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Titolo Data di pubblicazione Autori File
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss 1-gen-2015 VUCKOVIC, DRAGANAMORGAN, ANNADI STAZIO, MARIATERESAVOZZI, DiegoCONCAS, MARIA PINAGASPARINI, PAOLOGIROTTO, GIORGIA +
Rare coding variants and X-linked loci associated with age at menarche 1-gen-2015 BARBIERI, CATERINA MARIAGANDIN, ILARIAVOZZI, DIEGOEaston, Douglas F. +
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair 1-gen-2015 ROBINO, ANTONIETTAVUCKOVIC, DRAGANABARBIERI, CATERINA MARIAGANDIN, ILARIAGIROTTO, GIORGIAPIRASTU, NicolaVOZZI, DIEGOEaston, Douglas FGASPARINI, PAOLO +
Genetic variants linked to education predict longevity. 1-gen-2016 CONCAS, MARIA PINAGIROTTO, GIORGIAVUCKOVIC, DRAGANAGANDIN, ILARIAROBINO, ANTONIETTAULIVI, SHEILAVOZZI, DIEGOGASPARINI, PAOLOPIRASTU, Nicola +
Putative modifier genes in mevalonate kinase deficiency 1-gen-2016 MARCUZZI, ANNALISAVOZZI, DIEGOGIRARDELLI, MARTINATRICARICO, PAOLA MAURACROVELLA, SERGIOVUCH, JOSEFTOMMASINI, ALBERTOPISCIANZ, ELISABIANCO, ANNA MONICA ROSARIA +
Rare and low-frequency coding variants alter human adult height 1-gen-2017 COCCA, MASSIMILIANOEaston, Douglas F.Gandin, IlariaGASPARINI, PAOLOGIROTTO, GIORGIALA BIANCA, MARTINAMORGAN, ANNAROBINO, ANTONIETTAULIVI, SHEILAVOZZI, DIEGO +
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families 1-gen-2017 VOZZI, DIEGOMORGAN, ANNAGANDIN, ILARIAGASPARINI, PAOLOGIROTTO, GIORGIA +
Type i interferon-mediated autoinflammation due to DNase II deficiency 1-gen-2017 Tesser, AlessandraVOLPI, STEFANOBianco, Anna MonicaFaletra, FlavioMarcuzzi, AnnalisaPastore, SerenaPiscianz, ElisaStocco, GabrieleTaddio, AndreaValencic, EricaVozzi, DiegoTommasini, Alberto +
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders 1-gen-2018 Gandin I.Vozzi D.Concas M. P.Robino A. +
The Challenge of Next Generation Sequencing in a Boy with Severe Mononucleosis and EBV-related Lymphoma 1-gen-2018 Verzegnassi F.Valencic E.Kiren V.Giurici N.Bianco A. M.Marcuzzi A.Vozzi D.Tommasini A.Faletra F.
Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype 1-gen-2018 Girardelli M.Loganes C.Pin A.Decleva E.Vozzi D.Baj G.Tommasini A.Bianco A. M. +
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 +
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 +
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 identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss 1-gen-2019 Morgan, AnnaVuckovic, DraganaRubinato, ElisaVozzi, DiegoLa Bianca, MartinaCappellani, StefaniaDi Stazio, MariateresaGasparini, PaoloGirotto, Giorgia +
Analisi mediante metodiche di sequenziamente di nuova generazione di soggetti affetti da sordità genetica, finalizzata all’individuazione di alterazioni genomiche patogenetiche, non descritte in precedenza. 18-ott-2019 VOZZI, DIEGO
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals 1-gen-2022 Maria Pina ConcasGiorgia GirottoDragana VuckovicIlaria GandinAntonietta RobinoDiego VozziPaolo GaspariniNicola Pirastu +
Mostrati risultati da 21 a 37 di 37
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