J. Jaeken

3.9k total citations
90 papers, 2.8k citations indexed

About

J. Jaeken is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, J. Jaeken has authored 90 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 27 papers in Physiology and 26 papers in Clinical Biochemistry. Recurrent topics in J. Jaeken's work include Glycosylation and Glycoproteins Research (26 papers), Metabolism and Genetic Disorders (26 papers) and Lysosomal Storage Disorders Research (19 papers). J. Jaeken is often cited by papers focused on Glycosylation and Glycoproteins Research (26 papers), Metabolism and Genetic Disorders (26 papers) and Lysosomal Storage Disorders Research (19 papers). J. Jaeken collaborates with scholars based in Belgium, Netherlands and United States. J. Jaeken's co-authors include R. Eeckels, C. Jakobs, E. Eggermont, L Corbeel, K. Michael Gibson, Bengt Hagberg, Paul Casaer, Gert Matthijs, Helena Stibler and H.G. van Eijk and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Neurology.

In The Last Decade

J. Jaeken

87 papers receiving 2.7k citations

Author Peers

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

Author Last Decade Papers Cites
J. Jaeken 2.0k 649 606 467 427 90 2.8k
Paz Briones 2.1k 1.1× 420 0.6× 896 1.5× 245 0.5× 145 0.3× 70 2.7k
Belén Pérez 2.6k 1.3× 618 1.0× 2.0k 3.3× 412 0.9× 163 0.4× 160 3.5k
Saskia B. Wortmann 1.9k 0.9× 302 0.5× 1.0k 1.7× 539 1.2× 66 0.2× 122 2.7k
Lourdes R. Desviat 2.7k 1.4× 567 0.9× 2.1k 3.5× 415 0.9× 107 0.3× 154 3.7k
Kunihiko Suzuki 2.1k 1.1× 1.6k 2.4× 223 0.4× 101 0.2× 475 1.1× 56 3.1k
Magdalena Ugarte 3.3k 1.7× 753 1.2× 2.9k 4.8× 464 1.0× 143 0.3× 218 4.7k
Rohini Sidhu 1.3k 0.6× 1.1k 1.7× 114 0.2× 105 0.2× 289 0.7× 39 2.7k
Manuel Schiff 1.3k 0.7× 380 0.6× 870 1.4× 255 0.5× 33 0.1× 115 2.3k
Barbara Karten 1.0k 0.5× 822 1.3× 141 0.2× 150 0.3× 216 0.5× 34 2.2k
Hana Hansíková 1.6k 0.8× 291 0.4× 519 0.9× 197 0.4× 64 0.1× 131 2.0k

Countries citing papers authored by J. Jaeken

Since Specialization
Citations

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

Fields of papers citing papers by J. Jaeken

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Jaeken

This figure shows the co-authorship network connecting the top 25 collaborators of J. Jaeken. A scholar is included among the top collaborators of J. Jaeken 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 J. Jaeken. J. Jaeken 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.
Quelhas, Dulce, J. Jaeken, Ana María Fortuna, et al.. (2018). RFT1-CDG: Absence of Epilepsy and Deafness in Two Patients with Novel Pathogenic Variants. JIMD Reports. 43. 111–116. 5 indexed citations
2.
Régal, Luc, Peter M. van Hasselt, François Foulquier, et al.. (2014). ALG11-CDG: Three novel mutations and further characterization of the phenotype. Molecular Genetics and Metabolism Reports. 2. 16–19. 14 indexed citations
3.
Jaeken, J.. (2013). Congenital disorders of glycosylation. Handbook of clinical neurology. 113. 1737–1743. 75 indexed citations
4.
Tümer, Leyla, Fatih Süheyl Ezgü, Alev Hasanoğlu, et al.. (2012). SRD5A3-CDG: A patient with a novel mutation. European Journal of Paediatric Neurology. 16(5). 554–556. 25 indexed citations
5.
Guelbert, Norberto, Luisa Sturiale, Domenico Garozzo, et al.. (2011). Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?. JIMD Reports. 1. 65–72. 6 indexed citations
6.
Keldermans, Liesbeth, et al.. (2009). Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient. Glycobiology. 19(8). 910–917. 19 indexed citations
7.
Jaeken, J., et al.. (2008). Clinical and biochemical features in a Congolese infant with congenital disorder of glycosylation (CDG)-IIx. European Journal of Paediatric Neurology. 12(3). 257–261. 4 indexed citations
8.
Zeevaert, Renate, François Foulquier, Boyan Dimitrov, et al.. (2008). Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1. Human Molecular Genetics. 18(3). 517–524. 40 indexed citations
9.
Hagemans, M.L.C., et al.. (2007). Enzymatic replacement therapy with rhGAA in Brazilian Pompe patients. Neuromuscular Disorders. 17(9). 887.
10.
Hagemans, M.L.C., et al.. (2007). M.P.5.01 Two years follow-up of enzyme therapy in five children with Pompe disease. Neuromuscular Disorders. 17(9-10). 887–887.
11.
12.
Koning, Tom J. de, J. Jaeken, M. Pineda, et al.. (2000). Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency. Neuropediatrics. 31(6). 287–292. 54 indexed citations
13.
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
14.
Garel, Cathérine, et al.. (1998). Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex. Skeletal Radiology. 27(1). 43–45. 21 indexed citations
15.
Burda, Patricie, Lubor Borsig, Ron A. Wevers, et al.. (1998). A novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharide.. Journal of Clinical Investigation. 102(4). 647–652. 74 indexed citations
16.
Burgemeister, Renate, Wolf Gutensohn, Greet Van den Berghe, & J. Jaeken. (1995). Genetic and Clinical Heterogeneity in Hypoxanthine Phosphoribosyltransferase Deficiencies. Advances in experimental medicine and biology. 370. 331–335. 3 indexed citations
17.
Jaeken, J.. (1994). Cerebrospinal fluid as a tool in the diagnosis of neurometabolic diseases: amino acid analysis before and after acid hydrolysis. European Journal of Pediatrics. 153(S1). S86–S89. 4 indexed citations
18.
Devlieger, H., J. Jaeken, Ph. Moerman, et al.. (1994). Intractable asphyxia at birth: analysis of the underlying conditions. European Journal of Obstetrics & Gynecology and Reproductive Biology. 54(1). 21–24. 1 indexed citations
19.
Beckers, Christian, et al.. (1987). Iodine Intake of Breast-fed Versus Bottle-fed Healthy Newborns and Prematures. Annales d Endocrinologie. 48(2). 166–166. 3 indexed citations
20.
Jaeken, J., et al.. (1982). Fisher syndrome in childhood. Neurology. 32(9). 1075–1075. 1 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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