Nicolò Ghiringhelli Borsa

1.1k total citations
23 papers, 757 citations indexed

About

Nicolò Ghiringhelli Borsa is a scholar working on Immunology, Nephrology and Genetics. According to data from OpenAlex, Nicolò Ghiringhelli Borsa has authored 23 papers receiving a total of 757 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Immunology, 13 papers in Nephrology and 8 papers in Genetics. Recurrent topics in Nicolò Ghiringhelli Borsa's work include Complement system in diseases (17 papers), Renal Diseases and Glomerulopathies (12 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers). Nicolò Ghiringhelli Borsa is often cited by papers focused on Complement system in diseases (17 papers), Renal Diseases and Glomerulopathies (12 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (3 papers). Nicolò Ghiringhelli Borsa collaborates with scholars based in United States, Italy and France. Nicolò Ghiringhelli Borsa's co-authors include Richard J. Smith, Nicole C. Meyer, Yuzhou Zhang, Carla Nester, Fengxiao Bu, Ladan Zand, Samih H. Nasr, Fernando C. Fervenza, Sanjeev Sethi and Silvana Tedeschi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and Kidney International.

In The Last Decade

Nicolò Ghiringhelli Borsa

21 papers receiving 751 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicolò Ghiringhelli Borsa United States 13 552 514 247 164 122 23 757
Oliver Amon Germany 8 264 0.5× 137 0.3× 121 0.5× 101 0.6× 125 1.0× 17 543
Claire Hall United Kingdom 6 575 1.0× 328 0.6× 296 1.2× 41 0.3× 23 0.2× 6 692
Cynthia Abarrategui-Garrido Spain 7 536 1.0× 303 0.6× 290 1.2× 24 0.1× 26 0.2× 8 565
Nadia Arzouk France 12 261 0.5× 151 0.3× 114 0.5× 28 0.2× 10 0.1× 27 461
Scott J. Staniforth United Kingdom 4 430 0.8× 296 0.6× 231 0.9× 22 0.1× 23 0.2× 4 463
Weiju Wu United Kingdom 12 232 0.4× 112 0.2× 27 0.1× 136 0.8× 35 0.3× 19 468
Ortraud Beringer Germany 5 161 0.3× 78 0.2× 101 0.4× 106 0.6× 131 1.1× 6 423
Ww Bakker Netherlands 6 135 0.2× 264 0.5× 52 0.2× 53 0.3× 58 0.5× 18 388
L Allegri Italy 12 127 0.2× 252 0.5× 30 0.1× 80 0.5× 66 0.5× 24 441
Jeffrey Gryn United States 11 158 0.3× 63 0.1× 231 0.9× 119 0.7× 10 0.1× 14 392

Countries citing papers authored by Nicolò Ghiringhelli Borsa

Since Specialization
Citations

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

Fields of papers citing papers by Nicolò Ghiringhelli Borsa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicolò Ghiringhelli Borsa. 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 Nicolò Ghiringhelli Borsa. The network helps show where Nicolò Ghiringhelli Borsa may publish in the future.

