Matteo Breno

1.2k total citations
24 papers, 786 citations indexed

About

Matteo Breno is a scholar working on Immunology, Nephrology and Geometry and Topology. According to data from OpenAlex, Matteo Breno has authored 24 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Immunology, 9 papers in Nephrology and 6 papers in Geometry and Topology. Recurrent topics in Matteo Breno's work include Complement system in diseases (10 papers), Renal Diseases and Glomerulopathies (9 papers) and Morphological variations and asymmetry (6 papers). Matteo Breno is often cited by papers focused on Complement system in diseases (10 papers), Renal Diseases and Glomerulopathies (9 papers) and Morphological variations and asymmetry (6 papers). Matteo Breno collaborates with scholars based in Italy, Belgium and Denmark. Matteo Breno's co-authors include Herwig Leirs, Giuseppe Remuzzi, Marina Noris, Caterina Mele, Stefan Van Dongen, Ariela Benigni, Lorena Longaretti, Elisabetta Valoti, Jonas Reijniers and Kristijn RR Swinnen and has published in prestigious journals such as Nature Communications, The Journal of Immunology and PLoS ONE.

In The Last Decade

Matteo Breno

24 papers receiving 773 citations

Peers

Matteo Breno
Richard J. Reynolds United States
Hayat Dagher Australia
Ya‐Huan Lou United States
D.A. Male Australia
Matteo Breno
Citations per year, relative to Matteo Breno Matteo Breno (= 1×) peers Arnout F. Gerritsen

Countries citing papers authored by Matteo Breno

Since Specialization
Citations

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

Fields of papers citing papers by Matteo Breno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matteo Breno

This figure shows the co-authorship network connecting the top 25 collaborators of Matteo Breno. A scholar is included among the top collaborators of Matteo Breno 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 Breno. Matteo Breno 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.
Trionfini, Piera, Paola Rizzo, Sara Conti, et al.. (2025). PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells. Scientific Reports. 15(1). 10375–10375. 4 indexed citations
2.
Piras, Rossella, Elisabetta Valoti, Marta Alberti, et al.. (2023). CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome. Frontiers in Immunology. 13. 1011580–1011580. 9 indexed citations
3.
Gastoldi, Sara, Sistiana Aiello, Miriam Galbusera, et al.. (2023). An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndrome. Frontiers in Immunology. 14. 1112257–1112257. 9 indexed citations
4.
Valoti, Elisabetta, Rossella Piras, Caterina Mele, et al.. (2022). <b><i>Mycoplasma pneumoniae</i></b> Infection Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome. ˜The œNephron journals/Nephron journals. 146(6). 593–598. 2 indexed citations
5.
Piras, Rossella, Matteo Breno, Elisabetta Valoti, et al.. (2021). CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis. Frontiers in Genetics. 12. 670727–670727. 16 indexed citations
6.
Longaretti, Lorena, Piera Trionfini, Valerio Brizi, et al.. (2021). Unravelling the Role of PAX2 Mutation in Human Focal Segmental Glomerulosclerosis. Biomedicines. 9(12). 1808–1808. 5 indexed citations
7.
Valoti, Elisabetta, Marta Alberti, Matteo Breno, et al.. (2019). Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association. ˜The œNephron journals/Nephron journals. 142(3). 264–270. 2 indexed citations
8.
Valoti, Elisabetta, Marta Alberti, Paraskevas Iatropoulos, et al.. (2019). Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS. Frontiers in Immunology. 10. 853–853. 29 indexed citations
9.
Galbusera, Miriam, Marina Noris, Sara Gastoldi, et al.. (2019). An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome. American Journal of Kidney Diseases. 74(1). 56–72. 65 indexed citations
10.
Valoti, Elisabetta, Marina Noris, Annalisa Perna, et al.. (2019). Impact of a Complement Factor H Gene Variant on Renal Dysfunction, Cardiovascular Events, and Response to ACE Inhibitor Therapy in Type 2 Diabetes. Frontiers in Genetics. 10. 681–681. 9 indexed citations
11.
Breno, Matteo, Nicolò Ghiringhelli Borsa, Fengxiao Bu, et al.. (2018). Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. The Journal of Immunology. 200(7). 2464–2478. 119 indexed citations
12.
Perico, Luca, Marina Morigi, Cinzia Rota, et al.. (2017). Human mesenchymal stromal cells transplanted into mice stimulate renal tubular cells and enhance mitochondrial function. Nature Communications. 8(1). 983–983. 119 indexed citations
13.
Aiello, Sistiana, Lorena Longaretti, Silvia Faravelli, et al.. (2017). Extracellular vesicles derived from T regulatory cells suppress T cell proliferation and prolong allograft survival. Scientific Reports. 7(1). 11518–11518. 100 indexed citations
14.
Bots, Jessica, Matteo Breno, Luc De Schaepdrijver, & Stefan Van Dongen. (2016). Maternal Stress Affects Fetal Growth but Not Developmental Instability in Rabbits. Symmetry. 8(10). 101–101. 1 indexed citations
15.
Mele, Caterina, Mathieu Lemaire, Paraskevas Iatropoulos, et al.. (2015). Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. Clinical Journal of the American Society of Nephrology. 10(6). 1011–1019. 37 indexed citations
16.
Laudisoit, Anne, Dadi Falay, Dudu Akaibe, et al.. (2014). High Prevalence of Rickettsia typhi and Bartonella Species in Rats and Fleas, Kisangani, Democratic Republic of the Congo. American Journal of Tropical Medicine and Hygiene. 90(3). 463–468. 14 indexed citations
17.
Swinnen, Kristijn RR, Jonas Reijniers, Matteo Breno, & Herwig Leirs. (2014). A Novel Method to Reduce Time Investment When Processing Videos from Camera Trap Studies. PLoS ONE. 9(6). e98881–e98881. 60 indexed citations
18.
Meheretu, Yonas, et al.. (2013). Bartonella Prevalence and Genetic Diversity in Small Mammals from Ethiopia. Vector-Borne and Zoonotic Diseases. 13(3). 164–175. 22 indexed citations
19.
Breno, Matteo, Jessica Bots, & Stefan Van Dongen. (2013). Heritabilities of Directional Asymmetry in the Fore- and Hindlimbs of Rabbit Fetuses. PLoS ONE. 8(10). e76358–e76358. 7 indexed citations
20.
Breno, Matteo, Herwig Leirs, & Stefan Van Dongen. (2011). Traditional and geometric morphometrics for studying skull morphology during growth inMastomys natalensis(Rodentia: Muridae). Journal of Mammalogy. 92(6). 1395–1406. 40 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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