J Jaeken

1.0k total citations
19 papers, 760 citations indexed

About

J Jaeken is a scholar working on Genetics, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, J Jaeken has authored 19 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 5 papers in Clinical Biochemistry and 4 papers in Molecular Biology. Recurrent topics in J Jaeken's work include Genomic variations and chromosomal abnormalities (7 papers), Metabolism and Genetic Disorders (5 papers) and Lysosomal Storage Disorders Research (4 papers). J Jaeken is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Metabolism and Genetic Disorders (5 papers) and Lysosomal Storage Disorders Research (4 papers). J Jaeken collaborates with scholars based in Belgium, Spain and United States. J Jaeken's co-authors include Georges Berghe, Helena Stibler, Emile Van Schaftingen, Michel Detheux, Hubert Carchon, Lionel Van Maldergem, Ans T. van der Ploeg, W.F.M. Arts, Fryns Jp and E. Eggermont and has published in prestigious journals such as The Lancet, Neurology and Archives of Disease in Childhood.

In The Last Decade

J Jaeken

19 papers receiving 742 citations

Author Peers

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

Author						Papers	Cites
J Jaeken	421	194	162	147	146	19	760
Shlomo Almashanu	390 0.9×	271 1.4×	128 0.8×	88 0.6×	136 0.9×	45	838
Lock Hock Ngu	503 1.2×	299 1.5×	181 1.1×	62 0.4×	242 1.7×	59	899
N. U. Bosshard	338 0.8×	149 0.8×	446 2.8×	65 0.4×	163 1.1×	27	972
Clare Beesley	288 0.7×	189 1.0×	607 3.7×	83 0.6×	108 0.7×	29	980
Jakub Sikora	507 1.2×	71 0.4×	487 3.0×	83 0.6×	69 0.5×	48	1.1k
Maja Di Rocco	212 0.5×	122 0.6×	131 0.8×	124 0.8×	69 0.5×	20	459
Rosanna Gatti	298 0.7×	55 0.3×	422 2.6×	35 0.2×	140 1.0×	35	808
Daniel Beltrán-Valero de Bernabé	743 1.8×	360 1.9×	138 0.9×	135 0.9×	106 0.7×	16	972
Laura Gort	629 1.5×	247 1.3×	758 4.7×	61 0.4×	104 0.7×	67	1.3k
María Josep Coll	370 0.9×	158 0.8×	703 4.3×	33 0.2×	68 0.5×	37	1.1k

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

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19 of 19 papers shown

Mehta, Nitesh R., Valérie Race, François Foulquier, et al.. (2015). Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG. Glycobiology. 25(6). 669–682. 30 indexed citations

Aarsen, Femke K., Carin M. Van Gelder, Johanna M. P. van den Hout, et al.. (2012). Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy. Neurology. 78(19). 1512–1518. 58 indexed citations

Capelle, Carine I. van, Nadine A. M. E. van der Beek, M.L.C. Hagemans, et al.. (2010). Effect of enzyme therapy in juvenile patients with Pompe disease: A three-year open-label study. Neuromuscular Disorders. 20(12). 775–782. 45 indexed citations

Cassiman, David, Kathleen Claes, Raymond Oyen, et al.. (2007). Bilateral renal cell carcinoma development in long‐term Fabry disease. Journal of Inherited Metabolic Disease. 30(5). 830–831. 10 indexed citations

Pineda, M., Marina Vilaseca, Rafael Artuch, et al.. (2000). 3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome. Developmental Medicine & Child Neurology. 42(9). 629–633. 30 indexed citations

Pineda, M., Marina Vilaseca, Rafael Artuch, et al.. (2000). 3‐phosphoglycerate dehydrogenase deficiency in a patient with West syndrome. Developmental Medicine & Child Neurology. 42(9). 629–633. 9 indexed citations

Hove, Johan L.K. Van, Priya S. Kishnani, Philippe Demaerel, et al.. (2000). Acute hydrocephalus in nonketotic hyperglycinemia. Neurology. 54(3). 754–754. 34 indexed citations

Jaeken, J, et al.. (1996). 3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis.. Archives of Disease in Childhood. 74(6). 542–545. 135 indexed citations

Stibler, Helena & J Jaeken. (1990). Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.. Archives of Disease in Childhood. 65(1). 107–111. 127 indexed citations

10.

Jp, Fryns, et al.. (1989). Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.. PubMed. 32(3). 177–9. 5 indexed citations

11.

Kleczkowska, A, et al.. (1988). Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype.. PubMed. 43(3). 245–8. 4 indexed citations

12.

Kleczkowska, A., et al.. (1988). Complex chromosomal rearrangement involving chromosomes 11, 13 and 21.. PubMed. 31(2). 126–8. 5 indexed citations

13.

Kleczkowska, A, et al.. (1987). Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.. PubMed. 30(1). 47–51. 7 indexed citations

14.

Eyssen, H., E. Eggermont, J. Van Eldere, et al.. (1985). Bile Acid Abnormalities and the Diagnosis of Cerebro‐Hepato‐Renal Syndrome (Zellweger Syndrome). Acta Paediatrica. 74(4). 539–544. 21 indexed citations

15.

Jaeken, J & Georges Berghe. (1984). An Infantile Autistic Syndrome Characterized By the Presence of Succinyl Purines in Body-fluids. The Lancet. 2(8411). 1058–1061. 196 indexed citations

16.

Fryns, J. P., M Azou, J Jaeken, et al.. (1981). Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency. Human Genetics. 57(1). 108–110. 25 indexed citations

17.

Jaeken, J, et al.. (1980). De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).. PubMed. 23(2). 105–7. 15 indexed citations

18.

Jp, Fryns, et al.. (1979). Partial trisomy 22q with elevated arylsulfatase-A activity.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 168–70. 2 indexed citations

19.

Daele, Maria Casteels‐Van & J Jaeken. (1971). Primperan and its side-effects.. PubMed. 14(3). 205–15. 2 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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