Mariya Moosajee (M Moosajee)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 74

Top Venues

Genes

Therapeutic advances in ophthalmology

International journal of molecular sciences

Biomolecules

Francis Crick Institute

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Francis Crick Institute

United Kingdom

Professor and Group Leader :: Ocular Genomics and Therapeutics

UCL Institute of Ophthalmology, University College London Jan 01 2017

United Kingdom

Professor of Molecular Ophthalmology and Wellcome Trust Clinical Research Development Fellow :: Development, Ageing and Disease

Moorfields Eye Hospital NHS Foundation Trust

United Kingdom

Consultant Ophthalmologist :: Genetics

Great Ormond Street Hospital For Children NHS Foundation Trust

United Kingdom

Consultant Ophthalmologist :: Ophthalmology

Publications

Dalia Abdulhussein, Lee Jones, Sri Harsha Dintakurti, Mariya Moosajee
Practice patterns in reporting and documentation of Charles Bonnet syndrome: a retrospective review following COVID-19. Therapeutic advances in ophthalmology 16 (2024)
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, Mariya Moosajee
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic. Genes 15 (2) (2024)
Genevieve A Wright, Ana Catalina Rodriguez-Martinez, Hanne Conn, Mar Matarin, Pamela Thompson, Anthony T Moore, Rola Ba-Abbad, Andrew R Webster, Mariya Moosajee
Enhanced Learning and Memory in Patients with CRB1 Retinopathy. Genes 15 (6) (2024)
Michael Heyang, Joshua L Warren, Paulina Ocieczek, Jacque L Duncan, Mariya Moosajee, Lucian V Del Priore, Liangbo Linus Shen
Long-term natural history of ellipsoid zone width in USH2A -retinopathy. The British journal of ophthalmology (2024)
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, Mariya Moosajee
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic. Genes 15 (2) (2024)
Genevieve A Wright, Ana Catalina Rodriguez-Martinez, Hanne Conn, Mar Matarin, Pamela Thompson, Anthony T Moore, Rola Ba-Abbad, Andrew R Webster, Mariya Moosajee
Enhanced Learning and Memory in Patients with CRB1 Retinopathy. Genes 15 (6) (2024)
Paulina Ocieczek, Ngozi Oluonye, Cécile Méjécase, Elena R Schiff, Vijay K Tailor, Mariya Moosajee
Identification of a Novel Frameshift Variant in MYF5 Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies. Genes 15 (6) (2024)
Paulina Ocieczek, Ngozi Oluonye, Cécile Méjécase, Elena R Schiff, Vijay K Tailor, Mariya Moosajee
Identification of a Novel Frameshift Variant in MYF5 Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies. Genes 15 (6) (2024)
Paulina Ocieczek, Ngozi Oluonye, Cécile Méjécase, Elena R Schiff, Vijay K Tailor, Mariya Moosajee
Identification of a Novel Frameshift Variant in MYF5 Leading to External Ophthalmoplegia with Rib and Vertebral Anomalies. Genes 15 (6) (2024)
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, Mariya Moosajee
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic. Genes 15 (2) (2024)
Genevieve A Wright, Ana Catalina Rodriguez-Martinez, Hanne Conn, Mar Matarin, Pamela Thompson, Anthony T Moore, Rola Ba-Abbad, Andrew R Webster, Mariya Moosajee
Enhanced Learning and Memory in Patients with CRB1 Retinopathy. Genes 15 (6) (2024)
Dalia Abdulhussein, Lee Jones, Sri Harsha Dintakurti, Mariya Moosajee
Practice patterns in reporting and documentation of Charles Bonnet syndrome: a retrospective review following COVID-19. Therapeutic advances in ophthalmology 16 (2024)
Michael James Gilhooley, Naz Raoof, Patrick Yu-Wai-Man, Mariya Moosajee
Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic. Genes 15 (2) (2024)
Nicholas Owen, Maria Toms, Yuan Tian, Lyes Toualbi, Rose Richardson, Rodrigo Young, Dhani Tracey-White, Pawan Dhami, Stephan Beck, Mariya Moosajee
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. The Journal of pathology (2023)
Maria Toms, Natasha Ward, Mariya Moosajee
Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3): Role in Retinal Development and Disease. Genes 14 (7) (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Lyes Toualbi, Maria Toms, Patrick Vingadas Almeida, Richard Harbottle, Mariya Moosajee
