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M. P. Manitto · SciRah

Researcher profile · Semantic Scholar

M. P. Manitto

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M. P. Manitto — researcher profile on SciRah

h-index: 16
Works: 45
Citations: 822

Most-cited papers

Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian families
C. Ziviello, F. Simonelli, F. Testa, M. Anastasi +9 more
2005Journal of Medical Genetics88 citations Open access
Semantic Scholar
Apolipoprotein E Polymorphisms in Age-Related Macular Degeneration in an Italian Population
F. Simonelli, M. Margaglione, F. Testa, G. Cappucci +3 more
2001Ophthalmic Research88 citations
Semantic Scholar
Polymorphism p.402Y>H in the complement factor H protein is a risk factor for age related macular degeneration in an Italian population
F. Simonelli, G. Frisso, F. Testa, R. Di Fiore +5 more
2006British Journal of Ophthalmology71 citations Open access
Semantic Scholar
Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients
Antonella Fumagalli, M. Ferrari, N. Soriani, A. Gessi +7 more
2001Human Genetics60 citations
Semantic Scholar
Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art
A. Amato, A. Arrigo, E. Aragona, M. P. Manitto +3 more
2021Frontiers in Medicine59 citations Open access
Semantic Scholar
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families
F. Simonelli, G. Cennamo, C. Ziviello, F. Testa +7 more
2003British Journal of Ophthalmology46 citations Open access
Semantic Scholar
Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.
S. Stenirri, I. Fermo, S. Battistella, S. Galbiati +8 more
2004Clinical Chemistry41 citations Open access
Semantic Scholar
Spectral Domain Optical Coherence Tomography Findings in Patients with Retinitis Pigmentosa
Giacinto Triolo, L. Pierro, M. Parodi, U. de Benedetto +3 more
2013Ophthalmic Research40 citations
Semantic Scholar
VASCULAR ALTERATIONS REVEALED WITH OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN PATIENTS WITH CHOROIDEREMIA.
Maurizio Battaglia Parodi, A. Arrigo, R. MacLaren, E. Aragona +4 more
2019Retina32 citations Open access
Semantic Scholar
OPTICAL COHERENCE TOMOGRAPHY AND OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY EVALUATION OF COMBINED HAMARTOMA OF THE RETINA AND RETINAL PIGMENT EPITHELIUM
A. Arrigo, Eleonora Corbelli, E. Aragona, M. P. Manitto +3 more
2018Retina27 citations
Semantic Scholar
Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies
M. Cicinelli, A. Marchese, Alessandro Bordato, M. P. Manitto +2 more
2020Ophthalmology and Therapy26 citations Open access
Semantic Scholar
Morpho-functional correlation of fundus autofluorescence in Stargardt disease
M. Parodi, P. Iacono, Giacinto Triolo, C. La Spina +6 more
2015British Journal of Ophthalmology26 citations
Semantic Scholar
Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy.
Lorenzo Bianco, A. Arrigo, Alessio Antropoli, M. P. Manitto +4 more
2023JAMA ophthalmology21 citations Open access
Semantic Scholar
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients
A. Sodi, F. Menchini, M. P. Manitto, I. Passerini +3 more
2011Molecular Vision21 citations
Semantic Scholar
Neuron-Specific Enolase and Embryology of the Trabecular Meshwork of the Rat Eye: An Immunohistochemical Study
P. Nucci, G. Tredici, M. P. Manitto, G. Pizzini +1 more
1992International Journal of Biological Markers19 citations
Semantic Scholar
Resolution of cystoid macular edema following arginine-restricted diet and vitamin B6 supplementation in a case of gyrate atrophy.
G. Casalino, L. Pierro, M. P. Manitto, M. Michaelides +1 more
2018Journal of AAPOS17 citations Open access
Semantic Scholar
Are microarrays useful in the screening of ABCA4 mutations in Italian patients affected by macular degenerations?
S. Stenirri, G. Alaimo, M. P. Manitto, R. Brancato +2 more
2008Clinical Chemistry and Laboratory Medicine16 citations
Semantic Scholar
De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy
S. Stenirri, S. Battistella, I. Fermo, M. P. Manitto +4 more
2006Clinical Chemistry and Laboratory Medicine16 citations
Semantic Scholar
CAPILLARY NETWORK ALTERATIONS IN X-LINKED RETINOSCHISIS IMAGED ON OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY.
Francesco Romano, A. Arrigo, S. Ch'ng, Maurizio Battaglia Parodi +4 more
2019Retina14 citations
Semantic Scholar
Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.
G. Lavorgna, M. Lestingi, C. Ziviello, F. Testa +7 more
2003Biochemical and Biophysical Research Communications - BBRC14 citations
Semantic Scholar
Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype.
Firuzeh Rajabian, M. P. Manitto, Flavia Palombo, L. Caporali +9 more
2020Journal of neuro-ophthalmology13 citations Open access
Semantic Scholar
Macular dysplasia and pigmented paravenous retino-choroidal atrophy.
P. Nucci, M. P. Manitto, Andrea Piantanida, Rosario Brancato
