Stefania Lenarduzzi

981 total citations
17 papers, 132 citations indexed

About

Stefania Lenarduzzi is a scholar working on Molecular Biology, Sensory Systems and Otorhinolaryngology. According to data from OpenAlex, Stefania Lenarduzzi has authored 17 papers receiving a total of 132 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Sensory Systems and 3 papers in Otorhinolaryngology. Recurrent topics in Stefania Lenarduzzi's work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), Ear Surgery and Otitis Media (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Stefania Lenarduzzi is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (8 papers), Ear Surgery and Otitis Media (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Stefania Lenarduzzi collaborates with scholars based in Italy, Netherlands and United States. Stefania Lenarduzzi's co-authors include Giorgia Girotto, Anna Morgan, Claudio Graziano, Marcello Morgutti, Umberto Ambrosetti, Flavio Faletra, Paolo Gasparini, Stefania Cappellani, Marco Seri and Beatrice Spedicati and has published in prestigious journals such as Pflügers Archiv - European Journal of Physiology, European Journal of Heart Failure and Hearing Research.

In The Last Decade

Stefania Lenarduzzi

15 papers receiving 130 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefania Lenarduzzi Italy	7	64	61	28	26	22	17	132
Huanzheng Li China	8	158 2.5×	29 0.5×	25 0.9×	11 0.4×	63 2.9×	29	248
Christian Decker Germany	5	138 2.2×	52 0.9×	16 0.6×	11 0.4×	88 4.0×	5	187
Thomas Jaworek United States	5	73 1.1×	47 0.8×	15 0.5×	10 0.4×	27 1.2×	7	122
Radka Kremlíková Pourová Czechia	8	50 0.8×	45 0.7×	27 1.0×	23 0.9×	82 3.7×	18	168
Linyi Xie China	9	100 1.6×	128 2.1×	54 1.9×	16 0.6×	5 0.2×	20	174
Joana Rita Chora Portugal	5	37 0.6×	38 0.6×	8 0.3×	12 0.5×	34 1.5×	17	184
María Eugenia Foncuberta Argentina	5	99 1.5×	48 0.8×	16 0.6×	6 0.2×	18 0.8×	8	134
Faezeh Mojahedi Iran	6	82 1.3×	35 0.6×	14 0.5×	10 0.4×	64 2.9×	8	160
C. Calais France	6	30 0.5×	25 0.4×	37 1.3×	23 0.9×	10 0.5×	7	89
Jennifer Tarpinian United States	5	51 0.8×	20 0.3×	5 0.2×	11 0.4×	55 2.5×	5	117

Countries citing papers authored by Stefania Lenarduzzi

Since Specialization

Citations

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

Fields of papers citing papers by Stefania Lenarduzzi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Lenarduzzi

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Lenarduzzi. A scholar is included among the top collaborators of Stefania Lenarduzzi 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 Stefania Lenarduzzi. Stefania Lenarduzzi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Paldino, Alessia, Ilaria Gandin, Marta Gigli, et al.. (2025). Prediction and Prognostic Role of Left Ventricular Systolic Dysfunction in Family Screening for Dilated Cardiomyopathy and Non-Dilated Left Ventricular Cardiomyopathy. European Journal of Heart Failure. 27(12). 3260–3268.

Gialluisi, Alessandro, Beatrice Spedicati, Simona Costanzo, et al.. (2025). Normal hearing function genetics: have you heard all about it? An integrated approach of genome-wide association studies and transcriptome-wide association studies in three Italian cohorts. Frontiers in Genetics. 16. 1522338–1522338.

Busonero, Fabio, Stefania Lenarduzzi, Francesca Crobu, et al.. (2024). The Women4Health cohort: a unique cohort to study women-specific mechanisms of cardio-metabolic regulation. European Heart Journal Open. 4(2). oeae012–oeae012. 3 indexed citations

Spedicati, Beatrice, Anna Morgan, Stefania Lenarduzzi, et al.. (2023). Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort. Biomedicines. 11(8). 2122–2122. 7 indexed citations

Lenarduzzi, Stefania, Beatrice Spedicati, Paola Tesolin, et al.. (2023). Whole‐exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases. Molecular Genetics & Genomic Medicine. 11(5). e2143–e2143. 3 indexed citations

Tesolin, Paola, et al.. (2023). Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. Audiology Research. 13(6). 989–995. 3 indexed citations

Spedicati, Beatrice, Stefania Lenarduzzi, Claudio Graziano, et al.. (2023). The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population. Biomedicines. 11(3). 703–703. 5 indexed citations

Leoni, Loira, Elena Reffo, Giorgia Girotto, et al.. (2022). Long QT syndrome and left ventricular non-compaction in a family with KCNH2 mutation: A case report. Frontiers in Pediatrics. 10. 2 indexed citations

Tesolin, Paola, Stefania Lenarduzzi, Eva Orzan, et al.. (2021). Pendred Syndrome, or Not Pendred Syndrome? That Is the Question. Genes. 12(10). 1569–1569. 6 indexed citations

10.

Morgan, Anna, Stefania Lenarduzzi, Beatrice Spedicati, et al.. (2020). Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population. Genes. 11(11). 1237–1237. 18 indexed citations

11.

Lenarduzzi, Stefania, Anna Morgan, Flavio Faletra, et al.. (2019). Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss. Hearing Research. 381. 107769–107769. 8 indexed citations

12.

Morgan, Anna, Stefania Lenarduzzi, Stefania Cappellani, et al.. (2018). Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations. Frontiers in Genetics. 9. 681–681. 25 indexed citations

13.

Fontana, Paolo, Marcello Morgutti, Vanna Pecile, et al.. (2017). A novel OTOA mutation in an Italian family with hearing loss. Gene Reports. 9. 111–114. 5 indexed citations

14.

Corre, Tanguy, Eric Olinger, Sarah E. Harris, et al.. (2016). Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine. Pflügers Archiv - European Journal of Physiology. 469(1). 91–103. 20 indexed citations

15.

Lenarduzzi, Stefania, Diego Vozzi, Anna Morgan, et al.. (2015). Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis. Hearing Research. 320. 18–23. 22 indexed citations

16.

Lenarduzzi, Stefania, Marcello Morgutti, Sérgio Crovella, Alessandra Coiana, & Maria Cristina Rosatelli. (2014). Short Communication Novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients. Genetics and Molecular Research. 13(4). 9636–9641. 1 indexed citations

17.

Catamo, Eulalia, et al.. (2012). CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients. Genes and Immunity. 13(6). 489–495. 4 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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