Conferences

Poster Teasing Prize (2016) 17th doctoral school days, Université Pierre et Marie Curie, Paris, France 

Second runner-up oral presentation award (2023) IoO ECR Symposium, London, UK 

Best collaborative proposal (2023) Postdoc Symposium 2023 – Building Bridges in Research, The Francis Crick Institute, London, UK 

XVIIIth International Symposium on Retinal degeneration RD2018, Killarney, Ireland (2018)

Elizabeth Anderson Travel Grant (2017) The Association of Research of Vision and Ophthalmology, Baltimore, United States.

Méjécase C, Owen N, Cheloni R, Nair N, Sarkar H, Toualbi L, Moosajee M. Dominant and recessive pathogenic variants in RDH12 impair photoreceptor development and function in retinal organoids (2023) IoO ECR Symposium, London, United Kingdom

Méjécase C, Owen N, Sarkar H, Toualbi L, Moosajee M. Characterisation of induced pluripotent stem cell derived retinal organoid models of RDH12-retinopathies (2023) The Association of Research of Vision and Ophthalmology, New Orleans, United States

Méjécase C, Owen N, Sakar H, Toualbi L, Moosajee M. Characterisation of induced pluripotent stem cell derived retinal organoid models of RDH12-retinopathies (2022) Retina2022, Dublin, Ireland

Méjécase C, Moosajee M. When genetic testing reveals a dual diagnosis of two inherited retinal diseases (2022) UK EGG Annual Meeting, Bristol, United Kingdom

Méjécase C, Moosajee M. When genetic testing reveals a dual diagnosis of two inherited retinal diseases (2022) Women in Vision UK Annual Meeting (online)

Méjécase C, Toualbi L, Moosajee M. Investigating photoreceptor glycan-binding proteins to assist gene therapy (2021) UK EGG Annual Meeting, London, United Kingdom

Méjécase C, Toualbi L, Moosajee M. Immunolocalisation of glycan binding proteins in human retina and in mature retinal organoids derived from induced pluripotent stem cells (2021) 4th Crick Postdoc Symposium, London, United Kingdom

Méjécase C, Toualbi L, Moosajee M. Immunolocalisation of glycan binding proteins in human retina and in mature retinal organoids derived from induced pluripotent stem cells (2021) IoO ECR Symposium, London, United Kingdom

Méjécase C*, Way CM*, Owen N, Moosajee M. Ocular phenotype associated with DYRK1A variants (2021) UK EGG, London, United Kingdom (online)

Méjécase C, Wohschlegel J, Letellier C, […], Goureau O, Zeitz C, Audo I. Characterization of induced pluripotent stem cells derived from fibroblasts of a patient with rod-cone dystrophy and his unaffected brother (2019) IBPS International Symposium “Building, repairing, replacing organs”, Paris, France

Méjécase C, Mohand-Saïd S, Boulanger-Scemama E, […], Sahel JA, Zeitz C, Audo I. Treats and traps of next generation sequencing in resolving complex clinical cases. (2018) XVIIIth International Symposium on Retinal degeneration RD2018, Killarney, Ireland

Méjécase C*, Schalk A*, Mochel F, […], Sahel JA, Zeitz C, Audo I. A sporadic cone-rod dystrophy with cerebellar ataxia is associated with compound heterozygous variants in PATJ (2018) 19th doctoral school days, Université Pierre et Marie Curie, Paris, France

Méjécase C, Mohand-Saïd S, Hummel A, […], Sahel JA, Audo I, Zeitz C. CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy (2017) European Retina Meeting, Paris, France

Méjécase C, Mohand-Saïd S, Hummel A, […], Sahel JA, Audo I, Zeitz C. CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy (2017) The Association of Research of Vision and Ophthalmology, Baltimore, United States

Méjécase C, Mohand-Saïd S, Hummel A, […], Sahel JA, Audo I, Zeitz C. CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy (2017) 18th doctoral school days, Université Pierre et Marie Curie, Paris, France

Méjécase C, Laurent-Coriat C, Mayer C, […], Sahel JA, Audo I, Zeitz C. Identification of a novel homozygous nonsense mutation confirms the implication of GNAT1 in rod-cone dystrophy (2016) 17th doctoral school days, Université Pierre et Marie Curie, Paris, France 

Méjécase C, Owen N, Cheloni R, Nair N, Sarkar H, Toualbi L, Moosajee M. Dominant and recessive pathogenic variants in RDH12 impair photoreceptor development and function in retinal organoids (2023) IoO ECR Symposium, London, United Kingdom

Méjécase C, Owen N, Sakar H, Toualbi L, Moosajee M. Characterisation of induced pluripotent stem cell derived retinal organoid models of RDH12-retinopathies (2022) Women in Vision UK (WVUK) Winter Meeting, London, United Kingdom (Three Minute Thesis style presentation) 

Méjécase C, Owen N, Sakar H, Toualbi L, Moosajee M. Characterisation of induced pluripotent stem cell derived retinal organoid models of RDH12-retinopathies (2022) Development and Stem Cells group seminar, Francis Crick Institute, London, UK 

Méjécase C, Toualbi L, Moosajee M. Investigating photoreceptor glycan-binding proteins to assist gene therapy (2021) Genetics of Ocular Development (GoOD) meeting (online)

Méjécase C, Schalk A, Mochel F, […], Sahel JA, Audo I, Zeitz C. Identification of novel gene defects associated with a syndromic cone-rod dystrophy (2018) Société de Génétique Ophtalmologique Francophone, Lille, France

Méjécase C, Schalk A, Mochel F, […], Sahel JA, Audo I, Zeitz C. Identification of novel gene defects associated with a syndromic cone-rod dystrophy (2018) Paris-London Meeting, Paris, France

Méjécase C, Mohand-Saïd S, Hummel A, […], Sahel JA, Audo I, Zeitz C. CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy (2017) Société de Génétique Ophtalmologique Francophone, Tunis, Tunisia

Méjécase C, Mohand-Saïd S, Hummel A, […], Sahel JA, Audo I, Zeitz C. CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy (2017) Paris-London Meeting, London, United Kingdom

Méjécase C, Laurent-Coriat C, Mayer C, […], Sahel JA, Audo I, Zeitz C. Identification of a novel homozygous nonsense mutation confirms the implication of GNAT1 in rod-cone dystrophy (2016) Société de Génétique Ophtalmologique Francophone, Strasbourg, France

DYRK1A Families Meet Up Conference, organised by DYRK1A syndrome International Association (July 2022) The Wirral, United Kingdom

France Choroidérémie (2021) (online, in French)

RDH12 Global Community Call, organised by RDH12 Alliance (October 2021) (online)