Matteo Forloni

1.1k total citations
20 papers, 874 citations indexed

About

Matteo Forloni is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Matteo Forloni has authored 20 papers receiving a total of 874 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Matteo Forloni's work include Advanced biosensing and bioanalysis techniques (4 papers), CRISPR and Genetic Engineering (4 papers) and DNA and Nucleic Acid Chemistry (4 papers). Matteo Forloni is often cited by papers focused on Advanced biosensing and bioanalysis techniques (4 papers), CRISPR and Genetic Engineering (4 papers) and DNA and Nucleic Acid Chemistry (4 papers). Matteo Forloni collaborates with scholars based in Italy, United States and Singapore. Matteo Forloni's co-authors include Patrizio Giacomini, Doriana Fruci, Narendra Wajapeyee, Loredana Cifaldi, Renata Boldrini, Sonia Albini, Micol Eleonora Fiori, Valentina Federici, Alberto Donfrancesco and Serena Giovinazzi and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Cancer Research.

In The Last Decade

Matteo Forloni

18 papers receiving 855 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Matteo Forloni Italy 13 604 349 205 199 106 20 874
Alena Malyukova Sweden 14 669 1.1× 152 0.4× 190 0.9× 196 1.0× 40 0.4× 19 828
Xinyi Tu United States 16 627 1.0× 126 0.4× 220 1.1× 412 2.1× 39 0.4× 38 972
Walter Hanel United States 12 418 0.7× 225 0.6× 287 1.4× 436 2.2× 20 0.2× 39 910
Ileana Cuevas United States 17 516 0.9× 188 0.5× 120 0.6× 187 0.9× 29 0.3× 28 971
Sarah J. Hill United States 11 805 1.3× 111 0.3× 136 0.7× 391 2.0× 78 0.7× 36 1.2k
Francesco Boccalatte United States 12 536 0.9× 188 0.5× 156 0.8× 193 1.0× 30 0.3× 21 804
Dale O. Cowley United States 15 631 1.0× 170 0.5× 125 0.6× 202 1.0× 18 0.2× 29 875
Shin‐ichiro Numata Japan 11 559 0.9× 171 0.5× 109 0.5× 129 0.6× 115 1.1× 13 888
Toshina Ishiguro‐Oonuma Japan 9 234 0.4× 153 0.4× 68 0.3× 208 1.0× 50 0.5× 26 569
Adam Studebaker United States 13 396 0.7× 140 0.4× 146 0.7× 444 2.2× 37 0.3× 21 885

Countries citing papers authored by Matteo Forloni

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Forloni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Forloni

