Author

Saja Baheer Abdulwahhab

Observed names: Saja B. Abdulwahhab, Saja Baheer, Saja Baheer Abdul Wahhab

Institution: Sidra Medical and Research Center

Observed institution: Sidra Medical and Research Center

OpenAlex ID: A5112615154

The clinical and genotypic–phenotypic findings of mucopolysaccharidosis VI patients: an Iraqi single-study descriptive study

2023 · Saja Baheer Abdul Wahhab, Rabab Farhan Thejeal, et al. · Annals of Medicine and Surgery · 2

Acid sphingomyelinase deficiency: Phenotypic, biochemical, and molecular heterogeneity in a series of 47 Iraqi patients from a single center

2026 · Rabab Farhan, Mays Al-Tai, et al. · Molecular Genetics and Metabolism Reports

Incidental Detection of Glutamate Formiminotransferase Deficiency Through Newborn Screening in a Clinically Asymptomatic Infant: Molecular Findings and Counseling Considerations

2026 · Saja Baheer Abdulwahhab, Mohab Ben Omran, et al. · Cureus

Aicardi-Goutières Syndrome: Insights from a Middle Eastern Case Series

2026 · Osamah Alwalid, Marwa Al Subhi, et al. · American Journal of Neuroradiology

Unveiling alpha-mannosidosis in Iraqi children: A series of clinically and genetically characterized cases with novel MAN2B1 variant

2026 · Mays Riyadh Al Tai, Nebal Waill Saadi, et al. · Molecular Genetics and Metabolism Reports

Clinical and molecular spectrum of mucopolysaccharidosis IVA in Iraqi children: Allele-specific genotype–phenotype trends and novel GALNS variants

2025 · Saja Baheer Abdul Wahhab, Rabab Farhan Thejeal · Molecular Genetics and Metabolism Reports

Neonatal Presentation of a Case of Carbonic Anhydrase VA Deficiency

2025 · Saja Baheer Abdulwahhab, Amna Ahmed, et al. · Cureus

Pitfalls in the diagnosis of Gaucher disease in Iraq: A diagnostic experience from a developing country

2021 · Rabab Farhan Thejeal, Saja Baheer Abdulwahhab, et al. · Pakistan Journal of Medical Sciences

Works count: 8

Citation count: 2

H-index: 1

I10-index: