Saddek Mohand‐Saïd
0000-0002-0798-4802
Publication & Citation Trends
Publications
0 total
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries
Cited by 27
Semantic Scholar
Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy. OA
Cited by 11
Semantic Scholar
Computerized biofeedback to characterize Pupil Cycle Time (PCT) in neuropathies and retinopathies OA
Cited by 2
Semantic Scholar
Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort OA
Cited by 2
Semantic Scholar
Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity
Cited by 1
Semantic Scholar
Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy OA
Cited by 6
Semantic Scholar
CNGB1‐related rod‐cone dystrophy: A mutation review and update OA
Cited by 20
Semantic Scholar
CHM mutation spectrum and disease: An update at the time of human therapeutic trials OA
Cited by 12
Semantic Scholar
Research Topics
Retinal Development and Disorders
(137)
Retinal Diseases and Treatments
(88)
Retinal Imaging and Analysis
(31)
Photoreceptor and optogenetics research
(31)
Neuroscience and Neural Engineering
(28)
Affiliations
Centre National de la Recherche Scientifique
Institut de la Vision
Inserm
Institut Pasteur
University of Pittsburgh