Roberto Valli

982 total citations
46 papers, 542 citations indexed

About

Roberto Valli is a scholar working on Genetics, Immunology and Molecular Biology. According to data from OpenAlex, Roberto Valli has authored 46 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 18 papers in Immunology and 14 papers in Molecular Biology. Recurrent topics in Roberto Valli's work include Blood disorders and treatments (18 papers), Immunodeficiency and Autoimmune Disorders (15 papers) and Acute Myeloid Leukemia Research (9 papers). Roberto Valli is often cited by papers focused on Blood disorders and treatments (18 papers), Immunodeficiency and Autoimmune Disorders (15 papers) and Acute Myeloid Leukemia Research (9 papers). Roberto Valli collaborates with scholars based in Italy, United States and Latvia. Roberto Valli's co-authors include Emanuela Maserati, Francesco Pasquali, Annalisa Frattini, Francesco Lo Curto, Giuseppe Montalbano, Antonella Minelli, Marco Fabbri, Giovanni Porta, Cesare Danesino and Laura Gribaldo and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Roberto Valli

44 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberto Valli Italy 14 231 214 190 118 88 46 542
Francesca Ferrua Italy 14 241 1.0× 248 1.2× 167 0.9× 93 0.8× 65 0.7× 21 545
Roberta Zuntini Italy 14 145 0.6× 235 1.1× 278 1.5× 40 0.3× 61 0.7× 39 669
Michael Ehrhardt United States 13 166 0.7× 211 1.0× 295 1.6× 224 1.9× 44 0.5× 20 702
Mario Pujato United States 11 86 0.4× 250 1.2× 157 0.8× 44 0.4× 47 0.5× 20 594
Denise Petersen United States 12 340 1.5× 494 2.3× 127 0.7× 230 1.9× 56 0.6× 16 819
Yoji Ogasawara Japan 12 214 0.9× 428 2.0× 152 0.8× 255 2.2× 41 0.5× 47 817
Malin Melin Sweden 13 514 2.2× 236 1.1× 306 1.6× 44 0.4× 36 0.4× 20 799
Jennifer L. Gori United States 13 133 0.6× 372 1.7× 54 0.3× 65 0.6× 45 0.5× 23 625
Jenice D’Costa United States 10 152 0.7× 270 1.3× 75 0.4× 60 0.5× 77 0.9× 13 524
Séverine Charles France 13 468 2.0× 458 2.1× 107 0.6× 49 0.4× 113 1.3× 20 814

Countries citing papers authored by Roberto Valli

Since Specialization
Citations

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

Fields of papers citing papers by Roberto Valli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Valli

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Valli. A scholar is included among the top collaborators of Roberto Valli 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 Roberto Valli. Roberto Valli 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.
Danesino, Cesare, Federico Biglioli, Laura Moneghini, et al.. (2024). Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis. International Journal of Molecular Sciences. 25(19). 10664–10664.
2.
Nardo, Maddalena Di, Simonetta Astigiano, Silvia Baldari, et al.. (2024). The synergism of SMC1A cohesin gene silencing and bevacizumab against colorectal cancer. Journal of Experimental & Clinical Cancer Research. 43(1). 49–49. 4 indexed citations
3.
Terrinoni, Alessandro, Sabrina Caporali, Sergio Bernardini, et al.. (2023). OTX Genes in Adult Tissues. International Journal of Molecular Sciences. 24(23). 16962–16962. 2 indexed citations
4.
Campomenosi, Paola, Lorenzo Mortara, Barbara Bassani, et al.. (2023). The Potential Role of the T2 Ribonucleases in TME-Based Cancer Therapy. Biomedicines. 11(8). 2160–2160. 2 indexed citations
5.
6.
L’Abbate, Alberto, Ester Pungolino, Roberto Valli, et al.. (2023). Occurrence of L1M Elements in Chromosomal Rearrangements Associated to Chronic Myeloid Leukemia (CML): Insights from Patient-Specific Breakpoints Characterization. Genes. 14(7). 1351–1351. 1 indexed citations
7.
Bruno, Antonino, Douglas M. Noonan, Roberto Valli, et al.. (2022). Human RNASET2: A Highly Pleiotropic and Evolutionary Conserved Tumor Suppressor Gene Involved in the Control of Ovarian Cancer Pathogenesis. International Journal of Molecular Sciences. 23(16). 9074–9074. 5 indexed citations
8.
Azzolini, Claudio, Simone Donati, Roberto Valli, et al.. (2021). Expression of Otx Genes in Müller Cells Using an In Vitro Experimental Model of Retinal Hypoxia. Journal of Ophthalmology. 2021. 1–10. 5 indexed citations
9.
Khan, Abdul Waheed, Alyssa L. Kennedy, Elissa Furutani, et al.. (2021). The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations. Molecular Cytogenetics. 14(1). 54–54. 11 indexed citations
10.
Montalbano, Giuseppe, Francesco Acquati, Cristina Giaroni, et al.. (2021). Soy diet induces intestinal inflammation in adult Zebrafish: Role of OTX and P53 family. International Journal of Experimental Pathology. 103(1). 13–22. 9 indexed citations
11.
Marcozzi, Cristiana, et al.. (2020). Paracrine Effect of Human Adipose-Derived Stem Cells on Lymphatic Endothelial Cells. Regenerative Medicine. 15(9). 2085–2098. 13 indexed citations
12.
Khan, Abdul Waheed, Antonella Minelli, Annalisa Frattini, et al.. (2020). Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype. Molecular Cytogenetics. 13(1). 1–1. 2 indexed citations
13.
Angaroni, Fabrizio, Francesca D’Avila, Andrea Conti, et al.. (2018). gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML. Cell Death and Disease. 9(3). 349–349. 6 indexed citations
14.
Bosi, Annalisa, Marco Fabbri, Edoardo Pedrini, et al.. (2018). The human RNASET2 protein affects the polarization pattern of human macrophages in vitro. Immunology Letters. 203. 102–111. 20 indexed citations
15.
Maserati, Emanuela, et al.. (2017). Novel recurrent chromosome anomalies in Shwachman Diamond syndrome. IrInSubria (University of Insubria). 1 indexed citations
16.
Pangrazio, Alessandra, Annalisa Frattini, Roberto Valli, et al.. (2012). A Homozygous Contiguous Gene Deletion in Chromosome 16p13.3 Leads to Autosomal Recessive Osteopetrosis in a Jordanian Patient. Calcified Tissue International. 91(4). 250–254. 9 indexed citations
17.
Tassano, Elisa, Roberto Valli, Concetta Micalizzi, et al.. (2012). New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6. Leukemia & lymphoma. 53(12). 2434–2438. 1 indexed citations
18.
Valli, Roberto, et al.. (2011). Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula. Cancer Genetics. 204(4). 216–218. 21 indexed citations
19.
Porta, Giovanni, Elia Mattarucchi, Emanuela Maserati, et al.. (2007). Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR. Journal of Pediatric Hematology/Oncology. 29(3). 163–165. 4 indexed citations
20.
Minelli, Antonella, Emanuela Maserati, Gabriele Rossi, et al.. (2004). Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies. Genes Chromosomes and Cancer. 40(3). 165–171. 18 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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