Gert Matthijs
Impact in
- Molecular Biology top 0.5%
- Glycosylation and Glycoproteins Research
- Genetics top 0.2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 87
- Genetics and Neurodevelopmental Disorders 29
- Genomic variations and chromosomal abnormalities 24
-
- Glycosylation and Glycoproteins Research 120
- RNA modifications and cancer 21
- Co-authors
- Jaak JaekenEls SchollenEmile Van SchaftingenFrançois FoulquierKoenraad DevriendtEric LegiusJean‐Jacques CassimanG. Vantrappen
- Journals
- European Journal of Human Genetics (45 papers)The American Journal of Human Genetics (20 papers)Human Mutation (16 papers)Journal of Medical Genetics (8 papers)Glycobiology (8 papers)
- Partner nations
- BelgiumUnited StatesFrance
In The Last Decade
Gert Matthijs
326 papers receiving 12.7k citations
Hit Papers
Peers
Comparison fields: 5 of 164
- Molecular Biology 8.3k
- Genetics 3.3k
- Cell Biology 1.7k
- Physiology 2.0k
- Immunology 1.6k
Countries citing papers authored by Gert Matthijs
This map shows the geographic impact of Gert Matthijs'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 Gert Matthijs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gert Matthijs more than expected).
Fields of papers citing papers by Gert Matthijs
This network shows the impact of papers produced by Gert Matthijs. 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 Gert Matthijs. The network helps show where Gert Matthijs may publish in the future.
Co-authors
The 25 scholars most cited alongside Gert Matthijs, 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 | 2019 | 61 | |
| 2 | Exuberant myopathic phenotype in a DPAGT1-CDG patient | 2016 | 0 |
| 3 | MAN1B1-CDG: how stressed-out can the Golgi be? | 2014 | 1 |
| 4 | 2013 | 118 | |
| 5 | A novel mutation in cog7 expands the spectrum of cog deficiencies | 2009 | 1 |
| 6 | Congenital Disorder of Glycosylation type Ia: antisense therapeutics for an intronic variation causing exonization of an intronic sequence | 2008 | 1 |
| 7 | Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa | 2008 | 0 |
| 8 | 2007 | 80 | |
| 9 | Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation | 2007 | 4 |
| 10 | The Caregene Study: ACE gene I/D polymorphism and effect of physical training on aerobic power in coronary artery disease. | 2006 | 8 |
| 11 | CDG IB PRESENTING WITH HAEMORRHAGE AND THROMBOSIS | 2005 | 1 |
| 12 | 2003 | 20 | |
| 13 | Multicenter validation of a new reverse hybridization assay for CFTR mutation analysis | 2002 | 1 |
| 14 | Selective genetic screening in 250 Belgian breast and ovarian cancer families identifies BRCA1 or BRCA2 mutations in 20% of cases | 2002 | 1 |
| 15 | 2001 | 33 | |
| 16 | 2001 | 104 | |
| 17 | Carbohydrate electrophoresis on the DNA-sequencer: technology development and first applications | 2001 | 2 |
| 18 | Successful treatment with oral mannose of a patient with congenital disorder of glycosylation Ib (CDG Ib) | 2000 | 4 |
| 19 | FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 2000 | 2 |
| 20 | 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 |
About Gert Matthijs
Gert Matthijs is a scholar working on Genetics, Molecular Biology, Cell Biology, Immunology and Genetics, having authored 332 papers that have together received 13.1k indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (120 papers), Carbohydrate Chemistry and Synthesis (47 papers), Galectins and Cancer Biology (41 papers), Cellular transport and secretion (29 papers), Genetics and Neurodevelopmental Disorders (29 papers), Lysosomal Storage Disorders Research (29 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA modifications and cancer (21 papers). The work is most often cited by research in Molecular Biology (8.3k citations), Genetics (3.3k citations), Cell Biology (1.7k citations), Physiology (2.0k citations) and Immunology (1.6k citations). Gert Matthijs has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Jaak Jaeken, Els Schollen, Emile Van Schaftingen, François Foulquier, Koenraad Devriendt, Eric Legius, Jean‐Jacques Cassiman, G. Vantrappen, Thierry Hennet and Dirk J. Lefeber. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Mutation, Journal of Medical Genetics and Glycobiology.
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.