Eric Legius
- Neurology top 0.1%
- Neurofibromatosis and Schwannoma Cases 97
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 24
- BRCA gene mutations in cancer 19
- Rheumatology top 0.5%
- Soft tissue tumor case studies 20
- Genetics top 1%
- Genomic variations and chromosomal abnormalities 24
- BRCA gene mutations in cancer 19
- Pathology and Forensic Medicine top 0.5%
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- Prenatal Screening and Diagnostics 27
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- Meningioma and schwannoma management 24
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- Protein Tyrosine Phosphatases 22
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- Sarcoma Diagnosis and Treatment 20
- Co-authors
- Hilde BremsDouglas A. MarchukMie‐Jef DescheemaekerThomas W. GloverKoenraad DevriendtGert MatthijsThomy de RavelJ P Fryns
- Cited by
- NeurologyGeneticsRheumatology
- Journals
- European Journal of Human Genetics (18 papers)Journal of Medical Genetics (16 papers)Clinical Genetics (16 papers)
- Partner nations
- BelgiumUnited StatesNetherlands
In The Last Decade
Eric Legius
288 papers receiving 11.8k citations
Hit Papers
Peers
Comparison fields: 5 of 154
- Neurology 4.2k
- Genetics 3.1k
- Rheumatology 1.2k
- Genetics 820
- Pathology and Forensic Medicine 1.3k
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2024 | 0 | |
| 3 | 2024 | 0 | |
| 4 | 2023 | 2 | |
| 5 | 2023 | 10 | |
| 6 | 2023 | 7 | |
| 7 | 2022 | 16 | |
| 8 | 2021 | 3 | |
| 9 | 2019 | 12 | |
| 10 | 2018 | 45 | |
| 11 | 2016 | 41 | |
| 12 | 2009 | 92 | |
| 13 | Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association (vol 69, pg 7393, 2009) | 2009 | 4 |
| 14 | BRCA1/2 predictive testing and gender: uptake, motivation and psychological characteristics. | 2009 | 8 |
| 15 | 2005 | 52 | |
| 16 | Syndromic clefting : broadening the clinical spectrum of an “old” syndrome, confirmation of a rare syndrome and description of a novel entity | 2005 | 2 |
| 17 | Familial migraine with aura and partial epilepsy involving posterior brain regions caused by a mutation in SLC4A4, a sodium bicarbonate cotransporter gene | 2005 | 1 |
| 18 | 2004 | 39 | |
| 19 | Selective genetic screening in 250 Belgian breast and ovarian cancer families identifies BRCA1 or BRCA2 mutations in 20% of cases | 2002 | 1 |
| 20 | The Kabuki make-up (Niikawa-Kuroki) syndrome: 12 new patients, further delineation of the non-Japanese phenotype | 1994 | 4 |
About Eric Legius
Eric Legius is a scholar working on Neurology, Genetics and Pathology and Forensic Medicine, having authored 296 papers that have together received 12.1k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (97 papers), Prenatal Screening and Diagnostics (27 papers), Genomic variations and chromosomal abnormalities (24 papers), Meningioma and schwannoma management (24 papers), Protein Tyrosine Phosphatases (22 papers), Soft tissue tumor case studies (20 papers), Sarcoma Diagnosis and Treatment (20 papers) and BRCA gene mutations in cancer (19 papers). The work is most often cited by research in Neurology (4.2k citations), Genetics (3.1k citations) and Rheumatology (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, Thomas W. Glover, Koenraad Devriendt, Gert Matthijs, Thomy de Ravel, J P Fryns, Eline Beert and Karen Cichowski. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics, Genes Chromosomes and Cancer and Human Mutation.
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.