Aisha M Al-Shamsi (Aisha Al-Shamsi, Aisha Al Shamsi)

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 4

Top Topics

Mitochondrial Dna

Intellectual Disability

Top Venues

Molecular genetics & genomic medicine

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Omnia Elsayed, Aisha M Al-Shamsi
Mutation spectrum of non-syndromic hearing loss in the UAE, a retrospective cohort study and literature review. Molecular genetics & genomic medicine 10 (11) (2022)
Hanadi A Abdelrahman, Nadia Akawi, Aisha M Al-Shamsi, Amanat Ali, Fathiya Al-Murshedi, Anne John, Jozef Hertecant, Lihadh Al-Gazali, Bassam R Ali
Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive. Clinical genetics 101 (4) (2022)
Sirine Saleh, Ela Beyyumi, Aysha Al Kaabi, Jozef Hertecant, Doaa Barakat, Noura Salem AlDhaheri, Lihadh Al-Gazali, Aisha M Al-Shamsi
Spectrum of neuro-genetic disorders in the United Arab Emirates national population. Clinical genetics 100 (5) (2021)
Aisha M Al-Shamsi, Noura Al Hassani, Moustafa Hamchou, Raya Almazrouei, Aziz Mhanni
A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review. Molecular genetics & genomic medicine 8 (11) (2020)