Marisa Giani

647 total citations
24 papers, 413 citations indexed

About

Marisa Giani is a scholar working on Nephrology, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Marisa Giani has authored 24 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Nephrology, 9 papers in Molecular Biology and 9 papers in Immunology and Allergy. Recurrent topics in Marisa Giani's work include Cell Adhesion Molecules Research (9 papers), Renal Diseases and Glomerulopathies (8 papers) and Platelet Disorders and Treatments (5 papers). Marisa Giani is often cited by papers focused on Cell Adhesion Molecules Research (9 papers), Renal Diseases and Glomerulopathies (8 papers) and Platelet Disorders and Treatments (5 papers). Marisa Giani collaborates with scholars based in Italy, Switzerland and Argentina. Marisa Giani's co-authors include Alberto Edefonti, Antonio Mastrangelo, Luciana Ghio, Giovanni Montini, Sophie Guez, Alessandra Renieri, Maria Luisa Melzi, Piergiorgio Messa, B.M. Assael and Corinne Antignac and has published in prestigious journals such as PLoS ONE, Transplantation and Thrombosis and Haemostasis.

In The Last Decade

Marisa Giani

23 papers receiving 405 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marisa Giani Italy 14 172 118 113 112 62 24 413
Yoshitsugu Kaku Japan 11 260 1.5× 94 0.8× 50 0.4× 18 0.2× 52 0.8× 23 344
Riku Hamada Japan 12 237 1.4× 138 1.2× 38 0.3× 14 0.1× 79 1.3× 63 436
Staša Kaplan-Pavlovčič Slovenia 10 114 0.7× 45 0.4× 21 0.2× 45 0.4× 151 2.4× 19 286
L.H. Noël France 10 164 1.0× 71 0.6× 25 0.2× 22 0.2× 180 2.9× 16 452
Santiago Mendizábal Spain 12 346 2.0× 110 0.9× 87 0.8× 12 0.1× 83 1.3× 30 589
S Colon France 7 236 1.4× 94 0.8× 40 0.4× 15 0.1× 72 1.2× 27 352
Hidekazu Kamitsuji Japan 10 144 0.8× 63 0.5× 71 0.6× 12 0.1× 138 2.2× 35 335
Hiroko Chikamoto Japan 12 224 1.3× 41 0.3× 40 0.4× 8 0.1× 64 1.0× 30 381
A. Séchet France 8 175 1.0× 136 1.2× 40 0.4× 7 0.1× 33 0.5× 13 296
Jonathan Chemouny France 11 310 1.8× 103 0.9× 82 0.7× 6 0.1× 53 0.9× 31 524

Countries citing papers authored by Marisa Giani

Since Specialization
Citations

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

Fields of papers citing papers by Marisa Giani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marisa Giani

This figure shows the co-authorship network connecting the top 25 collaborators of Marisa Giani. A scholar is included among the top collaborators of Marisa Giani 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 Marisa Giani. Marisa Giani 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.
Mastrangelo, Antonio, Marisa Giani, Pierangela Castorina, et al.. (2020). X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases. Frontiers in Medicine. 7. 580376–580376. 13 indexed citations
2.
Mastrangelo, Antonio, Jessica Serafinelli, Marisa Giani, & Giovanni Montini. (2020). Clinical and Pathophysiological Insights Into Immunological Mediated Glomerular Diseases in Childhood. Frontiers in Pediatrics. 8. 205–205. 13 indexed citations
3.
Barozzi, Stefania, Marisa Giani, Mirko Aldè, et al.. (2020). Vestibular and audiological findings in the Alport syndrome. American Journal of Medical Genetics Part A. 182(10). 2345–2358. 4 indexed citations
4.
Brunini, Francesca, Barbara Zàina, Davide Gianfreda, et al.. (2018). Alport syndrome and pregnancy: a case series and literature review. Archives of Gynecology and Obstetrics. 297(6). 1421–1431. 18 indexed citations
5.
Chiereghin, Chiara, Antonio Mastrangelo, Pierangela Castorina, et al.. (2017). Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. PLoS ONE. 12(6). e0178630–e0178630. 22 indexed citations
6.
Mihatsch, Michael J., et al.. (2015). Ultrastructural Lesions of Henoch-Sch�nlein Syndrome and of IgA Nephropathy: Similarities and Differences. Contributions to nephrology. 40. 255–263.
7.
Giani, Marisa, Antonio Mastrangelo, Roberta Villa, et al.. (2013). Alport syndrome: the effects of spironolactone on proteinuria and urinary TGF-β1. Pediatric Nephrology. 28(9). 1837–1842. 11 indexed citations
8.
Rocco, Daniela De, Emanuele Panza, Valeria Bozzi, et al.. (2010). Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thrombosis and Haemostasis. 103(4). 826–832. 66 indexed citations
9.
Belingheri, Mirco, Patrizia Comoli, Franco Locatelli, et al.. (2009). Successful medical treatment of EBV smooth muscle tumor in a renal transplant recipient. Pediatric Transplantation. 14(8). E101–E104. 18 indexed citations
10.
Fogazzi, Giovanni B., Alberto Edefonti, Giuseppe Garigali, et al.. (2008). Urine erythrocyte morphology in patients with microscopic haematuria caused by a glomerulopathy. Pediatric Nephrology. 23(7). 1093–1100. 32 indexed citations
11.
Longo, Ilaria, Francesca Mari, Rossella Caselli, et al.. (2005). Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families. Nephrology Dialysis Transplantation. 21(3). 665–671. 38 indexed citations
12.
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
13.
Edefonti, Alberto, et al.. (1999). Dietary prescription based on estimated nitrogen balance during peritoneal dialysis. Pediatric Nephrology. 13(3). 253–258. 20 indexed citations
14.
Guez, Sophie, Marisa Giani, Maria Luisa Melzi, Corinne Antignac, & B.M. Assael. (1998). Adequate clinical control of congenital nephrotic syndrome by enalapril. Pediatric Nephrology. 12(2). 130–132. 32 indexed citations
15.
Giani, Marisa, Alberto Edefonti, Giuseppina Marra, et al.. (1996). Nephrotic syndrome in a mother and her infant: relationship with cytomegalovirus infection. Pediatric Nephrology. 10(1). 73–75. 13 indexed citations
16.
Edefonti, Alberto, et al.. (1995). Dialysis delivery in children on nightly intermittent and tidal peritoneal dialysis. Pediatric Nephrology. 9(3). 329–332. 11 indexed citations
17.
Renieri, Alessandra, Lucia Galli, Mirella Bruttini, et al.. (1995). Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome. American Journal of Medical Genetics. 59(3). 380–385. 17 indexed citations
18.
Giani, Marisa, et al.. (1994). Clinical Features and Prognosis in Childhood IgA Nephropathy. Renal Failure. 16(5). 629–636. 3 indexed citations
19.
Renieri, Alessandra, Maria Teresa Bassi, Lucia Galli, et al.. (1994). Deletion spanning the 5′ ends of both the COL4A5 and COL4A6 genes in a patient with Alport's syndrome and leiomyomatosis. Human Mutation. 4(3). 195–198. 17 indexed citations
20.
Ghio, Luciana, et al.. (1992). ADVANTAGES OF CYCLOSPORINE AS SOLE IMMUNOSUPPRESSIVE AGENT IN CHILDREN WITH TRANSPLANTED KIDNEYS. Transplantation. 54(5). 834–838. 22 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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