Daniela Perotti

1.8k citations
67 papers · 1.4k · h-index 20

Impact in

    • Renal and related cancers
    • Epigenetics and DNA Methylation
  • Genetics top 10%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities

Papers in

    • Renal and related cancers 45
    • Genetic Syndromes and Imprinting 4
    • Genomic variations and chromosomal abnormalities 3
    • Dermatological and Skeletal Disorders 2
    • Connective tissue disorders research 2

Daniela Perotti

65 papers receiving 1.3k citations

Peers

Daniela Perotti
Comparison fields: 5 of 59
  • Molecular Biology 805
  • Genetics 234
  • Cancer Research 65
  • Pulmonary and Respiratory Medicine 144
  • Pediatrics, Perinatology and Child Health 53
Replace Jeffrey S. Dome with:
Jeffrey S. Dome United States
Eric J. Gratias United States
Sonja Kiuru‐Kuhlefelt Finland
Hajime Takayasu Japan
Aurélie L. Vogt United States
Catherine Goudie Canada
Michihiro Yano Japan
Michelle A. Wood United States
Marieke Levitus Netherlands
Javier Suela Spain
Daniela Perotti relative to Jeffrey S. Dome United States Jeffrey S. Dome's profile →
Citations per field
00.5×2×4×5.8×
Jeffrey S. Dome · 1×
Citations per year

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

20 of 20 papers shown

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2018193
2 200894
3 200876
4 200472
5 200861
6 201552
7 202146
8 199645
9 201037
10 201335
11 200334
12 200433
13 200833
14 201431
15 201229
16 201228
17 201327
18 201626
19 202025
20 201723

About Daniela Perotti

Daniela Perotti is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine and Oncology, having authored 67 papers that have together received 1.4k indexed citations. Recurring topics across this work include Renal and related cancers (45 papers), Sarcoma Diagnosis and Treatment (5 papers), Genetic Syndromes and Imprinting (4 papers), Acute Lymphoblastic Leukemia research (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Lymphoma Diagnosis and Treatment (3 papers), Dermatological and Skeletal Disorders (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Molecular Biology (805 citations), Genetics (234 citations), Cancer Research (65 citations), Pulmonary and Respiratory Medicine (144 citations) and Pediatrics, Perinatology and Child Health (53 citations). Daniela Perotti has collaborated with scholars based in Italy, United Kingdom and Netherlands. Frequent co-authors include Filippo Spreafico, Paola Collini, Paolo Radice, Kathy Pritchard‐Jones, Monica Terenziani, Franca Fossati‐Bellani, Marry M. van den Heuvel‐Eibrink, Norbert M. Graf, Andrea Pession and Roberto Luksch. Their work appears in journals such as Pediatric Blood & Cancer, Genes Chromosomes and Cancer, Oncotarget, Nature Reviews Urology and Journal of Pediatric Hematology/Oncology.

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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