Eric Legius
Impact in
- Neurology top 0.1%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Gastroenterology top 0.5%
Papers in
- Co-authors
- Hilde Brems (68 shared papers)GERT L. MATTHIJS (27 shared papers)Koenraad Devriendt (38 shared papers)Douglas A. Marchuk (5 shared papers)Thomas W. Glover (9 shared papers)Thomy J.L. de Ravel (17 shared papers)Peter Marynen (19 shared papers)Karen Cichowski (4 shared papers)
- Journals
- European Journal of Human Genetics (21 papers)Clinical Genetics (17 papers)Journal of Medical Genetics (17 papers)Human Mutation (15 papers)Genes Chromosomes and Cancer (13 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Eric Legius
338 papers receiving 17.3k citations
Eric Legius's Hit Papers
Peers
Comparison fields: 5 of 162
- Neurology 5.6k
- Gastroenterology 692
- Genetics 3.4k
- Rheumatology 1.6k
- Pulmonary and Respiratory Medicine 3.1k
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 347 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up☆ Hit paper breakdown → | 2021 | 690 |
| 2 | SOX10 mutations in patients with Waardenburg-Hirschsprung disease Hit paper breakdown → | 1998 | 690 |
| 3 | 2004 | 600 | |
| 4 | 2005 | 491 | |
| 5 | Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Hit paper breakdown → | 2021 | 459 |
| 6 | 2014 | 372 | |
| 7 | Gastrointestinal stromal tumours: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up Hit paper breakdown → | 2021 | 371 |
| 8 | 2007 | 361 | |
| 9 | 1993 | 346 | |
| 10 | Bone sarcomas: ESMO–EURACAN–GENTURIS–ERN PaedCan Clinical Practice Guideline for diagnosis, treatment and follow-up Hit paper breakdown → | 2021 | 303 |
| 11 | 1997 | 302 | |
| 12 | 2009 | 265 | |
| 13 | 2003 | 235 | |
| 14 | 1999 | 230 | |
| 15 | 1997 | 217 | |
| 16 | 2004 | 210 | |
| 17 | 2002 | 209 | |
| 18 | 2002 | 207 | |
| 19 | 2011 | 196 | |
| 20 | 2015 | 175 |
About Eric Legius
Eric Legius is a scholar working on Neurology, Genetics, Molecular Biology, Pathology and Forensic Medicine and Rheumatology, having authored 347 papers that have together received 18.0k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (110 papers), Protein Tyrosine Phosphatases (30 papers), Prenatal Screening and Diagnostics (27 papers), Sarcoma Diagnosis and Treatment (23 papers), BRCA gene mutations in cancer (22 papers), Genomic variations and chromosomal abnormalities (19 papers), Soft tissue tumor case studies (18 papers) and Genetics and Neurodevelopmental Disorders (16 papers). The work is most often cited by research in Neurology (5.6k citations), Gastroenterology (692 citations), Genetics (3.4k citations), Rheumatology (1.6k citations) and Pulmonary and Respiratory Medicine (3.1k citations). Eric Legius has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Hilde Brems, GERT L. MATTHIJS, Koenraad Devriendt, Douglas A. Marchuk, Thomas W. Glover, Thomy J.L. de Ravel, Peter Marynen, Karen Cichowski, Eline Beert and Ludwine M. Messiaen. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Journal of Medical 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.