V. Peter Collins

28.7k citations
159 papers · 10.8k · 2 hit papers · h-index 58

Impact in

  • Genetics top 0.05%
    • Glioma Diagnosis and Treatment
    • Cancer Genomics and Diagnostics
    • Cancer, Hypoxia, and Metabolism

Papers in

    • Chromatin Remodeling and Cancer 9
    • Epigenetics and DNA Methylation 8
    • Glioma Diagnosis and Treatment 57

V. Peter Collins

158 papers receiving 10.3k citations

V. Peter Collins's Hit Papers

Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p. 1994 · 517 citations
5170+11+22Years since publication100200300400500

Peers

V. Peter Collins
Comparison fields: 5 of 148
  • Genetics 4.4k
  • Cancer Research 2.0k
  • Neurology 1.9k
  • Oncology 1.6k
  • Molecular Biology 4.2k
Replace Tarık Tihan with:
Tarık Tihan United States
S. Clifford Schold United States
Marc Sanson France
Kurt A. Jaeckle United States
Karima Mokhtari France
Sandra H. Bigner United States
Koichi Ichimura Japan
Marie‐France Hamou Switzerland
W.K. Alfred Yung United States
Erik P. Sulman United States
V. Peter Collins relative to Tarık Tihan United States Tarık Tihan's profile →
Citations per field
00.5×1.6×
Tarık Tihan · 1×
Citations per year

Countries citing papers authored by V. Peter Collins

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with V. Peter Collins Line = papers co-authored together V. Peter Collins links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 159 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.
Hit paper breakdown →
1994517
2 2009495
3
Amplified and rearranged epidermal growth factor receptor genes in human glioblastomas reveal deletions of sequences encoding portions of the N- and/or C-terminal tails.
Hit paper breakdown →
1992494
4 1994470
5 1997343
6 2015296
7 2013284
8 1989259
9 2009252
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.
1999225
11 2001219
12 2006206
13 1987190
14 1983189
15 2010188
16
Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q.
1998171
17 2015169
18
Molecular genetic analysis of chromosome 22 in 81 cases of meningioma.
1990148
19 2003146
20 2004142

About V. Peter Collins

V. Peter Collins is a scholar working on Molecular Biology, Genetics, Cancer Research, Neurology and Oncology, having authored 159 papers that have together received 10.8k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (57 papers), Neurofibromatosis and Schwannoma Cases (14 papers), Cancer Genomics and Diagnostics (13 papers), Microtubule and mitosis dynamics (11 papers), Meningioma and schwannoma management (10 papers), Neuroblastoma Research and Treatments (9 papers), Chromatin Remodeling and Cancer (9 papers) and Epigenetics and DNA Methylation (8 papers). The work is most often cited by research in Genetics (4.4k citations), Cancer Research (2.0k citations), Neurology (1.9k citations), Oncology (1.6k citations) and Molecular Biology (4.2k 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 A. Jonas Ekstrand. Their work appears in journals such as Journal of Neuropathology & Experimental Neurology, Genes Chromosomes and Cancer, Cancer, Proceedings of the National Academy of Sciences and Neuro-Oncology.

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.

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