Martin Ruttledge
Impact in
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Epidemiology top 5%
- Meningioma and schwannoma management
Papers in
- Neurology 13
- Neurofibromatosis and Schwannoma Cases 13
- Neuroblastoma Research and Treatments 2
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- Soft tissue tumors and treatment 3
- Trigeminal Neuralgia and Treatments 3
- Co-authors
- Jan P. Dumanski (9 shared papers)Guy A. Rouleau (9 shared papers)Magnus Nordenskjöld (5 shared papers)V. Peter Collins (4 shared papers)Catherine M. Phelan (5 shared papers)Olivier Delattre (4 shared papers)Gilles Thomas (3 shared papers)P. Merel (2 shared papers)
- Journals
- Human Molecular Genetics (4 papers)Genomics (3 papers)Nature Genetics (2 papers)Neurology (2 papers)The Journal of Headache and Pain (2 papers)
- Partner nations
- SwedenCanadaUnited States
In The Last Decade
Martin Ruttledge
26 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 90
- Neurology 922
- Epidemiology 711
- Rheumatology 299
- Genetics 149
- Pathology and Forensic Medicine 244
Countries citing papers authored by Martin Ruttledge
This map shows the geographic impact of Martin Ruttledge'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 Martin Ruttledge with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martin Ruttledge more than expected).
Fields of papers citing papers by Martin Ruttledge
This network shows the impact of papers produced by Martin Ruttledge. 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 Martin Ruttledge. The network helps show where Martin Ruttledge may publish in the future.
Co-authors
The 25 scholars most cited alongside Martin Ruttledge, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 433 | |
| 2 | Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. | 1996 | 196 |
| 3 | 1996 | 155 | |
| 4 | 1994 | 118 | |
| 5 | 2015 | 111 | |
| 6 | 1994 | 101 | |
| 7 | 1994 | 81 | |
| 8 | 1994 | 79 | |
| 9 | 1993 | 47 | |
| 10 | 1995 | 44 | |
| 11 | Neurofibromatosis type 2 appears to be a genetically homogeneous disease. | 1992 | 41 |
| 12 | 2021 | 40 | |
| 13 | 1996 | 29 | |
| 14 | 1993 | 28 | |
| 15 | 1993 | 22 | |
| 16 | 1990 | 18 | |
| 17 | 2003 | 15 | |
| 18 | 2021 | 15 | |
| 19 | 1988 | 12 | |
| 20 | 1996 | 12 |
About Martin Ruttledge
Martin Ruttledge is a scholar working on Neurology, Pathology and Forensic Medicine, Epidemiology, Rheumatology and Psychiatry and Mental health, having authored 27 papers that have together received 1.6k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (13 papers), Meningioma and schwannoma management (8 papers), Migraine and Headache Studies (6 papers), Bone Tumor Diagnosis and Treatments (5 papers), Soft tissue tumors and treatment (3 papers), Sympathectomy and Hyperhidrosis Treatments (3 papers), Trigeminal Neuralgia and Treatments (3 papers) and Neuroblastoma Research and Treatments (2 papers). The work is most often cited by research in Neurology (922 citations), Epidemiology (711 citations), Rheumatology (299 citations), Genetics (149 citations) and Pathology and Forensic Medicine (244 citations). Martin Ruttledge has collaborated with scholars based in Sweden, Canada and United States. Frequent co-authors include Jan P. Dumanski, Guy A. Rouleau, Magnus Nordenskjöld, V. Peter Collins, Catherine M. Phelan, Olivier Delattre, Gilles Thomas, P. Merel, Fei‐Yu Han and Ya‐Gang Xie. Their work appears in journals such as Human Molecular Genetics, Genomics, Nature Genetics, Neurology and The Journal of Headache and Pain.
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.