Liliana Mizrahi‐Meissonnier

A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews

Lina Zelinger, Eyal Banin, Alexey Obolensky et al. · The American Journal of Human Genetics · 2011 · 138 citations · Full text

Mendelian Disorder, Genetic Disorder, Ashkenazi Jews +7

BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome

Alejandro Estrada‐Cuzcano, Robert K. Koenekoop, Audrey Sénéćhal et al. · Archives of Ophthalmology · 2012 · 125 citations

Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

Dikla Bandah‐Rozenfeld, Liliana Mizrahi‐Meissonnier, Chen Farhy et al. · The American Journal of Human Genetics · 2010 · 103 citations · Full text

Engineering, Mendelian Disorder, Genetic Disorder +9

The Effect of Cone Opsin Mutations on Retinal Structure and the Integrity of the Photoreceptor Mosaic

Joseph Carroll, Alfredo Dubra, Jessica C. Gardner et al. · Investigative Ophthalmology & Visual Science · 2012 · 96 citations · Full text

A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome

Samer Khateb, Lina Zelinger, Liliana Mizrahi‐Meissonnier et al. · Journal of Medical Genetics · 2014 · 89 citations