Leen Abu Safieh

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa

Mai M. Abd El-Aziz, Isabel Barragán, C. O'Driscoll et al. · Nature Genetics · 2008 · 209 citations · Full text

Biology, Developmental Biology, Developmental Genetics +10

Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping

Leen Abu Safieh, Mohammed A. Aldahmesh, Hanan E. Shamseldin et al. · Journal of Medical Genetics · 2009 · 86 citations

Molecular characterization of retinitis pigmentosa in Saudi Arabia.

Mohammed A. Aldahmesh, Leen Abu Safieh, Hisham Alkuraya et al. · PubMed · 2009 · 80 citations · Full text

Molecular characterization of Joubert syndrome in Saudi Arabia

Anas M. Alazami, Muneera Alshammari, Mustafa A. Salih et al. · Human Mutation · 2012 · 59 citations

Mendelian Disorder, Joubert Syndrome, Saudi Arabia +13

ACVR1C/SMAD2 signaling promotes invasion and growth in retinoblastoma

Laura Asnaghi, David T. White, Nolan Key et al. · Oncogene · 2018 · 58 citations · Full text

Developmental Biology, Cell Regulation, Medicine +6