1994Ophthalmic Genetics12 citations Open access
Semantic Scholar
Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches
C. Di Resta, I. Spiga, S. Presi, S. Merella +6 more
2018EJIFCC10 citations
Semantic Scholar
Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy
M. P. Manitto, S. Roosing, C. Boon, E. Souied +2 more
2015European Journal of Human Genetics7 citations Open access
Semantic Scholar
Posterior Polymorphous Corneal Dystrophy Concomitant to Large Colloid Drusen
C. Del Turco, L. Pierro, G. Querques, M. Gagliardi +3 more
2015European Journal of Ophthalmology6 citations Open access
Semantic Scholar
Balanced translocation (t 2q; 10p) and ocular anomalies. A possible HOX gene defect.
P. Nucci, M. P. Manitto, A. Faiella, E. Boncinelli +1 more
1994Ophthalmic Genetics6 citations
Semantic Scholar
Non-neurological, non skeletal outcomes after hematopoietic stem and progenitor cell-gene therapy -OTL-203- for Hurler syndrome.
F. Tucci, M. L. Uria-Oficialdegui, G. Consiglieri, M. Cossutta +27 more
2025Molecular Therapy5 citations Open access
Semantic Scholar
Regressive Retinal Flecks in CRX-Mutated Early-Onset Retinal Dystrophy
M. Cicinelli, M. P. Manitto, M. Parodi, F. Bandello
2016Optometry and Vision Science5 citations
Semantic Scholar
Multimodal imaging in Schubert-Bornschein congenital stationary night blindness
M. Parodi, A. Arrigo, Firuzeh Rajabian, A. Mansour +6 more
2022Ophthalmic Genetics3 citations
Semantic Scholar
Ectopia Lentis et Pupillae with Patchy Depigmentation of the Skin, Hair and Lashes: A New Association
M. P. Manitto, R. Brancato, N. Lombardo, M. Zarrella +1 more
1998European Journal of Ophthalmology3 citations Open access
Semantic Scholar
[Neuron-specific enolase in ophthalmology].
P. Nucci, G. Tredici, M. P. Manitto, R. Alfarano +1 more
1991Archivio italiano di anatomia e di embriologia. Italian journal of anatomy and embryology3 citations
Semantic Scholar
Optical Coherence Tomography Angiography in CRB1-Associated Retinal Dystrophies
Firuzeh Rajabian, A. Arrigo, Lorenzo Bianco, Alessio Antropoli +5 more
2023Journal of Clinical Medicine2 citations Open access
Semantic Scholar
BENIGN FOVEAL DEPIGMENTATION: A MULTIMODAL IMAGING INVESTIGATION
M. Parodi, A. Arrigo, Elena Bruschi, M. P. Manitto +2 more
2020Retinal cases & brief reports2 citations
Semantic Scholar
Single nucleotide polymorphism and mutation identification by microelectronic chip technology
S. Stenirri, B. Foglieni, M. P. Manitto, Elisabetta Martina +3 more
20022 citations
Semantic Scholar
Ocular pharmacokinetics of rufloxacin a new fluoroquinolone antibiotic.
P. Nucci, N. Lombardo, F. Cremonesi, M. P. Manitto +2 more
1992Clinica Terapeutica2 citations
Semantic Scholar
Nummular Macular Depigmentation in Dandy-Walker Syndrome.
M. Parodi, A. Arrigo, M. P. Manitto, F. Bandello
2020Retina1 citations
Semantic Scholar
Hematopoietic stem cell gene therapy for mucopolysaccharidosis type I—Hurler syndrome (OTL-203): Interim skeletal, neurological and systemic outcomes from a phase I/II study
M. E. Bernardo, F. Tucci, G. Consiglieri, M. L. U. Oficialdegui +12 more
2025Molecular Genetics and Metabolism0 citations
Semantic Scholar
Multimodal imaging in pediatric arterial macroaneurysm: A case report
L. Pierro, Marco Battista, A. Arrigo, M. P. Manitto +1 more
2020European Journal of Ophthalmology0 citations
Semantic Scholar
Cystoid macular edema resolution following arginine-restricted diet and vitamin B6 supplementation in a case of gyrate atrophy from Italy
Gabriella Casalino, L. Pierro, M. P. Manitto, Paul Michel +2 more
20180 citations
Semantic Scholar
Molecular Genetic Variants Associated with AMD in Italian Patients
F. Testa, A. Sodi, G. Frisso, S. Rossi +6 more
20110 citations
Semantic Scholar
PON1 Gene Polymorphisms in Italian Age-Related Macular Degeneration Patients
F. Testa, F. Simonelli, M. Illiano, N. Tinto +4 more
20030 citations
Semantic Scholar
Subject Index Vol. 33, 2001
H. Dick, A. Frohn, A. Augustin, B. Wolters +56 more
2001Ophthalmic Research0 citations
Semantic Scholar
Contents Vol. 33, 2001
H. Dick, A. Frohn, A. Augustin, B. Wolters +56 more
2001Ophthalmic Research0 citations Open access
Semantic Scholar
La cefalea nell'infanzia e nell'età giovanile: qualcosa in più dell'approccio oculistico
P. Nucci, A. Piantanida, R. Alfarano, M. P. Manitto +1 more
19930 citations
Semantic Scholar
Guidelines for pediatricians. Sending patients to the ophthalmologist: Who and when
P. Nucci, M. P. Manitto, Rosario Brancato
19930 citations
Semantic Scholar

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Elisabetta Martina×12
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A. Arrigo×11
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F. Simonelli — researcher profile on SciRah

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Maurizio Battaglia Parodi×7

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