Publications by authors named "Inas Sayed"

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COL1-related overlap disorder: An emerging phenotype linked to mono- and bi-allelic COL1A1/2 variants.
Nehal F Hassib, Rasha M Elhossini, Inas S M Sayed, Mona S Aglan, Mohamed S Abdel-Hamid

Arch Oral Biol· October 2025

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Delineating the Clinical and Brain Imaging Characteristics of the Neonatal Form of CSTB -Related Neurodevelopmental Disorders.
Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar, Inas S M Sayed, Maha S Zaki, Ghada M H Abdel-Salam

Clin Genet· August 2025

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Elevated uric acid in gestational diabetes and its risk on pregnancy outcomes.
Marwa Mostafa Ahmed, Nagwa Eid Saad, Shimaa Mohamed Abbas, Tarek Mohamed Saeed El Azizi, Inas El Sayed

SAGE Open Med· April 2024

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A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.
Rasha M Elhossini, Inas M Sayed, Usama Saad Hellal, Sarah A M Mahmoud, Mona S Aglan

Am J Med Genet A· January 2024

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CHST3-related skeletal dysplasia in 14 patients: Identification of 8 novel variants and further expansion of the phenotypic spectrum.
Ghada A Otaify, Rasha M Elhossini, Sherif F Abdel-Ghafar, Inas M Sayed, Ghada M H Abdel-Salam

Am J Med Genet A· August 2023

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Further Evidence of a Continuum in the Clinical Spectrum of Dominant -Related Disorders and Implications in Cerebellar Anomalies.
Ghada M H Abdel-Salam, Hanan H Afifi, Sahar N Saleem, Mohamed I Gadelhak, Manar A El-Serafy, Inas S M Sayed

Mol Syndromol· December 2022

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A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia.
Ghada M H Abdel-Salam, Marian Girgis, Maha M Eid, Inas S M Sayed, Mohamed S Abdel-Hamid

J Hum Genet· November 2022

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Diagnosis of coronavirus disease 2019 and the potential role of deep learning: insights from the experience of Cairo University Hospitals.
Marwa M Ahmed, Amal M Sayed, Dina El Abd, Inas T El Sayed, Yasmine S Elkholy

J Int Med Res· July 2022

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Accuracy of the Traditional COVID-19 Phone Triaging System and Phone Triage-Driven Deep Learning Model.
Marwa M Ahmed, Amal M Sayed, Ghada M Khafagy, Inas T El Sayed, Yasmine S Elkholy, Radwa M Elsayed, Asmaa A Sayed

J Prim Care Community Health· July 2022

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Confirmation of a Phenotypic Entity for Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.
Eman A Rabie, Inas S M Sayed, Khalda Amr, Hoda A Ahmed, Mostafa I Mostafa, Heba El-Sayed

Genes (Basel)· June 2022

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Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9-associated disease trait.
Ghada M H Abdel-Salam, Ruizhi Duan, Mohamed S Abdel-Hamid, Inas S M Sayed, Shalini N Jhangiani

Am J Med Genet A· February 2022

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OTUD6B-associated intellectual disability: novel variants and genetic exclusion of retinal degeneration as part of a refined phenotype.
Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid, Inas S M Sayed, Ulrich Zechner, Hanno Jörn Bolz

J Hum Genet· January 2022

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Expansion of the phenotypic and mutational spectrum of Carpenter syndrome.
Rabab Khairat, Rasha Elhossini, Nara Sobreira, Elizabeth Wohler, Ghada Otaify, Inas Sayed

Eur J Med Genet· January 2022

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Gene Mutations of the Three Ectodysplasin Pathway Key Players (, , and ) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.
Hoda A Ahmed, Ghada Y El-Kamah, Eman Rabie, Mostafa I Mostafa, Maha R Abouzaid, Inas S M Sayed

Genes (Basel)· September 2021

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Effect of DASH Diet Versus Healthy Dietary Advice on the Estimated Atherosclerotic Cardiovascular Disease Risk.
Marwa S Said, Inas T El Sayed, Eman E Ibrahim, Ghada M Khafagy

J Prim Care Community Health· June 2021

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An Adapted Online Family Medicine Training for House Officers Amid Covid-19 Pandemic in Egypt.
Marwa M Ahmed, Samar Fares, Asmaa A Sayed, Inas T El Sayed

J Prim Care Community Health· May 2021

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Perceived Stress Scale Among Adolescents with Polycystic Ovary Syndrome.
Ghada Khafagy, Inas El Sayed, Shimaa Abbas, Saeed Soliman

Int J Womens Health· December 2020

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KBG syndrome in two patients from Egypt.
Inas S M Sayed, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam

Am J Med Genet A· June 2020

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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, Sherif F Abdel-Ghafar, Maha R Abouzaid

Am J Med Genet A· June 2020

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Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features.
Maha S Zaki, Ola M Eid, Maha M Eid, Amal M Mohamed, Inas S M Sayed

Cytogenet Genome Res· February 2020

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PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly.
Ranad Shaheen, Monika Tasak, Sateesh Maddirevula, Ghada M H Abdel-Salam, Inas S M Sayed

Hum Genet· March 2019

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Phenotypic and molecular insights into PQBP1-related intellectual disability.
Ghada M H Abdel-Salam, Noriko Miyake, Mohamed S Abdel-Hamid, Inas S M Sayed, Mohamed I Gadelhak

Am J Med Genet A· November 2018

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Philtrum length and intercommissural distance measurements at mixed dentition period.
Mostafa Mostafa, Nehal Hassib, Inas Sayed, Amany Neamat, Magda Ramzy

Am J Med Genet A· May 2018

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