V. Peter Collins

14.3k citations

77 papers · 7.7k indexed · 3 hit papers · h-index 40

Impact in

Genetics top 0.1%
- Glioma Diagnosis and Treatment
Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
- MicroRNA in disease regulation

Papers in

Genetics 28
- Glioma Diagnosis and Treatment 26
Cancer Research 19
- Cancer Genomics and Diagnostics 11

Co-authors: Koichi Ichimura Esther Schmidt C. David James A. Jonas Ekstrand Guido Reifenberger Christina Curtis Anestis Touloumis Colin Watts
Journals: Journal of Neuropathology & Experimental Neurology (4 papers)Genes Chromosomes and Cancer (3 papers)Oncogene (3 papers)The Journal of Pathology (2 papers)Brain Pathology (2 papers)
Partner nations: Sweden United Kingdom United States

In The Last Decade

V. Peter Collins

76 papers receiving 7.5k citations

Hit Papers

align trajectories log scale

Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics 2013 · 1.2k citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2013 Proceedings of the National Academy of Sciences
2008 Cancer Research
1991 PubMed

Peers

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

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20 of 20 papers shown

#	Work
1	Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics Proceedings of the National Academy of Sciences ·Andrea Sottoriva, Inmaculada Spiteri, Sara Piccirillo, Anestis Touloumis, V. Peter Collins, John C. Marioni, Christina Curtis, Colin Watts, Simon Tavaré Hit paper breakdown →	2013	1231
2	Tandem Duplication Producing a Novel Oncogenic BRAF Fusion Gene Defines the Majority of Pilocytic Astrocytomas Cancer Research ·David Jones, Sylvia Kocialkowski, Lu Liu, Danita M. Pearson, L. Magnus Bäcklund, Koichi Ichimura, V. Peter Collins Hit paper breakdown →	2008	609
3	Improved grading and survival prediction of human astrocytic brain tumors by artificial neural network analysis of gene expression microarray data Molecular Cancer Therapeutics ·JM Trejo, Anastasis Oulas, L. Magnus Bäcklund, Matthew T. Wayland, Lu Liu, Karen P. Plant, Lisa Happerfield, Tom C. Freeman, Panayiota Poirazi, V. Peter Collins	2008	64
4	Genome‐Wide Analysis of Subependymomas Shows Underlying Chromosomal Copy Number Changes Involving Chromosomes 6, 7, 8 and 14 in a Proportion of Cases Brain Pathology ·Kathreena M. Kurian, David Jones, Keigo Cho, Ya. E. Benson, Danita M. Pearson, Koichi Ichimura, V. Peter Collins	2008	12
5	Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint Genes Chromosomes and Cancer ·Martin G. McCabe, Koichi Ichimura, Danita M. Pearson, Lu Liu, Steven C. Clifford, David W. Ellison, V. Peter Collins	2008	9
6	Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes Oncogene ·Karen Howarth, Helena Braga Cruz, Bee Ling Ng, Kateryna Selcuk, Kozou Saeki, Susanna L. Cooke, Lai Xu-guang, Koichi Ichimura, V. Peter Collins, Charles Soares Braz, Paul A. Edwards	2007	55
7	Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH Oncogene ·Koichi Ichimura, Andrew J. Mungall, Heike Fiegler, Danita M. Pearson, Ian Dunham, Charles Soares Braz, V. Peter Collins	2005	54
8	Mutations in Rb1 pathway-related genes are associated with poor prognosis in Anaplastic Astrocytomas British Journal of Cancer ·L. Magnus Bäcklund, Bo Nilsson, Ju-Yup Lee, Koichi Ichimura, V. Peter Collins	2005	25
9	Allelic Gain and Amplification on the Long Arm of Chromosome 17 in Anaplastic Meningiomas Brain Pathology ·Rainer Büschges, Koichi Ichimura, Ruthild G. Weber, Guido Reifenberger, V. Peter Collins	2002	39
10	Cellular mechanisms targeted during astrocytoma progression Cancer Letters ·V. Peter Collins	2002	21
