Publications by authors named "Micol Busi"

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Diagnostic Yield and Genetic Variation in 85 Swedish Patients with Mild to Profound Hearing Loss Analyzed by Whole Genome Sequencing.
Johanna Elander, Tove Ullmark, Karolina Löwgren, Karin Stenfeldt, Karolina Falkenius-Schmidt, Micol Busi

J Otolaryngol Head Neck Surg· July 2025

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Navigating the Usher Syndrome Genetic Landscape: An Evaluation of the Associations between Specific Genes and Quality Categories of Cochlear Implant Outcomes.
Micol Busi, Alessandro Castiglione

Audiol Res· February 2024

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Cochlear Implant Outcomes and Genetic Mutations in Children with Ear and Brain Anomalies.
Micol Busi, Monica Rosignoli, Alessandro Castiglione, Federica Minazzi, Patrizia Trevisi

Biomed Res Int· May 2016

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Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects.
Valeria Guaran, Laura Astolfi, Alessandro Castiglione, Edi Simoni, Elena Olivetto, Micol Busi

Int J Mol Med· October 2013

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Novel mutations in the SLC26A4 gene.
Micol Busi, Alessandro Castiglione, Marina Taddei Masieri, Anna Ravani, Valeria Guaran

Int J Pediatr Otorhinolaryngol· September 2012

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Association of the 4 g/5 g polymorphism of plasminogen activator inhibitor-1 gene with sudden sensorineural hearing loss. A case control study.
Seong Ho Cho, Haimei Chen, Il Soo Kim, Chio Yokose, Joseph Kang, Micol Busi

BMC Ear Nose Throat Disord· June 2012

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LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.
Alberto Sensi, Stefano Ceruti, Patrizia Trevisi, Francesca Gualandi, Micol Busi

Am J Med Genet A· May 2011

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The universal newborn hearing screening program at the University Hospital of Ferrara: focus on costs and software solutions.
Andrea Ciorba, Stavros Hatzopoulos, Micol Busi, Piero Guerrini, Joseph Petruccelli

Int J Pediatr Otorhinolaryngol· June 2008

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