Ihab Siam

Mutation in <i>KANK2</i> , encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair

Yuval Ramot, Vered Molho‐Pessach, Tomer Meir et al. · Journal of Medical Genetics · 2014 · 51 citations

Medicine, Dermatology, Genetics +17

Excoriation (skin-picking) disorder in adults: a cross-cultural survey of Israeli Jewish and Arab samples

Vera Leibovici, Sari Murad, Ihab Siam et al. · Comprehensive Psychiatry · 2014 · 28 citations

Medicine, Dermatology, Psychology +5

Two Novel Homozygous Desmoplakin Mutations in Carvajal Syndrome

Vered Molho‐Pessach, Sivan Sheffer, Rula Siam et al. · Pediatric Dermatology · 2015 · 25 citations

Life Sciences, Cardiology, Genetics +17

Prevalence of tinea pedis in psoriasis, compared to atopic dermatitis and normal controls – a prospective study

Vera Leibovici, Yuval Ramot, Rula Siam et al. · Mycoses · 2014 · 15 citations

Medicine, Dermatology, Allergy +11

RETRACTED: Generalized verrucosis and abnormal T cell activation due to homozygous TAOK2 mutation

Vered Molho‐Pessach, Yuval Ramot, Maxim Mogilevsky et al. · Journal of Dermatological Science · 2017 · 12 citations

Life Sciences, Genetics, Immunology +10