C. Ziviello

发表

Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes

A. Ciccodicola, P. Formisano, V. Costa, 2016, International journal of molecular sciences.

Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

A. Ciccodicola, M. Ferrari, S. Banfi, 2003, Biochemical and biophysical research communications.

Clinical and molecular genetics of Leber's congenital amaurosis: a multicenter study of Italian patients.

A. Ciccodicola, F. Brancati, E. Valente, 2007, Investigative ophthalmology & visual science.

A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.

T. L. McGee, A. D. den Hollander, T. Dryja, 2009, Investigative ophthalmology & visual science.

Identification and expression analysis of novel Jakmip1 transcripts.

A. Ciccodicola, A. Casamassimi, S. Banfi, 2007, Gene.

Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families

A. Ciccodicola, S. Banfi, F. Testa, 2003, The British journal of ophthalmology.

Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration

Jean Bennett, Gui-Shuang Ying, Francesco Testa, 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

Molecular epidemiology of Usher syndrome in Italy

P. Gasparini, D. Vozzi, S. Banfi, 2011, Molecular vision.

BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome.

B. J. Klevering, E. Zrenner, T. de Ravel, 2012, Archives of ophthalmology.

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

Nicola Meola, S. Banfi, M. Pizzo, 2013, Orphanet Journal of Rare Diseases.

New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma

A. Ciccodicola, A. Fusco, V. Costa, 2015, Oncotarget.

Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies?

A. Ciccodicola, V. Costa, Carla Pollastro, 2015, PPAR research.

Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures

P. Gasparini, D. Vozzi, H. Scheffer, 2012, PloS one.

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.

E. Surace, S. Banfi, M. Bacci, 2011, Investigative ophthalmology & visual science.

BBS 1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome

B. J. Klevering, E. Zrenner, D. Sharon, 2012 .

Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations

Sandro Banfi, A. Ciccodicola, S. Banfi, 2003, European Journal of Human Genetics.

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families

A. Ciccodicola, S. Banfi, B. Falsini, 2005, Journal of Medical Genetics.

In the Shadow of the Genome : A Challenging Journey to Diversity in Leishmania donovani

Margherita, A. Ciccodicola, C. Angelini, 2012 .