Jessica Caprioli

4.1k citations

25 papers · 3.1k indexed · 2 hit papers · h-index 17

Immunology top 0.5%
Nephrology top 0.2%
Hematology top 0.5%
Genetics top 2%
Physiology top 0.5%

Co-authors: Giuseppe Remuzzi Marina Noris Elena Bresin Sara Gamba Peter F. Zipfel Federica Castelletti Erica Daina Gaia Pianetti
Topics: Complement system in diseases (21 papers)Renal Diseases and Glomerulopathies (11 papers)Blood groups and transfusion (10 papers)
Cited by: Nephrology Immunology Hematology
Journals: Proceedings of the National Academy of Sciences The Lancet Journal of Clinical Investigation
Partner nations: Italy Germany United Kingdom

In The Last Decade

Jessica Caprioli

25 papers receiving 3.0k 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 →
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

Countries citing papers authored by Jessica Caprioli

Since Specialization

Citations

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

Fields of papers citing papers by Jessica Caprioli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jessica Caprioli

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

#	Work	Indexed citations
1	Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype 2013 ·Journal of the American Society of Nephrology ·Elena Bresin,Erica Rurali,Jessica Caprioli,Pilar Sánchez‐Corral,Véronique Frémeaux‐Bacchi,Santiago Rodrı́guez de Córdoba,Sheila Pinto,Timothy H.J. Goodship,Marta Alberti,David Ribes,Elisabetta Valoti,Giuseppe Remuzzi,Marina Noris	263
2	Thrombotic Microangiopathies: From Animal Models to Human Disease and Cure 2011 ·Contributions to nephrology ·Jessica Caprioli,Giuseppe Remuzzi,Marina Noris	9
3	Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotypebreakdown → 2010 ·Clinical Journal of the American Society of Nephrology ·Marina Noris,Jessica Caprioli,Elena Bresin,(unknown),Gaia Pianetti,Sara Gamba,Erica Daina,(unknown),Federica Castelletti,(unknown),Rossella Piras,Roberta Donadelli,Ramona Maranta,(unknown),Edward M. Conway,Peter F. Zipfel,Timothy H.J. Goodship,Giuseppe Remuzzi	724
4	Mutations in FN1 cause glomerulopathy with fibronectin deposits 2008 ·Proceedings of the National Academy of Sciences ·Federica Castelletti,Roberta Donadelli,Federica Banterla,Friedhelm Hildebrandt,Peter F. Zipfel,Elena Bresin,Edgar A. Otto,Christine Skerka,Alessandra Renieri,Marta Todeschini,Jessica Caprioli,Rosa Caruso,Rosangela Artuso,Giuseppe Remuzzi,Marina Noris	98
5	Complement hyperactivation may cause atypical haemolytic uraemic syndrome gain-of-function mutations in factor B 2007 ·Nephrology Dialysis Transplantation ·Jessica Caprioli,Giuseppe Remuzzi	5
6	Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome 2006 ·Molecular Immunology ·(unknown),Simona Brioschi,Jessica Caprioli,Gaia Pianetti,Paola Bettinaglio,Elena Bresin,Giuseppe Remuzzi,Marina Noris	35
7	Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS13 Deficiency and Renal Involvement 2005 ·Journal of the American Society of Nephrology ·Marina Noris,(unknown),Miriam Galbusera,Roberta Donadelli,Elena Bresin,Federica Castelletti,Jessica Caprioli,Simona Brioschi,Friedrich Scheiflinger,Giuseppe Remuzzi	104
8	The hemolytic uremic syndromes 2005 ·Current Opinion in Critical Care ·Jessica Caprioli,Peng Li,Giuseppe Remuzzi	27
9	Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome 2003 ·Journal of Clinical Investigation ·Tamara Manuelian,Jens Hellwage,Seppo Meri,Jessica Caprioli,Marina Noris,Stefan Heinen,Mihály Józsi,Hartmut P.H. Neumann,Giuseppe Remuzzi,Peter F. Zipfel	288
