Morad Khayat

NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules

Meral Gunay‐Aygun, Tzipora C. Falik‐Zaccai, Thierry Vilboux et al. · Nature Genetics · 2011 · 255 citations · Full text

Blood Platelet, Genetics, Pathogenesis +8

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p

Meral Gunay‐Aygun, Yifat Zivony-Elboum, Fatma Gümrük et al. · Blood · 2010 · 153 citations · Full text

Chronic Diarrhea and Juvenile Cataracts: Think Cerebrotendinous Xanthomatosis and Treat

Vladimir M. Berginer, Bella Gross, Morad Khayat et al. · PEDIATRICS · 2008 · 96 citations

Hepatology, Ophthalmology, Biliary Tract +12

A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis

Yifat Zivony-Elboum, Wendy Westbroek, Nehama Cohen Kfir et al. · Journal of Medical Genetics · 2012 · 79 citations

Molecular Epidemiology of Hereditary Epidermolysis Bullosa in a Middle Eastern Population

Judeh Abu Sa'd, Margarita Indelman, Ellen G Pfendner et al. · Journal of Investigative Dermatology · 2006 · 73 citations · Full text

Hereditary Epidermolysis Bullosa, Molecular Epidemiology, Pathology +5