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A. Auricchio · SciRah

Researcher profile · Semantic Scholar

A. Auricchio

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A. Auricchio — researcher profile on SciRah

h-index: 62
Works: 221
Citations: 15K

Most-cited papers

AAV2 Gene Therapy Readministration in Three Adults with Congenital Blindness
J. Bennett, M. Ashtari, J. Wellman, Kathleen A. Marshall +16 more
2012Science Translational Medicine423 citations Open access
Semantic Scholar
Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutatons: a follow-on phase 1 trial
J. Bennett, J. Wellman, Kathleen A. Marshall, Sarah Mccague +18 more
2016The Lancet414 citations Open access
Semantic Scholar
Three Year Follow-Up after Unilateral Subretinal Delivery of Adeno-Associated Virus in Patients with Leber Congenital Amaurosis Type 2
F. Testa, A. Maguire, S. Rossi, E. Pierce +12 more
2013Ophthalmology (Rochester, Minn.)342 citations Open access
Semantic Scholar
Effective delivery of large genes to the retina by dual AAV vectors
I. Trapani, P. Colella, A. Sommella, Carolina Iodice +9 more
2013EMBO Molecular Medicine263 citations Open access
Semantic Scholar
Intein-mediated protein trans-splicing expands adeno-associated virus transfer capacity in the retina
P. Tornabene, I. Trapani, R. Minopoli, M. Centrulo +19 more
2019Science Translational Medicine169 citations Open access
Semantic Scholar
Vector platforms for gene therapy of inherited retinopathies
I. Trapani, Agostina Puppo, A. Auricchio
2014Progress in retinal and eye research169 citations Open access
Semantic Scholar
SEPN1, an endoplasmic reticulum-localized selenoprotein linked to skeletal muscle pathology, counteracts hyperoxidation by means of redox-regulating SERCA2 pump activity.
Marianna Marino, T. Stoilova, C. Giorgi, A. Bachi +4 more
2015Human Molecular Genetics126 citations Open access
Semantic Scholar
Triple Vectors Expand AAV Transfer Capacity in the Retina
A. Maddalena, P. Tornabene, P. Tiberi, R. Minopoli +7 more
2017Molecular Therapy124 citations Open access
Semantic Scholar
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
C. Bonnet, Z. Riahi, S. Chantot-Bastaraud, Luce Smagghe +33 more
2016European Journal of Human Genetics111 citations Open access
Semantic Scholar
Single Delivery of an Adeno-Associated Viral Construct to Transfer the CASQ2 Gene to Knock-In Mice Affected by Catecholaminergic Polymorphic Ventricular Tachycardia Is Able to Cure the Disease From Birth to Advanced Age
M. Denegri, R. Bongianino, F. Lodola, S. Boncompagni +15 more
2014Circulation111 citations Open access
Semantic Scholar
Seeing the Light after 25 Years of Retinal Gene Therapy.
I. Trapani, A. Auricchio
2018Trends in Molecular Medicine108 citations Open access
Semantic Scholar
Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors
P. Colella, I. Trapani, Giulia Cesi, Andrea Sommella +8 more
2014Gene Therapy108 citations Open access
Semantic Scholar
Improved dual AAV vectors with reduced expression of truncated proteins are safe and effective in the retina of a mouse model of Stargardt disease
I. Trapani, Elisabetta Toriello, S. de Simone, P. Colella +10 more
2015Human Molecular Genetics93 citations Open access
Semantic Scholar
Manufacturing and Characterization of a Recombinant Adeno-Associated Virus Type 8 Reference Standard Material
E. Ayuso, V. Blouin, Martin Lock, S. McGorray +32 more
2014Human Gene Therapy92 citations Open access
Semantic Scholar
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2)
R. Bongianino, M. Denegri, A. Mazzanti, F. Lodola +11 more
2017Circulation Research89 citations Open access
Semantic Scholar
Viral Gene Transfer Rescues Arrhythmogenic Phenotype and Ultrastructural Abnormalities in Adult Calsequestrin-Null Mice With Inherited Arrhythmias
M. Denegri, J. Avelino-Cruz, S. Boncompagni, S. A. De Simone +6 more
