Claudia Izzi

5.1k total citations
52 papers, 1.3k citations indexed

About

Claudia Izzi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Claudia Izzi has authored 52 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 26 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Claudia Izzi's work include Renal and related cancers (13 papers), Genetic and Kidney Cyst Diseases (13 papers) and Renal Diseases and Glomerulopathies (10 papers). Claudia Izzi is often cited by papers focused on Renal and related cancers (13 papers), Genetic and Kidney Cyst Diseases (13 papers) and Renal Diseases and Glomerulopathies (10 papers). Claudia Izzi collaborates with scholars based in Italy, United States and Germany. Claudia Izzi's co-authors include Francesco Scolari, Gian Marco Ghiggeri, Federico Prefumo, Gianluca Caridi, Simone Sanna‐Cherchi, Regina Tardanico, Pietro Ravani, Danio Somenzi, Landino Allegri and Francesca Romana Grati and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and Kidney International.

In The Last Decade

Claudia Izzi

50 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claudia Izzi Italy 19 565 536 341 311 219 52 1.3k
Vincent Morinière France 14 806 1.4× 323 0.6× 452 1.3× 497 1.6× 126 0.6× 27 1.3k
Larry T. Patterson United States 20 1.4k 2.6× 336 0.6× 350 1.0× 306 1.0× 154 0.7× 29 1.8k
Sarah Howles United Kingdom 13 313 0.6× 154 0.3× 140 0.4× 433 1.4× 33 0.2× 34 950
Ryan C. Hedgepeth United States 12 506 0.9× 56 0.1× 549 1.6× 88 0.3× 154 0.7× 18 1.1k
Jacqueline Aziza France 15 334 0.6× 224 0.4× 138 0.4× 33 0.1× 51 0.2× 32 770
Harley R. Powell Australia 14 253 0.4× 123 0.2× 108 0.3× 517 1.7× 36 0.2× 27 984
Ryuichiro Konda Japan 14 137 0.2× 199 0.4× 43 0.1× 68 0.2× 137 0.6× 44 474
Cécile Brachet Belgium 14 362 0.6× 171 0.3× 137 0.4× 63 0.2× 20 0.1× 36 845
Madeleine Joubert France 13 279 0.5× 215 0.4× 147 0.4× 20 0.1× 33 0.2× 36 682
France Ziereisen Belgium 12 146 0.3× 102 0.2× 118 0.3× 137 0.4× 13 0.1× 29 693

Countries citing papers authored by Claudia Izzi

Since Specialization
Citations

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

Fields of papers citing papers by Claudia Izzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Izzi

This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Izzi. A scholar is included among the top collaborators of Claudia Izzi 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 Claudia Izzi. Claudia Izzi 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.
Dordoni, Chiara, Letizia Zeni, Cinzia Mazza, et al.. (2024). Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease–spectrum phenotype. Clinical Kidney Journal. 17(2). sfae026–sfae026. 5 indexed citations
2.
Giacchè, Mara, et al.. (2024). Pheochromocytoma–Paraganglioma Syndrome: A Multiform Disease with Different Genotype and Phenotype Features. Biomedicines. 12(10). 2385–2385. 3 indexed citations
3.
Zeni, Letizia, Federica Mescia, Chiara Dordoni, et al.. (2024). Clinical Significance of the Cystic Phenotype in Alport Syndrome. American Journal of Kidney Diseases. 84(3). 320–328.e1. 5 indexed citations
4.
Schaeffer, Céline, Maurizio De Fusco, Elena Pasqualetto, et al.. (2023). Leader peptide or pro-segment mutants of renin are misrouted to mitochondria in autosomal dominant tubulointerstitial kidney disease. Disease Models & Mechanisms. 16(6). 2 indexed citations
5.
Bedeschi, Maria Francesca, Claudia Izzi, Chiara Dordoni, et al.. (2023). Identification of bi‐allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3. Clinical Genetics. 104(2). 230–237. 1 indexed citations
6.
Grati, Francesca Romana, José Carlos Ferreira, Peter Benn, et al.. (2020). Outcomes in Pregnancies With a Confined Placental Mosaicism and Implications for Prenatal Screening Using Cell-Free DNA. Obstetrical & Gynecological Survey. 75(7). 397–398. 1 indexed citations
7.
Dordoni, Chiara, Federico Prefumo, Maria Iascone, et al.. (2019). Prenatal findings in oral‐facial‐digital syndrome type VI: Report of three cases and literature review. Prenatal Diagnosis. 39(8). 652–655. 2 indexed citations
8.
Schaeffer, Céline, Claudia Izzi, Andrea Vettori, et al.. (2019). Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein. Scientific Reports. 9(1). 11601–11601. 12 indexed citations
9.
Delbarba, Elisa, et al.. (2016). [Hyperuricemia and Gout].. PubMed. 33(S68). 4 indexed citations
10.
Carrera, Paola, Riccardo Magistroni, Johan T. den Dunnen, et al.. (2016). Deciphering Variability of PKD1 and PKD2 in an Italian Cohort of 643 Patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD). Scientific Reports. 6(1). 30850–30850. 27 indexed citations
11.
Gregorini, Gina, Claudia Izzi, Pietro Ravani, et al.. (2015). Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis. Kidney International. 87(6). 1223–1229. 30 indexed citations
12.
Savoldi, Gianfranco, Claudia Izzi, Maria Pia Bondioni, et al.. (2013). Prenatal presentation and postnatal evolution of a patient with Jansen metaphyseal dysplasia with a novel missense mutation in PTH1R. American Journal of Medical Genetics Part A. 161(10). 2614–2619. 17 indexed citations
13.
Prefumo, Federico & Claudia Izzi. (2013). Fetal abdominal wall defects. Best Practice & Research Clinical Obstetrics & Gynaecology. 28(3). 391–402. 69 indexed citations
14.
Athanasakis, Emmanouil, Sophie Dahoun, Ambroise Wonkam, et al.. (2013). Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. European Journal of Medical Genetics. 56(8). 404–410. 7 indexed citations
15.
Schaeffer, Céline, Angela Cattaneo, Matteo Trudu, et al.. (2012). Urinary secretion and extracellular aggregation of mutant uromodulin isoforms. Kidney International. 81(8). 769–778. 18 indexed citations
16.
Izzi, Claudia, Pietro Maffei, Gabriella Milan, et al.. (2011). The Case ∣ Familial occurrence of retinitis pigmentosa, deafness, and nephropathy. Kidney International. 79(6). 691–692. 8 indexed citations
17.
Sanna‐Cherchi, Simone, Pietro Ravani, Valentina Corbani, et al.. (2009). Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney International. 76(5). 528–533. 247 indexed citations
18.
Sanna‐Cherchi, Simone, Gianluca Caridi, Patricia L. Weng, et al.. (2007). Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33. The American Journal of Human Genetics. 80(3). 539–549. 23 indexed citations
19.
Izzi, Claudia, Pietro Ravani, Diletta Domenica Torres, et al.. (2006). IgA Nephropathy: The Presence of Familial Disease Does Not Confer an Increased Risk for Progression. American Journal of Kidney Diseases. 47(5). 761–769. 22 indexed citations
20.
Scolari, Francesco, Gianluca Caridi, Luca Rampoldi, et al.. (2004). Uromodulin storage diseases: Clinical aspects and mechanisms. American Journal of Kidney Diseases. 44(6). 987–999. 94 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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