V. Peter Collins
Impact in
- Genetics top 0.05%
- Glioma Diagnosis and Treatment
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
Papers in
-
- Epigenetics and DNA Methylation 10
- Hedgehog Signaling Pathway Studies 9
- Genetics 59
- Glioma Diagnosis and Treatment 56
- Co-authors
- Koichi Ichimura (31 shared papers)C. David James (6 shared papers)Guido Reifenberger (9 shared papers)Magnus Nordenskjöld (10 shared papers)David Jones (8 shared papers)Jan P. Dumanski (12 shared papers)Danita M. Pearson (12 shared papers)Sylvia Kocialkowski (4 shared papers)
- Journals
- Journal of Neuropathology & Experimental Neurology (7 papers)Genes Chromosomes and Cancer (6 papers)Acta Neuropathologica (5 papers)Cancer (5 papers)Proceedings of the National Academy of Sciences (5 papers)
- Partner nations
- SwedenUnited KingdomUnited States
In The Last Decade
V. Peter Collins
154 papers receiving 9.9k citations
Peers
Comparison fields: 5 of 146
- Genetics 4.3k
- Cancer Research 2.2k
- Neurology 2.0k
- Molecular Biology 4.4k
- Oncology 1.7k
Countries citing papers authored by V. Peter Collins
This map shows the geographic impact of V. Peter Collins'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 V. Peter Collins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. Peter Collins more than expected).
Fields of papers citing papers by V. Peter Collins
This network shows the impact of papers produced by V. Peter Collins. 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 V. Peter Collins. The network helps show where V. Peter Collins may publish in the future.
Co-authors
The 25 scholars most cited alongside V. Peter Collins, 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 155 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. | 1994 | 491 |
| 2 | 1992 | 469 | |
| 3 | 2009 | 468 | |
| 4 | 1994 | 433 | |
| 5 | 1997 | 322 | |
| 6 | 2013 | 270 | |
| 7 | 2015 | 268 | |
| 8 | 1989 | 243 | |
| 9 | 2009 | 238 | |
| 10 | The dermatofibrosarcoma protuberans-associated collagen type Ialpha1/platelet-derived growth factor (PDGF) B-chain fusion gene generates a transforming protein that is processed to functional PDGF-BB. | 1999 | 212 |
| 11 | 2001 | 204 | |
| 12 | 2006 | 192 | |
| 13 | 1987 | 180 | |
| 14 | 2010 | 178 | |
| 15 | Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q. | 1998 | 168 |
| 16 | 1983 | 165 | |
| 17 | 2015 | 164 | |
| 18 | Molecular genetic analysis of chromosome 22 in 81 cases of meningioma. | 1990 | 142 |
| 19 | 2003 | 141 | |
| 20 | 1991 | 133 |
About V. Peter Collins
V. Peter Collins is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Neurology, having authored 155 papers that have together received 10.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (56 papers), Cancer Genomics and Diagnostics (14 papers), Neurofibromatosis and Schwannoma Cases (13 papers), Microtubule and mitosis dynamics (12 papers), Meningioma and schwannoma management (11 papers), Epigenetics and DNA Methylation (10 papers), Hedgehog Signaling Pathway Studies (9 papers) and Cancer, Hypoxia, and Metabolism (8 papers). The work is most often cited by research in Genetics (4.3k citations), Cancer Research (2.2k citations), Neurology (2.0k citations), Molecular Biology (4.4k citations) and Oncology (1.7k citations). V. Peter Collins has collaborated with scholars based in Sweden, United Kingdom and United States. Frequent co-authors include Koichi Ichimura, C. David James, Guido Reifenberger, Magnus Nordenskjöld, David Jones, Jan P. Dumanski, Danita M. Pearson, Sylvia Kocialkowski, L. Magnus Bäcklund and Noriaki Sugawa. Their work appears in journals such as Journal of Neuropathology & Experimental Neurology, Genes Chromosomes and Cancer, Acta Neuropathologica, Cancer and Proceedings of the National Academy of Sciences.
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.