Els Schollen
- Molecular Biology top 5%
- Glycosylation and Glycoproteins Research 34
- RNA modifications and cancer 8
- Ubiquitin and proteasome pathways 4
- Immunology top 5%
- Galectins and Cancer Biology 19
- Organic Chemistry top 5%
- Carbohydrate Chemistry and Synthesis 16
- Physiology top 5%
- Lysosomal Storage Disorders Research 9
- Cell Biology top 5%
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- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Gert MatthijsEmile Van SchaftingenJaak JaekenJean‐Jacques CassimanEric LegiusStephanie GrünewaldMaria Veiga‐da‐CunhaEls Pardon
- Journals
- The American Journal of Human Genetics (7 papers)European Journal of Human Genetics (6 papers)Human Mutation (4 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Els Schollen
57 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 92
- Molecular Biology 2.1k
- Immunology 604
- Organic Chemistry 676
- Physiology 540
- Cell Biology 316
Countries citing papers authored by Els Schollen
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
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
The 25 scholars most cited alongside Els Schollen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 163 | |
| 2 | 2007 | 34 | |
| 3 | 2005 | 21 | |
| 4 | 2004 | 57 | |
| 5 | 2003 | 19 | |
| 6 | Quality assurance of novel diagnostic technologies: a collaborative effort towards the generation of "generic SOPs" for DHPLC analysis | 2003 | 1 |
| 7 | 2003 | 44 | |
| 8 | Gross rearrangements in the MECP2 gene in two patients with Rett syndrome | 2002 | 2 |
| 9 | 2002 | 24 | |
| 10 | Carbohydrate electrophoresis on the DNA-sequencer: technology development and first applications | 2001 | 2 |
| 11 | 2001 | 83 | |
| 12 | Partial deficiency of phosphomannomutase: a pitfall in the diagnosis of congenital disorders of glycosylation (CDG-Ia) | 2000 | 1 |
| 13 | Successful treatment with oral mannose of a patient with congenital disorder of glycosylation Ib (CDG Ib) | 2000 | 4 |
| 14 | 2000 | 122 | |
| 15 | 2000 | 90 | |
| 16 | 1998 | 28 | |
| 17 | 1998 | 123 | |
| 18 | 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. | 1997 | 0 |
| 19 | 1996 | 48 | |
| 20 | 1995 | 8 |
About Els Schollen
Els Schollen is a scholar working on Immunology, Molecular Biology and Genetics, having authored 58 papers that have together received 2.6k indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (34 papers), Galectins and Cancer Biology (19 papers), Carbohydrate Chemistry and Synthesis (16 papers), Lysosomal Storage Disorders Research (9 papers), RNA modifications and cancer (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Ubiquitin and proteasome pathways (4 papers). The work is most often cited by research in Molecular Biology (2.1k citations), Immunology (604 citations) and Organic Chemistry (676 citations). Els Schollen has collaborated with scholars based in Belgium, Netherlands and United States. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Human Mutation, Glycobiology and Journal of Inherited Metabolic Disease.
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.