CAPPELLANI, STEFANIA

CAPPELLANI, STEFANIA  

Dipartimento Universitario Clinico di Scienze mediche, chirurgiche e della salute  

Personale esterno ed autonomi  

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Risultati 1 - 12 di 12 (tempo di esecuzione: 0.021 secondi).
Titolo Data di pubblicazione Autori File
Brain-derived neurotrophic factor serum levels in genetically isolated populations: Gender-specific association with anxiety disorder subtypes but not with anxiety levels or Val66Met polymorphism 1-gen-2015 CARLINO, DAVIDEBAJ, GabrieleD'ADAMO, ADAMO PIOULIVI, SHEILACAPPELLANI, STEFANIAGASPARINI, PAOLOTONGIORGI, Enrico +
Case Report: Two cases of apparent discordance between non-invasive prenatal testing (NIPT) and amniocentesis resulting in feto-placental mosaicism of trisomy 21. Issues in diagnosis, investigation and counselling 1-gen-2022 Feresin, AgneseStampalija, TamaraCappellani, StefaniaBussani, RossanaFaletra, FlavioBosio, BarbaraArdisia, Carmela +
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 1-gen-2018 Cappellani, StefaniaIorio, AnnamariaRobino, AntoniettaGasparini, PaoloSinagra, GianfrancoUlivi, Sheila +
A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma. 1-gen-2018 Crovella SergioCappellaniFulvio CelsiElisa TrevisanEnza Maria. NicastroFrancesca VitaVioletta Borelli +
Genome-wide analysis identifies 12 loci influencing human reproductive behavior. 1-gen-2016 BARBIERI, CATERINA MARIACONCAS, MARIA PINAGANDIN, ILARIAROBINO, ANTONIETTAULIVI, SHEILACAPPELLANI, STEFANIAGASPARINI, PAOLOGIROTTO, GIORGIALA BIANCA, MARTINATRAGLIA, MICHELAVUCKOVIC, DRAGANA +
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 +
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. +
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 +
Phenotypic expression of 19q13.32 microdeletions: Report of a new patient and review of the literature 1-gen-2017 TRAVAN, LAURANAVIGLIO, SAMUELEDE CUNTO, ANGELAPECILE, VANNACAPPELLANI, STEFANIAFALETRA, FLAVIO +
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity 1-gen-2018 Brumat, MarcoCappellani, StefaniaCatamo, EulaliaCocca, MassimilianoD'Eustacchio, AngelaGandin, IlariaGasparini, PaoloRobino, AntoniettaVuckovic, Dragana +
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (Nature Genetics, (2018), 50, 1, (26-41), 10.1038/s41588-017-0011-x) 1-gen-2019 Graff M.Allison M.Cappellani S.Catamo E.Gandin I.Gasparini P.Jia Y.Kim E.Lin H.Lind L.Palmer N. D.Robino A.Veronesi G.Wang F.Zhan X.Zhao W.Zhao W. +
What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian Study 1-gen-2022 Bianco, Anna MonicaFaletra, FlavioDi Stazio, MariateresaCappellani, StefaniaDibello, Danielad’Adamo, Adamo P. +