Faisal Almalki

4PUBLICATIONS
9CO-AUTHORS
Clinical nutritionEpigenetics (incl. genome methylation and epigenomics)Gene mappingNeurogenetics
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Publications (4)

|Sep 26, 2026
Identification of CD320-Associated Cobalamin Transport Deficiency Through Newborn Screening Caused by Novel Homozygous Candidate Variants.

|Aug 13, 2026
Integrative Clinical and Functional Characterization of the TCF7L2 rs7903146 Variant Reveals Regulatory Mechanisms Linking Genetic Susceptibility to Oxidative Stress in Type 2 Diabetes.

|Aug 27, 2025
A Novel Homozygous Splice Variant in the NUP188 Gene Causing Sandestig-Stefanova Syndrome in a Saudi Patient.

Faisal Almalki, Haifa Abdullah Alkorbi, Naglaa M Kamal

|Mar 22, 2024
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia.

Faisal Almalki

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Frequent Collaborators

1 joint publications

Jwaher Mesleh Althobiti

1 joint publications

Ahmed M Ahmed

1 joint publications

Hakeemah H Al-Nakhle

1 joint publications

Amjad M Yousuf