Daniela Perotti

1.8k citations

56 papers · 1.1k indexed · h-index 20

Impact in

Pediatrics, Perinatology and Child Health top 5%
- Ethics and Legal Issues in Pediatric Healthcare
- Prenatal Screening and Diagnostics
- Childhood Cancer Survivors' Quality of Life
Molecular Biology top 10%
- Renal and related cancers
- Epigenetics and DNA Methylation

Papers in ⓘ

Pediatrics, Perinatology and Child Health 17
- Ethics and Legal Issues in Pediatric Healthcare 9
- Prenatal Screening and Diagnostics 7
Molecular Biology 48
- Renal and related cancers 42
- Epigenetics and DNA Methylation 5

Co-authors: Paola Collini (29 shared papers)Filippo Spreafico (34 shared papers)Paolo Radice (26 shared papers)Monica Terenziani (18 shared papers)Kathy Pritchard‐Jones (6 shared papers)Franca Fossati‐Bellani (13 shared papers)Roberto Luksch (9 shared papers)Norbert Graf (5 shared papers)
Journals: Pediatric Blood & Cancer (6 papers)Oncotarget (4 papers)Genes Chromosomes and Cancer (4 papers)Journal of Pediatric Hematology/Oncology (3 papers)Scientific Reports (2 papers)
Partner nations: Italy United Kingdom United States

