Inas S. M. Sayed

PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly

Ranad Shaheen, Monika Tasak, Sateesh Maddirevula et al. · Human Genetics · 2019 · 91 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations

Hoda A. Ahmed, Ghada El‐Kamah, Eman Rabie et al. · Genes · 2021 · 21 citations · Full text

Medicine, Genetics, Molecular Genetics +16

KBG syndrome in two patients from Egypt

Inas S. M. Sayed, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam · American Journal of Medical Genetics Part A · 2020 · 12 citations

Dentistry, Oral Biology, Human Genetics +13

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

Ghada M. H. Abdel‐Salam, Inas S. M. Sayed, Hanan H. Afifi et al. · American Journal of Medical Genetics Part A · 2020 · 12 citations

Life Sciences, Genetics, Oral Biology +10

Phenotypic and molecular insights into <i>PQBP1</i>‐related intellectual disability

Ghada M. H. Abdel‐Salam, Noriko Miyake, Mohamed S. Abdel‐Hamid et al. · American Journal of Medical Genetics Part A · 2018 · 11 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17