Mariya Moosajee

72PUBLICATIONS
129CO-AUTHORS
NeonatologyGene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markersNeurogeneticsOptical technology
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Publications (72)

|Aug 27, 2026
Association of ABHD12 Variants with the Spectrum of PHARC Syndrome Phenotypes.

|May 04, 2026
Using Steady-State Visual Evoked Potentials to Characterize Wide-Ranging Retinopathy Linked to CRB1: Implications for Clinical Trials.

|Dec 11, 2025
GLI2 and FLNB Define Periocular Morphoeic Basal Cell Carcinoma.

John C Bladen, Jun Wang, Mariya Moosajee

|Sep 27, 2025
Genetic Basis of Non-Syndromic Childhood Glaucoma Associated with Anterior Segment Dysgenesis: A Narrative Review.

Nicola Cronbach, Cécile Méjécase, Mariya Moosajee

|Jul 09, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei

|May 22, 2025
DYRK1A syndrome presenting with a familial exudative vitreoretinopathy (FEVR)-like retinovascular phenotype.

Siying Lin, Eleanor Hay, Dorothy A Thompson

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Frequent Collaborators

10 joint publications

Lee Jones

7 joint publications

Nicholas Owen

7 joint publications

Cécile Méjécase

5 joint publications

Philippa Harding