Hadia Hijazi
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 16 publications
Optimizing outcomes with less than more: multi-institutional experience of fast-forward fractionation and the impact of dosimetric parameters on toxicity in breast cancer patients.
Journal: Frontiers in oncology
Published: April 21, 2026
TLE6 mutation causes the earliest known human embryonic lethality.
Journal: Genome biology
Published: August 18, 2015
ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.
Journal: Human genetics
Published: February 27, 2015
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
Journal: Journal of medical genetics
Published: December 18, 2014
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.
Journal: Cell reports
Published: August 21, 2014
Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome.
Journal: Clinical genetics
Published: April 07, 2014
NECAP1 loss of function leads to a severe infantile epileptic encephalopathy.
Journal: Journal of medical genetics
Published: January 09, 2014
Complete aniridia with central keratopathy and congenital glaucoma is a CYP1B1-related phenotype.
Journal: Ophthalmic genetics
Published: June 18, 2013
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus.
Journal: Journal of medical genetics
Published: April 27, 2013
Mutations in LRPAP1 are associated with severe myopia in humans.
Journal: American journal of human genetics
Published: April 02, 2013
Last Updated: 09/26/2026