GIROTTO, GIORGIA

GIROTTO, GIORGIA  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

Settore MED/03 - Genetica Medica  

Docenti di ruolo di IIa fascia  

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Risultati 1 - 20 di 116 (tempo di esecuzione: 0.025 secondi).
Titolo Data di pubblicazione Autori File
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 1-gen-2017 COCCA, MASSIMILIANOD'ADAMO, ADAMO PIOGASPARINI, PAOLOGIROTTO, GIORGIAPISTIS, GIORGIOROBINO, ANTONIETTAULIVI, SHEILAVUCKOVIC, DRAGANA +
A bird’s-eye view of Italian genomic variation through whole-genome sequencing 1-gen-2020 Robino A.Brumat M.Gandin I.Girotto G.Gasparini P.Mezzavilla M. +
A catalog of genetic loci associated with kidney function from analyses of a million individuals. 1-gen-2019 Cocca MBrumat MCAMPANA, ERICCatamo EConcas MPGasparini PGirotto GLa Bianca MRobino A +
A meta-analysis of genome-wide association studies identifies new genetic loci associated with all-cause and vascular dementia 1-gen-2022 Maria Pina ConcasGiorgia Girotto +
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 1-gen-2022 Morgan, AnnaConcas, Maria PinaGirotto, Giorgia +
A new case of TAR syndrome confirms the importance of noncoding variants in the etiopathogenesis of the disease 1-gen-2021 Morgan A.La Bianca M.Faletra F.Girotto G. +
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 1-gen-2017 GIROTTO, GIORGIAGIANGREGORIO, TANIAGASPARINI, PAOLOROMEO, GIOVANNI +
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 1-gen-2013 GIROTTO, GIORGIAD'ADAMO, ADAMO PIOVOZZI, DIEGOMORGAN, ANNAGASPARINI, PAOLO +
A saturated map of common genetic variants associated with human height 1-gen-2022; 1-gen-2022 Catamo, EulaliaCocca, MassimilianoConcas, Maria PinaFrancescatto, MargheritaMorgan, AnnaTesolin, PaolaGasparini, PaoloGirotto, Giorgia +
Age-related hearing loss and level of education: an epidemiological study on a large cohort of isolated popu-lations 1-gen-2014 VUCKOVIC, DRAGANAGASPARINI, PAOLOGIROTTO, GIORGIA +
Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population 1-gen-2022 Mezzavilla, MassimoCocca, MassimilianoGiorgia, GirottoGasparini, Paolo +
Association of SNPs in LCP1 and CTIF with hearing in 11 year old children: Findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort and the G-EAR consortium 1-gen-2015 VUCKOVIC, DRAGANAGIROTTO, GIORGIA +
Associations of autozygosity with a broad range of human phenotypes 1-gen-2019 Mason D.Pirastu N.Gandin I.Lin K.Hofer E.Jia Y.Viberti C.Wang L.Zhao W.Chen G.Concas M. P.Girotto G.Graff M.Liu J.Magi R.Mezzavilla M.Moore A.Robino A.Ruggiero D.Schmidt H.Shi Y.Zhang L.Carmi S.Ciullo M.Cornelis M.Gasparini P.Gonzalez C.Lea R. A.Palmer C. +
Benefit of cochlear implantation in a patient with Myhre syndrome 1-gen-2021 Girotto G. +
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures 1-gen-2022 Spedicati, BeatriceMorgan, AnnaRubinato, ElisaSantin, AuroraFaletra, FlavioGirotto, Giorgia +
Chronic Rhinosinusitis: T2r38 Genotyping and Nasal Cytology in Primary Ciliary Dyskinesia 1-gen-2023 Girotto, GiorgiaConcas, Maria P. +
Common Variants in UMOD Associate with Urinary Uromodulin Levels: A Meta-Analysis. 1-gen-2014 GASPARINI, PAOLOCOCCA, MASSIMILIANOGANDIN, ILARIAGIROTTO, GIORGIATRAGLIA, MICHELAVUCKOVIC, DRAGANA +
Consanguinity and Hereditary Hearing Loss in Qatar 1-gen-2014 GIROTTO, GIORGIAMEZZAVILLA, MASSIMOVUCKOVIC, DRAGANAVOZZI, DiegoGASPARINI, PAOLO +
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 1-gen-2017 Li, ManCocca, MassimilianoAdamo, Adamo Pio d'Gasparini, PaoloGirotto, GiorgiaPistis, GiorgioRobino, AntoniettaVuckovic, Dragana +
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 1-gen-2018 Ziraldo, GaiaBrumat, MarcoGirotto, GiorgiaGasparini, Paolo +