Stefania Cappellani

1.3k total citations
14 papers, 136 citations indexed

About

Stefania Cappellani is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Stefania Cappellani has authored 14 papers receiving a total of 136 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Sensory Systems and 4 papers in Genetics. Recurrent topics in Stefania Cappellani's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Congenital heart defects research (4 papers) and Prenatal Screening and Diagnostics (2 papers). Stefania Cappellani is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Congenital heart defects research (4 papers) and Prenatal Screening and Diagnostics (2 papers). Stefania Cappellani collaborates with scholars based in Italy, Qatar and Canada. Stefania Cappellani's co-authors include Paolo Gasparini, Anna Morgan, Pio D’Adamo, Vanna Pecile, Flavio Faletra, Giorgia Girotto, Marcello Morgutti, Martina La Bianca, Stefania Lenarduzzi and Umberto Ambrosetti and has published in prestigious journals such as Hearing Research, European Journal of Human Genetics and Frontiers in Genetics.

In The Last Decade

Stefania Cappellani

13 papers receiving 125 citations

Peers

Countries citing papers authored by Stefania Cappellani

Since Specialization

Citations

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

Fields of papers citing papers by Stefania Cappellani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Cappellani

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Polygenic score from MODY genes is associated with type 1 diabetes and disease characteristics 2025 ·Acta Diabetologica ·Eulalia Catamo, (unknown), Roberto Franceschi, Klemen Dovč, (unknown), Davide Tinti, (unknown), Stefania Cappellani, Gianluca Tamaro, Angela Zanfardino, Elena Faleschini, Ivana Rabbone, Riccardo Bonfanti, Tadej Battelino, Dario Iafusco, Gianluca Tornese, (unknown)	0
2	Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA‐A03:01* allele 2023 ·HLA ·Chiara Magri, Eleonora Marchina, (unknown), Pio D’Adamo, Stefania Cappellani, Carlo Bonfanti, (unknown), Giorgio Biasiotto, Isabella Zanella, Emma Sala, Arnaldo Caruso, Massimo Lombardo, Paolo Gasparini, Giuseppe De Palma, Massimo Gennarelli	8
3	High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis 2022 ·Journal of Personalized Medicine ·Paola Tesolin, Francesca Bertinetto, (unknown), Stefania Cappellani, Maria Pina Concas, Anna Morgan, (unknown), Alen Zabotti, Paolo Gasparini, Antonio Amoroso, Luca Quartuccio, Giorgia Girotto	4
4	Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling 2022 ·Frontiers in Genetics ·(unknown), Tamara Stampalija, Stefania Cappellani, Rossana Bussani, Flavio Faletra, (unknown), Sheila Ulivi, (unknown), (unknown), (unknown), (unknown), (unknown), Bárbara Bosio, Giovanni Savarese, (unknown)	1
5	What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study 2022 ·Genes ·Anna Monica Bianco, (unknown), (unknown), Flavio Faletra, Mariateresa Di Stazio, (unknown), Giovanni Trisolino, Stefania Cappellani, Maurizio De Pellegrin, (unknown), Giuseppe Carluccio, Sergio Monforte, Antonio Andreacchio, (unknown), Pio D’Adamo	4
6	Ten new cases of Balanced Reciprocal Translocation Mosaicism (BRTM): Reproductive implications, frequency and mechanism 2019 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), Maria Paola Recalcati, Ornella Rodeschini, Chiara Barone, (unknown), (unknown), Stefania Cappellani, (unknown), (unknown), (unknown), Vanna Pecile, Maria Carla Pittalis, Lorenza Romitti, Sabine Stioui, Lidia Larizza, Daniela Giardino	5
7	Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 2019 ·Hearing Research ·Stefania Lenarduzzi, Anna Morgan, Flavio Faletra, Stefania Cappellani, Marcello Morgutti, Massimo Mezzavilla, (unknown), Sara Ghiselli, Umberto Ambrosetti, Claudio Graziano, Marco Seri, Paolo Gasparini, Giorgia Girotto	8
8	Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 2018 ·European Journal of Human Genetics ·Anna Morgan, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, (unknown), Umberto Ambrosetti, Pierangela Castorina, Annamaria Franzè, Diego Vozzi, Martina La Bianca, Stefania Cappellani, Mariateresa Di Stazio, Paolo Gasparini, Giorgia Girotto	18
9	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 2018 ·Frontiers in Genetics ·Anna Morgan, Stefania Lenarduzzi, Stefania Cappellani, Vanna Pecile, Marcello Morgutti, Eva Orzan, Sara Ghiselli, Umberto Ambrosetti, Marco Brumat, (unknown), Martina La Bianca, Flavio Faletra, Enrico Grosso, Fabio Sirchia, Alberto Sensi, Claudio Graziano, Marco Seri, Paolo Gasparini, Giorgia Girotto	25
10	A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma 2017 ·Journal of Toxicology and Environmental Health ·Sérgio Crovella, Ronald Moura, Stefania Cappellani, Fulvio Celsi, Elisa Trevisan, (unknown), Alessandro Brollo, (unknown), Francesca Vita, (unknown), Giuliano Zabucchi, Violetta Borelli	8
11	Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literature 2017 ·American Journal of Medical Genetics Part A ·Laura Travan, Samuele Naviglio, Angela De Cunto, (unknown), Vanna Pecile, Alessandro Spinelli, Stefania Cappellani, Flavio Faletra	14
12	A novel OTOA mutation in an Italian family with hearing loss 2017 ·Gene Reports ·Paolo Fontana, Marcello Morgutti, Vanna Pecile, Stefania Lenarduzzi, Stefania Cappellani, Mariateresa Falco, (unknown), Fortunato Lonardo	5
13	Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss 2015 ·Molecular Cytogenetics ·(unknown), Valerio Costa, (unknown), (unknown), (unknown), Stefania Cappellani, (unknown), Giovanni Cennamo, Pio D’Adamo, Alessandra D’Amico, (unknown), Raimondo Forte, Paolo Gasparini, Carla Laria, Barbara Lombardo, Rita Malesci, Andrea Vitale, Elio Marciano, Annamaria Franzè	19
14	Brain-derived neurotrophic factor serum levels in genetically isolated populations: gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism 2015 ·PeerJ ·Davide Carlino, Ruggiero Francavilla, Gabriele Baj, (unknown), Pio D’Adamo, Sheila Ulivi, Stefania Cappellani, Paolo Gasparini, Enrico Tongiorgi	17

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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