Sawsan R Nowilaty

6PUBLICATIONS
6CO-AUTHORS
Vision scienceAnthropological geneticsOptical technologyCardiovascular medicine and haematology not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Apr 20, 2026
Unusual presentation of cone dysfunction consequent upon a homozygous FAM161A variant.

|Jun 27, 2024
The Clinical and Mutational Spectrum of Bardet-Biedl Syndrome in Saudi Arabia.

Doaa Milibari, Sawsan R Nowilaty, Rola Ba-Abbad

|Apr 03, 2023
Adjunctive Intravitreal Triamcinolone Acetonide for Exudative Retinal Detachment in Coats Disease.

Wael A Alsakran, Sawsan R Nowilaty, Nicola G Ghazi

|Jan 14, 2021
Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa.

Moustafa Magliyah, Abdulaziz A Alshamrani, Patrik Schatz

|Nov 27, 2020
A novel c.980C>G variant in OAT results in identifiable gyrate atrophy phenotype associated with retinal detachment in a young female.

Moustafa Magliyah, Abrar K Alsalamah, Majeedah AlOtaibi

|Aug 21, 2020
Evolution of macular hole in enhanced S-cone syndrome.

Moustafa S Magliyah, Sulaiman M AlSulaiman, Patrik Schatz

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Frequent Collaborators

1 joint publications

Abdulaziz A Alshamrani

1 joint publications

Patrik Schatz

1 joint publications

Abdulrahman AlZaid

1 joint publications

Doaa Milibari