M. Escarceller

651 citations
21 papers · 553 · h-index 13

Impact in

    • Carcinogens and Genotoxicity Assessment
    • DNA Repair Mechanisms
    • CRISPR and Genetic Engineering
    • DNA and Nucleic Acid Chemistry
    • Genomics and Chromatin Dynamics

Papers in

    • RNA modifications and cancer 6
    • DNA Repair Mechanisms 5
    • Genomics and Chromatin Dynamics 4
    • RNA Research and Splicing 4
    • Ubiquitin and proteasome pathways 4
    • Glycosylation and Glycoproteins Research 3
    • Congenital heart defects research 3

M. Escarceller

21 papers receiving 544 citations

Peers

M. Escarceller
Comparison fields: 5 of 59
  • Cancer Research 158
  • Molecular Biology 432
  • Cell Biology 91
  • Developmental Neuroscience 21
  • Genetics 125
Replace Megana Prasad with:
Megana Prasad United States
Elena Koulich United States
Irena N. Melnikova United States
Evgenya Y. Popova United States
Inês Amorim Monteiro Barbosa Austria
Hilger H. Ropers Germany
Erika Lorenzo-Vivas Spain
Kenji Kokura Japan
Giovanna M. Collu United States
Mariateresa Pizzo Italy
M. Escarceller relative to Megana Prasad United States Megana Prasad's profile →
Citations per field
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Megana Prasad · 1×
Citations per year

Countries citing papers authored by M. Escarceller

Since Specialization
Citations

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

Fields of papers citing papers by M. Escarceller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M. Escarceller, 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 M. Escarceller Line = papers co-authored together M. Escarceller links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1 199481
2 200373
3 199870
4 200068
5 199741
6 200038
7 200026
8 199921
9 200021
10 200121
11 199218
12 199917
13 200114
14 200112
15 200110
16 20017
17 19936
18 20005
19 20012
20 20001

About M. Escarceller

M. Escarceller is a scholar working on Molecular Biology, Genetics, Cell Biology, Cancer Research and Cellular and Molecular Neuroscience, having authored 21 papers that have together received 553 indexed citations. Recurring topics across this work include RNA modifications and cancer (6 papers), DNA Repair Mechanisms (5 papers), Genomics and Chromatin Dynamics (4 papers), RNA Research and Splicing (4 papers), Ubiquitin and proteasome pathways (4 papers), Carcinogens and Genotoxicity Assessment (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Cancer Research (158 citations), Molecular Biology (432 citations), Cell Biology (91 citations), Developmental Neuroscience (21 citations) and Genetics (125 citations). M. Escarceller has collaborated with scholars based in Spain, France and United Kingdom. Frequent co-authors include Xavier Estivill, Lauro Sumoy, D. Papadopoulo, Laura Carim‐Todd, E. Moustacchi, Núria Andreu, Danièlle Rouillard, Penny A. Jeggo, S Rousset and Belinda K. Singleton. Their work appears in journals such as Cytogenetic and Genome Research, Gene, Journal of Bacteriology, European Journal of Neuroscience and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

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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