Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Mutations in the 5′ UTR of ANKRD26, the Ankirin Repeat Domain 26 Gene, Cause an Autosomal-Dominant Form of Inherited Thrombocytopenia, THC2Pippucci, Tommaso ; Savoia, Anna ; Perrotta, Silverio ; Pujol-Moix, Núria ; Noris, Patrizia ; Castegnaro, Giovanni ; Pecci, Alessandro ; Gnan, Chiara ; Punzo, Francesca ; Marconi, Caterina ; Gherardi, Samuele ; Loffredo, Giuseppe ; De Rocco, Daniela ; Scianguetta, Saverio ; Barozzi, Serena ; Magini, Pamela ; Bozzi, Valeria ; Dezzani, Luca ; Di Stazio, Mariateresa ; Ferraro, Marcella ; Perini, Giovanni ; Seri, Marco ; Balduini, Carlo L.American journal of human genetics, 2011-01, Vol.88 (1), p.115-120 [Periódico revisado por pares]Cambridge, MA: Elsevier IncTexto completo disponível |
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2 |
Material Type: Artigo
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TBL1Y: a new gene involved in syndromic hearing lossDi Stazio, Mariateresa ; Collesi, Chiara ; Vozzi, Diego ; Liu, Wei ; Myers, Mike ; Morgan, Anna ; D Adamo, Pio Adamo ; Girotto, Giorgia ; Rubinato, Elisa ; Giacca, Mauro ; Gasparini, PaoloEuropean journal of human genetics : EJHG, 2019-03, Vol.27 (3), p.466-474 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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3 |
Material Type: Artigo
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New age-related hearing loss candidate genes in humans: an ongoing challengeDi Stazio, M. ; Morgan, A. ; Brumat, M. ; Bassani, S. ; Dell'Orco, D. ; Marino, V. ; Garagnani, P. ; Giuliani, C. ; Gasparini, P. ; Girotto, G.Gene, 2020-06, Vol.742, p.144561-144561, Article 144561 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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4 |
Material Type: Artigo
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Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing lossMorgan, Anna ; Vuckovic, Dragana ; Krishnamoorthy, Navaneethakrishnan ; Rubinato, Elisa ; Ambrosetti, Umberto ; Castorina, Pierangela ; Franzè, Annamaria ; Vozzi, Diego ; La Bianca, Martina ; Cappellani, Stefania ; Di Stazio, Mariateresa ; Gasparini, Paolo ; Girotto, GiorgiaEuropean journal of human genetics : EJHG, 2019-01, Vol.27 (1), p.70-79 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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5 |
Material Type: Artigo
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Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)Donaudy, Francesca ; Snoeckx, Rik ; Pfister, Markus ; Zenner, Hans-Peter ; Blin, Nikolaus ; Di Stazio, Mariateresa ; Ferrara, Antonella ; Lanzara, Carmen ; Ficarella, Romina ; Declau, Frank ; Pusch, Carsten M. ; Nürnberg, Peter ; Melchionda, Salvatore ; Zelante, Leopoldo ; Ballana, Ester ; Estivill, Xavier ; Van Camp, Guy ; Gasparini, Paolo ; Savoia, AnnaAmerican journal of human genetics, 2004-04, Vol.74 (4), p.770-776 [Periódico revisado por pares]Chicago, IL: Elsevier IncTexto completo disponível |
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6 |
Material Type: Artigo
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Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B -Associated DisordersDi Stazio, Mariateresa ; Zanus, Caterina ; Faletra, Flavio ; Pesaresi, Alessia ; Ziccardi, Ilaria ; Morgan, Anna ; Girotto, Giorgia ; Costa, Paola ; Carrozzi, Marco ; d'Adamo, Adamo P ; Musante, LucianaGenes, 2023-01, Vol.14 (2), p.250 [Periódico revisado por pares]Switzerland: MDPI AGTexto completo disponível |
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7 |
Material Type: Artigo
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What Is the Exact Contribution of PITX1 and TBX4 Genes in Clubfoot Development? An Italian StudyBianco, Anna Monica ; Ragusa, Giulia ; Di Carlo, Valentina ; Faletra, Flavio ; Di Stazio, Mariateresa ; Racano, Costantina ; Trisolino, Giovanni ; Cappellani, Stefania ; De Pellegrin, Maurizio ; d’Addetta, Ignazio ; Carluccio, Giuseppe ; Monforte, Sergio ; Andreacchio, Antonio ; Dibello, Daniela ; d’Adamo, Adamo P.Genes, 2022-10, Vol.13 (11), p.1958 [Periódico revisado por pares]Basel: MDPI AGTexto completo disponível |
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8 |
Material Type: Artigo
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Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing LossGirotto, Giorgia ; Morgan, Anna ; Krishnamoorthy, Navaneethakrishnan ; Cocca, Massimiliano ; Brumat, Marco ; Bassani, Sissy ; La Bianca, Martina ; Di Stazio, Mariateresa ; Gasparini, PaoloFrontiers in genetics, 2019-02, Vol.10, p.142-142 [Periódico revisado por pares]Switzerland: Frontiers Media S.ATexto completo disponível |
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9 |
Material Type: Artigo
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Mild neurological phenotype in a family carrying a novel N-terminal null GRIN2A variantDe Bernardi, Margherita Lucia ; Di Stazio, Agnese ; Romano, Alfonso ; Minardi, Raffaella ; Bisulli, Francesca ; Licchetta, Laura ; Aiello, Salvatore ; Carelli, Valerio ; Brunetti-Pierri, Nicola ; Cappuccio, Gerarda ; Terrone, GaetanoEuropean journal of medical genetics, 2022-05, Vol.65 (5), p.104500-104500, Article 104500 [Periódico revisado por pares]Netherlands: Elsevier Masson SASTexto completo disponível |
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10 |
Material Type: Artigo
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Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and lossVuckovic, Dragana ; Dawson, Sally ; Scheffer, Deborah I ; Rantanen, Taina ; Morgan, Anna ; Di Stazio, Mariateresa ; Vozzi, Diego ; Nutile, Teresa ; Concas, Maria P ; Biino, Ginevra ; Nolan, Lisa ; Bahl, Aileen ; Loukola, Anu ; Viljanen, Anne ; Davis, Adrian ; Ciullo, Marina ; Corey, David P ; Pirastu, Mario ; Gasparini, Paolo ; Girotto, GiorgiaHuman molecular genetics, 2015-10, Vol.24 (19), p.5655-5664 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |