Mariya Moosajee

Moorfields Eye Hospital NHS Foundation Trust — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

30h-index3.6kcitations260works3.32yr avg
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Research Topics

Retinal Development and Disorders(109), Retinal Diseases and Treatments(54), Ocular Disorders and Treatments(33), Connexins and lens biology(25), Glaucoma and retinal disorders(24)

Publications260 total

Management of Charles Bonnet syndrome in routine eye care services
Eye·2026Open Access
GLI2 and FLNB Define Periocular Morphoeic Basal Cell Carcinoma
International Journal of Molecular Sciences·2025Open Access
Novel Genotype–Phenotype Correlations in CRB1-Retinopathies
Ophthalmology Science·2025Open Access
Abnormal Splicing in the Final Intron of <i>PRX</i> Results in Dominant Congenital Cataract Without Neurological Phenotype
Investigative Ophthalmology & Visual Science·2025Open Access
#ECR-Paper-06 Visual acuities in patients with autosomal recessive retinitis pigmentosa associated with mutations in four phototransduction genes
2025Open Access
#ECR-Poster-04 Targeting an in-frame nonsense variant in<i>ABHD12</i>gene causing PHARC syndrome with translational read-through-inducing drugs (TRIDs)
2025Open Access
#ECR-Paper-01 Metabolic dysregulation without gut barrier dysfunction in<i>CRB1</i>-related retinopathies
2025Open Access
#ECR-Paper-04 Genotype-phenotype correlation of<i>CYP1B1</i>variants
2025Open Access
#ECR-Poster-03 Interrogation of open-access RNA-sequencing datasets of anterior segment tissues to potentially identify novel childhood glaucoma genes
2025Open Access
Genetic Basis of Non-Syndromic Childhood Glaucoma Associated with Anterior Segment Dysgenesis: A Narrative Review
Pharmaceuticals·2025Open Access
Genome-Wide Insights Into the Genes and Pathways Shaping Human Foveal Development: Redefining the Genetic Landscape of Foveal Hypoplasia
Investigative Ophthalmology & Visual Science·2025Open Access
Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis Pigmentosa
Investigative Ophthalmology & Visual Science·2025Open Access
MM-711: Safety Outcomes Following Frontline Daratumumab-Based Therapy in Multiple Myeloma: A Systematic Reviewand Meta-Analysis
Clinical Lymphoma Myeloma & Leukemia·2025
POSTER: MM-711 Safety Outcomes Following Frontline Daratumumab-Based Therapy in Multiple Myeloma: A Systematic Review and Meta-Analysis
Clinical Lymphoma Myeloma & Leukemia·2025
Retinal Degeneration Diagnosed at 12 and 13 Months and Sensorineural Hearing Loss in Two Unrelated Female Infants With <scp>PRS</scp> Deficiency
American Journal of Medical Genetics Part A·2025Open Access
Charles Bonnet syndrome: taking another look at visual hallucinations in sight loss
Therapeutic Advances in Ophthalmology·2025· 1 citedOpen Access
Genetic Basis of Non-Syndromic Childhood Glaucoma Associated with Anterior Segment Dysgenesis
Preprints.org·2025Open Access
Using ssVEPs to Characterise Wide-Ranging Retinopathy: implications for Clinical Trials
Journal of Vision·2025Open Access
Quantification of Optical Coherence Tomography Features in &gt;3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations
2025· 2 citedOpen Access
A Phenotypic Study of <i>CRB1</i> Retinopathy Secondary to the Variant p.(Pro836Thr) Prevalent in Those of Black African Ancestry
Investigative Ophthalmology & Visual Science·2025Open Access
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Frequent Co-authors

Andrew R. Webster(13), Dhani Tracey‐White(9), Maria Toms(8), Cheryl Y. Gregory‐Evans(8), Adam M. Dubis(7), Gavin Arno(6), Kevin Gregory‐Evans(6), Samantha Malka(5), Rose Richardson(5), Philippa Harding(5), Andreas Mitsios(4), Neringa Jurkutė(3), Patrick Yu‐Wai‐Man(3), Michel Michaelides(3), Dulce Lima Cunha(3), Maria Bitner‐Glindzicz(3), Matthew Smart(3), Miguel C. Seabra(3), Nicholas Owen(3), Cécile Méjécase(3)