Alessia Gozzini

1.2k total citations
34 papers, 833 citations indexed

About

Alessia Gozzini is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Alessia Gozzini has authored 34 papers receiving a total of 833 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Oncology. Recurrent topics in Alessia Gozzini's work include Cardiomyopathy and Myosin Studies (5 papers), Parathyroid Disorders and Treatments (4 papers) and Bone health and treatments (4 papers). Alessia Gozzini is often cited by papers focused on Cardiomyopathy and Myosin Studies (5 papers), Parathyroid Disorders and Treatments (4 papers) and Bone health and treatments (4 papers). Alessia Gozzini collaborates with scholars based in Italy, United States and Hungary. Alessia Gozzini's co-authors include Maria Luisa Brandi, L. Giovannini, Annalisa Tanini, A Bertelli, A Bertelli, Alberto Falchetti, Sílvia Carbonell Sala, Carmelo Mavilia, Francesca Del Monte and Francesca Marini and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biomaterials and Journal of Bone and Joint Surgery.

In The Last Decade

Alessia Gozzini

31 papers receiving 801 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessia Gozzini Italy 17 259 217 193 142 124 34 833
Xiaoyan Wu China 23 532 2.1× 107 0.5× 74 0.4× 212 1.5× 89 0.7× 47 1.1k
Zhengzhe Li China 19 471 1.8× 117 0.5× 82 0.4× 160 1.1× 67 0.5× 33 1.1k
Luisa Salvatori Italy 20 477 1.8× 182 0.8× 174 0.9× 114 0.8× 50 0.4× 33 1.1k
Jinghuan Lv China 18 409 1.6× 147 0.7× 61 0.3× 90 0.6× 62 0.5× 37 885
Jingyan Xu China 18 311 1.2× 203 0.9× 63 0.3× 96 0.7× 237 1.9× 79 845
Jeong Kyu Kim South Korea 17 782 3.0× 197 0.9× 49 0.3× 185 1.3× 97 0.8× 59 1.2k
Feiyu Zhang China 15 376 1.5× 170 0.8× 56 0.3× 89 0.6× 56 0.5× 61 1.0k
Raghunatha R. Yammani United States 21 633 2.4× 107 0.5× 50 0.3× 100 0.7× 57 0.5× 35 1.3k
Jonas Feilchenfeldt Switzerland 12 389 1.5× 204 0.9× 61 0.3× 87 0.6× 68 0.5× 14 868

Countries citing papers authored by Alessia Gozzini

Since Specialization
Citations

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

Fields of papers citing papers by Alessia Gozzini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessia Gozzini

