Research Output per year
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
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
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 journal › Article
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. 70-79Research output: Contribution to journal › Article
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 journal › Article
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 journal › Article
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 journal › Article
Exome
Connexin 43
Genome-Wide Association Study
Gap Junctions
Sudden Cardiac Death