Rossella Piras

2.4k total citations · 1 hit paper
24 papers, 1.3k citations indexed

About

Rossella Piras is a scholar working on Immunology, Nephrology and Hematology. According to data from OpenAlex, Rossella Piras has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Immunology, 16 papers in Nephrology and 13 papers in Hematology. Recurrent topics in Rossella Piras's work include Complement system in diseases (19 papers), Renal Diseases and Glomerulopathies (16 papers) and Blood groups and transfusion (7 papers). Rossella Piras is often cited by papers focused on Complement system in diseases (19 papers), Renal Diseases and Glomerulopathies (16 papers) and Blood groups and transfusion (7 papers). Rossella Piras collaborates with scholars based in Italy, United States and Germany. Rossella Piras's co-authors include Elena Bresin, Giuseppe Remuzzi, Marina Noris, Roberta Donadelli, Erica Daina, Sara Gamba, Gaia Pianetti, Federica Castelletti, Ramona Maranta and Edward M. Conway and has published in prestigious journals such as Journal of the American Society of Nephrology, Frontiers in Immunology and American Journal of Kidney Diseases.

In The Last Decade

Rossella Piras

24 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

2010 724 citations Marina Noris, Jessica Caprioli et al. Clinical Journal of the American Society of Nephrology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rossella Piras Italy	13	1.1k	908	418	216	147	24	1.3k
Elisabetta Valoti Italy	13	1.1k 1.0×	844 0.9×	429 1.0×	176 0.8×	157 1.1×	21	1.2k
Marie-Alice Macher France	7	1.2k 1.1×	965 1.1×	545 1.3×	151 0.7×	159 1.1×	8	1.4k
Sheila Pinto Spain	13	911 0.8×	664 0.7×	402 1.0×	129 0.6×	120 0.8×	20	1.0k
Rubén Martínez-Barricarte Spain	13	1.3k 1.2×	815 0.9×	582 1.4×	108 0.5×	156 1.1×	19	1.6k
Ramona Maranta Italy	5	717 0.7×	531 0.6×	263 0.6×	171 0.8×	208 1.4×	5	960
Simona Brioschi Italy	5	863 0.8×	535 0.6×	401 1.0×	148 0.7×	181 1.2×	7	961
Kirsten L. Rose United Kingdom	6	678 0.6×	394 0.4×	227 0.5×	57 0.3×	92 0.6×	7	742
Dineke Westra Netherlands	15	451 0.4×	311 0.3×	199 0.5×	86 0.4×	69 0.5×	43	725
Anthony Nicholls United Kingdom	5	423 0.4×	237 0.3×	200 0.5×	64 0.3×	80 0.5×	8	590
Bernadette Obert France	17	653 0.6×	303 0.3×	896 2.1×	28 0.1×	276 1.9×	31	1.2k

Countries citing papers authored by Rossella Piras

Since Specialization

Citations

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

Fields of papers citing papers by Rossella Piras

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rossella Piras

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

Piras, Rossella, et al.. (2024). Cognitive Impairment in People Living with HIV and the Impact of Mood: Results from a Cross-Sectional Study. Journal of Clinical Medicine. 13(6). 1631–1631. 4 indexed citations

Piras, Rossella, Elisabetta Valoti, Marta Alberti, et al.. (2023). CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome. Frontiers in Immunology. 13. 1011580–1011580. 9 indexed citations

Valoti, Elisabetta, Rossella Piras, Caterina Mele, et al.. (2022). <b><i>Mycoplasma pneumoniae</i></b> Infection Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome. The Nephron journals/Nephron journals. 146(6). 593–598. 2 indexed citations

Piras, Rossella, Matteo Breno, Elisabetta Valoti, et al.. (2021). CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis. Frontiers in Genetics. 12. 670727–670727. 16 indexed citations

Piras, Rossella, Paraskevas Iatropoulos, Elena Bresin, et al.. (2020). Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant. Frontiers in Medicine. 7. 579418–579418. 9 indexed citations

Podestà, Manuel Alfredo, Mauro Abbate, Paola Rizzo, et al.. (2020). Morphofunctional Effects of C5 Convertase Blockade in Immune Complex-Mediated Membranoproliferative Glomerulonephritis: Report of Two Cases with Evidence of Terminal Complement Activation. The Nephron journals/Nephron journals. 144(4). 195–203. 4 indexed citations

Galbusera, Miriam, Marina Noris, Sara Gastoldi, et al.. (2019). An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome. American Journal of Kidney Diseases. 74(1). 56–72. 65 indexed citations

Valoti, Elisabetta, Marta Alberti, Paraskevas Iatropoulos, et al.. (2019). Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS. Frontiers in Immunology. 10. 853–853. 29 indexed citations

Donadelli, Roberta, Rossella Piras, Paraskevas Iatropoulos, et al.. (2018). Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN. Frontiers in Immunology. 9. 2329–2329. 37 indexed citations

10.

Piras, Rossella, et al.. (2017). Fibronectin Glomerulopathy - A Sporadic Case with Unusual Clinical Manifestation. Saudi Journal of Kidney Diseases and Transplantation. 28(6). 1416–1420. 1 indexed citations

11.

Vivarelli, Marina, Manuela Colucci, Francesca Diomedi‐Camassei, et al.. (2016). Nephrotic-Range Proteinuria and Peripheral Edema in a Child: Not Only Idiopathic Nephrotic Syndrome. Case Reports in Nephrology and Dialysis. 6(3). 120–127. 4 indexed citations

12.

Iatropoulos, Paraskevas, Marina Noris, Caterina Mele, et al.. (2016). Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. Molecular Immunology. 71. 131–142. 115 indexed citations

13.

Mele, Caterina, Mathieu Lemaire, Paraskevas Iatropoulos, et al.. (2015). Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome. Clinical Journal of the American Society of Nephrology. 10(6). 1011–1019. 37 indexed citations

14.

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

15.

Alberti, Marta, Elisabetta Valoti, Rossella Piras, et al.. (2013). Two Patients With History of STEC-HUS, Posttransplant Recurrence and Complement Gene Mutations. American Journal of Transplantation. 13(8). 2201–2206. 40 indexed citations

16.

Baydar, Dilek Ertoy, et al.. (2012). A Case of Familial Glomerulopathy With Fibronectin Deposits Caused by the Y973C Mutation in Fibronectin. American Journal of Kidney Diseases. 61(3). 514–518. 17 indexed citations

17.

Yasuda, Keiko, Koichi Sasaki, Masaya Yamato, et al.. (2012). Atypical hemolytic uremic syndrome with MCP mutations preceded by respiratory infection. CEN Case Reports. 2(1). 34–37. 2 indexed citations

18.

Nadamuni, Mridula, et al.. (2012). Fibronectin Glomerulopathy: An Unusual Cause of Adult-Onset Nephrotic Syndrome. American Journal of Kidney Diseases. 60(5). 839–842. 18 indexed citations

19.

Noris, Marina, Jessica Caprioli, Elena Bresin, et al.. (2010). Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype. Clinical Journal of the American Society of Nephrology. 5(10). 1844–1859. 724 indexed citations breakdown →

20.

Frigerio, Carlo Sala, Paola Piscopo, Emma Calabrese, et al.. (2005). PEN–2 gene mutation in a familial Alzheimer’s disease case. Journal of Neurology. 252(9). 1033–1036. 25 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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