Luciana Chessa

6.6k total citations
75 papers, 2.7k citations indexed

About

Luciana Chessa is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Luciana Chessa has authored 75 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 27 papers in Cancer Research and 19 papers in Oncology. Recurrent topics in Luciana Chessa's work include DNA Repair Mechanisms (49 papers), Carcinogens and Genotoxicity Assessment (26 papers) and Cancer-related Molecular Pathways (19 papers). Luciana Chessa is often cited by papers focused on DNA Repair Mechanisms (49 papers), Carcinogens and Genotoxicity Assessment (26 papers) and Cancer-related Molecular Pathways (19 papers). Luciana Chessa collaborates with scholars based in Italy, United States and Japan. Luciana Chessa's co-authors include Richard A. Gatti, Domenico Delia, Yosef Shiloh, Patrick Concannon, Özden Sanal, Maria Piane, Sara Becker-Catania, Ewa Bernatowska, Mauro Magnani and Shuki Mizutani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Luciana Chessa

73 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Luciana Chessa Italy	28	2.1k	722	693	371	319	75	2.7k
Anna Merlos‐Suárez Spain	16	1.2k 0.6×	577 0.8×	1.2k 1.7×	306 0.8×	231 0.7×	18	2.5k
Ferenc Boldog United States	21	1.8k 0.9×	445 0.6×	517 0.7×	500 1.3×	232 0.7×	36	2.5k
Mathew J. Thayer United States	29	3.5k 1.6×	375 0.5×	477 0.7×	624 1.7×	192 0.6×	49	3.9k
Miller Huang United States	21	1.9k 0.9×	690 1.0×	483 0.7×	467 1.3×	106 0.3×	30	2.9k
Marcus Schuermann Germany	24	2.2k 1.0×	274 0.4×	626 0.9×	440 1.2×	343 1.1×	43	3.0k
Pierre Roux France	27	1.6k 0.8×	332 0.5×	656 0.9×	258 0.7×	171 0.5×	49	2.4k
Yosef Buganim Israel	26	2.3k 1.1×	401 0.6×	417 0.6×	275 0.7×	93 0.3×	47	2.9k
Mark Duquette United States	25	1.4k 0.7×	496 0.7×	359 0.5×	141 0.4×	204 0.6×	37	2.1k
Roel de Weger Netherlands	14	2.9k 1.4×	559 0.8×	649 0.9×	407 1.1×	97 0.3×	23	3.7k
Jason Howitt Australia	23	1.7k 0.8×	541 0.7×	201 0.3×	216 0.6×	335 1.1×	34	2.2k

Countries citing papers authored by Luciana Chessa

Since Specialization

Citations

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

Fields of papers citing papers by Luciana Chessa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luciana Chessa

This figure shows the co-authorship network connecting the top 25 collaborators of Luciana Chessa. A scholar is included among the top collaborators of Luciana Chessa 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 Luciana Chessa. Luciana Chessa 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

Menotta, Michele, Sara Biagiotti, Luigia Rossi, et al.. (2017). ATM splicing variants as biomarkers for low dose dexamethasone treatment of A-T. Orphanet Journal of Rare Diseases. 12(1). 126–126. 14 indexed citations

Menotta, Michele, Sara Biagiotti, Luigia Rossi, et al.. (2017). In vivo effects of dexamethasone on blood gene expression in ataxia telangiectasia. Molecular and Cellular Biochemistry. 438(1-2). 153–166. 19 indexed citations

Chessa, Luciana, Roberto Micheli, & Anna Molinaro. (2016). Focusing New Ataxia Telangiectasia Therapeutic Approaches. 2(2). 6 indexed citations

Piane, Maria, Anna Molinaro, Annarosa Soresina, et al.. (2016). Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders. Journal of the Neurological Sciences. 371. 48–53. 4 indexed citations

Rubattu, Speranza, Cristina Bozzao, Erika Pagannone, et al.. (2016). A Next-Generation Sequencing Approach to Identify Gene Mutations in Early- and Late-Onset Hypertrophic Cardiomyopathy Patients of an Italian Cohort. International Journal of Molecular Sciences. 17(8). 1239–1239. 21 indexed citations

