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Fingerprint Dive into the research topics where Umberto Ambrosetti is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Hearing Loss Medicine & Life Sciences
Tinnitus Medicine & Life Sciences
Hearing Medicine & Life Sciences
Genes Medicine & Life Sciences
Sensorineural Hearing Loss Medicine & Life Sciences
Mutation Medicine & Life Sciences
Deafness Medicine & Life Sciences
Sudden Hearing Loss Medicine & Life Sciences

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Research Output 1980 2019

  • 1392 Citations
  • 20 h-Index
  • 59 Article
  • 3 Chapter

Diagnosis of congenital CMV infection via DBS samples testing and neonatal hearing screening: An observational study in Italy

Pellegrinelli, L., Galli, C., Primache, V., Alde, M., Fagnani, E., Di Berardino, F., Zanetti, D., Pariani, E., Ambrosetti, U. & Binda, S., Jul 22 2019, In : BMC Infectious Diseases. 19, 1, 652.

Research output: Contribution to journalArticle

Open Access
Dried Blood Spot Testing
Neonatal Screening
Italy
Hearing
Observational Studies
Sudden Hearing Loss
Sensorineural Hearing Loss
Emergencies
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss

Morgan, A., Vuckovic, D., Krishnamoorthy, N., Rubinato, E., Ambrosetti, U., Castorina, P., Franzè, A., Vozzi, D., La Bianca, M., Cappellani, S., Di Stazio, M., Gasparini, P. & Girotto, G., Jan 2019, In : European Journal of Human Genetics. 27, 1, p. 70-79 10 p.

Research output: Contribution to journalArticle

Hearing Loss
Age of Onset
Genes
Hearing
Central Asia
3 Citations (Scopus)

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss

Morgan, A., Vuckovic, D., Krishnamoorthy, N., Rubinato, E., Ambrosetti, U., Castorina, P., Franzè, A., Vozzi, D., La Bianca, M., Cappellani, S., Di Stazio, M., Gasparini, P. & Girotto, G., 2019, In : European Journal of Human Genetics. 27, 1, p. 70-79

Research output: Contribution to journalArticle

Hearing Loss
Age of Onset
Genes
Hearing
Central Asia

Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss

Lenarduzzi, S., Morgan, A., Faletra, F., Cappellani, S., Morgutti, M., Mezzavilla, M., Peruzzi, A., Ghiselli, S., Ambrosetti, U., Graziano, C., Seri, M., Gasparini, P. & Girotto, G., Sep 15 2019, In : Hearing Research. 381, 107769.

Research output: Contribution to journalArticle

Hearing Loss
Alleles
Genes
Single Nucleotide Polymorphism
Usher Syndromes