This figure shows the co-authorship network connecting the top 25 collaborators of Matteo Forloni. A scholar is included among the top collaborators of Matteo Forloni based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Matteo Forloni. Matteo Forloni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Forloni, Matteo, et al.. (2019). Oligonucleotide-Directed Mutagenesis by Elimination of a Unique Restriction Site (USE Mutagenesis). Cold Spring Harbor Protocols. 2019(1). pdb.prot097782–pdb.prot097782. 4 indexed citations
2.
Forloni, Matteo, et al.. (2019). Methods for In Vitro Mutagenesis. Cold Spring Harbor Protocols. 2019(12). pdb.top097733–pdb.top097733. 4 indexed citations
3.
Forloni, Matteo, et al.. (2019). Saturation Mutagenesis by Codon Cassette Insertion. Cold Spring Harbor Protocols. 2019(1). pdb.prot097790–pdb.prot097790. 5 indexed citations
4.
Forloni, Matteo, et al.. (2019). Random Scanning Mutagenesis. Cold Spring Harbor Protocols. 2019(6). pdb.prot097808–pdb.prot097808. 1 indexed citations
5.
Forloni, Matteo, et al.. (2019). Multisite-Directed Mutagenesis. Cold Spring Harbor Protocols. 2019(12). pdb.prot097816–pdb.prot097816. 3 indexed citations
6.
Forloni, Matteo, et al.. (2019). Megaprimer Polymerase Chain Reaction (PCR)-Based Mutagenesis. Cold Spring Harbor Protocols. 2019(6). pdb.prot097824–pdb.prot097824. 16 indexed citations
7.
Forloni, Matteo, et al.. (2018). Random Mutagenesis Using Error-Prone DNA Polymerases. Cold Spring Harbor Protocols. 2018(3). pdb.prot097741–pdb.prot097741. 4 indexed citations
8.
Forloni, Matteo, et al.. (2018). In Vitro Mutagenesis Using Double-Stranded DNA Templates: Selection of Mutants with DpnI. Cold Spring Harbor Protocols. 2018(3). pdb.prot097766–pdb.prot097766. 14 indexed citations
9.
Forloni, Matteo, et al.. (2018). Creating Insertions or Deletions Using Overlap Extension Polymerase Chain Reaction (PCR) Mutagenesis. Cold Spring Harbor Protocols. 2018(8). pdb.prot097758–pdb.prot097758. 13 indexed citations
10.
Forloni, Matteo, et al.. (2018). Altered β-Lactamase Selection Approach for Site-Directed Mutagenesis. Cold Spring Harbor Protocols. 2018(8). pdb.prot097774–pdb.prot097774. 1 indexed citations
11.
Gupta, Romi, Matteo Forloni, Malik Bisserier, et al.. (2016). Interferon alpha-inducible protein 6 regulates NRASQ61K-induced melanomagenesis and growth. eLife. 5. 21 indexed citations
12.
Forloni, Matteo, Romi Gupta, Arvindhan Nagarajan, et al.. (2016). Oncogenic EGFR Represses the TET1 DNA Demethylase to Induce Silencing of Tumor Suppressors in Cancer Cells. Cell Reports. 16(2). 457–471. 55 indexed citations
13.
Forloni, Matteo, Shaillay Kumar Dogra, Darryl Conte, et al.. (2014). miR-146a promotes the initiation and progression of melanoma by activating Notch signaling. eLife. 3. e01460–e01460. 98 indexed citations
14.
Lorenzi, Silvia, Matteo Forloni, Loredana Cifaldi, et al.. (2012). IRF1 and NF-kB Restore MHC Class I-Restricted Tumor Antigen Processing and Presentation to Cytotoxic T Cells in Aggressive Neuroblastoma. PLoS ONE. 7(10). e46928–e46928. 76 indexed citations
15.
Cifaldi, Loredana, Elisa Lo Monaco, Matteo Forloni, et al.. (2011). Natural Killer Cells Efficiently Reject Lymphoma Silenced for the Endoplasmic Reticulum Aminopeptidase Associated with Antigen Processing. Cancer Research. 71(5). 1597–1606. 64 indexed citations
16.
Lizardi, Paul M., Matteo Forloni, & Narendra Wajapeyee. (2011). Genome-wide approaches for cancer gene discovery. Trends in biotechnology. 29(11). 558–568. 19 indexed citations
17.
Forloni, Matteo, Sonia Albini, Loredana Cifaldi, et al.. (2010). NF-κB, and not MYCN, Regulates MHC Class I and Endoplasmic Reticulum Aminopeptidases in Human Neuroblastoma Cells. Cancer Research. 70(3). 916–924. 62 indexed citations
18.
Fontana, Laura, Micol Eleonora Fiori, Sonia Albini, et al.. (2008). Antagomir-17-5p Abolishes the Growth of Therapy-Resistant Neuroblastoma through p21 and BIM. PLoS ONE. 3(5). e2236–e2236. 308 indexed citations
19.
Fruci, Doriana, Patrizio Giacomini, Maria Rita Nicotra, et al.. (2008). Altered expression of endoplasmic reticulum aminopeptidases ERAP1 and ERAP2 in transformed non‐lymphoid human tissues. Journal of Cellular Physiology. 216(3). 742–749. 79 indexed citations
20.
Guffanti, Elisa, Roberto Ferrari, Milena Preti, et al.. (2006). A Minimal Promoter for TFIIIC-dependent in Vitro Transcription of snoRNA and tRNA Genes by RNA Polymerase III. Journal of Biological Chemistry. 281(33). 23945–23957. 27 indexed citations

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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