Loconte, Daria Carmela, Valentina Grossi, Cristina Bozzao, et al.. (2015). Molecular and Functional Characterization of Three Different Postzygotic Mutations in PIK3CA-Related Overgrowth Spectrum (PROS) Patients: Effects on PI3K/AKT/mTOR Signaling and Sensitivity to PIK3 Inhibitors. PLoS ONE. 10(4). e0123092–e0123092. 52 indexed citations

Chessa, Luciana, Vincenzo Leuzzi, Alessandro Plebani, et al.. (2014). Intra-Erythrocyte Infusion of Dexamethasone Reduces Neurological Symptoms in Ataxia Teleangiectasia Patients: Results of a Phase 2 Trial. Orphanet Journal of Rare Diseases. 9(1). 5–5. 106 indexed citations

Grippaudo, Francesca Romana, Maria Piane, Matteo Amoroso, et al.. (2013). Cutaneous Venous Malformations Related to KRIT1 Mutation: Case Report and Literature Review. Journal of Molecular Neuroscience. 51(2). 442–445. 15 indexed citations

Folgori, Laura, Alessia Scarselli, Giulia Angelino, et al.. (2010). Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 36(1). 29–29. 20 indexed citations

10.

Lulli, Patrizia, Valentina Mangano, Chiara Batini, et al.. (2009). HLA-DRB1 and -DQB1 loci in three west African ethnic groups: Genetic relationship with sub-Saharan African and European populations. Human Immunology. 70(11). 903–909. 16 indexed citations

11.

Piane, Maria, Matteo Della Monica, Gianluca Piatelli, et al.. (2009). Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: Report of a novel mutation of the PCNT gene. American Journal of Medical Genetics Part A. 149A(11). 2452–2456. 29 indexed citations

12.

Masci, A., Daniela Mastronicola, Marzia Arese, et al.. (2007). Control of cell respiration by nitric oxide in Ataxia Telangiectasia lymphoblastoid cells. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1777(1). 66–73. 10 indexed citations

13.

Saviozzi, Silvia, Maria Piane, Sabrina Prudente, et al.. (2003). Six novel ATM mutations in Italian patients with classical ataxia-telangiectasia. Human Mutation. 21(4). 450–450. 9 indexed citations

14.

Sun, Xia, Sara Becker-Catania, Helen H. Chun, et al.. (2002). Early diagnosis of ataxia-telangiectasia using radiosensitivity testing. The Journal of Pediatrics. 140(6). 724–731. 95 indexed citations

15.

Becker-Catania, Sara, Gang Chen, Zhijun Wang, et al.. (2000). Ataxia-Telangiectasia: Phenotype/Genotype Studies of ATM Protein Expression, Mutations, and Radiosensitivity. Molecular Genetics and Metabolism. 70(2). 122–133. 88 indexed citations

16.

Teraoka, Sharon N., Milhan Telatar, Sara Becker-Catania, et al.. (1999). Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences. The American Journal of Human Genetics. 64(6). 1617–1631. 239 indexed citations

17.

Gilad, Shlomit, Rami Khosravi, Yael Ziv, et al.. (1998). Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel. Human Mutation. 11(1). 69–75. 30 indexed citations

18.

Telatar, Milhan, Sharon N. Teraoka, Zhijun Wang, et al.. (1998). Ataxia-Telangiectasia: Identification and Detection of Founder-Effect Mutations in the ATM Gene in Ethnic Populations. The American Journal of Human Genetics. 62(1). 86–97. 121 indexed citations

19.

Chessa, Luciana, Fiorella Nuzzo, Martina Stefanini, P. Lagomarsini, & G. Del Porto. (1991). Xeroderma pigmentosum: clonal chromosomal rearrangements in a pre-cancerous skin lesion.. PubMed. 8(3). 125–36. 2 indexed citations

20.

Cascino, Isabella, A. Benedetto, Maria Cristina Mazzilli, et al.. (1986). A Nonneutralizing Human IgM Monoclonal Antibody Inhibiting Hemagglutination of H3N2 Influenza A Strains. PubMed. 5(4). 307–318. 3 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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