Elena Bresin

5.6k total citations · 2 hit papers
61 papers, 3.9k citations indexed

About

Elena Bresin is a scholar working on Immunology, Hematology and Nephrology. According to data from OpenAlex, Elena Bresin has authored 61 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Immunology, 30 papers in Hematology and 28 papers in Nephrology. Recurrent topics in Elena Bresin's work include Complement system in diseases (45 papers), Renal Diseases and Glomerulopathies (28 papers) and Blood groups and transfusion (16 papers). Elena Bresin is often cited by papers focused on Complement system in diseases (45 papers), Renal Diseases and Glomerulopathies (28 papers) and Blood groups and transfusion (16 papers). Elena Bresin collaborates with scholars based in Italy, United States and Spain. Elena Bresin's co-authors include Giuseppe Remuzzi, Marina Noris, Jessica Caprioli, Federica Castelletti, Erica Daina, Sara Gamba, Gaia Pianetti, Roberta Donadelli, Timothy H.J. Goodship and Elisabetta Valoti and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and The Journal of Immunology.

In The Last Decade

Elena Bresin

59 papers receiving 3.8k 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. 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. profile →

Peers

Countries citing papers authored by Elena Bresin

Since Specialization

Citations

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

Fields of papers citing papers by Elena Bresin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Bresin

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Bresin. A scholar is included among the top collaborators of Elena Bresin 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 Elena Bresin. Elena Bresin 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	C3 glomerulopathy in children: a European longitudinal study evaluating outcome 2024 ·Pediatric Nephrology ·(unknown), (unknown), (unknown), Gema Ariceta, (unknown), Gian Marco Ghiggeri, Dieter Haffner, Nele Kanzelmeyer, Elena Levtchenko, Andrea Pasini, Aoife Waters, José Aguilera, Licia Peruzzi, Marina Noris, Elena Bresin, Antonio Gargiulo, Francesco Emma, Marina Vivarelli	1
2	<b><i>Mycoplasma pneumoniae</i></b> Infection Associated with Anti-Factor H Autoantibodies in Atypical Hemolytic Uremic Syndrome 2022 ·The Nephron journals/Nephron journals ·Elisabetta Valoti, Rossella Piras, Caterina Mele, Marta Alberti, Lucia Liguori, Matteo Breno, Cristina Bertulli, Elena Bresin, Roberta Donadelli	2
3	Peripheral nervous system manifestations of Shiga toxin-producing E. coli-induced haemolytic uremic syndrome in children 2021 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown), Giuseppe Stefano Netti, Diletta Domenica Torres, (unknown), (unknown), Luciana Losito, (unknown), (unknown), (unknown), (unknown), Maria Chironna, Federica Spadaccino, Elena Bresin, Antonio Trabacca, Elena Ranieri, Mario Giordano	5
4	CFH and CFHR Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis 2021 ·Frontiers in Genetics ·Rossella Piras, Matteo Breno, Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, Caterina Mele, Elena Bresin, Roberta Donadelli, Paola Cuccarolo, Richard J. Smith, Ariela Benigni, Giuseppe Remuzzi, Marina Noris	16
5	Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association 2019 ·The Nephron journals/Nephron journals ·Elisabetta Valoti, Marta Alberti, (unknown), Matteo Breno, (unknown), Elena Bresin, Paola Cuccarolo, (unknown), Ariela Benigni, Marina Noris, Giuseppe Remuzzi, Caterina Mele	2
6	Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS 2019 ·Frontiers in Immunology ·Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, Rossella Piras, Caterina Mele, Matteo Breno, (unknown), Elena Bresin, Roberta Donadelli, (unknown), Antonio Amoroso, Ariela Benigni, Giuseppe Remuzzi, Marina Noris	29
7	An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome 2019 ·American Journal of Kidney Diseases ·Miriam Galbusera, Marina Noris, Sara Gastoldi, Elena Bresin, Caterina Mele, Matteo Breno, Paola Cuccarolo, Marta Alberti, Elisabetta Valoti, Rossella Piras, Roberta Donadelli, Marina Vivarelli, Luisa Murer, Carmine Pecoraro, Elisa Ferrari, Annalisa Perna, Ariela Benigni, Valentina Portalupi, Giuseppe Remuzzi	65
8	Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome 2016 ·Molecular Immunology ·Paraskevas Iatropoulos, Marina Noris, Caterina Mele, Rossella Piras, Elisabetta Valoti, Elena Bresin, (unknown), (unknown), Anna Zito, Sara Gamba, Serena Bettoni, Luisa Murer, Véronique Frémeaux‐Bacchi, Marina Vivarelli, Francesco Emma, Erica Daina, Giuseppe Remuzzi	115
9	Successful long-term outcome after renal transplantation in a patient with atypical haemolytic uremic syndrome with combined membrane cofactor protein CD46 and complement factor I mutations 2013 ·Pediatric Nephrology ·(unknown), Thomas J. Neuhaus, (unknown), Elena Bresin, (unknown), (unknown)	3
10	A Case of Familial Glomerulopathy With Fibronectin Deposits Caused by the Y973C Mutation in Fibronectin 2012 ·American Journal of Kidney Diseases ·Dilek Ertoy Baydar, (unknown), Elena Bresin, Rossella Piras	17
11	Atypical hemolytic uremic syndrome with MCP mutations preceded by respiratory infection 2012 ·CEN Case Reports ·Keiko Yasuda, Koichi Sasaki, Masaya Yamato, Hiromi Rakugi, Yoshitaka Isaka, Terumasa Hayashi, Rossella Piras, Elena Bresin	2
12	Congenital thrombotic thrombocytopenic purpura (cTTP) with two novel mutations 2012 ·Pediatric Blood & Cancer ·(unknown), Erica Rurali, Louis D. Wadsworth, John K. Wu, Jane C. Moore, Elena Bresin	5
13	A case of atypical hemolytic uremic syndrome due to anti-factor H antibody in a patient presenting with a factor XII deficiency identified two novel mutations 2011 ·Clinical and Experimental Nephrology ·Eiji Matsukuma, Yoshimitsu Gotoh, (unknown), Takuji Yamada, Mitsuji Iwasa, Satoshi Yamakawa, Takuhito Nagai, Nobuaki Takagi, (unknown), Kenji Iijima, Elena Bresin	13
14	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
15	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
16	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
17	Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families 2005 ·Nephrology Dialysis Transplantation ·Ilaria Longo, (unknown), Francesca Mari, Rossella Caselli, Chiara Pescucci, Maria Antonietta Mencarelli, (unknown), Marisa Giani, Elena Bresin, (unknown), (unknown), Komudi Siriwardena, Ingrid Winship, Alessandra Renieri, Ilaria Meloni	38
18	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
19	Molecular Genetic Investigations in Autosomal Dominant Polycystic Kidney Disease. Gene Mutation Detection, Linkage Analysis, and Preliminary ACE Gene I/D Polymorphism Association Studies: An Update 1997 ·Contributions to nephrology ·Alberto Turco, Elena Bresin, Sandro Rossetti, (unknown), Pier Franco Pignatti, Linda Gammaro, Giuseppe Maschio, (unknown), Maurizio Vecchi, Angelo Ferrantelli, Giovanni Cerasola, (unknown), (unknown)	3
20	Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 gene 1996 ·American Journal of Medical Genetics ·Sandro Rossetti, Elena Bresin, Gabriella Restagno, A. O. Carbonara, (unknown), (unknown), Pier Franco Pignatti, Alberto Turco	40

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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