Publications by authors named "Maha Eid"

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Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.
Asmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud, Amira Nabil, Mona M Aboulghar, Maha Mohamed Eid

Clin Genet· October 2025

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Maternal vaping and pregnancy adverse outcomes: A systematic review and meta-analysis.
Alexandre Vallée, Maha Eid, Anis Feki, Jean-Marc Ayoubi

Women Birth· September 2025

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Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort.
Sara H El-Dessouky, Wessam E Sharaf-Eldin, Mona M Aboulghar, Hatem A Mousa, Maha S Zaki, Maha M Eid

Clin Genet· July 2025

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New Phenotypes Associated With Pathogenic RNASEH2B and SAMHD1 Variants.
Ghada M H Abdel-Salam, Maha Eid, Manar A El-Serafy, Heba El-Sayed, Mohamed S Abdel-Hamid

Int J Dev Neurosci· May 2025

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Celiac disease risk HLA-DQ haplotypes in an Egyptian cohort using multiplex ligation-dependent probe amplification.
Marwa Farid, Ola M Eid, Rania M A Abdel Kader, Rana Mahrous, Khaled M Refaat, Maha M Eid

Egypt J Immunol· April 2025

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Generation of Dual-Color FISH probes targeting 9p21, Xp21, and 17p13.1 loci as diagnostic markers for some genetic disorders and cancer in Egypt.
Amal M Mohamed, Maha Eid, Ola Eid, Shymaa H Hussein, Wael Mahmoud

J Genet Eng Biotechnol· March 2025

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Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect.
Sara H El-Dessouky, Wessam E Sharaf-Eldin, Mona M Aboulghar, Alaa Ebrashy, Sameh M Senousy, Maha M Eid

Prenat Diagn· February 2025

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Screening for Variants in Egyptian Patients with Pontocerebellar Malformations.
Bayoumi A Emam, Mohamed S Abdel-Hamid, Maha Eid, Marian Girgis, Omar A Ragab

Mol Syndromol· December 2024

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DNA phenotyping and mapping intragenic deletion mutations in Fanconi anemia: Patterns and diagnostic inferences.
Rehab Mosaad, Ghada El-Kamah, Maha Eid, Khalda Amr

J Genet Eng Biotechnol· December 2024

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Pain after oocyte retrieval in women with endometriosis undergoing fertility preservation or IVF.
Maha Eid, Adrien Lemoine, Lena Bardet, Lise Selleret, Sophie Stout

Reprod Biomed Online· September 2024

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Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors.
Ghada M H Abdel-Salam, Susanne Hellmuth, Elise Gradhand, Stephan Käseberg, Jennifer Winter, Maha M Eid, Heidi Rossmann, Dominik T Schneider

JCI Insight· November 2023

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Detection of AZFc gene deletion in a cohort of Egyptian patients with idiopathic male infertility.
Maha M Eid, Ola M Eid, Amany H Abdelrahman, Islam F S Abdelrahman, Elshaimaa A F Aboelkomsan

J Genet Eng Biotechnol· November 2023

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Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients.
Mona F Sokkar, Mona Hamdy, Peter Sf Erian, Rehab M Mosaad, Nesma M Elaraby, Maha M Eid

J Genet Eng Biotechnol· November 2023

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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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[Conservative treatments for endometrial cancer].
Maha Eid, Clémentine Gonthier, Margot Bucau, Martin Koskas

Rev Prat· September 2022

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MLPA as a genetic assay for the prenatal diagnosis of common aneuploidy: the first Egyptian experience.
Ola M Eid, Maha M Eid, Marwa Farid, Rania M A Abdel Kader, Rana Mahrous

J Genet Eng Biotechnol· July 2022

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Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly.
Amal M Mohamed, Alaa K Kamel, Maha M Eid, Ola M Eid, Mona Mekkawy

Mol Genet Genomic Med· November 2021

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Identification of Gene Signature as Diagnostic and Prognostic Blood Biomarker for Early Hepatocellular Carcinoma Using Integrated Cross-Species Transcriptomic and Network Analyses.
Olfat Al-Harazi, Ibrahim H Kaya, Maha Al-Eid, Lina Alfantoukh, Ali Saeed Al Zahrani

Front Genet· September 2021

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Evaluation of MLPA as a comprehensive molecular cytogenetic tool to detect cytogenetic markers of chronic lymphocytic leukemia in Egyptian patients.
Ola M Eid, Rania M A Abdel Kader, Lamiaa A Fathalla, Amany H Abdelrahman, Ahmed Rabea, Maha M Eid

J Genet Eng Biotechnol· June 2021

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Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic Aberrations.
Hanaa R M Attia, Amany H Abdelrahman, Mona H Ibrahim, Maha M Eid, Ola M Eid

Curr Pharm Biotechnol· December 2020

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Response to letter from Okoye JO and Ngokere AA "Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?".
Ghada M H Abdel-Salam, Sara H El-Dessouky, Mona M Aboulghar, Maha M Eid

Prenat Diagn· December 2020

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Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.
Maha M Eid, Ola M Eid, Sawsan Abdel-Hadi, Nehal Hassib, Abdelrahman Madian

J Pediatr Genet· September 2020

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Erratum: Clinical Variability of Pallister-Killian Syndrome in Two Egyptian Patients.
Maha M Eid, Ola M Eid, Sawsan Abdel-Hadi, Nehal Hassib, Abdelrahman Madian

J Pediatr Genet· September 2020

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Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation.
Amal M Mohamed, Maha M Eid, Ola M Eid, Shymaa H Hussein, Aida M Mossaad

Cytogenet Genome Res· 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, Maha Eid

Am J Med Genet A· June 2020

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