Mice Lacking Gpr179 with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia von Wilmet, Baptiste, Callebert, Jacques, Duvoisin, Robert, Goulet, Ruben, Tourain, Christophe, Michiels, Christelle, Frederiksen, Helen, Schaeffel, Frank, Marre, Olivier, Sahel, José Alain, Audo, Isabelle, Picaud, Serge, Zeitz, Christina

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Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation von Boulanger-Scemama, Elise, El Shamieh, Said, Démontant, Vanessa, Condroyer, Christel, Antonio, Aline, Michiels, Christelle, Boyard, Fiona, Saraiva, Jean-Paul, Letexier, Mélanie, Souied, Eric, Mohand-Saïd, Saddek, Sahel, José-Alain, Zeitz, Christina, Audo, Isabelle

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Identification and characterization of novel TRPM1 autoantibodies from serum of patients with melanoma-associated retinopathy von Varin, Juliette, Reynolds, Margaret M, Bouzidi, Nassima, Tick, Sarah, Wohlschlegel, Juliette, Becquart, Ondine, Michiels, Christelle, Dereure, Olivier, Duvoisin, Robert M, Morgans, Catherine W, Sahel, José-Alain, Samaran, Quentin, Guillot, Bernard, Pulido, José S, Audo, Isabelle, Zeitz, Christina

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Establishment and measurement of myopia in mice with ON‐bipolar cell defects von Baptiste, Wilmet, Robert, Duvoisin, Jacques, Callebert, Ruben, Goulet, Christophe, Tourain, Christelle, Michiels, Julie, Degardin, Helen, Frederiksen, Quenol, Cesar, Manuel, Simonutti, Olivier, Marre, José‐Alain, Sahel, Audo, Isabelle, Serge, Picaud, Zeitz, Christina

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Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies von Boulanger-Scemama, Elise, Mohand-Saïd, Saddek, El Shamieh, Said, Démontant, Vanessa, Condroyer, Christel, Antonio, Aline, Michiels, Christelle, Boyard, Fiona, Saraiva, Jean-Paul, Letexier, Mélanie, Sahel, José-Alain, Zeitz, Christina, Audo, Isabelle

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LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation von Neuillé, Marion, Morgans, Catherine W., Cao, Yan, Orhan, Elise, Michiels, Christelle, Sahel, José-Alain, Audo, Isabelle, Duvoisin, Robert M., Martemyanov, Kirill A., Zeitz, Christina

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A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency von Orhan, Elise, Neuillé, Marion, de Sousa Dias, Miguel, Pugliese, Thomas, Michiels, Christelle, Condroyer, Christel, Antonio, Aline, Sahel, José-Alain, Audo, Isabelle, Zeitz, Christina

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Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases von Audo, Isabelle, Bujakowska, Kinga M, Léveillard, Thierry, Mohand-Saïd, Saddek, Lancelot, Marie-Elise, Germain, Aurore, Antonio, Aline, Michiels, Christelle, Saraiva, Jean-Paul, Letexier, Mélanie, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina

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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness von Audo, Isabelle, Bujakowska, Kinga, Orhan, Elise, Poloschek, Charlotte M., Defoort-Dhellemmes, Sabine, Drumare, Isabelle, Kohl, Susanne, Luu, Tien D., Lecompte, Odile, Zrenner, Eberhart, Lancelot, Marie-Elise, Antonio, Aline, Germain, Aurore, Michiels, Christelle, Audier, Claire, Letexier, Mélanie, Saraiva, Jean-Paul, Leroy, Bart P., Munier, Francis L., Mohand-Saïd, Saddek, Lorenz, Birgit, Friedburg, Christoph, Preising, Markus, Kellner, Ulrich, Renner, Agnes B., Moskova-Doumanova, Veselina, Berger, Wolfgang, Wissinger, Bernd, Hamel, Christian P., Schorderet, Daniel F., De Baere, Elfride, Sharon, Dror, Banin, Eyal, Jacobson, Samuel G., Bonneau, Dominique, Zanlonghi, Xavier, Le Meur, Guylene, Casteels, Ingele, Koenekoop, Robert, Long, Vernon W., Meire, Francoise, Prescott, Katrina, de Ravel, Thomy, Simmons, Ian, Nguyen, Hoan, Dollfus, Hélène, Poch, Olivier, Léveillard, Thierry, Nguyen-Ba-Charvet, Kim, Sahel, José-Alain, Bhattacharya, Shomi S., Zeitz, Christina

