Publications by authors named "Randa Bassiouni"

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Mapping autism in Egypt: population-based insights into prevalence, risk determinants, and severity among children aged 1-12 years.
Ammal M Metwally, Ebtissam M Salah El-Din, Samia M Sami, Ehab R Abdelraouf, Sara F Sallam, Randa I Bassiouni

Mol Autism· May 2025

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National screening for developmental delays and their determinants among Egyptian school age children: A step towards implementing life skills programs.
Ammal M Metwally, Maysa S Nassar, Ebtissam M Salah El-Din, Ali M Abdallah, Zeinab Khadr, Randa I Bassiouni

PLoS One· September 2023

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A national screening for the prevalence and profile of disability types among Egyptian children aged 6-12 years: a community-based population study.
Ammal M Metwally, Ebtissam M Salah El-Din, Ghada A Abdel-Latif, Dina A Nagi, Lobna A El Etreby, Randa I Bassiouni

BMC Public Health· August 2023

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National screening for Egyptian children aged 1 year up to 12 years at high risk of Autism and its determinants: a step for determining what ASD surveillance needs.
Ammal M Metwally, Mona A Helmy, Ebtissam M Salah El-Din, Rehan M Saleh, Ehab R Abdel Raouf, Randa I Bassiouni

BMC Psychiatry· June 2023

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Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family.
Muhammad I Naseer, Mahmood Rasool, Angham A Abdulkareem, Randa I Bassiouni, Hussein Algahtani

Neurosciences (Riyadh)· October 2018

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Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Ibtessam R Hussein, Rima S Bader, Adeel G Chaudhary, Randa Bassiouni, Maha Alquaiti

Pediatr Cardiol· June 2018

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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.
Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Zuhair Alhassnan, Maha Alotaibi, Randa Bassiouni

Hum Genet· August 2017

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Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015.
Jerry W. Shay, Noriko Homma, Ruyun Zhou, Muhammad Imran Naseer, Adeel G. Chaudhary, Randa Bassiouni, Randa I. Bassiouni, Randa Ibrahim Bassiouni

BMC Genomics· July 2016

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Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
Adeel G Chaudhary, Ibtessam R Hussein, Adel Abuzenadah, Mamdouh Gari, Randa Bassiouni

Pediatr Neurol· April 2014

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Mutational Analysis of the alpha-L-iduronidase gene in three Egyptian families: identification of three novel mutations and five novel polymorphisms.
Khalda Amr, Ahmed Katoury, Mohamed Abdel-Hamid, Randa Bassiouni, Mona Ibrahim

Genet Test Mol Biomarkers· December 2009

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Sensitivity of DCSR3/GAPDH ratio using quantitative real-time PCR in the rapid prenatal diagnosis for down syndrome.
Sanaa M H Helmy, Somaya Ismail, Randa Bassiouni, Khaled R Gaber

Fetal Diagn Ther· November 2009

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