Andrés Lanzós

14.5k citations
29 papers · 9.6k · 10 hit papers · h-index 25

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
  • Oncology top 2%
    • Cancer Immunotherapy and Biomarkers

Papers in

    • Cancer Genomics and Diagnostics 20
    • Cancer-related molecular mechanisms research 6
    • Genomic variations and chromosomal abnormalities 5

Andrés Lanzós

29 papers receiving 9.5k citations

Andrés Lanzós's Hit Papers

Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition 2020 · 315 citations
3150+2+4Years since publication5001k1.5k2k

Peers

Andrés Lanzós
Comparison fields: 5 of 130
  • Cancer Research 4k
  • Oncology 1.4k
  • Molecular Biology 2.9k
  • Genetics 1.3k
  • Aging 47
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Citations per field
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Citations per year

Countries citing papers authored by Andrés Lanzós

Since Specialization
Citations

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

Fields of papers citing papers by Andrés Lanzós

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 10 scholars most cited alongside Andrés Lanzós, 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 Andrés Lanzós Line = papers co-authored together Andrés Lanzós links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 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 →
20202401
2
Pan-cancer analysis of whole genomes
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20202169
3
The evolutionary history of 2,658 cancers
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2020730
4
Patterns of somatic structural variation in human cancer genomes
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2020564
5
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
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2020489
6
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
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2020428
7
Comprehensive molecular characterization of mitochondrial genomes in human cancers
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2020319
8
Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Hit paper breakdown →
2020315
9
Genomic basis for RNA alterations in cancer
Hit paper breakdown →
2020310
10
The landscape of viral associations in human cancers
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2020293
11 2020190
12 2019175
13 2020167
14 2020161
15 2020153
16 2020109
17 201794
18 202094
19 202086
20 202077

About Andrés Lanzós

Andrés Lanzós is a scholar working on Cancer Research, Genetics, Molecular Biology, Information Systems and Management and Oncology, having authored 29 papers that have together received 9.6k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (20 papers), Cancer-related molecular mechanisms research (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Chromatin Remodeling and Cancer (2 papers), Cervical Cancer and HPV Research (1 paper), Telomeres, Telomerase, and Senescence (1 paper), Mitochondrial Function and Pathology (1 paper) and Bioinformatics and Genomic Networks (1 paper). The work is most often cited by research in Cancer Research (4k citations), Oncology (1.4k citations), Molecular Biology (2.9k citations), Genetics (1.3k citations) and Aging (47 citations). Andrés Lanzós has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Rory Johnson, Taisia Polidori, Roberta Esposito, Carlos Pulido-Quetglas, Roderic Guigó, Loris Mularoni, Ferrán Reverter, Joana Carlevaro-Fita, Adrienne Vancura and Simon Haefliger. Their work appears in journals such as Nature Communications, Nature, Nature Genetics, Cell Genomics and Cancer Cell.

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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