Daniela Perotti

1.8k total citations
56 papers, 1.1k citations indexed

About

Daniela Perotti is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Daniela Perotti has authored 56 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 17 papers in Pediatrics, Perinatology and Child Health and 15 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Daniela Perotti's work include Renal and related cancers (42 papers), Renal cell carcinoma treatment (14 papers) and Ethics and Legal Issues in Pediatric Healthcare (9 papers). Daniela Perotti is often cited by papers focused on Renal and related cancers (42 papers), Renal cell carcinoma treatment (14 papers) and Ethics and Legal Issues in Pediatric Healthcare (9 papers). Daniela Perotti collaborates with scholars based in Italy, United Kingdom and United States. Daniela Perotti's co-authors include Paola Collini, Filippo Spreafico, Paolo Radice, Monica Terenziani, Kathy Pritchard‐Jones, Franca Fossati‐Bellani, Roberto Luksch, Norbert Graf, Paolo D’Angelo and Marry M. van den Heuvel‐Eibrink and has published in prestigious journals such as PLoS ONE, Cancer and Oncogene.

In The Last Decade

Daniela Perotti

55 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniela Perotti Italy	20	867	345	280	259	100	56	1.1k
Tino D. Piscione Canada	16	829 1.0×	188 0.5×	175 0.6×	252 1.0×	38 0.4×	21	1.1k
Boo Messahel United Kingdom	14	409 0.5×	223 0.6×	105 0.4×	54 0.2×	78 0.8×	24	582
Surya P. Rednam United States	11	322 0.4×	132 0.4×	137 0.5×	150 0.6×	70 0.7×	31	766
Jiarui Pu China	23	793 0.9×	144 0.4×	132 0.5×	51 0.2×	61 0.6×	45	1.4k
Linda King‐Underwood United Kingdom	15	629 0.7×	103 0.3×	130 0.5×	64 0.2×	65 0.7×	16	828
Diem Dao United States	9	669 0.8×	56 0.2×	239 0.9×	356 1.4×	48 0.5×	9	871
Fiona E. McRonald United Kingdom	14	467 0.5×	330 1.0×	40 0.1×	80 0.3×	40 0.4×	17	890
Montserrat Domènech Spain	17	317 0.4×	250 0.7×	24 0.1×	259 1.0×	60 0.6×	70	882
Oddrun Elise Olsen Norway	12	302 0.3×	114 0.3×	69 0.2×	52 0.2×	23 0.2×	24	556
Amy E. Schuster United States	9	321 0.4×	213 0.6×	32 0.1×	96 0.4×	62 0.6×	9	550

Countries citing papers authored by Daniela Perotti

Since Specialization

Citations

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

Fields of papers citing papers by Daniela Perotti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Perotti

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Perotti. A scholar is included among the top collaborators of Daniela Perotti 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 Daniela Perotti. Daniela Perotti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bertolotti, Alessia, Annalisa Serra, Giovanna Gattuso, et al.. (2024). Widening the spectrum of players affected by genetic changes in Wilms tumor relapse. iScience. 27(9). 110684–110684.

Fiore, Michele, Valentina Indio, Salvatore Nicola Bertuccio, et al.. (2023). Molecular Signature of Biological Aggressiveness in Clear Cell Sarcoma of the Kidney (CCSK). International Journal of Molecular Sciences. 24(4). 3743–3743. 6 indexed citations

Uno, Kaname, Caroline Jansson, Geoffroy Durand, et al.. (2023). A Gradual Transition Toward Anaplasia in Wilms Tumor Through Tolerance to Genetic Damage. Modern Pathology. 37(1). 100382–100382. 4 indexed citations

Spreafico, Filippo, Ronald R. de Krijger, Jarno Drost, et al.. (2021). Prognostic Factors for Wilms Tumor Recurrence: A Review of the Literature. Cancers. 13(13). 3142–3142. 34 indexed citations

