Simona Brioschi

1.4k total citations · 1 hit paper
7 papers, 961 citations indexed

About

Simona Brioschi is a scholar working on Immunology, Hematology and Molecular Biology. According to data from OpenAlex, Simona Brioschi has authored 7 papers receiving a total of 961 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Immunology, 3 papers in Hematology and 2 papers in Molecular Biology. Recurrent topics in Simona Brioschi's work include Complement system in diseases (5 papers), Blood groups and transfusion (3 papers) and Renal Diseases and Glomerulopathies (2 papers). Simona Brioschi is often cited by papers focused on Complement system in diseases (5 papers), Blood groups and transfusion (3 papers) and Renal Diseases and Glomerulopathies (2 papers). Simona Brioschi collaborates with scholars based in Italy, Austria and United Kingdom. Simona Brioschi's co-authors include Marina Noris, Jessica Caprioli, Elena Bresin, Giuseppe Remuzzi, Federica Castelletti, Paola Bettinaglio, Gaia Pianetti, Sara Gamba, Celia J. Fang and Linda Cassis and has published in prestigious journals such as Blood, PLoS ONE and Journal of the American Society of Nephrology.

In The Last Decade

Simona Brioschi

7 papers receiving 947 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.

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

2006 531 citations Jessica Caprioli, Marina Noris et al. Blood profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simona Brioschi Italy	5	863	535	401	181	148	7	961
Sheila Pinto Spain	13	911 1.1×	664 1.2×	402 1.0×	120 0.7×	129 0.9×	20	1.0k
Elisabetta Valoti Italy	13	1.1k 1.2×	844 1.6×	429 1.1×	157 0.9×	176 1.2×	21	1.2k
Rossella Piras Italy	13	1.1k 1.3×	908 1.7×	418 1.0×	147 0.8×	216 1.5×	24	1.3k
Claire Hall United Kingdom	6	575 0.7×	328 0.6×	296 0.7×	201 1.1×	98 0.7×	6	692
Kirsten L. Rose United Kingdom	6	678 0.8×	394 0.7×	227 0.6×	92 0.5×	57 0.4×	7	742
Paula Vieira‐Martins France	9	505 0.6×	311 0.6×	237 0.6×	130 0.7×	92 0.6×	10	588
Isabel Y. Pappworth United Kingdom	11	703 0.8×	349 0.7×	284 0.7×	62 0.3×	76 0.5×	25	790
Anthony Nicholls United Kingdom	5	423 0.5×	237 0.4×	200 0.5×	80 0.4×	64 0.4×	8	590
Lori Shafner United States	5	596 0.7×	355 0.7×	238 0.6×	207 1.1×	140 0.9×	7	687
Fanny Tabarin France	5	268 0.3×	184 0.3×	191 0.5×	79 0.4×	20 0.1×	7	540

Countries citing papers authored by Simona Brioschi

Since Specialization

Citations

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

Fields of papers citing papers by Simona Brioschi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simona Brioschi

This figure shows the co-authorship network connecting the top 25 collaborators of Simona Brioschi. A scholar is included among the top collaborators of Simona Brioschi 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 Simona Brioschi. Simona Brioschi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Bovolenta, Matteo, Emanuele Valli, Simona Brioschi, et al.. (2012). The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms. PLoS ONE. 7(9). e45328–e45328. 43 indexed citations

2.

Caprioli, Jessica, Simona Brioschi, & Giuseppe Remuzzi. (2012). Molecular basis of familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.. PubMed. 14(3). 342–50. 1 indexed citations

3.

Gualandi, Francesca, Simona Brioschi, Maria Sofia Falzarano, et al.. (2011). P1.19 Whole genetic and protein characterisation in DMD symptomatic female carriers excludes correlation with X-inactivation and transcriptional DMD allele balancing. Neuromuscular Disorders. 21(9-10). 647–647. 1 indexed citations

4.

Brioschi, Simona, Jessica Caprioli, Gaia Pianetti, et al.. (2006). Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome. Molecular Immunology. 44(7). 1704–1708. 35 indexed citations

5.

Caprioli, Jessica, Marina Noris, Simona Brioschi, et al.. (2006). Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood. 108(4). 1267–1279. 531 indexed citations breakdown →

6.

Noris, Marina, Miriam Galbusera, Roberta Donadelli, et al.. (2005). Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS13 Deficiency and Renal Involvement. Journal of the American Society of Nephrology. 16(5). 1177–1183. 104 indexed citations

7.

Caprioli, Jessica, Federica Castelletti, Paola Bettinaglio, et al.. (2003). Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease. Human Molecular Genetics. 12(24). 3385–3395. 246 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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