Dikla Bandah‐Rozenfeld

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 · 139 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Mutations in IMPG2, Encoding Interphotoreceptor Matrix Proteoglycan 2, Cause Autosomal-Recessive Retinitis Pigmentosa

Dikla Bandah‐Rozenfeld, Rob W.J. Collin, Eyal Banin et al. · The American Journal of Human Genetics · 2010 · 106 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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

Life Sciences, Genetics, Molecular Genetics +12

FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies

Silvio Alessandro Di Gioia, Stef J.F. Letteboer, Corinne Kostic et al. · Human Molecular Genetics · 2012 · 69 citations · Full text

Medicine, Genetics, Molecular Biology +17

Molecular Anthropology Meets Genetic Medicine to Treat Blindness in the North African Jewish Population: Human Gene Therapy Initiated in Israel

Eyal Banin, Dikla Bandah‐Rozenfeld, Alexey Obolensky et al. · Human Gene Therapy · 2010 · 69 citations

Medicine, Genetics, Molecular Genetics +15