle Germany	9	557 1.3×	56 0.4×	38 0.3×	47 0.4×	27 0.3×	14	925
Matthew J. Toth United States	17	1.0k 2.4×	134 0.9×	47 0.4×	153 1.4×	15 0.2×	20	1.3k

Countries citing papers authored by Rudy N. Van Coster

Since Specialization

Citations

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

Fields of papers citing papers by Rudy N. Van Coster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rudy N. Van Coster. 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 Rudy N. Van Coster. The network helps show where Rudy N. Van Coster may publish in the future.

Co-authorship network of co-authors of Rudy N. Van Coster

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

All Works

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18 of 18 papers shown

Celie, Bert, An Mariman, Jan Boone, et al.. (2018). Near-Infrared Spectroscopy Screening to Allow Detection of Pathogenic Mitochondrial DNA Variants in Individuals with Unexplained Abnormal Fatigue: A Preliminary Study. Applied Spectroscopy. 72(5). 715–724. 1 indexed citations

Celie, Bert, Jan Boone, Joél Smet, et al.. (2015). Forearm Deoxyhemoglobin and Deoxymyoglobin (Deoxy[Hb + Mb]) Measured by Near-Infrared Spectroscopy (NIRS) Using a Handgrip Test in Mitochondrial Myopathy. Applied Spectroscopy. 69(3). 342–347. 13 indexed citations

Zecic, Alexandra, Joél Smet, Piet Vanhaesebrouck, et al.. (2009). Lactic Acidosis in a Newborn With Adrenal Calcifications. Pediatric Research. 66(3). 317–322. 3 indexed citations

Verhelst, Hélène, et al.. (2008). Hippocampal atrophy and developmental regression as first sign of linear scleroderma “en coup de sabre”. European Journal of Paediatric Neurology. 12(6). 508–511. 14 indexed citations

Engelke, Udo F. H., Jörn Oliver Sass, Rudy N. Van Coster, et al.. (2007). NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism. NMR in Biomedicine. 21(2). 138–147. 37 indexed citations

Päivä, Hannu, Karin Thelen, Rudy N. Van Coster, et al.. (2005). High-dose statins and skeletal muscle metabolism in humans: A randomized, controlled trial. Clinical Pharmacology & Therapeutics. 78(1). 60–68. 249 indexed citations

Coster, Rudy N. Van, E. Gerlo, Thierry Giardina, et al.. (2005). Aminoacylase I deficiency: A novel inborn error of metabolism. Biochemical and Biophysical Research Communications. 338(3). 1322–1326. 44 indexed citations

Volker, C., et al.. (2002). Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb). Glycobiology. 12(8). 473–483. 36 indexed citations

Leroy, Jules G., Raili Seppälä, Marjan Huizing, et al.. (2001). Dominant Inheritance of Sialuria, an Inborn Error of Feedback Inhibition. The American Journal of Human Genetics. 68(6). 1419–1427. 41 indexed citations

10.

Gerwig, Gerrit J., Ernst Bause, Lieve Nuytinck, et al.. (2000). A Novel Disorder Caused by Defective Biosynthesis of N-Linked Oligosaccharides Due to Glucosidase I Deficiency. The American Journal of Human Genetics. 66(6). 1744–1756. 139 indexed citations

11.

Loeys, Bart, Rudy N. Van Coster, Luc Defreyne, & J. G. Leroy. (1999). Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis. European Journal of Pediatrics. 158(8). 650–652. 21 indexed citations

12.

Vanzieleghem, Bart, Marc Lemmerling, & Rudy N. Van Coster. (1999). Neurocutaneous melanosis presenting with intracranial amelanotic melanoma.. PubMed. 20(3). 457–60. 37 indexed citations

13.

Coster, Rudy N. Van, Sandra Janssens, Jean‐Paul Misson, Alain Verloès, & J. G. Leroy. (1998). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Prenatal Diagnosis. 18(10). 1041–1044. 10 indexed citations

14.

Coster, Rudy N. Van, et al.. (1998). MRI findings in a neonate with cerebellar agenesis. Pediatric Neurology. 19(2). 139–142. 6 indexed citations

15.

Coster, Rudy N. Van, et al.. (1996). Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome. American Journal of Medical Genetics. 65(3). 205–208. 5 indexed citations

16.

Fujii, Tatsuya, Rudy N. Van Coster, R. Medori, et al.. (1994). Pyruvate dehydrogenase deficiency: Molecular basis for intrafamilial heterogeneity. Annals of Neurology. 36(1). 83–89. 17 indexed citations

17.

Coster, Rudy N. Van, Paul M. Fernhoff, & Darryl C. De Vivo. (1991). Pyruvate Carboxylase Deficiency: A Benign Variant with Normal Development. Pediatric Research. 30(1). 1–4. 37 indexed citations

18.

Coster, Rudy N. Van, et al.. (1991). Adult Reye's syndrome. Neurology. 41(11). 1815–1815. 13 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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