Fathiya Al-Murshedi (Fatma Al-Jasmi)

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 3

Top Topics

Mitochondrial Dna

Genome Wide Analysis

Top Venues

Molecular genetics & genomic medicine

Orphanet journal of rare diseases

Clinical genetics

United Arab Emirates University

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

Affiliation History

United Arab Emirates University

United Arab Emirates

Associate Professor :: Department of Genetics & Genomics

Publications

Feda E Mohamed, Feda E Mohamed, Eiman Al-Ajmi, Nadia Al Hashmi, Khalid Al-Thihli, Amna Al Futaisi, Watfa Al Mamari, Fathiya Al-Murshedi, Fatma Al-Jasmi
Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families. Orphanet journal of rare diseases 18 (1) (2023)
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)
Nuha Al Zaabi, Noora Al Menhali, Fathiya Al-Murshedi
SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure. Molecular genetics & genomic medicine 6 (1) (2017)