Eric Legius
Impact in
Papers in
- Neurology 104
- Neurofibromatosis and Schwannoma Cases 98
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- Protein Tyrosine Phosphatases 22
- Co-authors
- Hilde Brems (70 shared papers)Douglas A. Marchuk (5 shared papers)Mie‐Jef Descheemaeker (15 shared papers)Koenraad Devriendt (35 shared papers)Thomas W. Glover (9 shared papers)Gert Matthijs (26 shared papers)Thomy de Ravel (17 shared papers)J P Fryns (6 shared papers)
- Journals
- European Journal of Human Genetics (18 papers)Journal of Medical Genetics (16 papers)Clinical Genetics (16 papers)Human Mutation (13 papers)Genes Chromosomes and Cancer (13 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Eric Legius
296 papers receiving 12.6k citations
Eric Legius's Hit Papers
Peers
Comparison fields: 5 of 151
- Neurology 4.3k
- Genetics 2.9k
- Genetics 804
- Rheumatology 1.1k
- Pathology and Forensic Medicine 1.2k
Countries citing papers authored by Eric Legius
This map shows the geographic impact of Eric Legius'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 Eric Legius with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Legius more than expected).
Fields of papers citing papers by Eric Legius
This network shows the impact of papers produced by Eric Legius. 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 Eric Legius. The network helps show where Eric Legius may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Legius, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 306 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | SOX10 mutations in patients with Waardenburg-Hirschsprung disease Hit paper breakdown → | 1998 | 668 |
| 2 | A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4) Hit paper breakdown → | 2004 | 576 |
| 3 | 2005 | 472 | |
| 4 | 1993 | 346 | |
| 5 | 2014 | 343 | |
| 6 | 2007 | 330 | |
| 7 | 1997 | 296 | |
| 8 | 2009 | 254 | |
| 9 | 2012 | 238 | |
| 10 | 1999 | 223 | |
| 11 | 2003 | 222 | |
| 12 | 1997 | 209 | |
| 13 | 2002 | 202 | |
| 14 | 2002 | 192 | |
| 15 | 2011 | 178 | |
| 16 | 2006 | 167 | |
| 17 | 1994 | 163 | |
| 18 | The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. | 1999 | 159 |
| 19 | 2015 | 146 | |
| 20 | 2003 | 146 |
About Eric Legius
Eric Legius is a scholar working on Neurology, Molecular Biology, Genetics, Pathology and Forensic Medicine and Surgery, having authored 306 papers that have together received 13.2k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (98 papers), Prenatal Screening and Diagnostics (24 papers), Protein Tyrosine Phosphatases (22 papers), BRCA gene mutations in cancer (19 papers), Sarcoma Diagnosis and Treatment (18 papers), Genomic variations and chromosomal abnormalities (17 papers), Soft tissue tumor case studies (16 papers) and Meningioma and schwannoma management (14 papers). The work is most often cited by research in Neurology (4.3k citations), Genetics (2.9k citations), Genetics (804 citations), Rheumatology (1.1k citations) and Pathology and Forensic Medicine (1.2k citations). Eric Legius has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Hilde Brems, Douglas A. Marchuk, Mie‐Jef Descheemaeker, Koenraad Devriendt, Thomas W. Glover, Gert Matthijs, Thomy de Ravel, J P Fryns, Peter Marynen and Eline Beert. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, Human Mutation and Genes Chromosomes and Cancer.
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.