Paola Tesolin

942 total citations
12 papers, 33 citations indexed

About

Paola Tesolin is a scholar working on Sensory Systems, Neurology and Otorhinolaryngology. According to data from OpenAlex, Paola Tesolin has authored 12 papers receiving a total of 33 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Sensory Systems, 3 papers in Neurology and 2 papers in Otorhinolaryngology. Recurrent topics in Paola Tesolin's work include Hearing, Cochlea, Tinnitus, Genetics (5 papers), Vestibular and auditory disorders (3 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers). Paola Tesolin is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (5 papers), Vestibular and auditory disorders (3 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (2 papers). Paola Tesolin collaborates with scholars based in Italy, Austria and Lithuania. Paola Tesolin's co-authors include Anna Morgan, Giorgia Girotto, Maria Pina Concas, Stefania Lenarduzzi, Michela Notarangelo, Claudio Granata, Alessandro Mangogna, Eva Orzan, Federico Romano and Giovanni Di Lorenzo and has published in prestigious journals such as Life Sciences, Molecular Medicine and Frontiers in Genetics.

In The Last Decade

Paola Tesolin

9 papers receiving 32 citations

Peers

Paola Tesolin

MB

SS

RM

GENET

PHEOH

Tasnim Fadl Qatar

Sreenath Chandran Ireland

Saleh Shekari United Kingdom

D. Cyr Canada

Mark McIntyre United Kingdom

Julie Firmin France

Guoyun Yu United States

Dayuan Shi China

Anne Ndungu United Kingdom

Jianping Jin United Kingdom

Tasnim Fadl Qatar

Paola Tesolin

11 ×1.1

MB

10 ×1.0

SS

2 ×0.2

RM

14 ×2.3

GENET

9 ×1.8

PHEOH

Citations per year, relative to Paola Tesolin Paola Tesolin (= 1×) peers Tasnim Fadl

Countries citing papers authored by Paola Tesolin

Since Specialization

Citations

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

Fields of papers citing papers by Paola Tesolin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paola Tesolin

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

All Works

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12 of 12 papers shown

1.

Tesolin, Paola, et al.. (2025). Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct. Molecular Medicine. 31(1). 111–111.

2.

Tesolin, Paola, et al.. (2025). Expanding the Molecular Spectrum of MMP21 Missense Variants: Clinical Insights and Literature Review. Genes. 16(1). 62–62.

3.

Campisciano, Giuseppina, Silvia Pegoraro, Gabriella Zito, et al.. (2025). A possible association between low MBL/lectin pathway functionality and microbiota dysbiosis in endometriosis patients. Life Sciences. 364. 123427–123427. 2 indexed citations

4.

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.

5.

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

6.

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

7.

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

8.

Concas, Maria Pina, et al.. (2022). Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals. Foods. 11(5). 735–735. 3 indexed citations

9.

Tesolin, Paola, Francesca Bertinetto, Stefania Cappellani, et al.. (2022). High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis. Journal of Personalized Medicine. 12(10). 1618–1618. 4 indexed citations

10.

Concas, Maria Pina, Alessandra Minelli, Anna Morgan, et al.. (2021). Genetic Dissection of Temperament Personality Traits in Italian Isolates. Genes. 13(1). 4–4. 1 indexed citations

11.

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

12.

Tesolin, Paola, Anna Morgan, Michela Notarangelo, et al.. (2021). Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene. Genes. 12(7). 1043–1043. 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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