11	Mutational Profile of the PTEN Gene in Primary Human Astrocytic Tumors and Cultivated Xenografts Journal of Neuropathology & Experimental Neurology ·Esther Schmidt, Koichi Ichimura, Helena Goike, Yaw-Kwan Chiu, Lu Liu, V. Peter Collins	1999	63
12	Relation Between Polymerase Chain Reaction Findings and Morphological Changes During Cytomegalovirus Infection in Transplanted Lung Diagnostic Molecular Pathology ·Petros Petsinis, Tomas Bergström, Gunnar Mårtensson, Anne Ricksten, Folke Nilsson, Sigvard Olofsson, V. Peter Collins	1997	6
13	Epidermal Growth Factor Receptor Gene and Its Transcripts in Glioblastomas Recent results in cancer research ·V. Peter Collins	1994	6
14	Characterization of a new member of the human /-adaptin gene family from chromosome 22q12, a candidate meningioma gene Human Molecular Genetics ·Myriam Peyrard, Ingegerd Fransson, Ya‐Gang Xie, Fei‐Yu Han, Martin Ruttledge, H. Haeser, Thavi Masmondana, Ian Dunham, V. Peter Collins, Jan P. Dumanski	1994	81
15	Amplification and overexpression of the MDM2 gene in a subset of human malignant gliomas without p53 mutations. PubMed ·G. Reifenberger, Ju-Yup Lee, Koichi Ichimura, Esther Schmidt, V. Peter Collins	1993	494
16	Effect of exposure to 2,5-hexanediol in light or darkness on the retina of albino and pigmented rats. II. Electrophysiology Archives of Toxicology ·Per Nylén, Ian Blanes Garcia, Maud Hagman, Ann‐Chrístin Johnson, V. Peter Collins, G. Höglund	1993	5
17	Recessive Genetic Mechanisms in the Oncogenesis of Prostatic Carcinoma Scandinavian Journal of Urology and Nephrology ·Ulf S.R. Bergerheim, V. Peter Collins, Peter Ekman, Kazuto Kunimi	1991	9
18	Expression of the Ganglioside GD3 in Human Meningiomas Is Associated with Monosomy of Chromosome 22 Journal of Neurochemistry ·Pam Fredman, Jan P. Dumanski, Pia Davidsson, Lars Svennerholm, V. Peter Collins	1990	18
19	Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter Human Genetics ·Jan P. Dumanski, A.H.M. Geurts van Kessel, Martin Ruttledge, Andreas Wladis, Noriaki Sugawa, V. Peter Collins, Magnus Nordenskjöld	1990	18
20	Stereotactic Biopsy in Acoustic Tumors Stereotactic and Functional Neurosurgery ·Georg Norén, V. Peter Collins	1980	5

About V. Peter Collins

V. Peter Collins is a scholar working on Genetics, Cancer Research, Neurology, Oncology and Cell Biology, having authored 77 papers that have together received 7.7k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (26 papers), Cancer Genomics and Diagnostics (11 papers), Cancer-related Molecular Pathways (11 papers), Microtubule and mitosis dynamics (8 papers), Neuroblastoma Research and Treatments (6 papers), Neurofibromatosis and Schwannoma Cases (6 papers), Genomics and Chromatin Dynamics (5 papers) and Meningioma and schwannoma management (5 papers). The work is most often cited by research in Genetics (3.2k citations), Cancer Research (2.1k citations), Oncology (2.4k citations), Neurology (977 citations) and Molecular Biology (3.9k citations). V. Peter Collins has collaborated with scholars based in Sweden, United Kingdom and United States. Frequent co-authors include Koichi Ichimura, Esther Schmidt, C. David James, A. Jonas Ekstrand, Guido Reifenberger, Christina Curtis, Anestis Touloumis, Colin Watts, John C. Marioni and Sara Piccirillo. Their work appears in journals such as Journal of Neuropathology & Experimental Neurology, Genes Chromosomes and Cancer, Oncogene, The Journal of Pathology and Brain Pathology.

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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