10	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 2003 ·Human Molecular Genetics ·Jessica Caprioli,Federica Castelletti,(unknown),Paola Bettinaglio,Elena Bresin,Gaia Pianetti,Sara Gamba,Simona Brioschi,Erica Daina,Giuseppe Remuzzi,Marina Noris	246
11	Combined kidney and liver transplantation for familial haemolytic uraemic syndrome 2002 ·The Lancet ·Giuseppe Remuzzi,Piero Ruggenenti,Daniela Codazzi,Marina Noris,Jessica Caprioli,Giuseppe Locatelli,Bruno Gridelli	113
12	Single strand conformation polymorphism (SSCP) as a quick and reliable method to genotype M235T polymorphism of angiotensinogen gene 2002 ·Clinical Biochemistry ·Paola Bettinaglio,(unknown),Jessica Caprioli,Silvia Orisio,Annalisa Perna,(unknown),(unknown),Marina Noris	11
13	von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome 2002 ·Blood ·Giuseppe Remuzzi,Miriam Galbusera,Marina Noris,Maria Teresa Canciani,Erica Daina,Elena Bresin,(unknown),Jessica Caprioli,Sara Gamba,Piero Ruggenenti,Norberto Perico,Pier Mannuccio Mannucci	148
14	Complement factor H and hemolytic uremic syndrome 2001 ·International Immunopharmacology ·Peter F. Zipfel,Christine Skerka,Jessica Caprioli,Tamara Manuelian,(unknown),Marina Noris,Giuseppe Remuzzi	22
15	The Molecular Basis of Familial Hemolytic Uremic Syndrome 2001 ·Journal of the American Society of Nephrology ·Jessica Caprioli,Paola Bettinaglio,Peter F. Zipfel,Barbara Amadei,Erica Daina,Sara Gamba,Christine Skerka,Nicola Marziliano,Giuseppe Remuzzi,Marina Noris	224
16	Mutations of factor H (HF) in familial Hemolytic Uremic Syndrome (HUS) / Thrombotic Thrombocytopenic Purpura (TTP) 2000 ·Immunopharmacology ·Jessica Caprioli,Paola Bettinaglio,Peter F. Zipfel,Beatrice Vasile,Sara Gamba,Barbara Amadei,Silvia Orisio,Giuseppe Remuzzi,Marina Noris	2
17	Pathophysiology of thrombotic microangiopathies 2000 ·Marina Noris,Jessica Caprioli,Giuseppe Remuzzi	1
18	Hypocomplementemia Discloses Genetic Predisposition to Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura 1999 ·Journal of the American Society of Nephrology ·Marina Noris,Piero Ruggenenti,Annalisa Perna,Silvia Orisio,Jessica Caprioli,Christine Skerka,Beatrice Vasile,Peter F. Zipfel,Giuseppe Remuzzi	114
19	Increased Fragmentation of von Willebrand Factor, Due to Abnormal Cleavage of the Subunit, Parallels Disease Activity in Recurrent Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura and Discloses Predisposition in Families 1999 ·Blood ·Miriam Galbusera,Marina Noris,Chiara Rossi,Silvia Orisio,Jessica Caprioli,Zaverio M. Ruggeri,Barbara Amadei,Piero Ruggenenti,Beatrice Vasile,Giorgio Casari,Giuseppe Remuzzi	1
20	Condensation anomalies and exclusion in micronuclei of rearranged chromosomes in human fibroblasts cultured in vitro 1995 ·Chromosoma ·(unknown),Roberta Riboni,Jessica Caprioli,Fiorella Nuzzo,Chiara Mondello	6

About Jessica Caprioli

Jessica Caprioli is a scholar working on Nephrology, Hematology and Immunology, having authored 25 papers that have together received 3.1k indexed citations. Recurring topics across this work include Complement system in diseases (21 papers), Renal Diseases and Glomerulopathies (11 papers) and Blood groups and transfusion (10 papers). The work is most often cited by research in Nephrology (1.7k citations), Immunology (2.7k citations) and Hematology (1.2k citations). Jessica Caprioli has collaborated with scholars based in Italy, Germany and United Kingdom. Frequent co-authors include Giuseppe Remuzzi, Marina Noris, Elena Bresin, Sara Gamba, Peter F. Zipfel, Federica Castelletti, Erica Daina, Gaia Pianetti, Paola Bettinaglio and Simona Brioschi. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Investigation.

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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