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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 - 9 of 9
- PublicationNon-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the NCOA3 Gene
;Tesolin Paola; ;Notarangelo Michela ;Ortore Rocco Pio; ;Notarangelo Angelantonio - PublicationGenetic dissection of temperament personality traits in Italian isolates
; ;Minelli Alessandra ;Aere Susanna; ;Tesolin Paola; ;Gennarelli Massimo - PublicationHearing function: Identification of new candidate genes further explaining the complexity of this sensory ability
; ; ; ;Nagtegaal A.P. ;Oosterloo B.C. ;Seshadri S. ;Heard-Costa N. ;Van Camp G. ;Fransen E. ;Francescatto M. ;Logroscino G. ;Sardone R. ;Quaranta N.; - PublicationNatural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates
;Spedicati Beatrice; ;Palmisano Roberto; ;Barbieri Caterina ;Francescatto Margherita; ; ;Pelliccione Giulia; ; - PublicationNon-syndromic sensorineural prelingual and postlingual hearing loss due to col11a1 gene mutation
;Ciorba Andrea ;Corazzi Virginia ;Melegatti Michela; ;Pelliccione Giulia; Bigoni Stefania - PublicationPendred syndrome, or not pendred syndrome? That is the question
;Tesolin Paola ;Fiorino Sofia; ; ; ;Ammar Lydie ;Castro Veronica; ; ;Dell¿orco Daniele; - PublicationGenome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
;Simcoe Mark ;Valdes Ana ;Liu Fan ;Furlotte Nicholas A. ;Evans David M. ;Hemani Gibran ;Ring Susan M. ;Smith George Davey ;Duffy David L. ;Zhu Gu ;Gordon Scott D. ;Medland Sarah E. ;Vuckovic Dragana; ;Sala Cinzia; ; ;Brumat Marco; ;Toniolo Daniela; ; ;Yazar Seyhan ;Hewitt Alex ;Wu Wenting ;Kraft Peter ;Hammond Christopher J. ;Shi Yuan ;Chen Yan ;Zeng Changqing ;Klaver Caroline C.W. ;Uitterlinden Andre G. ;Ikram M. Arfan ;Hamer Merel A. ;van Duijn Cornelia M. ;Nijsten Tamar ;Han Jiali ;Mackey David A. ;Martin Nicholas G. ;Cheng Ching Yu ;the 23andMe Research Team ;the International Visible Trait Genetics Consortium Gruppo ;Hinds David A. ;Spector Timothy D. ;Kayser ManfredHysi Pirro G. - PublicationThe power of genetic diversity in genome-wide association studies of lipids
;Graham S.E. ;Clarke S.L. ;Wu K.-H.H. ;Kanoni S. ;Zajac G.J.M. ;Ramdas S. ;Surakka I. ;Ntalla I. ;Vedantam S. ;Winkler T.W. ;Locke A.E. ;Marouli E. ;Hwang M.Y. ;Han S. ;Narita A. ;Choudhury A. ;Bentley A.R. ;Ekoru K. ;Verma A. ;Trivedi B. ;Martin H.C. ;Hunt K.A. ;Hui Q. ;Klarin D. ;Zhu X. ;Thorleifsson G. ;Helgadottir A. ;Gudbjartsson D.F. ;Holm H. ;Olafsson I. ;Akiyama M. ;Sakaue S. ;Terao C. ;Kanai M. ;Zhou W. ;Brumpton B.M. ;Rasheed H. ;Ruotsalainen S.E. ;Havulinna A.S. ;Veturi Y. ;Feng Q.P. ;Rosenthal E.A. ;Lingren T. ;Wang Y.X. ;Ruggiero D. ;Gorski M.; ; ;Joshi P.K.Ciullo M. - PublicationVariants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
;Bassani Sissy ;Van Beelen Edward ;Rossel Mireille ;Voisin Norine; ;Arribat Yoan ;Chatron Nicolas ;Chrast Jacqueline; ;Delprat Benjamin; ;Giannuzzi Giuliana ;Guex Nicolas ;Machavoine Roxane ;Pradervand Sylvain ;Smits Jeroen J. ;Van De Kamp Jiddeke M. ;Ziegler Alban ;Amati Francesca ;Marlin Sandrine ;Kremer Hannie ;Locher Heiko ;Maurice Tangui; ; Reymond Alexandre