Els Schollen

3.6k total citations
58 papers, 2.6k citations indexed

About

Els Schollen is a scholar working on Molecular Biology, Immunology and Organic Chemistry. According to data from OpenAlex, Els Schollen has authored 58 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 20 papers in Immunology and 16 papers in Organic Chemistry. Recurrent topics in Els Schollen's work include Glycosylation and Glycoproteins Research (34 papers), Galectins and Cancer Biology (19 papers) and Carbohydrate Chemistry and Synthesis (16 papers). Els Schollen is often cited by papers focused on Glycosylation and Glycoproteins Research (34 papers), Galectins and Cancer Biology (19 papers) and Carbohydrate Chemistry and Synthesis (16 papers). Els Schollen collaborates with scholars based in Belgium, Netherlands and United States. Els Schollen's co-authors include Gert Matthijs, Emile Van Schaftingen, Jaak Jaeken, Jean‐Jacques Cassiman, Eric Legius, Stephanie Grünewald, Maria Veiga‐da‐Cunha, Els Pardon, Koenraad Devriendt and Michel Pirard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Els Schollen

57 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Els Schollen Belgium 30 2.1k 676 604 540 530 58 2.6k
Torben Lübke Germany 22 985 0.5× 299 0.4× 311 0.5× 734 1.4× 162 0.3× 44 1.9k
Gerard Merkx Netherlands 25 1.6k 0.7× 336 0.5× 416 0.7× 71 0.1× 570 1.1× 52 2.2k
Livia Poënaru France 26 1.0k 0.5× 368 0.5× 100 0.2× 1.1k 2.0× 576 1.1× 86 2.1k
Babette Gwynn United States 22 1.2k 0.6× 80 0.1× 217 0.4× 1.2k 2.3× 459 0.9× 36 2.5k
Tobias Willer United States 23 1.8k 0.8× 184 0.3× 169 0.3× 266 0.5× 229 0.4× 32 2.0k
Ida Annunziata United States 22 1.1k 0.5× 160 0.2× 131 0.2× 865 1.6× 204 0.4× 42 2.1k
Rachel Myerowitz United States 19 941 0.4× 347 0.5× 98 0.2× 1.0k 1.9× 186 0.4× 31 1.8k
Wendy Westbroek United States 29 1.3k 0.6× 285 0.4× 225 0.4× 997 1.8× 87 0.2× 57 3.0k
Nancy Galvin United States 25 826 0.4× 134 0.2× 98 0.2× 967 1.8× 238 0.4× 37 2.1k
Frans W. Verheijen Netherlands 25 850 0.4× 156 0.2× 89 0.1× 722 1.3× 300 0.6× 47 1.8k

Countries citing papers authored by Els Schollen

Since Specialization
Citations

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

Fields of papers citing papers by Els Schollen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Els Schollen

