Marco Foppoli

1.9k citations
30 papers · 748 · h-index 12

Impact in

  • Neurology top 2%
    • CNS Lymphoma Diagnosis and Treatment
  • Genetics top 5%
    • Glioma Diagnosis and Treatment

Papers in

Marco Foppoli

28 papers receiving 727 citations

Peers

Marco Foppoli
Comparison fields: 5 of 54
  • Neurology 369
  • Genetics 222
  • Pathology and Forensic Medicine 311
  • Immunology 135
  • Rheumatology 71
Replace Stephan Kreher with:
Stephan Kreher Germany
Erdwine Klinker Germany
Kirsten Herbert Australia
Chae H. Koo United States
Nazan Özsan Türkiye
Akihiro Kitadate Japan
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Letizia Gandolfi Italy
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Citations per field
00.5×3.4×
Stephan Kreher · 1×
Citations per year

Countries citing papers authored by Marco Foppoli

Since Specialization
Citations

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

Fields of papers citing papers by Marco Foppoli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 30 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1996135
2 201477
3 201575
4 200472
5 200665
6 201259
7 201756
8 201454
9
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases.
200548
10 200725
11 201124
12 201013
13 20156
14 19916
15 20205
16 20214
17 19964
18 20133
19
Questions and answers in the management of primary central nervous system and ocular lymphomas.
20033
20 20173

About Marco Foppoli

Marco Foppoli is a scholar working on Neurology, Pathology and Forensic Medicine, Genetics, Oncology and Cardiology and Cardiovascular Medicine, having authored 30 papers that have together received 748 indexed citations. Recurring topics across this work include CNS Lymphoma Diagnosis and Treatment (16 papers), Lymphoma Diagnosis and Treatment (15 papers), Viral-associated cancers and disorders (5 papers), Glioma Diagnosis and Treatment (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), Acute Lymphoblastic Leukemia research (2 papers), Cardiac Fibrosis and Remodeling (2 papers) and CAR-T cell therapy research (1 paper). The work is most often cited by research in Neurology (369 citations), Genetics (222 citations), Pathology and Forensic Medicine (311 citations), Immunology (135 citations) and Rheumatology (71 citations). Marco Foppoli has collaborated with scholars based in Italy, Switzerland and Belgium. Frequent co-authors include Andrés J.M. Ferreri, Giovanni Citterio, Michele Reni, Maurilio Ponzoni, Luca Gianotti, Giuseppe Consogno, Laura Galli, Marco Braga, Claudio Fortis and Oreste ­Gentilini. Their work appears in journals such as Hematological Oncology, British Journal of Haematology, Cancer Letters, Journal of Clinical Oncology and Blood.

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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