François Eyskens

1.7k total citations
38 papers, 779 citations indexed

About

François Eyskens is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, François Eyskens has authored 38 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Physiology, 16 papers in Molecular Biology and 16 papers in Clinical Biochemistry. Recurrent topics in François Eyskens's work include Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (10 papers) and Diet and metabolism studies (6 papers). François Eyskens is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Lysosomal Storage Disorders Research (10 papers) and Diet and metabolism studies (6 papers). François Eyskens collaborates with scholars based in Belgium, United Kingdom and Netherlands. François Eyskens's co-authors include Rudy Van Coster, Joél Smet, Sara Seneca, Willy Lissens, E. Gerlo, Inge De Clercq, Linda De Meırleır, Dirk Van West, Günter Scheuerbrandt and Stuart J. Moat and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biochemical Journal.

In The Last Decade

François Eyskens

35 papers receiving 764 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
François Eyskens Belgium 17 462 331 158 94 83 38 779
Joy Yaplito‐Lee Australia 17 653 1.4× 575 1.7× 193 1.2× 144 1.5× 78 0.9× 29 1.1k
Emma Footitt United Kingdom 17 387 0.8× 412 1.2× 92 0.6× 78 0.8× 126 1.5× 29 735
Ubaldo Caruso Italy 15 349 0.8× 338 1.0× 136 0.9× 48 0.5× 89 1.1× 21 662
J. M. Saudubray France 18 717 1.6× 615 1.9× 164 1.0× 73 0.8× 84 1.0× 49 1.0k
María Teresa García‐Silva Spain 12 392 0.8× 234 0.7× 83 0.5× 71 0.8× 80 1.0× 24 595
Zuhair N. Al‐Hassnan Saudi Arabia 18 549 1.2× 291 0.9× 166 1.1× 248 2.6× 57 0.7× 78 1.0k
François‐Guillaume Debray Belgium 14 305 0.7× 211 0.6× 84 0.5× 84 0.9× 25 0.3× 26 507
Elena Martín‐Hernández Spain 16 408 0.9× 331 1.0× 77 0.5× 97 1.0× 52 0.6× 41 596
Daniela Verrigni Italy 17 484 1.0× 210 0.6× 102 0.6× 32 0.3× 46 0.6× 25 715
Ángela Arias Spain 18 290 0.6× 278 0.8× 146 0.9× 74 0.8× 83 1.0× 31 673

Countries citing papers authored by François Eyskens

Since Specialization
Citations

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

Fields of papers citing papers by François Eyskens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of François Eyskens

This figure shows the co-authorship network connecting the top 25 collaborators of François Eyskens. A scholar is included among the top collaborators of François Eyskens 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 François Eyskens. François Eyskens 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.
2.
Bruyndonckx, Luc, et al.. (2023). Severe dilated cardiomyopathy as an unusual clinical presentation in an infant with sialidosis type II. JIMD Reports. 64(2). 156–160. 2 indexed citations
3.
Eyskens, François, et al.. (2021). Vertebral Tongue-Like Deformity in Mucopolysaccharidosis VI. SHILAP Revista de lepidopterología. 105(1). 54–54.
4.
Yperzeele, Laetitia, et al.. (2018). Galactosidase Alpha p.A143T Variant Fabry Disease May Result in a Phenotype With Multifocal Microvascular Cerebral Involvement at a Young Age. Frontiers in Neurology. 9. 336–336. 11 indexed citations
5.
Muntau, Ania C., Alberto Burlina, François Eyskens, et al.. (2017). Efficacy, safety and population pharmacokinetics of sapropterin in PKU patients <4 years: results from the SPARK open-label, multicentre, randomized phase IIIb trial. Orphanet Journal of Rare Diseases. 12(1). 47–47. 29 indexed citations
6.
Jahja, Rianne, Stephan C. J. Huijbregts, Anne Daly, et al.. (2016). Neurocognitive outcome in tyrosinemia type 1 patients compared to healthy controls. Orphanet Journal of Rare Diseases. 11(1). 87–87. 54 indexed citations
7.
Welling, Lindsey, Sandra C. Van Calcar, Artemis Doulgeraki, et al.. (2016). Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis. JIMD Reports. 35. 87–96. 17 indexed citations
8.
Eyskens, François, et al.. (2014). Long-term follow-up on the effect of combined therapy of bile acids and statins in the treatment of cerebrotendinous xanthomatosis: A case report. Clinical Neurology and Neurosurgery. 118. 9–11. 19 indexed citations
9.
Bolar, Nikhita, Arnaud Vanlander, Nathalie Van der Aa, et al.. (2013). Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy. Human Molecular Genetics. 22(13). 2590–2602. 90 indexed citations
10.
Bulcke, Tim Van den, Viviane Van Hoof, Kristien Wouters, et al.. (2010). Data mining methods for classification of Medium-Chain Acyl-CoA dehydrogenase deficiency (MCADD) using non-derivatized tandem MS neonatal screening data. Journal of Biomedical Informatics. 44(2). 319–325. 19 indexed citations
11.
Roels, Frank, Patrick Verloo, François Eyskens, et al.. (2009). Mitochondrial mosaics in the liver of 3 infants with mtDNA defects. BMC Clinical Pathology. 9(1). 4–4. 12 indexed citations
12.
Boudewyns, An, Frank Declau, Koenraad Smets, et al.. (2009). Cytomegalovirus DNA Detection in Guthrie Cards. Otology & Neurotology. 30(7). 943–949. 21 indexed citations
13.
Eyskens, François. (2009). RARE INBORN ERRORS OF METABOLISM IN ADULTS: THE LYSOSOMAL STORAGE DISORDERS. Acta Clinica Belgica. 64(6). 534–539. 2 indexed citations
14.
Ebberink, Merel S., P. A. W. Mooyer, Janet Koster, et al.. (2008). Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines. Human Mutation. 30(1). 93–98. 16 indexed citations
15.
Bever, Yolande van, Wendy Balemans, E Duval, et al.. (2007). Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome. American Journal of Medical Genetics Part A. 143A(7). 763–767. 5 indexed citations
16.
Jaeken, Jaak, Kevin Martens, Inge François, et al.. (2005). Deletion of PREPL, a Gene Encoding a Putative Serine Oligopeptidase, in Patients with Hypotonia-Cystinuria Syndrome. The American Journal of Human Genetics. 78(1). 38–51. 61 indexed citations
17.
Meırleır, Linda De, Sara Seneca, Willy Lissens, et al.. (2004). Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12. Journal of Medical Genetics. 41(2). 120–124. 143 indexed citations
18.
Roels, Frank, Jean‐Marie Saudubray, M. Girós, et al.. (2003). Peroxisome Mosaics. Advances in experimental medicine and biology. 544. 97–106. 7 indexed citations
19.
Gootjes, Jeannette, Orly Elpeleg, François Eyskens, et al.. (2003). Novel Mutations in the PEX2 Gene of Four Unrelated Patients with a Peroxisome Biogenesis Disorder. Pediatric Research. 55(3). 431–436. 16 indexed citations
20.
Acker, K. J. Van, François Eyskens, Robert Verkerk, & Simon Scharpé. (1993). Urinary Excretion of Purine and Pyrimidine Metabolites in the Neonate. Pediatric Research. 34(6). 762–766. 9 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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