Brok, Jesper, Annelies M. C. Mavinkurve‐Groothuis, Jarno Drost, et al.. (2020). Unmet needs for relapsed or refractory Wilms tumour: Mapping the molecular features, exploring organoids and designing early phase trials – A collaborative SIOP-RTSG, COG and ITCC session at the first SIOPE meeting. European Journal of Cancer. 144. 113–122. 19 indexed citations

Vujanić, Gordan, Manfred Gessler, Ariadne H.A.G. Ooms, et al.. (2019). Publisher Correction: The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nature Reviews Urology. 16(9). 563–563. 4 indexed citations

Vujanić, Gordan, Manfred Gessler, Ariadne H.A.G. Ooms, et al.. (2018). The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nature Reviews Urology. 15(11). 693–701. 151 indexed citations

Roversi, Gaia, M. Crippa, Daniela Perotti, et al.. (2015). Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors. Scientific Reports. 5(1). 15454–15454. 7 indexed citations

Perotti, Daniela, Filippo Spreafico, Federica Torri, et al.. (2012). Genomic profiling by whole‐genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse. Genes Chromosomes and Cancer. 51(7). 644–653. 20 indexed citations

10.

Zicari, Anna Maria, Luigi Tarani, Daniela Perotti, et al.. (2012). WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features. The Italian Journal of Pediatrics/Italian journal of pediatrics. 38(1). 27–27. 16 indexed citations

11.

Daidone, Maria Grazia, Paola Collini, Filippo Spreafico, et al.. (2011). Telomere maintenance in wilms tumors: First evidence for the presence of alternative lengthening of telomeres mechanism. Genes Chromosomes and Cancer. 50(10). 823–829. 13 indexed citations

12.

Cerrato, Flavia, Angela Sparago, Gaetano Verde, et al.. (2008). Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. Human Molecular Genetics. 17(10). 1427–1435. 66 indexed citations

13.

Terenziani, Monica, M. Testi, Filippo Spreafico, et al.. (2008). A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor. Pediatric Nephrology. 24(7). 1413–1417. 2 indexed citations

14.

Murrell, Adele, Yoko Itō, Gaetano Verde, et al.. (2008). Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer. PLoS ONE. 3(3). e1849–e1849. 83 indexed citations

15.

Renzo, Francesca Di, Luisa Doneda, Elena Menegola, et al.. (2006). The Murine Pou6f2 Gene is Temporally and Spatially Regulated During Kidney Embryogenesis and its Human Homolog is Overexpressed in a Subset of Wilms Tumors. Journal of Pediatric Hematology/Oncology. 28(12). 791–797. 8 indexed citations

16.

Spreafico, Filippo, Monica Terenziani, Elena Lualdi, et al.. (2006). Non‐chromosome 11‐p syndromes in Wilms tumor patients: Clinical and cytogenetic report of two Down syndrome cases and one Turner syndrome case. American Journal of Medical Genetics Part A. 143A(1). 85–88. 5 indexed citations

17.

Manoukian, Siranoush, John A. Crolla, M. Testi, et al.. (2005). Bilateral preaxial polydactyly in a WAGR syndrome patient. American Journal of Medical Genetics Part A. 134A(4). 426–429. 4 indexed citations

18.

Terenziani, Monica, Filippo Spreafico, Paola Collini, et al.. (2004). Adult Wilms' tumor: A monoinstitutional experience and a review of the literature. Cancer. 101(2). 289–293. 58 indexed citations

19.

Perotti, Daniela, P Mondini, Roberto Giardini, et al.. (1998). No evidence of WT1 involvement in a Burkitt’s lymphoma in a patient with Denys–Drash syndrome. Annals of Oncology. 9(6). 627–631. 5 indexed citations

20.

Ferrari, Andrea, Daniela Perotti, Roberto Giardini, et al.. (1997). Disseminated Burkitt's Lymphoma After Kidney Transplantation: A Case Report in a Boy with Drash Syndrome. The American journal of pediatric hematology/oncology. 19(2). 151–155. 5 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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