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Author

Ashraf H. Aboelanine

Institution: Ministry of Health
ORCID: 0009-0006-2953-5334
Observed ORCID: 0009-0006-2953-5334
OpenAlex ID: A5092659602
Human ‘knockouts’ of CSF3 display severe congenital neutropenia
2023 · Ebtissal Khouj, Dana Marafi, et al. · British Journal of Haematology · 10
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Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis
2023 · Fatima Alabdulrazzaq, Talal Alanzi, et al. · Molecular Genetics & Genomic Medicine · 8
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Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement
2026 · Valentina Galassi Deforie, Reza Maroofian, et al. · Genetics in Medicine · 3
Tribal Founder EMC1 Variant in 5 Kuwaiti Families Expands Phenotypic Spectrum of EMC1 -Related Disorder
2024 · Nada T. Alzayed, Abdullah H. Alzuabi, et al. · Neurology Genetics · 3
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Works count: 4
Citation count: 24
H-index: 3
I10-index: 1
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