Isabelle Meunier (I Meunier)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 18

Top Venues

Genes

International journal of molecular sciences

Journal of personalized medicine

Scientific reports

National center in rare diseases (PHD)

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

Education History

National center in rare diseases

France

PHD :: Ophthalmology and unit INSERM 1053

Publications

Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, Ipek Selen Kocabaş, Isabelle Meunier, Francesca Simonelli, Marianthi Karali, Frans P M Cremers, Rebekkah J Hitti-Malin
Novel and Recurrent Copy Number Variants in ABCA4 -Associated Retinopathy. International journal of molecular sciences 25 (11) (2024)
Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, Ipek Selen Kocabaş, Isabelle Meunier, Francesca Simonelli, Marianthi Karali, Frans P M Cremers, Rebekkah J Hitti-Malin
Novel and Recurrent Copy Number Variants in ABCA4 -Associated Retinopathy. International journal of molecular sciences 25 (11) (2024)
Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, Ipek Selen Kocabaş, Isabelle Meunier, Francesca Simonelli, Marianthi Karali, Frans P M Cremers, Rebekkah J Hitti-Malin
Novel and Recurrent Copy Number Variants in ABCA4 -Associated Retinopathy. International journal of molecular sciences 25 (11) (2024)
Emmanuelle Moret, Raphaël Lejoyeux, Sophie Bonnin, Georges Georges Azar, Jessica Guillaume, Chloé Le Cossec, Justine Lafolie, Anne-Sophie Alonso, Catherine Favard, Isabelle Meunier, Vivien Vasseur, Martine Mauget-Faÿsse
Atypical Foveal Hypoplasia in Best Disease. Journal of personalized medicine 13 (2) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Emmanuelle Moret, Raphaël Lejoyeux, Sophie Bonnin, Georges Georges Azar, Jessica Guillaume, Chloé Le Cossec, Justine Lafolie, Anne-Sophie Alonso, Catherine Favard, Isabelle Meunier, Vivien Vasseur, Martine Mauget-Faÿsse
Atypical Foveal Hypoplasia in Best Disease. Journal of personalized medicine 13 (2) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Sara Geada, Francisco Teixeira-Marques, Bruno Teixeira, Ana Luísa Carvalho, Nuno Lousan, Jorge Saraiva, Joaquim Murta, Rufino Silva, Xavier Zanlonghi, Sabine Defoort-Dhellemmes, Vasily M Smirnov, Claire-Marie Dhaenens, Catherine Blanchet, Isabelle Meunier, João Pedro Marques
Mutational Spectrum, Ocular and Olfactory Phenotypes of CNGB1 -Related RP-Olfactory Dysfunction Syndrome in a Multiethnic Cohort. Genes 14 (4) (2023)
Emmanuelle Moret, Raphaël Lejoyeux, Sophie Bonnin, Georges Georges Azar, Jessica Guillaume, Chloé Le Cossec, Justine Lafolie, Anne-Sophie Alonso, Catherine Favard, Isabelle Meunier, Vivien Vasseur, Martine Mauget-Faÿsse
Atypical Foveal Hypoplasia in Best Disease. Journal of personalized medicine 13 (2) (2023)
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)
Bernd Wissinger, Britta Baumann, Elena Buena-Atienza, Zeinab Ravesh, Artur V Cideciyan, Katarina Stingl, Isabelle Audo, Isabelle Meunier, Béatrice Bocquet, Elias I Traboulsi, Alison J Hardcastle, Jessica C Gardner, Michel Michaelides, Kari E Branham, Thomas Rosenberg, Sten Andreasson, Hélène Dollfus, David Birch, Andrea L Vincent, Loreto Martorell, Jaume Catala, Ulrich Kellner, Klaus Rüther, Birgit Lorenz, Markus N Preising, Emanuela Manfredini, Yuri A Zarate, Raymon Vijzelaar, Eberhart Zrenner, Samuel G Jacobson, Susanne Kohl
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America 119 (27) (2022)
Christina Zeitz, Marco Nassisi, Caroline Laurent-Coriat, Camille Andrieu, Fiona Boyard, Christel Condroyer, Vanessa Démontant, Aline Antonio, Marie-Elise Lancelot, Helen Frederiksen, Barbara Kloeckener-Gruissem, Said El Shamieh, Xavier Zanlonghi, Isabelle Meunier, Anne-Françoise Roux, Saddek Mohand-Saïd, José Alain Sahel, Isabelle Audo
CHM mutation spectrum and disease: An update at the time of human therapeutic trials. Human mutation 42 (4) (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)
M G Bah, Diana Rodriguez, C Cazeneuve, Fanny Mochel, David Devos, Agnese Suppiej, Agathe Roubertie, Isabelle Meunier, Cyril Gitiaux, Aurore Curie, F Klapczynski, N Allani-Essid, M Carneiro, R Van Minkelen, Anneke J A Kievit, Joël Fluss, B Leheup, Ilham Ratbi, D Héron, D Gras, Jeremy Do Cao, S Pichard, I Strubi-Villaume, Isabelle Audo, Gaëtan Lesca, Perrine Charles, F Dubois, P Comet-Didierjean, Y Capri, C Barondiot, M Barathon, Claire Ewenczyk, Alexandra Dürr, Mignot Cyril
Deciphering the natural history of SCA7 in children. European journal of neurology 27 (11) (2020)
Laura Poujade, Quentin Samaran, Frédéric Mura, Bernard Guillot, Isabelle Meunier, Aurélie Du-Thanh
Melanoma-associated retinopathy during pembrolizumab treatment probably controlled by intravitreal injections of dexamethasone. Documenta ophthalmologica. Advances in ophthalmology 142 (2) (2020)
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)

Isabelle Meunier.css-eqlu8i{font-size:small;padding-left:4px;} (I Meunier)

Publication Activity (10 Years)

Top Topics

Top Venues

Isabelle Meunier (I Meunier)