Gene Augmentation of CHM Using Non-Viral Episomal Vectors in Models of Choroideremia. International journal of molecular sciences 24 (20) (2023)
Nicholas Owen, Maria Toms, Yuan Tian, Lyes Toualbi, Rose Richardson, Rodrigo Young, Dhani Tracey-White, Pawan Dhami, Stephan Beck, Mariya Moosajee
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. The Journal of pathology 259 (4) (2023)
Nicholas Owen, Maria Toms, Yuan Tian, Lyes Toualbi, Rose Richardson, Rodrigo Young, Dhani Tracey-White, Pawan Dhami, Stephan Beck, Mariya Moosajee
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. The Journal of pathology (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Nicholas Owen, Maria Toms, Yuan Tian, Lyes Toualbi, Rose Richardson, Rodrigo Young, Dhani Tracey-White, Pawan Dhami, Stephan Beck, Mariya Moosajee
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. The Journal of pathology 259 (4) (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Hajrah Sarkar, Manuela Lahne, Neelima Nair, Mariya Moosajee
Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for Choroideremia. Antioxidants (Basel, Switzerland) 12 (9) (2023)
Riccardo Cheloni, Neil Clough, Daniel Jackson, Mariya Moosajee
Longitudinal structure-function analysis of molecularly-confirmed CYP4V2 Bietti Crystalline Dystrophy. Eye (London, England) (2023)
Nicholas Owen, Maria Toms, Yuan Tian, Lyes Toualbi, Rose Richardson, Rodrigo Young, Dhani Tracey-White, Pawan Dhami, Stephan Beck, Mariya Moosajee
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. The Journal of pathology 259 (4) (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Violeta Trejo-Reveles, Nicholas Owen, Brian Ho Ching Chan, Maria Toms, Jeffrey Joseph Schoenebeck, Mariya Moosajee, Joe Rainger, null null
Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species. Biomolecules 13 (2) (2023)
Ana Catalina Rodriguez-Martinez, Bethany Elora Higgins, Vijay K Tailor, Samantha Malka, Riccardo Cheloni, Alexander Mark Collins, John Bladen, Robert Henderson, Mariya Moosajee
Foveal Hypoplasia in CRB1 -Related Retinopathies. International journal of molecular sciences 24 (18) (2023)
Riccardo Cheloni, Daniel Jackson, Mariya Moosajee
A Natural History Study of RP2 -Related Retinopathy. Journal of clinical medicine 11 (23) (2022)
Raquel R Martins, Mazen Zamzam, Dhani Tracey-White, Mariya Moosajee, Ryan Thummel, Catarina M Henriques, Ryan B MacDonald
Müller Glia maintain their regenerative potential despite degeneration in the aged zebrafish retina. Aging cell 21 (4) (2022)
Daniel J Jackson, Adam Michael Dubis, Mariya Moosajee
The Natural History of CNGB1 -Related Retinopathy: A Longitudinal Phenotypic Analysis. International journal of molecular sciences 23 (12) (2022)
Riccardo Cheloni, Daniel Jackson, Mariya Moosajee
A Natural History Study of RP2 -Related Retinopathy. Journal of clinical medicine 11 (23) (2022)
Riccardo Cheloni, Daniel Jackson, Mariya Moosajee
A Natural History Study of RP2 -Related Retinopathy. Journal of clinical medicine 11 (23) (2022)
Philippa Harding, Sri Gore, Samantha Malka, Jayashree Rajkumar, Ngozi Oluonye, Mariya Moosajee
Real-world clinical and molecular management of 50 prospective patients with microphthalmia, anophthalmia and/or ocular coloboma. The British journal of ophthalmology (2022)
Thomas Burgoyne, Maria Toms, Chris Way, Dhani Tracey-White, Clare E Futter, Mariya Moosajee
Changes in Mitochondrial Size and Morphology in the RPE and Photoreceptors of the Developing and Ageing Zebrafish. Cells 11 (22) (2022)
Jasdeep Singh Gill, Vasileios Theofylaktopoulos, Andreas Mitsios, Sarah Houston, Ahmed M Hagag, Adam Michael Dubis, Mariya Moosajee
Investigating Biomarkers for USH2A Retinopathy Using Multimodal Retinal Imaging. International journal of molecular sciences 23 (8) (2022)
Riccardo Cheloni, Daniel Jackson, Mariya Moosajee
A Natural History Study of RP2 -Related Retinopathy. Journal of clinical medicine 11 (23) (2022)
Daniel F P Larkin, Ludwig M Heindl, Mingguang He, Mariya Moosajee
