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Mostrati risultati da 41 a 60 di 122
Titolo Data di pubblicazione Autori File
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney 1-gen-2017 VUCKOVIC, DRAGANAGandin, IBrumat, MMORGAN, ANNAGIROTTO, GIORGIAGASPARINI, PAOLO +
Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway 1-gen-2018 Ziraldo, GaiaBrumat, MarcoGirotto, GiorgiaGasparini, Paolo +
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss 1-gen-2018 Girotto, GiorgiaVuckovic, DraganaMezzavilla, MassimoGasparini, Paolo +
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection 1-gen-2018 Vuckovic, DraganaMezzavilla, MassimoCocca, MassimilianoMorgan, AnnaBrumat, MarcoCatamo, EulaliaConcas, Maria PinaGasparini, PaoloGirotto, Giorgia +
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability 1-gen-2018 Vuckovic, DraganaGirotto, GiorgiaGandin, IlariaConcas, Maria PinaBrumat, MarcoGasparini, PaoloCocca, MassimilianoRobino, AntoniettaChen, Yan +
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals 1-gen-2018 Concas, Maria PinaGirotto, GiorgiaVuckovic, DraganaGandin, IlariaRobino, AntoniettaUlivi, SheilaVozzi, DiegoGasparini, PaoloPirastu, Nicola +
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) 1-gen-2018 Barbieri C. M.Gandin I.Gasparini P.Girotto G.Hofer E.Lind L.Robino A.Traglia M. +
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits 1-gen-2018 Barbieri, Caterina MBrumat, MarcoCocca, MassimilianoGandin, IlariaGasparini, PaoloGirotto, GiorgiaMorgan, AnnaRobino, AntoniettaTraglia, MichelaVuckovic, Dragana +
Sordità da cause genetiche 1-gen-2018 Gasparini P.Girotto G. +
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations 1-gen-2018 Morgan, AnnaLenarduzzi, StefaniaCappellani, StefaniaPecile, VannaMorgutti, MarcelloBrumat, MarcoLa Bianca, MartinaFaletra, FlavioGasparini, PaoloGirotto, Giorgia +
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution 1-gen-2019 Easton, Douglas F.Gandin, IlariaGasparini, PaoloGirotto, GiorgiaMorgan, AnnaRobino, AntoniettaVuckovic, Dragana +
Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals. 1-gen-2019 Catamo EConcas MPBrumat MCampana ERobino AGirotto G +
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels 1-gen-2019 Noce D.Horn K.Brumat M.Campana E.Catamo E.Ciullo M.Concas M. P.Gasparini P.Girotto G.La Bianca M.Liu J.Magi R.Martin N. G.Pirastu N.Pistis G.Robino A.Ruggiero D.Salvi E.Schmidt H.Teren A. +
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences 1-gen-2019 Concas, Maria PinaGirotto, GiorgiaVuckovic, DraganaGandin, IlariaRobino, AntoniettaVozzi, DiegoGasparini, PaoloPirastu, Nicola +
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss 1-gen-2019 Girotto, GiorgiaMorgan, AnnaCocca, MassimilianoBrumat, MarcoBASSANI, SISSYLa Bianca, MartinaDi Stazio, MariateresaGasparini, Paolo +
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss 1-gen-2019 Mezzavilla M.Faletra F.Gasparini P.Girotto G. +
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. +
TBL1Y: a new gene involved in syndromic hearing loss 1-gen-2019 Mariateresa Di StazioChiara CollesiDiego VozziAnna MorganPio Adamo D′AdamoGiorgia GirottoElisa RubinatoMauro GiaccaPaolo Gasparini +
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss 1-gen-2019 Faletra F.Cappellani S.Morgutti M.Mezzavilla M.Peruzzi A.Graziano C.Gasparini P.Girotto G. +
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment 1-gen-2019 Brumat M.Cocca M.Vuckovic D.Gasparini P.Girotto G. +
Mostrati risultati da 41 a 60 di 122
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