This figure shows the co-authorship network connecting the top 25 collaborators of Alessia Gozzini. A scholar is included among the top collaborators of Alessia Gozzini 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 Alessia Gozzini. Alessia Gozzini 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.
Bonanni, Fernando, Alessia Gozzini, Alberto Marchi, et al.. (2025). Autosomal recessive hypertrophic cardiomyopathy associated with variants in TRIM63. International Journal of Cardiology. 444. 134010–134010.
2.
Girolami, Francesca, Alessia Gozzini, Alessia Tomberli, et al.. (2023). Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked Questions. Journal of Clinical Medicine. 12(7). 2489–2489. 5 indexed citations
3.
Zampieri, Mattia, Chiara Zocchi, Gaia Spaziani, et al.. (2023). Focus on Paediatric Restrictive Cardiomyopathy: Frequently Asked Questions. Diagnostics. 13(24). 3666–3666.
4.
Girolami, Francesca, et al.. (2022). Clinical Exome Sequencing Revealed a De Novo FLNC Mutation in a Child with Restrictive Cardiomyopathy. SHILAP Revista de lepidopterología. 12(2). 206–211. 1 indexed citations
5.
Girolami, Francesca, Alessia Gozzini, Silvia Passantino, et al.. (2022). 263 GENETIC CAUSES OF CARDIOMYOPATHIES IN CHILDREN. European Heart Journal Supplements. 24(Supplement_K). 1 indexed citations
6.
Masi, Laura, Giovanni Beltrami, Serena Ottanelli, et al.. (2015). Human Preosteoblastic Cell Culture from a Patient with Severe Tumoral Calcinosis-Hyperphosphatemia Due to a New GALNT3 Gene Mutation: Study of In Vitro Mineralization. Calcified Tissue International. 96(5). 438–452. 10 indexed citations
7.
Pinchi, Vilma, Martina Focardi, Gian‐Aristide Norelli, et al.. (2013). DNA extraction method from teeth using QIAcube. Forensic science international. Genetics supplement series. 4(1). e276–e277. 6 indexed citations
8.
Falchetti, Alberto, Alessia Gozzini, Annalisa Terranegra, et al.. (2012). A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia. European Journal of Endocrinology. 166(5). 933–940. 3 indexed citations
9.
Anglani, Franca, Antonia Fabris, Alessia Gozzini, et al.. (2010). Identification of GDNF Gene Sequence Variations in Patients with Medullary Sponge Kidney Disease. Clinical Journal of the American Society of Nephrology. 5(7). 1205–1210. 30 indexed citations
10.
Masi, Laura, Alessia Gozzini, Alessandro Franchi, et al.. (2009). A Novel Recessive Mutation of Fibroblast Growth Factor-23 in Tumoral Calcinosis. Journal of Bone and Joint Surgery. 91(5). 1190–1198. 25 indexed citations
11.
Masi, Laura, Sílvia Carbonell Sala, Alessia Gozzini, et al.. (2007). A novel mutation of PHEX causes a dominant X-linked hypophosphatemic rickets. Bone. 40(6). S62–S62. 2 indexed citations
12.
Carossino, Anna Maria, Alessia Gozzini, Valentina Martineti, et al.. (2007). Methodological models for in vitro amplification and maintenance of human articular chondrocytes from elderly patients. Biogerontology. 8(5). 483–498. 19 indexed citations
13.
Cepollaro, C., Fulvio Lauretani, Alessia Gozzini, et al.. (2007). Relationship of Volumetric Bone Mineral Density and Structural Parameters with ERα Gene Polymorphisms. Calcified Tissue International. 80(5). 307–315. 6 indexed citations
14.
Picariello, Lucia, Sílvia Carbonell Sala, Valentina Martineti, et al.. (2006). A comparison of methods for the analysis of low abundance proteins in desmoid tumor cells. Analytical Biochemistry. 354(2). 205–212. 19 indexed citations
15.
Falchetti, Alberto, C. Cepollaro, Alessia Gozzini, et al.. (2006). FokI Polymorphism of the Vitamin D Receptor Gene Correlates with Parameters of Bone Mass and Turnover in a Female Population of the Italian Island of Lampedusa. Calcified Tissue International. 80(1). 15–20. 21 indexed citations
16.
Marini, Francesca, Alberto Falchetti, Francesca Del Monte, et al.. (2006). Multiple endocrine neoplasia type 1. Orphanet Journal of Rare Diseases. 1(1). 38–38. 115 indexed citations
17.
Thomsen, Anne Bloch, et al.. (2006). Estrogen receptor α and β polymorphisms. Menopause The Journal of The North American Menopause Society. 13(3). 451–461. 39 indexed citations
18.
Martineti, Valentina, Lucia Picariello, Isabella Tognarini, et al.. (2005). ERβ is a potent inhibitor of cell proliferation in the HCT8 human colon cancer cell line through regulation of cell cycle components. Endocrine Related Cancer. 12(2). 455–469. 82 indexed citations
19.
Falchetti, Alberto, Marco Di Stefano, Francesca Marini, et al.. (2005). Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family. Arthritis Research & Therapy. 7(6). R1289–95. 17 indexed citations
20.
Masi, Laura, Rolando Cimaz, Gabriele Simonini, et al.. (2002). Association of low bone mass with vitamin d receptor gene and calcitonin receptor gene polymorphisms in juvenile idiopathic arthritis.. PubMed. 29(10). 2225–31. 20 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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