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Edoardo Peroni · SciRah

Researcher profile · Semantic Scholar

Edoardo Peroni

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Edoardo Peroni — researcher profile on SciRah

h-index: 11
Works: 32
Citations: 338

Most-cited papers

Acute myeloid leukemia: from NGS, through scRNA-seq, to CAR-T. dissect cancer heterogeneity and tailor the treatment
Edoardo Peroni, M. Randi, A. Rosato, S. Cagnin
2023Journal of experimental & clinical cancer research : CR44 citations Open access
Semantic Scholar
Impact of mutational status on pregnancy outcome in patients with essential thrombocytemia
E. Rumi, I. Bertozzi, I. Casetti, E. Roncoroni +11 more
2015Haematologica39 citations Open access
Semantic Scholar
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohort
M. Randi, Giulia Geranio, I. Bertozzi, C. Micalizzi +18 more
2015British Journal of Haematology31 citations Open access
Semantic Scholar
Idiopathic erythrocytosis: a study of a large cohort with a long follow-up
M. Randi, I. Bertozzi, E. Cosi, C. Santarossa +2 more
2015Annals of Hematology30 citations
Semantic Scholar
Mutational profile of childhood myeloproliferative neoplasms
A. Karow, R. Nienhold, P. Lundberg, Edoardo Peroni +3 more
2015Leukemia29 citations
Semantic Scholar
Insights on Metabolic Reprogramming and Its Therapeutic Potential in Acute Leukemia
Ludovica Di Martino, V. Tosello, Edoardo Peroni, E. Piovan
2021International Journal of Molecular Sciences20 citations Open access
Semantic Scholar
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis
Marine Delamare, Amandine Le Roy, M. Pacault, Loïc Schmitt +38 more
2023Haematologica17 citations Open access
Semantic Scholar
Thrombotic risk correlates with mutational status in true essential thrombocythemia
I. Bertozzi, Edoardo Peroni, G. Coltro, G. Bogoni +4 more
2016European Journal of Clinical Investigation17 citations
Semantic Scholar
Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature
A. Girolami, Valentina Tasinato, L. Sambado, Edoardo Peroni +1 more
2015Blood Coagulation and Fibrinolysis15 citations
Semantic Scholar
Bone marrow histology for the diagnosis of essential thrombocythemia in children: a multicenter Italian study.
M. Putti, M. Pizzi, I. Bertozzi, E. Sabattini +9 more
2017Blood14 citations Open access
Semantic Scholar
Spatial-transcriptomic profiling: a new lens for understanding myelofibrosis pathophysiology
Edoardo Peroni, Elisabetta Calistri, Rosario Amato, M. Gottardi +1 more
2024Cell Communication and Signaling12 citations Open access
Semantic Scholar
Hematologic Neoplasms Associated with Down Syndrome: Cellular and Molecular Heterogeneity of the Diseases
Edoardo Peroni, M. Gottardi, L. D'Antona, M. Randi +2 more
2023International Journal of Molecular Sciences11 citations Open access
Semantic Scholar
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiency
A. Girolami, Giulia Berti de Marinis, I. Bertozzi, Edoardo Peroni +2 more
2013European Journal of Haematology11 citations
Semantic Scholar
Myocardial Infarctions and Other Acute Coronary Syndromes in Rare Congenital Bleeding Disorders
A. Girolami, S. Ferrari, L. Sambado, Edoardo Peroni +1 more
2015Clinical and applied thrombosis/hemostasis10 citations
Semantic Scholar
Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficiencies
A. Girolami, E. Cosi, Valentina Tasinato, Edoardo Peroni +2 more
2016Blood Coagulation and Fibrinolysis8 citations
Semantic Scholar
The Old and the New in Prekallikrein Deficiency: Historical Context and a Family from Argentina with PK Deficiency due to a New Mutation (Arg541Gln) in Exon 14 Associated with a Common Polymorphysm (Asn124Ser) in Exon 5
J. Vidal, Marcela Salagh, Nora Gervan, Maria Parody +4 more
2014Seminars in Thrombosis and Hemostasis8 citations
Semantic Scholar
Congenital factor XI and factor VII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: An intriguing observation†
