Leah Rizel

Mutations in C2ORF71 Cause Autosomal-Recessive Retinitis Pigmentosa

Rob W.J. Collin, Christine Safieh, Karin W. Littink et al. · The American Journal of Human Genetics · 2010 · 88 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

Lonneke Haer‐Wigman, Horatio Hackett Newman, Rina Leibu et al. · Human Molecular Genetics · 2015 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping

Liat Benayoun, Ronen Spiegel, Noa Auslender et al. · American Journal of Medical Genetics Part A · 2009 · 39 citations

Life Sciences, Genetics, Ophthalmology +14

Abetalipoproteinemia in Israel: Evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient

Liat Benayoun, Esther Granot, Leah Rizel et al. · Molecular Genetics and Metabolism · 2007 · 37 citations

Life Sciences, Genetics, Molecular Genetics +6

Four <i>USH2A</i> Founder Mutations Underlie the Majority of Usher Syndrome Type 2 Cases among Non-Ashkenazi Jews

Noa Auslender, Dikla Bandah, Leah Rizel et al. · Genetic Testing · 2008 · 34 citations

Life Sciences, Genetics, Molecular Genetics +13