Claudia Izzi

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Also affiliated with University of Brescia

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis”.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

Nature Communications(2020)10.1038/s41467-020-15383-w

N/A

4.6DataRank · unranked

223 citations

Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang +95 more

Exome analysis links kidney malformations to developmental disorders and reveals causal genes

Nature Communications(2025)10.1038/s41467-025-62319-3

N/A

0.345DataRank · unranked

9 citations

Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Miguel Verbitsky +95 more

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Kidney International(2020)10.1016/j.kint.2020.06.041

N/A

0DataRank · unranked

43 citations

Kendrah Kidd, Mohamad Zaidan, Petr Vyleťal, Veronika Barešová, Kateřina Hodaňová +51 more

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age

American Journal of Obstetrics and Gynecology(2023)10.1016/j.ajog.2023.09.005

N/A

0DataRank · unranked

15 citations

Stephanie Galloway, T. Blaine Crowley, Julie S. Moldenhauer, Ann Swillen, Jeroen Breckpot +57 more

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

Journal of the American Society of Nephrology(2023)10.1681/asn.0000000000000132

N/A

0DataRank · unranked

15 citations

Tze Yin Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Monica Bodria +77 more

Genome-wide studies define new genetic mechanisms of IgA vasculitis

medRxiv(2024)10.1101/2024.10.10.24315041

N/A

0DataRank · unranked

5 citations

Li Zhu, Sara Monteiro-Martins, Aaron T. Griffin, Lukas Vlahos, Masashi Fujita +88 more

Eight-Fold Increased COVID-19 Mortality in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations: An Observational Study

medRxiv(2024)10.1101/2024.07.03.24309887

N/A

0DataRank · unranked

0 citations

Adrienne H. Williams, Abbigail Taylor, Lauren Martin, Victoria Robins, John A. Sayer +21 more

Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

Kidney International Reports(2020)10.1016/j.ekir.2020.06.029

N/A

0DataRank · unranked

54 citations

Petr Vyleťal, Céline Schaeffer, Eric Olinger, Martina Živná, Kateřina Hodaňová +37 more