Somaya K. Alzelaye
Mecca, Saudi Arabia
Last Updated: 09/26/2026
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Found 8 publications
Molecular Genetics of 1α-Hydroxylase Deficiency in the Saudi Population.
Journal: Journal of the Endocrine Society
Published: August 15, 2025
Burden of Illness of Type 2 Diabetes Mellitus in the Kingdom of Saudi Arabia: A Five-Year Longitudinal Study.
Journal: Advances in therapy
Published: November 03, 2023
Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia.
Journal: Journal of epidemiology and global health
Published: October 17, 2023
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa.
Journal: Orphanet journal of rare diseases
Published: April 06, 2023
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Journal: American journal of human genetics
Published: October 05, 2019
A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families.
Journal: Annals of pediatric endocrinology & metabolism
Published: May 12, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Journal: American journal of human genetics
Published: December 19, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026