Mohamed H. Hamed-Al
Riyadh, 11533, Saudi Arabia
Last Updated: 09/26/2026
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Found 33 publications
Genetics and clinical landscape of pediatric monogenic diabetes in consanguineous cohort: high diagnostic yield and recessive burden.
Journal: Diabetes research and clinical practice
Published: May 23, 2026
Phenotype and genotype of hypophosphatasia cases in Saudi Arabia: multi-center case cohort.
Journal: Frontiers in genetics
Published: October 04, 2025
Transforming Prenatal Care in a Highly Inbred Population: Impact of a Multidisciplinary Board.
Journal: Prenatal diagnosis
Published: September 11, 2025
Network-based framework for studying etiology and phenotypic diversity in primary ciliopathies.
Journal: Genome biology
Published: January 08, 2025
Long-term outcomes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a retrospective study from a tertiary care center in Saudi Arabia.
Journal: Frontiers in endocrinology
Published: October 16, 2024
ANKS6 Variants Underlie Polycystic Kidneys in Prenatal and Neonatal Cases.
Journal: Genes
Published: August 02, 2024
Genetics of Primary Adrenal Insufficiency Beyond CAH in Saudi Arabian Population.
Journal: Molecular genetics & genomic medicine
Published: July 09, 2024
Use of Whole-Exome Sequencing and Pedigree Analysis to Identify X-linked Hypophosphatemia in Saudi Arabian Families.
Journal: Journal of the Endocrine Society
Published: June 18, 2024
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.
Journal: medRxiv : the preprint server for health sciences
Published: April 02, 2024
Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment.
Journal: Nature communications
Published: February 07, 2024
Last Updated: 09/26/2026