Co-authorship network of co-authors of Nicolò Ghiringhelli Borsa

This figure shows the co-authorship network connecting the top 25 collaborators of Nicolò Ghiringhelli Borsa. A scholar is included among the top collaborators of Nicolò Ghiringhelli Borsa 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 Nicolò Ghiringhelli Borsa. Nicolò Ghiringhelli Borsa 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.
Meyer, Nicole C., Nicolò Ghiringhelli Borsa, Amanda Taylor, et al.. (2025). Complement factor I functional assay for assessing CFI variants. Immunobiology. 230(4). 152938–152938.
2.
Borsa, Nicolò Ghiringhelli, et al.. (2024). Functional evaluation of rare variants in complement factor I using a minigene assay. Frontiers in Immunology. 15. 1446081–1446081. 1 indexed citations
3.
Taylor, Amanda, Nicole C. Meyer, Sarah M. Roberts, et al.. (2023). Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy. Kidney International Reports. 9(2). 464–477. 8 indexed citations
4.
Zhang, Yuzhou, Nicolò Ghiringhelli Borsa, Nicole C. Meyer, et al.. (2022). Complement Factor I Variants in Complement-Mediated Renal Diseases. Frontiers in Immunology. 13. 866330–866330. 11 indexed citations
5.
Zhang, Yuzhou, C. John Sperati, Kammi Henriksen, et al.. (2020). A Mutation in Complement Factor B Causing Massive Fluid-Phase Dysregulation of the Alternative Complement Pathway Can Result in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 31(10S). 682–682.
6.
Zhang, Yuzhou, Nicolò Ghiringhelli Borsa, Nicole C. Meyer, et al.. (2020). Factor H Autoantibodies and Complement-Mediated Diseases. Frontiers in Immunology. 11. 607211–607211. 27 indexed citations
7.
Zhang, Yuzhou, C. John Sperati, Kammi Henriksen, et al.. (2020). Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome. Kidney International. 98(5). 1265–1274. 8 indexed citations
8.
Bu, Fengxiao, Yuzhou Zhang, Kai Wang, et al.. (2018). Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome. Journal of the American Society of Nephrology. 29(12). 2809–2819. 48 indexed citations
9.
Breno, Matteo, Nicolò Ghiringhelli Borsa, Fengxiao Bu, et al.. (2018). Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. The Journal of Immunology. 200(7). 2464–2478. 119 indexed citations
10.
Meyer, Nicole C., et al.. (2018). Novel FHR fusion genes identified by MLPA and Western blot analysis. Molecular Immunology. 102. 199–199. 1 indexed citations
11.
Bu, Fengxiao, Nicolò Ghiringhelli Borsa, M. B. Jones, et al.. (2015). High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies. Journal of the American Society of Nephrology. 27(4). 1245–1253. 74 indexed citations
12.
Peyvandi, Flora, Paolo Rossi, Barbara Ferrari, et al.. (2015). Thrombotic microangiopathy without renal involvement: two novel mutations in complement‐regulator genes. Journal of Thrombosis and Haemostasis. 14(2). 340–345. 4 indexed citations
13.
Zhang, Yuzhou, Carla Nester, Mikkel‐Ole Skjoedt, et al.. (2014). Defining the Complement Biomarker Profile of C3 Glomerulopathy. Clinical Journal of the American Society of Nephrology. 9(11). 1876–1882. 66 indexed citations
14.
Sethi, Sanjeev, Fernando C. Fervenza, Yuzhou Zhang, et al.. (2012). Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement. Kidney International. 83(2). 293–299. 139 indexed citations
15.
Bu, Fengxiao, Nicolò Ghiringhelli Borsa, Gianluigi Ardissino, & Richard J. Smith. (2012). Familial Atypical Hemolytic Uremic Syndrome: A Review of Its Genetic and Clinical Aspects. SHILAP Revista de lepidopterología. 2012. 1–9. 31 indexed citations
16.
Crovetto, F., Nicolò Ghiringhelli Borsa, Barbara Acaia, et al.. (2012). The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndrome. The Journal of Maternal-Fetal & Neonatal Medicine. 25(11). 2322–2325. 33 indexed citations
17.
Kimberling, William J., Nicolò Ghiringhelli Borsa, & Richard J. Smith. (2011). Hearing Loss Disorders Associated with Renal Disease. Advances in oto-rhino-laryngology. 70. 75–83. 8 indexed citations
18.
Puricelli, Edela, Alberto Bettinelli, Nicolò Ghiringhelli Borsa, et al.. (2010). Long-term follow-up of patients with Bartter syndrome type I and II. Nephrology Dialysis Transplantation. 25(9). 2976–2981. 45 indexed citations
19.
Bettinelli, Alberto, Nicolò Ghiringhelli Borsa, Marie‐Louise Syrén, et al.. (2007). Patients With Biallelic Mutations in the Chloride Channel Gene CLCNKB: Long-Term Management and Outcome. American Journal of Kidney Diseases. 49(1). 91–98. 47 indexed citations
20.
Bettinelli, Alberto, Nicolò Ghiringhelli Borsa, Marie‐Louise Syrén, et al.. (2005). Simultaneous Mutations in the CLCNKB and SLC12A3 Genes in Two Siblings with Phenotypic Heterogeneity in Classic Bartter Syndrome. Pediatric Research. 58(6). 1269–1273. 17 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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