2012Circulation Research86 citations Open access
Semantic Scholar
Genetic Analysis Reveals a Longevity-Associated Protein Modulating Endothelial Function and Angiogenesis
Francesco Villa, Albino Carrizzo, C. Spinelli, A. Ferrario +21 more
2015Circulation Research85 citations Open access
Semantic Scholar
Effective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathy
I. Di Meo, A. Auricchio, C. Lamperti, A. Burlina +2 more
2012EMBO Molecular Medicine82 citations Open access
Semantic Scholar
Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer.
G. Cotugno, P. Annunziata, A. Tessitore, Thomas M. O'Malley +14 more
2011Molecular Therapy76 citations Open access
Semantic Scholar
Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy.
F. Testa, S. Rossi, A. Sodi, I. Passerini +7 more
2012Investigative Ophthalmology and Visual Science71 citations Open access
Semantic Scholar
Single systemic transfer of a human gene associated with exceptional longevity halts the progression of atherosclerosis and inflammation in ApoE knockout mice through a CXCR4-mediated mechanism
A. Puca, Albino Carrizzo, C. Spinelli, A. Damato +26 more
2019European Heart Journal70 citations Open access
Semantic Scholar
Gene therapy using a liver-targeted AAV vector restores nucleoside and nucleotide homeostasis in a murine model of MNGIE.
Javier Torres-Torronteras, C. Viscomi, R. Cabrera-Pérez, Yolanda Cámara +7 more
2014Molecular Therapy69 citations Open access
Semantic Scholar
AAV2/8 Vectors Purified from Culture Medium with a Simple and Rapid Protocol Transduce Murine Liver, Muscle, and Retina Efficiently
M. Dòria, Antonella Ferrara, A. Auricchio
2013Human Gene Therapy Methods60 citations Open access
Semantic Scholar
Retinal transduction profiles by high-capacity viral vectors
Agostina Puppo, G. Cesi, E. Marrocco, Pasquale Piccolo +9 more
2014Gene Therapy57 citations Open access
Semantic Scholar
AAV-mediated liver-specific MPV17 expression restores mtDNA levels and prevents diet-induced liver failure
Emanuela Bottani, C. Giordano, G. Civiletto, I. Di Meo +7 more
2013Molecular Therapy57 citations Open access
Semantic Scholar
Gene Therapy of Inherited Retinopathies: A Long and Successful Road from Viral Vectors to Patients
P. Colella, A. Auricchio
2012Human Gene Therapy56 citations Open access
Semantic Scholar
The Future Looks Brighter After 25 Years of Retinal Gene Therapy
A. Auricchio, Alexander J. Smith, R. Ali
2017Human Gene Therapy50 citations Open access
Semantic Scholar
Gene Therapy of Inherited Retinal Degenerations: Prospects and Challenges
I. Trapani, S. Banfi, F. Simonelli, E. Surace +1 more
2015Human Gene Therapy49 citations Open access
Semantic Scholar
Low incidence of hepatocellular carcinoma in mice and cats treated with systemic adeno-associated viral vectors
R. Ferla, M. Alliegro, Margherita Dell’Anno, E. Nusco +13 more
2020Molecular Therapy: Methods & Clinical Development47 citations Open access
Semantic Scholar
Has retinal gene therapy come of age? From bench to bedside and back to bench
I. Trapani, A. Auricchio
2019Human Molecular Genetics47 citations Open access
Semantic Scholar
Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.
F. Testa, E. Surace, S. Rossi, E. Marrocco +11 more
2011Investigative Ophthalmology and Visual Science47 citations
Semantic Scholar
Cross-talk between androgen receptor/filamin A and TrkA regulates neurite outgrowth in PC12 cells
M. Di Donato, A. Bilancio, L. D'Amato, Pamela Claudiani +7 more
2015Molecular Biology of the Cell46 citations Open access
Semantic Scholar
Non-clinical Safety and Efficacy of an AAV2/8 Vector Administered Intravenously for Treatment of Mucopolysaccharidosis Type VI
R. Ferla, M. Alliegro, J. Marteau, Margherita Dell’Anno +6 more
2017Molecular Therapy: Methods & Clinical Development45 citations Open access
Semantic Scholar
Gene Therapy for Mucopolysaccharidosis Type VI Is Effective in Cats Without Pre-Existing Immunity to AAV8
