Andrea Finocchi

6.6k total citations
84 papers, 1.8k citations indexed

About

Andrea Finocchi is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Andrea Finocchi has authored 84 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Immunology, 20 papers in Genetics and 16 papers in Molecular Biology. Recurrent topics in Andrea Finocchi's work include Immunodeficiency and Autoimmune Disorders (33 papers), Immune Cell Function and Interaction (17 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (13 papers). Andrea Finocchi is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (33 papers), Immune Cell Function and Interaction (17 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (13 papers). Andrea Finocchi collaborates with scholars based in Italy, United States and Sweden. Andrea Finocchi's co-authors include Paolo Rossi, Valerio Sanguigni, Pasquale Pignatelli, Caterina Cancrini, Francesco Violi, Maria Serena Chiriacò, Gigliola Di Matteo, Silvia Di Cesare, Maria Cristina Pietrogrande and Roberto Carnevale and has published in prestigious journals such as Circulation, SHILAP Revista de lepidopterología and The EMBO Journal.

In The Last Decade

Andrea Finocchi

82 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrea Finocchi Italy	24	886	505	330	286	269	84	1.8k
Jeng‐Hsien Yen Taiwan	29	1.3k 1.5×	556 1.1×	234 0.7×	223 0.8×	125 0.5×	132	2.7k
Lidan Zhao China	23	712 0.8×	536 1.1×	184 0.6×	144 0.5×	221 0.8×	85	1.9k
Ullrich Schwertschlag United States	18	811 0.9×	323 0.6×	321 1.0×	501 1.8×	179 0.7×	50	1.9k
Helen M. McGuire Australia	21	1.2k 1.4×	443 0.9×	291 0.9×	300 1.0×	209 0.8×	86	2.2k
Steven E. Carsons United States	27	908 1.0×	486 1.0×	230 0.7×	123 0.4×	316 1.2×	92	2.6k
Jeremy A. Sullivan United States	23	838 0.9×	626 1.2×	219 0.7×	135 0.5×	206 0.8×	49	2.2k
Atsuhisa Ueda Japan	28	560 0.6×	1.1k 2.1×	269 0.8×	145 0.5×	176 0.7×	90	2.6k
Kari Otterdal Norway	27	818 0.9×	553 1.1×	296 0.9×	121 0.4×	106 0.4×	63	2.2k
Mirko Ritter Germany	18	685 0.8×	497 1.0×	336 1.0×	114 0.4×	247 0.9×	23	1.8k
Bjarne Kuno Møller Denmark	24	552 0.6×	541 1.1×	259 0.8×	162 0.6×	138 0.5×	114	2.3k

Countries citing papers authored by Andrea Finocchi

Since Specialization

Citations

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

Fields of papers citing papers by Andrea Finocchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Finocchi

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

Rivalta, Beatrice, Paola Zangari, Lucia Pacillo, et al.. (2024). Epstein–Barr virus‐associated smooth muscle tumor in a female with ataxia telangiectasia: A case report. Pediatric Blood & Cancer. 71(7). e31019–e31019.

Romani, Lorenza, Maia De Luca, Paolo Palma, et al.. (2023). Novel Beta Lactam Antibiotics for the Treatment of Multidrug-Resistant Gram-Negative Infections in Children: A Narrative Review. Microorganisms. 11(7). 1798–1798. 10 indexed citations

Asperti, Claudia, Daniele Canarutto, Simona Porcellini, et al.. (2023). Scalable GMP-compliant gene correction of CD4+ T cells with IDLV template functionally validated in vitro and in vivo. Molecular Therapy — Methods & Clinical Development. 30. 546–557. 3 indexed citations

Canarutto, Daniele, Claudia Asperti, Valentina Vavassori, et al.. (2023). Unbiased assessment of genome integrity and purging of adverse outcomes at the target locus upon editing of CD4 ⁺ T‐cells for the treatment of Hyper IgM1. The EMBO Journal. 42(23). e114188–e114188. 5 indexed citations

Rotulo, Gioacchino Andrea, Giulia Ceglie, Carmela Giancotta, et al.. (2023). The Clinical Course of SARS-CoV-2 Infection in Patients With Autoimmune Neutropenia: A Retrospective Case Series Study. The Pediatric Infectious Disease Journal. 42(11). e403–e406.