Publication objectives and processes at the British Journal of Ophthalmology: what authors and readers need to know. The British journal of ophthalmology 105 (8) (2021)
Michael James Gilhooley, Nicholas Owen, Mariya Moosajee, Patrick Yu Wai Man
From Transcriptomics to Treatment in Inherited Optic Neuropathies. Genes 12 (2) (2021)
Cécile Méjécase, Chandni Nigam, Mariya Moosajee, John C Bladen
The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome. Genes 12 (3) (2021)
Suzannah J Bell, Samantha Malka, Ian Christopher Lloyd, Mariya Moosajee
Clinical Spectrum and Genetic Diagnosis of 54 Consecutive Patients Aged 0-25 with Bilateral Cataracts. Genes 12 (2) (2021)
Elena R Schiff, Vijay K Tailor, Hwei Wuen Chan, Maria Theodorou, Andrew R Webster, Mariya Moosajee
Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia. International journal of molecular sciences 22 (3) (2021)
Philippa Harding, Maria Toms, Elena R Schiff, Nicholas Owen, Suzannah J Bell, Ian Christopher Lloyd, Mariya Moosajee
EPHA2 Segregates with Microphthalmia and Congenital Cataracts in Two Unrelated Families. International journal of molecular sciences 22 (4) (2021)
Hwei Wuen Chan, Elena R Schiff, Vijay K Tailor, Samantha Malka, Magella M Neveu, Maria Theodorou, Mariya Moosajee
Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism. Genes 12 (4) (2021)
Lee Jones, Lara Ditzel-Finn, Judith Potts, Mariya Moosajee
Exacerbation of visual hallucinations in Charles Bonnet syndrome due to the social implications of COVID-19. BMJ open ophthalmology 6 (1) (2021)
Jian Lee Yeong, Peter Benjamin Michael Thomas, James Buller, Mariya Moosajee
Correction: A Newly Developed Web-Based Resource on Genetic Eye Disorders for Users With Visual Impairment (Gene.Vision): Usability Study. Journal of medical Internet research 23 (1) (2021)
Hajrah Sarkar, Maria Toms, Mariya Moosajee
Involvement of Oxidative and Endoplasmic Reticulum Stress in RDH12-Related Retinopathies. International journal of molecular sciences 22 (16) (2021)
Cécile Méjécase, Christopher M Way, Nicholas Owen, Mariya Moosajee
Ocular Phenotype Associated with DYRK1A Variants. Genes 12 (2) (2021)
Usman Mahmood, Cécile Méjécase, Syed M A Ali, Mariya Moosajee, Igor Kozak
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness. Genes 12 (2) (2021)
Lyes Toualbi, Maria Toms, Mariya Moosajee
The Landscape of Non-Viral Gene Augmentation Strategies for Inherited Retinal Diseases. International journal of molecular sciences 22 (5) (2021)
Alessandro Abbouda, Filippo Avogaro, Mariya Moosajee, Enzo Maria Vingolo
Update on Gene Therapy Clinical Trials for Choroideremia and Potential Experimental Therapies. Medicina (Kaunas, Lithuania) 57 (1) (2021)
Adam Michael Dubis, Wei S Lim, Jasleen K Jolly, Maria Toms, Robert E MacLaren, Andrew R Webster, Mariya Moosajee
Longitudinal Study to Assess the Quantitative Use of Fundus Autofluorescence for Monitoring Disease Progression in Choroideremia. Journal of clinical medicine 10 (2) (2021)
Lee Jones, Lara Ditzel-Finn, Jamie Enoch, Mariya Moosajee
An overview of psychological and social factors in Charles Bonnet syndrome. Therapeutic advances in ophthalmology 13 (2021)
Jian Lee Yeong, Peter Benjamin Michael Thomas, James Buller, Mariya Moosajee
A Newly Developed Web-Based Resource on Genetic Eye Disorders for Users With Visual Impairment (Gene.Vision): Usability Study. Journal of medical Internet research 23 (1) (2021)
Natalia Jaroszynska, Philippa Harding, Mariya Moosajee
Metabolism in the Zebrafish Retina. Journal of developmental biology 9 (1) (2021)
Suzannah J Bell, Urvi Karamchandani, Kirsten Malcolmson, Mariya Moosajee
Acceptability of Telegenetics for Families with Genetic Eye Diseases. Genes 12 (2) (2021)
Lee Jones, Mariya Moosajee
Visual hallucinations and sight loss in children and young adults: a retrospective case series of Charles Bonnet syndrome. The British journal of ophthalmology 105 (11) (2020)
Cécile Méjécase, Igor Kozak, Mariya Moosajee
The genetic landscape of inherited eye disorders in 74 consecutive families from the United Arab Emirates. American journal of medical genetics. Part C, Seminars in medical genetics 184 (3) (2020)
