Selwa F. Hazzaa-Al

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 15 publications

Perception of integrating an AI teaching module into medical education curriculum.

Perception of integrating an AI teaching module into medical education curriculum.

Journal: Frontiers in medicine

Published: December 24, 2025

Knowledge and attitude of medical students towards artificial intelligence in ophthalmology in Riyadh, Saudi Arabia: a cross-sectional study.

Knowledge and attitude of medical students towards artificial intelligence in ophthalmology in Riyadh, Saudi Arabia: a cross-sectional study.

Journal: Annals of medicine and surgery (2012)

Published: March 18, 2024

The application of artificial intelligence in diabetic retinopathy screening: a Saudi Arabian perspective.

The application of artificial intelligence in diabetic retinopathy screening: a Saudi Arabian perspective.

Journal: Frontiers in medicine

Published: September 28, 2023

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss.

Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss.

Journal: Genes

Published: November 01, 2020

Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series.

Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series.

Journal: The American journal of case reports

Published: April 07, 2020

Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center.

Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center.

Journal: The American journal of case reports

Published: April 29, 2018

Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.

Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations.

Journal: International journal of pediatric otorhinolaryngology

Published: November 16, 2017

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 18, 2015

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.

ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population.

Journal: European journal of medical genetics

Published: November 06, 2013

COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.

COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.

Journal: International journal of pediatric otorhinolaryngology

Published: October 03, 2013

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes.

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes.

Journal: Genome research

Published: October 30, 2012

Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.

Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia.

Journal: American journal of human genetics

Published: September 15, 2012

Showing 1-12 of 15

Last Updated: 09/26/2026