Rivalta, Beatrice, Donato Amodio, Carmela Giancotta, et al.. (2022). Case Report: Successful Treatment With Monoclonal Antibodies in One APDS Patient With Prolonged SARS-CoV-2 Infection Not Responsive to Previous Lines of Treatment. Frontiers in Immunology. 13. 891274–891274. 4 indexed citations

Romani, Lorenza, Peter R. Williamson, Silvia Di Cesare, et al.. (2021). Cryptococcal Meningitis and Post-Infectious Inflammatory Response Syndrome in a Patient With X-Linked Hyper IgM Syndrome: A Case Report and Review of the Literature. Frontiers in Immunology. 12. 708837–708837. 9 indexed citations

Renga, Giorgia, Vasileios Oikonomou, Silvia Moretti, et al.. (2019). Thymosin β4 promotes autophagy and repair via HIF-1α stabilization in chronic granulomatous disease. Life Science Alliance. 2(6). e201900432–e201900432. 14 indexed citations

Pulvirenti, Federica, Alessandro Plebani, Annarosa Soresina, et al.. (2019). Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet). Journal of Clinical Immunology. 40(2). 289–298. 9 indexed citations

10.

Matteo, Gigliola Di, Maria Serena Chiriacò, Alessia Scarselli, et al.. (2018). JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long‐known gene. Molecular Genetics & Genomic Medicine. 6(5). 713–721. 9 indexed citations

11.

Cifaldi, Cristina, Maria Serena Chiriacò, Gigliola Di Matteo, et al.. (2017). Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ+ T and B Cells. Frontiers in Immunology. 8. 1893–1893. 5 indexed citations

12.

Chiriacò, Maria Serena, Giada Farinelli, Valentina Capo, et al.. (2014). Dual-regulated Lentiviral Vector for Gene Therapy of X-linked Chronic Granulomatosis. Molecular Therapy. 22(8). 1472–1483. 49 indexed citations

13.

Zuntini, Roberta, Caterina Cancrini, Andrea Finocchi, et al.. (2014). Consanguinity and Polygenic Diseases: A Model for Antibody Deficiencies. Human Heredity. 77(1-4). 144–149. 3 indexed citations

14.

Ariganello, Paola, Giulia Angelino, Alessia Scarselli, et al.. (2013). RelapsingCampylobacter jejuniSystemic Infections in a Child with X-Linked Agammaglobulinemia. SHILAP Revista de lepidopterología. 2013. 1–3. 13 indexed citations

15.

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

16.

Violi, Francesco, Valerio Sanguigni, Roberto Carnevale, et al.. (2009). Hereditary Deficiency of gp91 ^phox Is Associated With Enhanced Arterial Dilatation. Circulation. 120(16). 1616–1622. 109 indexed citations

17.

Chiriacò, Maria Serena, Gigliola Di Matteo, Emiliano Giardina, et al.. (2009). Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. Genetic Testing and Molecular Biomarkers. 13(6). 785–789. 7 indexed citations

18.

Matangkasombut, Ponpan, Muriel Pichavant, Silvia Giliani, et al.. (2007). Lack of iNKT cells in patients with combined immune deficiency due to hypomorphic RAG mutations. Blood. 111(1). 271–274. 24 indexed citations

19.

Bottini, Nunzio, et al.. (2001). Maternal-Fetal Interaction in the ABO System: A Comparative Analysis of Healthy Mothers and Couples with Recurrent Spontaneous Abortion Suggests a Protective Effect of B Incompatibility. Human Biology. 73(2). 167–174. 10 indexed citations

20.

Panunzi, C, Maria Luisa Manca Bitti, Ambrogio Di Paolo, et al.. (1998). [Goiter prevalence and urinary excretion of iodine in a sample of school age children in the city of Rome].. PubMed. 34(3). 409–12. 6 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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