Vasiliki Kalatzis

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Venues

Scientific reports

European journal of human genetics : EJHG

International journal of molecular sciences

Diagnostics (Basel, Switzerland)

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

Publications

Christel Vaché, Valérie Faugère, David Baux, Luke Mansard, Charles Van Goethem, Claire-Marie Dhaenens, Olivier Grunewald, Isabelle Audo, Christina Zeitz, Isabelle Meunier, Béatrice Bocquet, Mireille Cossee, Anne Bergougnoux, Vasiliki Kalatzis, Anne-Françoise Roux
Validation of Nanopore long-read sequencing to resolve RPGR ORF15 genotypes in individuals with X-linked retinitis pigmentosa. European journal of human genetics : EJHG (2024)
Christel Vaché, Nicolas Cubedo, Luke Mansard, Jérôme Sarniguet, David Baux, Valérie Faugère, Corinne Baudoin, Melody Moclyn, Renaud Touraine, Geneviève Lina-Granade, Mireille Cossée, Anne Bergougnoux, Vasiliki Kalatzis, Mireille Rossel, Anne-Françoise Roux
Identification and in vivo functional investigation of a HOMER2 nonstop variant causing hearing loss. European journal of human genetics : EJHG (2023)
Carla Sanjurjo-Soriano, Nejla Erkilic, Krishna Damodar, Hassan Boukhaddaoui, Michalitsa Diakatou, Marcela Garita-Hernandez, Daria Mamaeva, Gregor Dubois, Zhour Jazouli, Carla Jimenez-Medina, Olivier Goureau, Isabelle Meunier, Vasiliki Kalatzis
Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid. Stem cell research & therapy 13 (1) (2022)
Luke Mansard, Christel Vaché, Julie Bianchi, Corinne Baudoin, Isabelle Perthus, Bertrand Isidor, Catherine Blanchet, David Baux, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss. Diagnostics (Basel, Switzerland) 12 (1) (2022)
Guillaume Olivier, Philippe Brabet, Nelly Pirot, Morgane Broyon, Laurent Guillou, Chantal Cazevieille, Chamroeun Sar, Melanie Quiles, Emmanuelle Sarzi, Marie Pequignot, Ervann Andreo, Agathe Roubertie, Isabelle Meunier, Agnès Muller, Vasiliki Kalatzis, Gaël Manes
SPACR Encoded by IMPG1 Is Essential for Photoreceptor Survival by Interplaying between the Interphotoreceptor Matrix and the Retinal Pigment Epithelium. Genes 13 (9) (2022)
Daria Mamaeva, Zhour Jazouli, Mattia L DiFrancesco, Nejla Erkilic, Gregor Dubois, Cecile Hilaire, Isabelle Meunier, Hassan Boukhaddaoui, Vasiliki Kalatzis
Novel roles for voltage-gated T-type Ca2+ and ClC-2 channels in phagocytosis and angiogenic factor balance identified in human iPSC-derived RPE. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 35 (4) (2021)
Luke Mansard, David Baux, Christel Vaché, Catherine Blanchet, Isabelle Meunier, Marjolaine Willems, Valérie Faugère, Corinne Baudoin, Melody Moclyn, Julie Bianchi, Helene Dollfus, Brigitte Gilbert-Dussardier, Delphine Dupin-Deguine, Dominique Bonneau, Isabelle Drumare, Sylvie Odent, Xavier Zanlonghi, Mireille Claustres, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
The Study of a 231 French Patient Cohort Significantly Extends the Mutational Spectrum of the Two Major Usher Genes MYO7A and USH2A . International journal of molecular sciences 22 (24) (2021)
Michalitsa Diakatou, Gregor Dubois, Nejla Erkilic, Carla Sanjurjo-Soriano, Isabelle Meunier, Vasiliki Kalatzis
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. International journal of molecular sciences 22 (5) (2021)
Kevin Mairot, Vasily Smirnov, Béatrice Bocquet, Gilles Labesse, Carl Arndt, Sabine Defoort-Dhellemmes, Xavier Zanlonghi, Dalil Hamroun, Danièle Denis, Marie-Christine Picot, Thierry David, Olivier Grunewald, Mako Pégart, Hélèna Huguet, Anne-Françoise Roux, Vasiliki Kalatzis, Claire-Marie Dhaenens, Isabelle Meunier
CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms. International journal of molecular sciences 22 (23) (2021)
Christel Vaché, David Baux, Julie Bianchi, Corinne Baudoin, Valérie Faugère, Christine Francannet, Michel Koenig, Vasiliki Kalatzis, Anne-Françoise Roux
Reclassification of a TMC1 synonymous substitution as a variant disrupting splicing regulatory elements associated with recessive hearing loss. European journal of human genetics : EJHG (2021)
Vasiliki Kalatzis, Anne-Françoise Roux, Isabelle Meunier
Molecular Therapy for Choroideremia: Pre-clinical and Clinical Progress to Date. Molecular diagnosis & therapy 25 (6) (2021)
Neus Bayó-Puxan, Ana Paula Terrasso, Sophie Creyssels, Daniel Simão, Christina Begon-Pescia, Marina Lavigne, Sara Salinas, Florence Bernex, Assumpció Bosch, Vasiliki Kalatzis, Thierry Levade, Ana Maria Cuervo, Philippe Lory, Antonella Consiglio, Catarina Brito, Eric J Kremer
Lysosomal and network alterations in human mucopolysaccharidosis type VII iPSC-derived neurons. Scientific reports 8 (1) (2018)
Simona Torriano, Nejla Erkilic, David Baux, Nicolas Cereso, Valerie De Luca, Isabelle Meunier, Mariya Moosajee, Anne-Francoise Roux, Christian P Hamel, Vasiliki Kalatzis
The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapy. Scientific reports 8 (1) (2018)
Aymeric Douillard, Marie-Christine Picot, Cécile Delcourt, Sabine Defoort-Dhellemmes, Nour Al-Dain Marzouka, Annie Lacroux, Xavier Zanlonghi, Isabelle Drumare, Elsa Jozefowicz, Béatrice Bocquet, Corinne Baudoin, Sarah Perez-Roustit, Sophie Arsène, Valérie Gissot, François Devin, Carl Arndt, Benjamin Wolff, Martine Mauget-Faÿsse, Maddalena Quaranta, Thibault Mura, Dominique Deplanque, Hassiba Oubraham, Salomon Yves Cohen, Pierre Gastaud, Olivia Zambrowski, Catherine Creuzot-Garcher, Saddek Mohand Saïd, José-Alain Sahel, Eric Souied, Solange Milazzo, Rocio Blanco Garavito, Vasiliki Kalatzis, Bernard Puech, Christian Hamel, Isabelle Audo, Isabelle Meunier
Dietary, environmental, and genetic risk factors of Extensive Macular Atrophy with Pseudodrusen, a severe bilateral macular atrophy of middle-aged patients. Scientific reports 8 (1) (2018)
Carla Sanjurjo-Soriano, Vasiliki Kalatzis
Guiding Lights in Genome Editing for Inherited Retinal Disorders: Implications for Gene and Cell Therapy. Neural plasticity 2018 (2018)

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Publication Activity (10 Years)

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Vasiliki Kalatzis