Sabina Nasti

1.3k total citations
24 papers, 783 citations indexed

About

Sabina Nasti is a scholar working on Molecular Biology, Oncology and Dermatology. According to data from OpenAlex, Sabina Nasti has authored 24 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Oncology and 9 papers in Dermatology. Recurrent topics in Sabina Nasti's work include Cancer and Skin Lesions (9 papers), Hedgehog Signaling Pathway Studies (6 papers) and Ear and Head Tumors (4 papers). Sabina Nasti is often cited by papers focused on Cancer and Skin Lesions (9 papers), Hedgehog Signaling Pathway Studies (6 papers) and Ear and Head Tumors (4 papers). Sabina Nasti collaborates with scholars based in Italy, United States and France. Sabina Nasti's co-authors include Lorenza Pastorino, Paola Ghiorzo, Silvano Garibaldi, Paola Altieri, Paolo Spallarossa, G Ghigliotti, Valeria Manca, Patrizia Fabbi, Pierfranco Rossettin and Alberto Ballestrero and has published in prestigious journals such as Human Molecular Genetics, Journal of Molecular and Cellular Cardiology and Human Mutation.

In The Last Decade

Sabina Nasti

23 papers receiving 762 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabina Nasti Italy 14 409 326 191 140 132 24 783
Tomoyuki Aoyama Japan 14 188 0.5× 229 0.7× 68 0.4× 85 0.6× 15 0.1× 38 652
Savita Sankar United States 10 532 1.3× 134 0.4× 77 0.4× 130 0.9× 8 0.1× 12 833
Åse Bratland Norway 16 277 0.7× 510 1.6× 457 2.4× 58 0.4× 9 0.1× 43 1.0k
Thomas Pap Switzerland 6 246 0.6× 144 0.4× 32 0.2× 137 1.0× 45 0.3× 7 689
Jon M. Carthy Canada 12 296 0.7× 102 0.3× 66 0.3× 40 0.3× 22 0.2× 20 598
Quancai Cui China 20 411 1.0× 281 0.9× 36 0.2× 76 0.5× 7 0.1× 61 1.0k
Arja Jukkola‐Vuorinen Finland 15 196 0.5× 202 0.6× 10 0.1× 43 0.3× 38 0.3× 40 687
Lucia Zanatta Italy 11 173 0.4× 175 0.5× 47 0.2× 83 0.6× 8 0.1× 19 651
Marcos Gelos Germany 9 689 1.7× 256 0.8× 14 0.1× 134 1.0× 25 0.2× 17 1.1k
Sam D. Molyneux Canada 9 433 1.1× 209 0.6× 13 0.1× 35 0.3× 35 0.3× 11 710

Countries citing papers authored by Sabina Nasti

Since Specialization
Citations

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

Fields of papers citing papers by Sabina Nasti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabina Nasti

This figure shows the co-authorship network connecting the top 25 collaborators of Sabina Nasti. A scholar is included among the top collaborators of Sabina Nasti 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 Sabina Nasti. Sabina Nasti 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.
Argenziano, Giuseppe, Giovanni Ponti, Sabina Nasti, et al.. (2014). A novel CYLD germline mutation in Brooke‐Spiegler syndrome. Journal of the European Academy of Dermatology and Venereology. 29(3). 457–462. 7 indexed citations
2.
Ponti, Giovanni, Cristel Ruini, Giampiero Girolomoni, et al.. (2014). Brooke–Spiegler Syndrome Tumor Spectrum Beyond the Skin: A Patient Carrying Germline R936X CYLD Mutation and a Somatic CYLD Mutation in Brenner tumor. Future Oncology. 10(3). 345–350. 6 indexed citations
3.
Ghiorzo, Paola, Lorenza Pastorino, Paola Queirolo, et al.. (2012). Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. Pigment Cell & Melanoma Research. 26(2). 259–262. 66 indexed citations
4.
Ponti, Giovanni, Annamaria Pollio, Lorenza Pastorino, et al.. (2012). Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report. Oncology Letters. 4(2). 241–244. 10 indexed citations
5.
Ponti, Giovanni, Lorenza Pastorino, Annamaria Pollio, et al.. (2012). Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome. Familial Cancer. 11(3). 411–418. 18 indexed citations
6.
Ponti, Giovanni, Sabina Nasti, Lorena Losi, et al.. (2011). Brooke‐Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor‐suppressor genes. Journal of Cutaneous Pathology. 39(3). 366–371. 18 indexed citations
7.
Ghiorzo, Paola, Valeria Pensotti, Giuseppe Fornarini, et al.. (2011). Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. Familial Cancer. 11(1). 41–47. 22 indexed citations
8.
Bisio, Alessandra, Sabina Nasti, Lorenza Pastorino, et al.. (2010). 655 Functional analysis of CDKN2A/p16INK4a 5 UTR variants predisposing to melanoma. European Journal of Cancer Supplements. 8(5). 165–166. 5 indexed citations
9.
Bisio, Alessandra, Sabina Nasti, Jennifer Jordan, et al.. (2010). Functional analysis of CDKN2A/p16INK4a 5′-UTR variants predisposing to melanoma. Human Molecular Genetics. 19(8). 1479–1491. 39 indexed citations
10.
Pastorino, Lorenza, Paola Ghiorzo, Sabina Nasti, et al.. (2009). Identification of aSUFUgermline mutation in a family with Gorlin syndrome. American Journal of Medical Genetics Part A. 149A(7). 1539–1543. 128 indexed citations
11.
Ghiorzo, Paola, Lorenza Pastorino, Maria Antonietta Pizzichetta, et al.. (2009). CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. Melanoma Research. 19(3). 142–145. 20 indexed citations
12.
Gargiulo, Sara, Saara Ollila, Sabina Nasti, et al.. (2009). Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. Familial Cancer. 8(4). 547–553. 29 indexed citations
13.
Pastorino, Lorenza, L Bonelli, Paola Ghiorzo, et al.. (2008). CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma. Pigment Cell & Melanoma Research. 21(6). 700–709. 35 indexed citations
14.
Perfumo, Chiara, L Bonelli, Paola Menichini, et al.. (2006). Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the <i>p53</i> PIN3 A2-Pro72 Haplotype. Digestion. 74(3-4). 228–235. 19 indexed citations
15.
Ghiorzo, Paola, Sara Gargiulo, Lorenza Pastorino, et al.. (2006). Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. Human Molecular Genetics. 15(18). 2682–2689. 28 indexed citations
16.
Nasti, Sabina, Paolo Spallarossa, Paola Altieri, et al.. (2006). C242T Polymorphism in CYBA Gene (p22phox) and Risk of Coronary Artery Disease in a Population of Caucasian Italians. Disease Markers. 22(3). 167–173. 26 indexed citations
17.
Pastorino, Lorenza, Roberto Cusano, Chiara Baldo, et al.. (2005). Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. Child Care Health and Development. 31(3). 351–354. 8 indexed citations
18.
Pastorino, Lorenza, Roberto Cusano, Sabina Nasti, et al.. (2005). Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients. Human Mutation. 25(3). 322–323. 45 indexed citations
19.
Spallarossa, Paolo, Silvano Garibaldi, Paola Altieri, et al.. (2004). Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. Journal of Molecular and Cellular Cardiology. 37(4). 837–846. 237 indexed citations
20.
Nasti, Sabina, Manrico Balbi, Patrizia Fabbi, et al.. (2002). CYBA polymorphism associated with oxidative stress in Italian patients with early onset of coronary artery disease. CINECA IRIS Institutial Research Information System (University of Genoa). 3(10). 52–54. 1 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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