Fathiya Al-Murshedi (Fatma Al-Jasmi)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 8

Top Venues

Briefings in bioinformatics

Molecular genetics & genomic medicine

Human genomics

Orphanet journal of rare diseases

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

Rahaf M Ahmad, Bassam R Ali, Fathiya Al-Murshedi, Noura Salem AlDhaheri, Saeed H Al Turki, Praseetha Kizhakkedath, Mohd Saberi Mohamad
AI-derived comparative assessment of the performance of pathogenicity prediction tools on missense variants of breast cancer genes. Human genomics 18 (1) (2024)
Rahaf M Ahmad, Bassam R Ali, Fathiya Al-Murshedi, Richard O Sinnott, Noura Salem AlDhaheri, Mohd Saberi Mohamad
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancer. Briefings in bioinformatics 25 (1) (2023)
Rahaf M Ahmad, Bassam R Ali, Fathiya Al-Murshedi, Richard O Sinnott, Noura Salem AlDhaheri, Mohd Saberi Mohamad
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancer. Briefings in bioinformatics 25 (1) (2023)
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)
Rahaf M Ahmad, Bassam R Ali, Fathiya Al-Murshedi, Richard O Sinnott, Noura Salem AlDhaheri, Mohd Saberi Mohamad
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancer. Briefings in bioinformatics 25 (1) (2023)
Rahaf M Ahmad, Bassam R Ali, Fathiya Al-Murshedi, Richard O Sinnott, Noura Salem AlDhaheri, Mohd Saberi Mohamad
A review of genetic variant databases and machine learning tools for predicting the pathogenicity of breast cancer. Briefings in bioinformatics 25 (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)

Fathiya Al-Murshedi.css-eqlu8i{font-size:small;padding-left:4px;} (Fatma Al-Jasmi)

Publication Activity (10 Years)

Top Topics

Top Venues

Fathiya Al-Murshedi (Fatma Al-Jasmi)