Francesco Testa

University of Foggia — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

37h-index7.4kcitations182works7.32yr avg
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Research Topics

Retinal Development and Disorders(103), Retinal Diseases and Treatments(76), Glaucoma and retinal disorders(25), Retinal Imaging and Analysis(23), Retinal and Macular Surgery(22)

Publications181 total

Improved Prognostic Accuracy of NEWS2 Score with Triage Data in Adults with Bacterial Sepsis: A Retrospective Cohort Study
International Journal of Translational Medicine·2025Open Access
Cystoid Macular Edema in Non-Syndromic Retinitis Pigmentosa: Associations With Causative Genes in a Large Cohort
Investigative Ophthalmology & Visual Science·2025· 1 citedOpen Access
Orthodontic Management of a Pediatric Patient Affected by Congenital Adrenal Hyperplasia: Case Report
Special Care in Dentistry·2025
Analysis of choriocapillaris vascular density in patients with retinitis pigmentosa caused by RPGR gene mutations
BMC Ophthalmology·2025Open Access
A Novel Variant in <scp><i>TUBB4B</i></scp> Causes Progressive Cone‐Rod Dystrophy and Early Onset Sensorineural Hearing Loss
Molecular Genetics & Genomic Medicine·2025· 4 citedOpen Access
Genetic complexity of inherited retinal diseases in a large italian cohort
Acta Ophthalmologica·2025
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss
European Journal of Human Genetics·2024· 2 citedOpen Access
PHOTOBIOMODULATION THERAPY FOR SEROUS PIGMENT EPITHELIUM DETACHMENT IN CHRONIC CENTRAL SEROUS CHORIORETINOPATHY
Retinal Cases & Brief Reports·2024· 1 citedOpen Access
Ocular Biomarkers in Alzheimer's Disease: Insights into Early Detection Through Eye-Based Diagnostics - A Literature Review.
PubMed·2024· 8 citedOpen Access
Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations
European Journal of Human Genetics·2024· 50 citedOpen Access
Multicentric Longitudinal Prospective Study in a European Cohort of <i>MYO7A</i> Patients: Disease Course and Implications for Gene Therapy
Investigative Ophthalmology & Visual Science·2024· 6 citedOpen Access
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients
Human Genetics and Genomics Advances·2024· 8 citedOpen Access
Voretigene neparvovec for inherited retinal dystrophy due to RPE65 mutations: a scoping review of eligibility and treatment challenges from clinical trials to real practice
Eye·2024· 26 citedOpen Access
Objective Outcomes to Evaluate Voretigene Neparvovec Treatment Effects in Clinical Practice
Ophthalmology Retina·2024· 4 citedOpen Access
Rare Eye Diseases Automatic Classification: A Deep Learning Approach
World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany·2024
Navigated yellow subthreshold micropulse laser for refractory cystoid macular edema following rhegmatogenous retinal detachment surgery
American Journal of Ophthalmology Case Reports·2023· 3 citedOpen Access
Late‐onset mucopolysaccharidosis type <scp>IIIA</scp> mimicking Usher syndrome
American Journal of Medical Genetics Part A·2023· 6 citedOpen Access
Ten Years of Experience With a Telemedicine Platform Dedicated to Health Care Personnel: Implementation Report
JMIR Medical Informatics·2023· 2 citedOpen Access
OPTIMIZATION AND CLINICAL VALIDATION OF A VIDEOFLUOROGRAPHIC PROTOCOL FOR SWALLOWING DISEASES
Physica Medica·2023
A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice
Orphanet Journal of Rare Diseases·2023· 35 citedOpen Access
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Frequent Co-authors

Francesca Simonelli(47), Settimio Rossi(23), Sandro Banfi(19), Valentina Di Iorio(15), Paolo Melillo(11), Alberto Auricchio(10), Enrico Maria Surace(9), E. Rinaldi(9), Michele Della Corte(7), Jean Bennett(5), Carmela Ziviello(5), Rando Allikmets(5), Alfredo Ciccodicola(5), Michele D’Urso(5), Raffaella Brunetti‐Pierri(5), Albert M. Maguire(4), Eric A. Pierce(4), Kathleen Marshall(4), Junwei Sun(4), J. Fraser Wright(4)