J Jaeken

1.0k citations
19 papers · 760 indexed · h-index 11
Topics
Genomic variations and chromosomal abnormalities (7 papers)Metabolism and Genetic Disorders (5 papers)Lysosomal Storage Disorders Research (4 papers)

In The Last Decade

J Jaeken

19 papers receiving 742 citations

Peers

J Jaeken
Comparison fields: 5 of 71
  • Molecular Biology 421
  • Clinical Biochemistry 194
  • Physiology 162
  • Biochemistry 147
  • Genetics 146
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Citations per field
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Citations per year

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

19 of 19 papers shown
#WorkIndexed citations
1 30
2 58
3 45
4 10
5 9
6 30
7 34
8 135
9 127
10
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.
5
11
Trisomy 3q2 and Pierre-Robin sequence in a boy with unbalanced 46,XY, der(10), t(3;10)(q23;q26.3) de novo karyotype.
4
12
Complex chromosomal rearrangement involving chromosomes 11, 13 and 21.
5
13
Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.
7
14 21
15
An Infantile Autistic Syndrome Characterized By the Presence of Succinyl Purines in Body-fluids
196
16 25
17
De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24).
15
18
Partial trisomy 22q with elevated arylsulfatase-A activity.
2
19
Primperan and its side-effects.
2

About J Jaeken

J Jaeken is a scholar working on Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 19 papers that have together received 760 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Metabolism and Genetic Disorders (5 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Clinical Biochemistry (194 citations), Biochemistry (147 citations) and Physiology (42 citations). J Jaeken has collaborated with scholars based in Belgium, Spain and United States. Frequent co-authors include Georges Berghe, Helena Stibler, Emile Van Schaftingen, Lionel Van Maldergem, Hubert Carchon, Michel Detheux, W.F.M. Arts, Ans T. van der Ploeg, E. Eggermont and Fryns Jp. Their work appears in journals such as The Lancet, Neurology and Archives of Disease in Childhood.

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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