R. Ferla, Thomas M. O'Malley, R. Calcedo, P. O'Donnell +6 more
2013Human Gene Therapy44 citations Open access
Semantic Scholar
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model
Clarissa Patrizi, Manel Llado, D. Benati, Carolina Iodice +6 more
2021American Journal of Human Genetics42 citations Open access
Semantic Scholar
AAV-mediated transcription factor EB (TFEB) gene delivery ameliorates muscle pathology and function in the murine model of Pompe Disease
F. Gatto, Barbara Rossi, Antonietta Tarallo, Elena Polishchuk +10 more
2017Scientific Reports42 citations Open access
Semantic Scholar
Gene Therapy of ABCA4-Associated Diseases.
A. Auricchio, I. Trapani, R. Allikmets
2015Cold Spring Harbor Perspectives in Medicine42 citations Open access
Semantic Scholar
Combined Rod and Cone Transduction by Adeno-Associated Virus 2/8
A. Manfredi, E. Marrocco, Agostina Puppo, G. Cesi +9 more
2013Human Gene Therapy41 citations Open access
Semantic Scholar
Therapeutic homology-independent targeted integration in retina and liver
P. Tornabene, R. Ferla, Manel Llado-Santaeularia, M. Centrulo +19 more
2022Nature Communications39 citations Open access
Semantic Scholar
Light‐responsive microRNA miR‐211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearance
Federica Naso, Daniela Intartaglia, Danila Falanga, C. Soldati +16 more
2020EMBO Journal36 citations Open access
Semantic Scholar
CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A
F. Testa, P. Melillo, C. Bonnet, V. Marcelli +10 more
2017Retina36 citations
Semantic Scholar
Myosin7a Deficiency Results in Reduced Retinal Activity Which Is Improved by Gene Therapy
P. Colella, A. Sommella, E. Marrocco, U. di Vicino +5 more
2013PLoS ONE36 citations Open access
Semantic Scholar
Novel Adeno-associated Viruses Derived From Pig Tissues Transduce Most Major Organs in Mice
A. Bello, A. Chand, J. Aviles, G. Soule +2 more
2014Scientific Reports32 citations Open access
Semantic Scholar
Large gene delivery to the retina with AAV vectors: are we there yet?
I. Trapani, P. Tornabene, A. Auricchio
2020Gene Therapy30 citations
Semantic Scholar
Similar Therapeutic Efficacy Between a Single Administration of Gene Therapy and Multiple Administrations of Recombinant Enzyme in a Mouse Model of Lysosomal Storage Disease
R. Ferla, Pamela Claudiani, G. Cotugno, Paola Saccone +2 more
2014Human Gene Therapy28 citations Open access
Semantic Scholar
Full-length ATP7B reconstituted through protein trans-splicing corrects Wilson disease in mice
Agnese Padula, Raffaella Petruzzelli, Sasha A. Philbert, Stephanie J Church +11 more
2022Molecular Therapy: Methods & Clinical Development27 citations Open access
Semantic Scholar
En Face Spectral-Domain Optical Coherence Tomography for the Monitoring of Lesion Area Progression in Stargardt Disease
P. Melillo, F. Testa, S. Rossi, V. Di Iorio +3 more
2016Investigative Ophthalmology and Visual Science26 citations Open access
Semantic Scholar
Prevalence of Anti–Adeno-Associated Virus Serotype 8 Neutralizing Antibodies and Arylsulfatase B Cross-Reactive Immunologic Material in Mucopolysaccharidosis VI Patient Candidates for a Gene Therapy Trial
R. Ferla, Pamela Claudiani, M. Savarese, K. Kozarsky +13 more
2015Human Gene Therapy26 citations Open access
Semantic Scholar
The longevity-associated variant of BPIFB4 improves a CXCR4-mediated striatum–microglia crosstalk preventing disease progression in a mouse model of Huntington’s disease
A. Di Pardo, E. Ciaglia, M. Cattaneo, A. Maciąg +14 more
2020Cell Death and Disease25 citations Open access
Semantic Scholar
Current Status on Clinical Development of Adeno-Associated Virus-Mediated Liver-Directed Gene Therapy for Inborn Errors of Metabolism
V. M. Ginocchio, R. Ferla, A. Auricchio, N. Brunetti-Pierri
2019Human Gene Therapy25 citations
Semantic Scholar

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