This figure shows the co-authorship network connecting the top 25 collaborators of Els Schollen. A scholar is included among the top collaborators of Els Schollen 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 Els Schollen. Els Schollen 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.
Foulquier, François, Mustapha Amyere, Jaak Jaeken, et al.. (2012). TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation. The American Journal of Human Genetics. 91(1). 15–26. 163 indexed citations
2.
Casaer, Paul, A.A.W. Peters, Alina T. Midro, et al.. (2004). Rett syndrome in females with CTS hot spot deletions: A disorder profile. American Journal of Medical Genetics Part A. 132A(2). 117–120. 57 indexed citations
3.
Matthijs, Gert, Elisabeth Dequeker, Els Schollen, et al.. (2003). Quality assurance of novel diagnostic technologies: a collaborative effort towards the generation of "generic SOPs" for DHPLC analysis. The American Journal of Human Genetics. 73(5). 414–414. 1 indexed citations
4.
Schollen, Els, Gert Matthijs, & Jean‐Pierre Fryns. (2003). PTPN11 mutation in a young man with Noonan syndrome and retinitis pigmentosa.. PubMed. 14(2). 259–259. 5 indexed citations
5.
Hove, Johan L.K. Van, Ron A. Wevers, Johan Van Cleemput, et al.. (2003). Late‐Onset visceral presentation with cardiomyopathy and without neurological symptoms of adult Sanfilippo A syndrome. American Journal of Medical Genetics Part A. 118A(4). 382–387. 19 indexed citations
6.
7.
Schollen, Els, et al.. (2002). Gross rearrangements in the MECP2 gene in two patients with Rett syndrome. The American Journal of Human Genetics. 71(4). 550–550. 2 indexed citations
8.
Schollen, Els, Gert Matthijs, Eric Legius, & Jean‐Pierre Fryns. (2002). Mutation in the gene for protein tyrosine phosphatase SHP-2 (PTPN11) in a large family with Noonan/cardio-facio-cutaneous syndrome. European Journal of Human Genetics. 10. 238–238. 2 indexed citations
9.
Callewaert, Nico, Annelies Van Hecke, Els Schollen, Gert Matthijs, & Roland Contreras. (2001). Carbohydrate electrophoresis on the DNA-sequencer: technology development and first applications. Glycobiology. 11(10). 922–923. 2 indexed citations
10.
Hendriksz, Christian J., Paula L. McClean, Geoffrey Keir, et al.. (2000). Successful treatment with oral mannose of a patient with congenital disorder of glycosylation Ib (CDG Ib). Glycobiology. 10(10). 1115–1116. 4 indexed citations
11.
Matthijs, Gert, et al.. (2000). Partial deficiency of phosphomannomutase: a pitfall in the diagnosis of congenital disorders of glycosylation (CDG-Ia). The American Journal of Human Genetics. 67(4). 36–36. 1 indexed citations
12.
Schollen, Els, L. Dorland, Tom J. de Koning, et al.. (2000). Genomic organization of the human phosphomannose isomerase (MPI) gene and mutation analysis in patients with congenital disorders of glycosylation type Ib (CDG-Ib). Human Mutation. 16(3). 247–252. 32 indexed citations
13.
Matthijs, Gert, Els Schollen, Cecilia Bjursell, et al.. (2000). Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia). Human Mutation. 16(5). 386–394. 122 indexed citations
14.
15.
Legius, Eric, Els Schollen, Gert Matthijs, & Jean‐Pierre Fryns. (1998). Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family. European Journal of Human Genetics. 6(1). 32–37. 47 indexed citations
16.
Matthijs, Gert, Els Schollen, Emile Van Schaftingen, Jean‐Jacques Cassiman, & Jaak Jaeken. (1998). Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A. The American Journal of Human Genetics. 62(3). 542–550. 123 indexed citations
17.
Matthijs, Gert, Els Schollen, Jaak Jaeken, Emile Van Schaftingen, & JJ Cassiman. (1997). Exhaustive mutation analysis of the PMM2 gene in patients with the carbohydrate-deficient glycoprotein syndrome type I (CDG1 or Jaeken syndrome) and cloning of the mouse Pmm1 and Pmm2 genes.. The American Journal of Human Genetics. 61(4).
18.
Matthijs, Gert, Eric Legius, Els Schollen, et al.. (1996). Evidence for Genetic Heterogeneity in the Carbohydrate-Deficient Glycoprotein Syndrome Type I (CDG1). Genomics. 35(3). 597–599. 26 indexed citations
19.
Devriendt, Koenraad, et al.. (1996). Clinical and molecular genetic features of congenital spinal muscular atrophy. Annals of Neurology. 40(5). 731–738. 48 indexed citations
20.
Jaspers, Martine, et al.. (1994). Stable expression of VLA‐4 and increased maturation of the β1‐integrin precursor after transfection of CHO cells with α4m cDNA. FEBS Letters. 353(3). 239–242. 7 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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