Lucia Pedace

1.1k total citations
27 papers, 391 citations indexed

About

Lucia Pedace is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lucia Pedace has authored 27 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lucia Pedace's work include Glioma Diagnosis and Treatment (7 papers), Epigenetics and DNA Methylation (6 papers) and Sarcoma Diagnosis and Treatment (5 papers). Lucia Pedace is often cited by papers focused on Glioma Diagnosis and Treatment (7 papers), Epigenetics and DNA Methylation (6 papers) and Sarcoma Diagnosis and Treatment (5 papers). Lucia Pedace collaborates with scholars based in Italy, Lebanon and United States. Lucia Pedace's co-authors include Evelina Miele, Marco Tartaglia, Andrea Ciolfi, Angela Mastronuzzi, Franco Locatelli, Giuseppe Aiello, Elisabetta Ferretti, Francesca Gianno, Marina Cardano and Claudio Ballabio and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Lucia Pedace

23 papers receiving 388 citations

Peers

Lucia Pedace
Antje Arnold United States
Mark W. Youngblood United States
Ali Jalali United States
Sean Tsao United States
T. Schweitzer Germany
Anke Leinhaas Germany
Da‐Young Chang South Korea
Michele Kyle United States
Wojciech Przylecki United States
S U Kim South Korea
Antje Arnold United States
Lucia Pedace
Citations per year, relative to Lucia Pedace Lucia Pedace (= 1×) peers Antje Arnold

Countries citing papers authored by Lucia Pedace

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Pedace

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Pedace

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Pedace. A scholar is included among the top collaborators of Lucia Pedace 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 Lucia Pedace. Lucia Pedace 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.
Barresi, Sabina, Matteo Cassandri, Isabella Giovannoni, et al.. (2025). Age-linked DNA methylation and gene expression patterns in parameningeal head and neck alveolar rhabdomyosarcoma reveal CDK9 as a promising therapeutic target. Pharmacological Research. 216. 107767–107767.
2.
Rossi, Marcelo, Andrea Ciolfi, Lucia Pedace, et al.. (2025). Genome-wide DNA methylation analysis identifies kidney epigenetic dysregulation in a cystinosis mouse model. Frontiers in Cell and Developmental Biology. 13. 1638123–1638123. 1 indexed citations
3.
Abballe, Luana, Lucia Pedace, Sabina Barresi, et al.. (2025). DNA methylation profiling from cerebrospinal fluid as a diagnostic tool for pineoblastoma. Acta Neuropathologica Communications. 13(1). 52–52.
4.
Barresi, Valeria, Evelina Miele, Lucia Pedace, et al.. (2024). CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors. Acta Neuropathologica Communications. 12(1). 8–8. 5 indexed citations
5.
Barresi, Sabina, Laura S. Hiemcke‐Jiwa, Lennart Kester, et al.. (2024). Spindle Cell Lesions with Oncogenic EGFR Kinase Domain Aberrations: Expanding the Spectrum of Protein Kinase–Related Mesenchymal Tumors. Modern Pathology. 37(9). 100539–100539. 3 indexed citations
6.
Pedace, Lucia, Sabina Barresi, Isabella Giovannoni, et al.. (2024). Quantification of tumour-infiltrating immune cells through deconvolution of DNA methylation data in Ewing sarcomas. SHILAP Revista de lepidopterología. 2.
7.
8.
Fragale, Alessandra, Emilia Stellacci, Giulia Romagnoli, et al.. (2023). Reversing vemurafenib‐resistance in primary melanoma cells by combined romidepsin and type I IFN treatment through blocking of tumorigenic signals and induction of immunogenic effects. International Journal of Cancer. 153(5). 1080–1095. 4 indexed citations
9.
Salgado, Cláudia, Rita Alaggio, Andrea Ciolfi, et al.. (2023). Pediatric BCOR-Altered Tumors From Soft Tissue/Kidney Display Specific DNA Methylation Profiles. Modern Pathology. 36(2). 100039–100039. 8 indexed citations
10.
Ballabio, Claudio, Marica Anderle, Evelina Miele, et al.. (2020). Modeling medulloblastoma in vivo and with human cerebellar organoids. Nature Communications. 11(1). 583–583. 118 indexed citations
11.
Ciolfi, Andrea, Erfan Aref‐Eshghi, Simone Pizzi, et al.. (2020). Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature. Clinical Epigenetics. 12(1). 7–7. 28 indexed citations
12.
Colafati, Giovanna Stefania, Francesca Diomedi‐Camassei, Andrea Ciolfi, et al.. (2019). Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review. Frontiers in Genetics. 10. 391–391. 20 indexed citations
13.
Kaji, Seiji, Toshitaka Kawarai, Ryosuke Miyamoto, et al.. (2016). Late-onset spastic paraplegia type 10 (SPG10) family presenting with bulbar symptoms and fasciculations mimicking amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 364. 45–49. 13 indexed citations
14.
Pedace, Lucia, Temistocle Lo Giudice, Fabrizio Gaudiello, et al.. (2015). ALS5/SPG11/KIAA1840mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease. Brain. 139(1). 73–85. 75 indexed citations
15.
Pedace, Lucia, Paola De Simone, Marco Castori, et al.. (2011). Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma. Cancer Epidemiology. 35(6). e116–e120. 18 indexed citations
16.
Cozzolino, Angela Maria, Lucia Pedace, Marco Castori, et al.. (2011). Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening. Familial Cancer. 11(2). 201–208. 9 indexed citations
17.
Pedace, Lucia, A. Amantea, Giovanna Zambruno, et al.. (2011). Molecular characterization of 11 Italian patients with Darier Disease. European Journal of Dermatology. 21(3). 334–338. 9 indexed citations
18.
Castori, Marco, Luigi Laino, Vito Briganti, et al.. (2010). Jejunal atresia and anterior chamber anomalies: Further delineation of the Strømme syndrome. European Journal of Medical Genetics. 53(3). 149–152. 5 indexed citations
19.
Castori, Marco, Evelina Silvestri, Lucia Pedace, et al.. (2009). Fontaine–Farriaux syndrome: A recognizable craniosynostosis syndrome with nail, skeletal, abdominal, and central nervous system anomalies. American Journal of Medical Genetics Part A. 149A(10). 2193–2199. 9 indexed citations
20.
Pedace, Lucia, Silvia Majore, Francesca Megiorni, et al.. (2008). Identification of a novel duplication in the APC gene using multiple ligation probe amplification in a patient with familial adenomatous polyposis. Cancer Genetics and Cytogenetics. 182(2). 130–135. 2 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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