A. Girolami, Edoardo Peroni, B. Girolami, Silvia Ferrari +1 more
2016Hematology7 citations Open access
Semantic Scholar
High ETV6 Levels Support Aggressive B Lymphoma Cell Survival and Predict Poor Outcome in Diffuse Large B-Cell Lymphoma Patients
D. Marino, M. Pizzi, Iuliia Kotova, R. Schmidt +11 more
2022Cancers6 citations Open access
Semantic Scholar
Two novel missense mutations in EPOR gene causes erythrocytosis in two unrelated patients
Edoardo Peroni, I. Bertozzi, F. Gherlinzoni, P. Stefani +4 more
2018British Journal of Haematology5 citations Open access
Semantic Scholar
Darboux transformations and related non-Abelian integrable differential-difference systems of the derivative nonlinear Schrödinger type
Edoardo Peroni, Jing-Ping Wang
2025Physica A: Statistical Mechanics and its Applications3 citations
Semantic Scholar
Associated risk factors and arterial occlusions in patients with von Willebrand disease: Analysis of the literature and report of two cases
A. Girolami, S. Ferrari, A. Bertomoro, Edoardo Peroni +2 more
20141 citations Open access
Semantic Scholar
Effect of busulfan on JAK2V617F allele burden
M. Randi, C. Santarossa, Edoardo Peroni, E. Cosi +3 more
2014Haematologica1 citations Open access
Semantic Scholar
Spatially resolved transcriptomic profiling of myelofibrosis spleen reveals compartment specific niche programs
Edoardo Peroni, Marco Pizzi, Marco Basso, Alessandro Atanasio +3 more
2026Experimental Hematology & Oncology0 citations Open access
Semantic Scholar
Antigen recognition licenses therapeutic CD8+ T cells to organize a multicellular myeloid interaction network in the tumor microenvironment
Alfredo Pherez-Farah, W. de Koning, Wei-Sha Qi, Gioia Boncompagni +10 more
2026bioRxiv0 citations Open access
Semantic Scholar
The spatial and multi-omic landscape of Down syndrome leukemogenesis: moving beyond cellular heterogeneity
Edoardo Peroni, Rosario Amato, M. Bado, Mosé Favarato +1 more
2026Experimental Hematology & Oncology0 citations Open access
Semantic Scholar
Isoform-Specific TRIOBP Truncating Variants in Deafness, Autosomal Recessive 28: A Case Study of Postlingual Moderate Sensorineural Hearing Loss.
D. Degiorgio, E. Greco, M. Beggio, Edoardo Peroni +7 more
2026The Journal of Applied Laboratory Medicine0 citations Open access
Semantic Scholar
Methodological Assessment of High-Throughput Sequencing Platforms: Illumina vs. MGI in Clinical-Grade CFTR Genotyping
M. Beggio, Edoardo Peroni, E. Greco, Giulia Favretto +3 more
2025International Journal of Molecular Sciences0 citations
Semantic Scholar
Hamiltonian and recursion operators for a discrete analogue of the Kaup-Kupershmidt equation
Edoardo Peroni, Jing-Ping Wang
2023Open Communications in Nonlinear Mathematical Physics0 citations Open access
Semantic Scholar
Sequencing of the hypoxia pathway genes in patients with congenital erythrocytoses by next generation sequencing
F. Girodon, F. Pacault, M. Airaud, C. Garrec +10 more
20170 citations
Semantic Scholar
CONGENITAL ERYTHROCYTOSIS ARE RARE DISORDERS WITH MANY GENES INVOLVED. FUNCTIONAL EVALUATION OF NOVEL PHD2 AND EPOR MUTATIONS.
Edoardo Peroni
20160 citations
Semantic Scholar
Anche la mutazione di Calr è rara nelle trombocitemie essenziali pediatriche
Giulia Geranio, Edoardo Peroni, M. L. Randi, I. Bertozzi +13 more
20140 citations
Semantic Scholar
A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15
A. Girolami, L. Sambado, Edoardo Peroni, L. Santarossa +1 more
2014Blood Coagulation and Fibrinolysis0 citations
Semantic Scholar
The Old and the New in Prekallikrein Deficiency: Historical Context and a Family from Argentina with PK Deficiency due to a New Mutation (Arg541Gln) in Exon 14 Associated with a Common Polymorphysm (Asn124Ser) in Exon 5
J. Vidal, Marcela Sabagh, Nora Gervan, Maria Parody +4 more
2014Seminars in Thrombosis and Hemostasis0 citations Open access
Semantic Scholar

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