Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies? by Ciccodicola, Alfredo, Costa, Valerio, Ziviello, Carmela, Pollastro, Carla

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Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes by Costa, Valerio, Federico, Antonio, Pollastro, Carla, Ziviello, Carmela, Cataldi, Simona, Formisano, Pietro, Ciccodicola, Alfredo

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Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures by Licastro, Danilo, Mutarelli, Margherita, Peluso, Ivana, Neveling, Kornelia, Wieskamp, Nienke, Rispoli, Rossella, Vozzi, Diego, Athanasakis, Emmanouil, D'Eustacchio, Angela, Pizzo, Mariateresa, D'Amico, Francesca, Ziviello, Carmela, Simonelli, Francesca, Fabretto, Antonella, Scheffer, Hans, Gasparini, Paolo, Banfi, Sandro, Nigro, Vincenzo

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The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy by Peluso, Ivana, Conte, Ivan, Testa, Francesco, Dharmalingam, Gopuraja, Pizzo, Mariateresa, Collin, Rob W J, Meola, Nicola, Barbato, Sara, Mutarelli, Margherita, Ziviello, Carmela, Barbarulo, Anna Maria, Nigro, Vincenzo, Melone, Mariarosa A B, Simonelli, Francesca, Banfi, Sandro

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Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration by Simonelli, Francesca, Maguire, Albert M, Testa, Francesco, Pierce, Eric A, Mingozzi, Federico, Bennicelli, Jeannette L, Rossi, Settimio, Marshall, Kathleen, Banfi, Sandro, Surace, Enrico M, Sun, Junwei, Redmond, T Michael, Zhu, Xiaosong, Shindler, Kenneth S, Ying, Gui-Shuang, Ziviello, Carmela, Acerra, Carmela, Wright, J Fraser, McDonnell, Jennifer Wellman, High, Katherine A, Bennett, Jean, Auricchio, Alberto

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New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma by Costa, Valerio, Esposito, Roberta, Ziviello, Carmela, Sepe, Romina, Bim, Larissa Valdemarin, Cacciola, Nunzio Antonio, Decaussin-Petrucci, Myriam, Pallante, Pierlorenzo, Fusco, Alfredo, Ciccodicola, Alfredo

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Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients by Simonelli, Francesca, Ziviello, Carmela, Testa, Francesco, Rossi, Settimio, Fazzi, Elisa, Bianchi, Paolo Emilio, Fossarello, Maurizio, Signorini, Sabrina, Bertone, Chiara, Galantuomo, Silvana, Brancati, Francesco, Valente, Enza Maria, Ciccodicola, Alfredo, Rinaldi, Ernesto, Auricchio, Alberto, Banfi, Sandro

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A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa by den Hollander, Anneke I, McGee, Terri L, Ziviello, Carmela, Banfi, Sandro, Dryja, Thaddeus P, Gonzalez-Fernandez, Federico, Ghosh, Debashis, Berson, Eliot L

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Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy by Testa, Francesco, Surace, Enrico Maria, Rossi, Settimio, Marrocco, Elena, Gargiulo, Annagiusi, Di Iorio, Valentina, Ziviello, Carmela, Nesti, Anna, Fecarotta, Simona, Bacci, Maria Laura, Giunti, Massimo, Della Corte, Michele, Banfi, Sandro, Auricchio, Alberto, Simonelli, Francesca

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Molecular epidemiology of Usher syndrome in Italy by Vozzi, Diego, Aaspõllu, Anu, Athanasakis, Emmanouil, Berto, Anna, Fabretto, Antonella, Licastro, Danilo, Külm, Maigi, Testa, Francesco, Trevisi, Patrizia, Vahter, Marju, Ziviello, Carmela, Martini, Alessandro, Simonelli, Francesca, Banfi, Sandro, Gasparini, Paolo

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Identification and expression analysis of novel Jakmip1 transcripts by Costa, Valerio, Conte, Ivan, Ziviello, Carmela, Casamassimi, Amelia, Alfano, Giovanna, Banfi, Sandro, Ciccodicola, Alfredo

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Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa by Lavorgna, Giovanni, Lestingi, Marta, Ziviello, Carmela, Testa, Francesco, Simonelli, Francesca, Manitto, Maria Pia, Brancato, Rosario, Ferrari, Maurizio, Rinaldi, Ernesto, Ciccodicola, Alfredo, Banfi, Sandro

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