Lucas Fares‐Taie
Inserm(FR)Université Paris Cité(FR)Institut des Maladies Génétiques Imagine(FR)
Publications by Year
Research Areas
Retinal Development and Disorders, Ocular Disorders and Treatments, Retinal Diseases and Treatments, Genetic and Kidney Cyst Diseases, Mitochondrial Function and Pathology
Most-Cited Works
- → Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy(2012)145 cited
- → Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome(2016)144 cited
- → TMEM126A, Encoding a Mitochondrial Protein, Is Mutated in Autosomal-Recessive Nonsyndromic Optic Atrophy(2009)101 cited
- → ALDH1A3 Mutations Cause Recessive Anophthalmia and Microphthalmia(2013)100 cited
- → Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies(2015)73 cited
- → Implication of non-coding PAX6 mutations in aniridia(2018)54 cited
- → Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with mutations