David Viskochil
Impact in
- Neurology top 0.1%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Vascular Malformations Diagnosis and Treatment
- Rheumatology top 0.5%
- Soft tissue tumor case studies
- Bone Tumor Diagnosis and Treatments
Papers in
- Neurology 94
- Neurofibromatosis and Schwannoma Cases 93
- Neuroblastoma Research and Treatments 21
- Rheumatology 37
- Soft tissue tumor case studies 22
- Bone Tumor Diagnosis and Treatments 11
- Co-authors
- Richard CawthonP. O’ConnellJohn C. CareyR. WhiteMelanie CulverMargaret RobertsonRobert B. WeissGangfeng Xu
- Journals
- Journal of Pediatric Orthopaedics (6 papers)Molecular Genetics and Metabolism (5 papers)Genomics (5 papers)The American Journal of Human Genetics (4 papers)Journal of Medical Genetics (4 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David Viskochil
154 papers receiving 8.4k citations
Hit Papers
Peers
Comparison fields: 5 of 123
- Neurology 5.0k
- Rheumatology 1.6k
- Pulmonary and Respiratory Medicine 1.7k
- Genetics 536
- Pathology and Forensic Medicine 893
Countries citing papers authored by David Viskochil
This map shows the geographic impact of David Viskochil'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 David Viskochil with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Viskochil more than expected).
Fields of papers citing papers by David Viskochil
This network shows the impact of papers produced by David Viskochil. 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 David Viskochil. The network helps show where David Viskochil may publish in the future.
Co-authorship network
The 25 scholars most cited alongside David Viskochil, 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 | 2024 | 6 | |
| 2 | 2024 | 5 | |
| 3 | 2022 | 4 | |
| 4 | 2020 | 13 | |
| 5 | 2019 | 51 | |
| 6 | 2016 | 15 | |
| 7 | 2014 | 13 | |
| 8 | 2014 | 36 | |
| 9 | 2013 | 44 | |
| 10 | 2009 | 88 | |
| 11 | 2005 | 12 | |
| 12 | 2003 | 34 | |
| 13 | 2003 | 32 | |
| 14 | 2000 | 141 | |
| 15 | 1999 | 96 | |
| 16 | 1997 | 49 | |
| 17 | 1991 | 98 | |
| 18 | 1991 | 92 | |
| 19 | The neurofibromatosis type 1 gene encodes a protein related to GAP Hit paper breakdown → | 1990 | 907 |
| 20 | Model systems for studies on androgen-dependent gene expression in the rat prostate. | 1981 | 11 |
About David Viskochil
David Viskochil is a scholar working on Neurology, Rheumatology, Pulmonary and Respiratory Medicine, Genetics and Epidemiology, having authored 159 papers that have together received 8.6k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (93 papers), Sarcoma Diagnosis and Treatment (30 papers), Soft tissue tumor case studies (22 papers), Neuroblastoma Research and Treatments (21 papers), Meningioma and schwannoma management (17 papers), Lysosomal Storage Disorders Research (15 papers), Chromatin Remodeling and Cancer (11 papers) and Bone Tumor Diagnosis and Treatments (11 papers). The work is most often cited by research in Neurology (5.0k citations), Rheumatology (1.6k citations), Pulmonary and Respiratory Medicine (1.7k citations), Genetics (536 citations) and Pathology and Forensic Medicine (893 citations). David Viskochil has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Richard Cawthon, P. O’Connell, John C. Carey, R. White, Melanie Culver, Margaret Robertson, Robert B. Weiss, Gangfeng Xu, Jeff Stevens and R F Gesteland. Their work appears in journals such as Journal of Pediatric Orthopaedics, Molecular Genetics and Metabolism, Genomics, The American Journal of Human Genetics and Journal of Medical Genetics.
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.