Cécile Méjécase, Samantha Malka, Zeyu Guan, Amy Slater, Gavin Arno, Mariya Moosajee
Practical guide to genetic screening for inherited eye diseases. Therapeutic advances in ophthalmology 12 (2020)
Dulce Lima Cunha, Nicholas Owen, Vijay K Tailor, Marta Corton, Maria Theodorou, Mariya Moosajee
PAX6 missense variants in two families with isolated foveal hypoplasia and nystagmus: evidence of paternal postzygotic mosaicism. European journal of human genetics : EJHG 29 (2) (2020)
Daniel Jackson, Samantha Malka, Philippa Harding, Juliana Palma, Hannah Dunbar, Mariya Moosajee
Molecular diagnostic challenges for non-retinal developmental eye disorders in the United Kingdom. American journal of medical genetics. Part C, Seminars in medical genetics 184 (3) (2020)
Eszter Balogh, Jennifer C Chandler, Máté Varga, Mona Tahoun, Dóra K Menyhárd, Gusztáv Schay, Tomas Goncalves, Renáta Hamar, Regina Légrádi, Ákos Szekeres, Olivier Gribouval, Robert Kleta, Horia Stanescu, Detlef Bockenhauer, Andrea Kerti, Hywel Williams, Veronica Kinsler, Wei-Li Di, David Curtis, Maria Kolatsi-Joannou, Hafsa Hammid, Anna Szőcs, Kristóf Perczel, Erika Maka, Gergely Toldi, Florentina Sava, Christelle Arrondel, Magdolna Kardos, Attila Fintha, Ahmed Hossain, Felice D'Arco, Marios Kaliakatsos, Jutta Koeglmeier, William Mifsud, Mariya Moosajee, Ana Faro, Eszter Jávorszky, Gábor Rudas, Marwa H Saied, Salah Marzouk, Kata Kelen, Judit Götze, George S Reusz, Tivadar Tulassay, François Dragon, Geraldine Mollet, Susanne Motameny, Holger Thiele, Guillaume Dorval, Peter Nürnberg, András Perczel, Attila J Szabo, David A Long, Kazunori Tomita, Corinne Antignac, Aoife M Waters, Kálmán Tory
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proceedings of the National Academy of Sciences of the United States of America 117 (26) (2020)
Ahmed M Hagag, Andreas Mitsios, Akshay Narayan, Alessandro Abbouda, Andrew R Webster, Adam M Dubis, Mariya Moosajee
Prospective deep phenotyping of choroideremia patients using multimodal structure-function approaches. Eye (London, England) 35 (3) (2020)
Jonathan Eintracht, Marta Corton, David FitzPatrick, Mariya Moosajee
CUGC for syndromic microphthalmia including next-generation sequencing-based approaches. European journal of human genetics : EJHG 28 (5) (2020)
Maria Toms, Waheeda Pagarkar, Mariya Moosajee
Usher syndrome: clinical features, molecular genetics and advancing therapeutics. Therapeutic advances in ophthalmology 12 (2020)
Nicholas Owen, Mariya Moosajee
RNA-sequencing in ophthalmology research: considerations for experimental design and analysis. Therapeutic advances in ophthalmology 11 (2019)
Dulce Lima Cunha, Gavin Arno, Marta Corton, Mariya Moosajee
The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the Eye. Genes 10 (12) (2019)
Philippa Harding, Brian P Brooks, David FitzPatrick, Mariya Moosajee
Anophthalmia including next-generation sequencing-based approaches. European journal of human genetics : EJHG 28 (3) (2019)
Joanne Best, Pui Y Liu, Dominic Ffytche, Judith Potts, Mariya Moosajee
Think sight loss, think Charles Bonnet syndrome. Therapeutic advances in ophthalmology 11 (2019)
Maria Toms, Thomas Burgoyne, Dhani Tracey-White, Rose Richardson, Adam M Dubis, Andrew R Webster, Clare Futter, Mariya Moosajee
Phagosomal and mitochondrial alterations in RPE may contribute to KCNJ13 retinopathy. Scientific reports 9 (1) (2019)
Jasdeep Singh Gill, Mariya Moosajee, Adam M Dubis
Cellular imaging of inherited retinal diseases using adaptive optics. Eye (London, England) 33 (11) (2019)
R Richardson, N Owen, M Toms, Rodrigo M Young, D Tracey-White, Mariya Moosajee
Transcriptome profiling of zebrafish optic fissure fusion. Scientific reports 9 (1) (2019)
Andreas Mitsios, Adam M Dubis, Mariya Moosajee
Choroideremia: from genetic and clinical phenotyping to gene therapy and future treatments. Therapeutic advances in ophthalmology 10 (2018)

Mariya Moosajee.css-eqlu8i{font-size:small;padding-left:4px;} (M Moosajee)

Publication Activity (10 Years)

Top Topics

Top Venues

Mariya Moosajee (M Moosajee)