Author

Bayoumi A. Emam

Observed names: B.A., Emam, Bayoumi A Emam, Bayoumi Emam

Observed institution: National Research Centre

OpenAlex ID: A5010841865

Mutation in WDR4 impairs tRNA m7G46 methylation and causes a distinct form of microcephalic primordial dwarfism

2015 · Ranad Shaheen, Ghada M H Abdel-Salam, et al. · Genome biology · 193

Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations

2017 · Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam, et al. · Journal of Human Genetics · 25

Long‐term survival in microcephalic osteodysplastic primordial dwarfism type I: Evaluation of an 18‐year‐old male with g.55G>A homozygous mutation in RNU4ATAC

2015 · Ghada M.H. Abdel‐Salam, Bayoumi A. Emam, et al. · American Journal of Medical Genetics Part A · 6

A Rare Case of a Child with X-linked Opitz G/BBB Syndrome Caused by a Novel Partial Microduplication in the MID1 gene: Implications for Genetic Diagnosis.

2025 · Mishal Alsulami, Hatem Elghezal, et al. · Journal of Biochemical and Clinical Genetics

Screening for TSEN54 Variants in Egyptian Patients with Pontocerebellar Malformations

2024 · Bayoumi A. Emam, Mohamed S. Abdel-Hamid, et al. · Molecular Syndromology

Additional file 2: Table S2. of Mutation in WDR4 impairs tRNA m7G46 methylation and causes a distinct form of microcephalic primordial dwarfism

2015 · Ranad Shaheen, Abdel-Salam, Ghada, et al. · Figshare

Additional file 1: Table S1. of Mutation in WDR4 impairs tRNA m7G46 methylation and causes a distinct form of microcephalic primordial dwarfism

2015 · Ranad Shaheen, Abdel-Salam, Ghada, et al. · Figshare

Works count: 9

Citation count: 224

H-index: 3

I10-index: 2