Javier Temes

15.3k citations
28 papers · 9.1k · 7 hit papers · h-index 25

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
    • RNA modifications and cancer
    • Epigenetics and DNA Methylation
    • DNA Repair Mechanisms
    • Genomics and Chromatin Dynamics
    • CRISPR and Genetic Engineering

Papers in

Javier Temes

28 papers receiving 9.0k citations

Javier Temes's Hit Papers

The evolutionary history of 2,658 cancers 2020 · 705 citations
7050+2+4Years since publication50010001.5k2.0k

Peers

Javier Temes
Comparison fields: 5 of 148
  • Cancer Research 4.1k
  • Molecular Biology 5.0k
  • Oncology 1.8k
  • Pathology and Forensic Medicine 1.0k
  • Genetics 1.3k
Replace Alicia L. Bruzos with:
Alicia L. Bruzos Canada
David Ocaña Canada
Karolina M. Czajka Canada
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Javier Temes relative to Alicia L. Bruzos Canada Alicia L. Bruzos's profile →
Citations per field
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Citations per year

Countries citing papers authored by Javier Temes

Since Specialization
Citations

This map shows the geographic impact of Javier Temes'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 Javier Temes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Javier Temes more than expected).

Fields of papers citing papers by Javier Temes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Javier Temes. 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 Javier Temes. The network helps show where Javier Temes may publish in the future.

Co-authors

The 14 scholars most cited alongside Javier Temes, 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 Javier Temes Line = papers co-authored together Javier Temes links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#Work
1
The repertoire of mutational signatures in human cancer
Hit paper breakdown →
20202339
2
Pan-cancer analysis of whole genomes
Hit paper breakdown →
20202109
3
The evolutionary history of 2,658 cancers
Hit paper breakdown →
2020705
4
Patterns of somatic structural variation in human cancer genomes
Hit paper breakdown →
2020550
5
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Hit paper breakdown →
2020476
6
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Hit paper breakdown →
2020419
7 2020317
8
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020309
9 2020301
10 2020293
11 2020184
12 2020160
13 2020159
14 2020152
15 2020104
16 202092
17 202083
18 202077
19 202057
20 202042

About Javier Temes

Javier Temes is a scholar working on Cancer Research, Pathology and Forensic Medicine, Molecular Biology, Genetics and Oncology, having authored 28 papers that have together received 9.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (15 papers), Genetic factors in colorectal cancer (8 papers), Genomics and Phylogenetic Studies (4 papers), Genomics and Chromatin Dynamics (4 papers), RNA modifications and cancer (4 papers), RNA Research and Splicing (4 papers), Genomics and Rare Diseases (3 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Cancer Research (4.1k citations), Molecular Biology (5.0k citations), Oncology (1.8k citations), Pathology and Forensic Medicine (1.0k citations) and Genetics (1.3k citations). Javier Temes has collaborated with scholars based in Canada, United Kingdom and Germany. Frequent co-authors include Mónica Martínez‐Fernández, Jorge Zamora, Martín Santamarina, Daniel García Souto, Jorge Rodríguez‐Castro, Eva G. Álvarez, Ana Pequeño‐Valtierra, Miguel G. Blanco, Peter Van Loo and Gaël Cristofari. Their work appears in journals such as Nature Communications, Nature Genetics, Nature, Science and Communications Biology.

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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