• 282 Citations
  • 4 h-Index
20152019
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Fingerprint Dive into the research topics where Stefania Cappellani is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Hearing Loss Medicine & Life Sciences
Reproductive Behavior Medicine & Life Sciences
Birth Order Medicine & Life Sciences
Genes Medicine & Life Sciences
Genome-Wide Association Study Medicine & Life Sciences
Genome Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Age of Onset Medicine & Life Sciences

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Research Output 2015 2019

  • 282 Citations
  • 4 h-Index
  • 17 Article

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

A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma

Crovella, S., Moura, R. R., Cappellani, S., Celsi, F., Trevisan, E., Schneider, M., Brollo, A., Nicastro, E. M., Vita, F., Finotto, L., Zabucchi, G. & Borelli, V., 2018, In : Journal of Toxicology and Environmental Health - Part A: Current Issues. 81, 5, p. 98-105 8 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Gasparini P, Jul 17 2018, In : Genome Biology. 19, 1, 87.

Research output: Contribution to journalArticle

Exome
Connexin 43
Genome-Wide Association Study
Gap Junctions
Sudden Cardiac Death