Alberto Magi

3.4k citations
86 papers · 2.0k · h-index 25

Impact in

    • Cancer Genomics and Diagnostics
    • Cancer-related molecular mechanisms research
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Genomics and Phylogenetic Studies 17
    • RNA modifications and cancer 6
    • Gene expression and cancer classification 5
    • Epigenetics and DNA Methylation 4
    • Genomic variations and chromosomal abnormalities 18
    • Genomics and Rare Diseases 16

Alberto Magi

82 papers receiving 2.0k citations

Peers

Alberto Magi
Comparison fields: 5 of 133
  • Cancer Research 466
  • Genetics 683
  • Molecular Biology 1.1k
  • Sensory Systems 47
  • Pathology and Forensic Medicine 159
Replace Patrick Tarpey with:
Patrick Tarpey United Kingdom
Steven Flygare United States
Tristan Shaffer United States
Koh-ichiro Yoshiura Japan
Ahmet Nayır Türkiye
Daniel M. Jordan United States
Wenwu Cui United States
Vasily Ramensky Russia
Peggy D. Robertson United States
Małgorzata Rydzanicz Poland
Alberto Magi relative to Patrick Tarpey United Kingdom Patrick Tarpey's profile →
Citations per field
00.5×1.7×
Patrick Tarpey · 1×
Citations per year

Countries citing papers authored by Alberto Magi

Since Specialization
Citations

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

Fields of papers citing papers by Alberto Magi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 86 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013159
2 2015157
3 2012126
4 2017108
5 201473
6 201670
7 201160
8 200858
9 201154
10 201752
11 200650
12 201050
13 200548
14 201648
15 202045
16 201244
17 201243
18 201540
19 200938
20 201029

About Alberto Magi

Alberto Magi is a scholar working on Molecular Biology, Genetics, Cancer Research, Pulmonary and Respiratory Medicine and Plant Science, having authored 86 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genomics and Phylogenetic Studies (17 papers), Genomics and Rare Diseases (16 papers), Cancer Genomics and Diagnostics (13 papers), Chromosomal and Genetic Variations (7 papers), RNA modifications and cancer (6 papers), Gene expression and cancer classification (5 papers) and Epigenetics and DNA Methylation (4 papers). The work is most often cited by research in Cancer Research (466 citations), Genetics (683 citations), Molecular Biology (1.1k citations), Sensory Systems (47 citations) and Pathology and Forensic Medicine (159 citations). Alberto Magi has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Betti Giusti, Lorenzo Tattini, Romina D’Aurizio, Matteo Benelli, Francesca Torricelli, Tommaso Pippucci, Rosanna Abbate, Roberto Semeraro, Giuseppina Marseglia and Chiara Pescucci. Their work appears in journals such as Bioinformatics, PLoS ONE, BMC Genomics, Frontiers in Genetics and Scientific Reports.

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.

Explore authors with similar magnitude of impact