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Girotto, Giorgia
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Preferred name
Girotto, Giorgia
Main Affiliation
Email
giorgia.girotto@burlo.trieste.it
ORCID
Scopus Author ID
35503194200
Researcher ID
I-9452-2018
Research Output
Now showing 1 - 10 of 19
- PublicationHearing function: Identification of new candidate genes further explaining the complexity of this sensory ability
; ; ; ; - PublicationNatural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates
; ; ; ; ; ; - PublicationNon-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation
; ; Bigoni Stefania - PublicationPendred syndrome, or not pendred syndrome? That is the question
; ; ; ; ; ; - PublicationGenome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
; ; ; ; ; ; - PublicationThe power of genetic diversity in genome-wide association studies of lipids
; ; - PublicationVariants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
; ; ; ; ; Reymond Alexandre - PublicationNon-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene
; ; - PublicationGenetic dissection of temperament personality traits in Italian isolates
; ; ; - PublicationDifferential and shared genetic effects on kidney function between diabetic and non-diabetic individuals
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