In The Last Decade

Daniela Perotti

55 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Daniela Perotti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Daniela Perotti Line = papers co-authored together Daniela Perotti links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol Nature Reviews Urology ·(unknown), Gordan Vujanić, Manfred Gessler, Ariadne H.A.G. Ooms, Paola Collini, Aurore Coulomb L’Herminé, Ellen D’Hooghe, Ronald R. de Krijger, Daniela Perotti, Kathy Pritchard‐Jones, Christian Vokuhl, Marry M. van den Heuvel‐Eibrink, Norbert Graf	2018	151
2	Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer PLoS ONE ·Adele Murrell, Yoko Itō, Gaetano Verde, Joanna E. Huddleston, Kathryn Woodfine, Margherita Silengo, Filippo Spreafico, Daniela Perotti, Agostina De Crescenzo, Angela Sparago, Flavia Cerrato, Andrea Riccio	2008	83
3	Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour Human Molecular Genetics ·Flavia Cerrato, Angela Sparago, Gaetano Verde, Agostina De Crescenzo, Valentina Citro, Maria Vittoria Cubellis, M M Rinaldi, Luigi Boccuto, Giampiero Neri, Corrado Magnani, Paolo D’Angelo, Paola Collini, Daniela Perotti, Gianfranco Sebastio, Eamonn R. Maher, Andrea Riccio	2008	66
4	Adult Wilms' tumor: A monoinstitutional experience and a review of the literature Cancer ·Monica Terenziani, Filippo Spreafico, Paola Collini, Luigi Piva, Daniela Perotti, Marta Podda, Lorenza Gandola, Maura Massimino, Stefano Cereda, Graziella Cefalo, Roberto Luksch, Michela Casanova, Andrea Ferrari, Daniela Polastri, Pinuccia Valagussa, Franca Fossati‐Bellani	2004	58
5	Functional inactivation of the WTX gene is not a frequent event in Wilms’ tumors Oncogene ·Daniela Perotti, Beatrice Gamba, Michele Sardella, Filippo Spreafico, Monica Terenziani, Paola Collini, Andrea Pession, Marilina Nantron, Franca Fossati‐Bellani, Paolo Radice, (unknown)	2008	48
6	Lipoprotein(a) and other lipids after oophorectomy and estrogen replacement therapy Obstetrics and Gynecology ·F. Bruschi, Michele Meschìa, Maurizio R. Soma, Daniela Perotti, R. Paoletti, P GIORGIOCROSIGNANI	1996	46
7	Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney Oncotarget ·Annalisa Astolfi, Fraia Melchionda, Daniela Perotti, Maura Fois, Valentina Indio, Milena Urbini, Chiara Giusy Genovese, Paola Collini, Nunzio Salfi, Marilina Nantron, Paolo D’Angelo, Filippo Spreafico, Andrea Pession	2015	45
8	Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors Genomics ·Monica Miozzo, Daniela Perotti, Fabiola Minoletti, P Mondini, Silvana Pilotti, Roberto Luksch, Franca Fossati-Bellani, Marco A. Pierotti, Gabriella Sozzi, Paolo Radice	1996	41
9	Prognostic Factors for Wilms Tumor Recurrence: A Review of the Literature Cancers ·Alissa Groenendijk, Filippo Spreafico, Ronald R. de Krijger, Jarno Drost, Jesper Brok, Daniela Perotti, Harm van Tinteren, Rajkumar Venkatramani, Jan Godziński, Christian Rübe, James I. Geller, Norbert Graf, Marry M. van den Heuvel‐Eibrink, Annelies M. C. Mavinkurve‐Groothuis	2021	34
10	Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome Epigenetics ·Mariarosaria Calvello, Silvia Tabano, Patrizia Colapietro, Silvia Maitz, Alessandra Pansa, Claudia Augello, Faustina Lalatta, Barbara Gentilin, Filippo Spreafico, Luciano Calzari, Daniela Perotti, Lidia Larizza, Silvia Russo, Angelo Selicorni, Silvia Maria Sirchia, Monica Miozzo	2013	31
11	Germline mutations of thePOU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14 Human Mutation ·Daniela Perotti, Giovanna De Vecchi, M. Testi, Elena Lualdi, Piergiorgio Modena, P Mondini, Fernando Ravagnani, Paola Collini, Francesca Di Renzo, Filippo Spreafico, Monica Terenziani, Gabriella Sozzi, Franca Fossati‐Bellani, Paolo Radice	2004	30
12	Immunomodulation in a Treatment Program Including Pre- and Post-Operative Interleukin-2 and Chemotherapy for Childhood Osteosarcoma Tumori Journal ·Roberto Luksch, Daniela Perotti, Graziella Cefalo, Carlo Gambacorti‐Passerini, Maura Massimino, Filippo Spreafico, Michela Casanova, Andrea Ferrari, Monica Terenziani, Daniela Polastri, Felicita Gambirasio, Marta Podda, Fabio Bozzi, F. Ravagnani, Giorgio Parmiani, Franca Fossati Bellani	2003	29
13	The IGF signalling pathway in Wilms tumours - A report from the ENCCA Renal Tumours Biology-driven drug development workshop Oncotarget ·Mariana Maschietto, Jocelyn Charlton, Daniela Perotti, Paolo Radice, James I. Geller, Kathy Pritchard‐Jones, Mark C. Willingham	2014	27
14	Treatment of high‐risk relapsed Wilms tumor with dose‐intensive chemotherapy, marrow‐ablative chemotherapy, and autologous hematopoietic stem cell support: Experience by the Italian association of pediatric hematology and oncology Pediatric Blood & Cancer ·Filippo Spreafico, Gianni Bisogno, Paola Collini, Alessandro Jenkner, Lorenza Gandola, Paolo D’Angelo, Gabriella Casazza, Luigi Piva, Roberto Luksch, Daniela Perotti, Andrea Pession, Franca Fagioli, Sandro Dallorso	2008	26
15	Loss of Heterozygosity Analysis at Different Chromosome Regions in Wilms Tumor Confirms 1p Allelic Loss as a Marker of Worse Prognosis: A Study from the Italian Association of Pediatric Hematology and Oncology The Journal of Urology ·Filippo Spreafico, Beatrice Gamba, Luigi Mariani, Paola Collini, Paolo D’Angelo, Andrea Pession, Andrea Di Cataldo, Paolo Indolfi, Marilina Nantron, Monica Terenziani, Carlo Morosi, Paolo Radice, Daniela Perotti, (unknown)	2012	26
16	Is Wilms Tumor a Candidate Neoplasia for Treatment with WNT/β-Catenin Pathway Modulators?—A Report from the Renal Tumors Biology-Driven Drug Development Workshop Molecular Cancer Therapeutics ·Daniela Perotti, Peter Hohenstein, Italia Bongarzone, Mariana Maschietto, Mark C. Willingham, Paolo Radice, Kathy Pritchard‐Jones	2013	23
17	Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: Cytogenetic, molecular and clinico‐pathological studies American Journal of Medical Genetics Part A ·Massimo Carella, Filippo Spreafico, Orazio Palumbo, Clelia Tiziana Storlazzi, Silvia Tabano, Monica Miozzo, L Miglionico, Savino Calvano, Giulia Sindici, Beatrice Gamba, Luciana Impera, Paola Collini, Leopoldo Zelante, Paolo Radice, Daniela Perotti	2010	21
18	Genomic profiling by whole‐genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse Genes Chromosomes and Cancer ·Daniela Perotti, Filippo Spreafico, Federica Torri, Beatrice Gamba, Pio D’Adamo, Sara Pizzamiglio, Monica Terenziani, Serena Catania, Paola Collini, Marilina Nantron, Andrea Pession, Maurizio Bianchi, Paolo Indolfi, Paolo D’Angelo, Franca Fossati‐Bellani, Paolo Verderio, Fabìo Macciardi, Paolo Radice, (unknown)	2012	20
19	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 ·Jesper Brok, Annelies M. C. Mavinkurve‐Groothuis, Jarno Drost, Daniela Perotti, James I. Geller, Amy L. Walz, Birgit Geoerger, Claudia Pasqualini, Arnauld Verschuur, Angela Polanco, K. Pritchard-Jones, Marry van den Heuvel‐Eibrink, Norbert Graf, Filippo Spreafico	2020	19
20	Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11 Genomics ·Paolo Radice, Daniela Perotti, Virna De Benedetti, P Mondini, Maria Teresa Radice, Silvana Pilotti, Roberto Luksch, Franca Fossati Bellani, Marco A. Pierotti	1995	19

About Daniela Perotti

Daniela Perotti is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology, Pathology and Forensic Medicine, Urology and Developmental Biology, having authored 56 papers that have together received 1.1k indexed citations. Recurring topics across this work include Renal and related cancers (42 papers), Renal cell carcinoma treatment (14 papers), Ethics and Legal Issues in Pediatric Healthcare (9 papers), Prenatal Screening and Diagnostics (7 papers), Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (5 papers), Lymphoma Diagnosis and Treatment (4 papers) and Tumors and Oncological Cases (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (280 citations), Molecular Biology (867 citations), Urology (79 citations), Pulmonary and Respiratory Medicine (345 citations) and Genetics (259 citations). Daniela Perotti has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Paola Collini, Filippo Spreafico, Paolo Radice, Monica Terenziani, Kathy Pritchard‐Jones, Franca Fossati‐Bellani, Roberto Luksch, Norbert Graf, Marry M. van den Heuvel‐Eibrink and Paolo D’Angelo. Their work appears in journals such as Pediatric Blood & Cancer, Oncotarget, Genes Chromosomes and Cancer, Journal of Pediatric Hematology/Oncology and Scientific Reports.

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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