Duane Superneau
Impact in
- Neurology top 2%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Vascular Malformations Diagnosis and Treatment
- Epidemiology top 10%
- Meningioma and schwannoma management
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
- Craniofacial Disorders and Treatments 4
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- Peroxisome Proliferator-Activated Receptors 2
- Co-authors
- Wladimir Wertelecki (9 shared papers)Guy A. Rouleau (3 shared papers)Jonathan L. Haines (3 shared papers)James F. Gusella (3 shared papers)Robert L. Martuza (2 shared papers)Bernd R. Seizinger (2 shared papers)Wendy Hobbs (1 shared paper)P. Michael Conneally (1 shared paper)
- Journals
- Clinical Genetics (1 paper)American Journal of Medical Genetics (9 papers)Nature (1 paper)Journal of Biosocial Science (1 paper)Congenital Heart Disease (1 paper)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
Duane Superneau
22 papers receiving 808 citations
Peers
Comparison fields: 5 of 71
- Neurology 408
- Epidemiology 274
- Developmental Biology 17
- Rheumatology 105
- Genetics 189
Countries citing papers authored by Duane Superneau
This map shows the geographic impact of Duane Superneau'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 Duane Superneau with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Duane Superneau more than expected).
Fields of papers citing papers by Duane Superneau
This network shows the impact of papers produced by Duane Superneau. 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 Duane Superneau. The network helps show where Duane Superneau may publish in the future.
Co-authors
The 25 scholars most cited alongside Duane Superneau, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 350 | |
| 2 | 1988 | 123 | |
| 3 | Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22. | 1990 | 75 |
| 4 | 2001 | 46 | |
| 5 | 1999 | 44 | |
| 6 | 2004 | 27 | |
| 7 | 1998 | 27 | |
| 8 | 1981 | 23 | |
| 9 | 1993 | 21 | |
| 10 | 1999 | 21 | |
| 11 | 1985 | 20 | |
| 12 | 2008 | 16 | |
| 13 | 1988 | 16 | |
| 14 | 1993 | 8 | |
| 15 | Angiomas and von Recklinghausen neurofibromatosis. | 1988 | 7 |
| 16 | 2002 | 6 | |
| 17 | 1995 | 5 | |
| 18 | 2011 | 5 | |
| 19 | 1996 | 2 | |
| 20 | 1998 | 2 |
About Duane Superneau
Duane Superneau is a scholar working on Genetics, Molecular Biology, Neurology, Surgery and Pediatrics, Perinatology and Child Health, having authored 22 papers that have together received 846 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Craniofacial Disorders and Treatments (4 papers), Fetal and Pediatric Neurological Disorders (3 papers), Meningioma and schwannoma management (3 papers), Neuroblastoma Research and Treatments (2 papers), Peroxisome Proliferator-Activated Receptors (2 papers) and Congenital Anomalies and Fetal Surgery (2 papers). The work is most often cited by research in Neurology (408 citations), Epidemiology (274 citations), Developmental Biology (17 citations), Rheumatology (105 citations) and Genetics (189 citations). Duane Superneau has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Wladimir Wertelecki, Guy A. Rouleau, Jonathan L. Haines, James F. Gusella, Robert L. Martuza, Bernd R. Seizinger, Wendy Hobbs, P. Michael Conneally, James A. Trofatter and John M. Opitz. Their work appears in journals such as Clinical Genetics, American Journal of Medical Genetics, Nature, Journal of Biosocial Science and Congenital Heart Disease.
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.