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Genotypic and phenotypic characterization of P23H line 1 rat model von Orhan, Elise, Dalkara, Deniz, Neuillé, Marion, Lechauve, Christophe, Michiels, Christelle, Picaud, Serge, Léveillard, Thierry, Sahel, José-Alain, Naash, Muna I, Lavail, Matthew M, Zeitz, Christina, Audo, Isabelle

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Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB) von Neuillé, Marion, El Shamieh, Said, Orhan, Elise, Michiels, Christelle, Antonio, Aline, Lancelot, Marie-Elise, Condroyer, Christel, Bujakowska, Kinga, Poch, Olivier, Sahel, José-Alain, Audo, Isabelle, Zeitz, Christina

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Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy von Zeitz, Christina, Méjécase, Cécile, Michiels, Christelle, Condroyer, Christel, Wohlschlegel, Juliette, Foussard, Marine, Antonio, Aline, Démontant, Vanessa, Emmenegger, Lisa, Schalk, Audrey, Neuillé, Marion, Orhan, Elise, Augustin, Sébastien, Bonnet, Crystel, Estivalet, Amrit, Blond, Frédéric, Blanchard, Steven, Andrieu, Camille, Chantot-Bastaraud, Sandra, Léveillard, Thierry, Mohand-Saïd, Saddek, Sahel, José-Alain, Audo, Isabelle

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Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy von Méjécase, Cécile, Laurent-Coriat, Caroline, Mayer, Claudine, Poch, Olivier, Mohand-Saïd, Saddek, Prévot, Camille, Antonio, Aline, Boyard, Fiona, Condroyer, Christel, Michiels, Christelle, Blanchard, Steven, Letexier, Mélanie, Saraiva, Jean-Paul, Sahel, José-Alain, Audo, Isabelle, Zeitz, Christina

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Substantial restoration of night vision in adult mice with congenital stationary night blindness von Varin, Juliette, Bouzidi, Nassima, Gauvain, Gregory, Joffrois, Corentin, Desrosiers, Melissa, Robert, Camille, De Sousa Dias, Miguel Miranda, Neuillé, Marion, Michiels, Christelle, Nassisi, Marco, Sahel, José-Alain, Picaud, Serge, Audo, Isabelle, Dalkara, Deniz, Zeitz, Christina

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Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother von Wohlschlegel, Juliette, Letellier, Camille, Liu, Bingqian, Méjécase, Cécile, Slembrouck-Brec, Amélie, Condroyer, Christel, Michiels, Christelle, Sahel, José-Alain, Reichman, Sacha, Zeitz, Christina, Goureau, Olivier, Audo, Isabelle

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A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness von Riazuddin, S. Amer, Shahzadi, Amber, Zeitz, Christina, Ahmed, Zubair M., Ayyagari, Radha, Chavali, Venkata R.M., Ponferrada, Virgilio G., Audo, Isabelle, Michiels, Christelle, Lancelot, Marie-Elise, Nasir, Idrees A., Zafar, Ahmad U., Khan, Shaheen N., Husnain, Tayyab, Jiao, Xiaodong, MacDonald, Ian M., Riazuddin, Sheikh, Sieving, Paul A., Katsanis, Nicholas, Hejtmancik, J. Fielding

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Pharmacological inhibition of Stearoyl-CoA Desaturase 1 improves insulin sensitivity in insulin-resistant rat models von Issandou, Marc, Bouillot, Anne, Brusq, Jean-Marie, Forest, Marie-Claire, Grillot, Didier, Guillard, Raphaelle, Martin, Sandrine, Michiels, Christelle, Sulpice, Thierry, Daugan, Alain

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Loss of ON-Pathway Function in Mice Lacking Lrit3 Decreases Recovery From Lens-Induced Myopia von Wilmet, Baptiste, Michiels, Christelle, Zhang, Jingyi, Callebert, Jacques, Sahel, José Alain, Picaud, Serge, Audo, Isabelle, Zeitz, Christina

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Restoration of mGluR6 Localization Following AAV-Mediated Delivery in a Mouse Model of Congenital Stationary Night Blindness von Varin, Juliette, Bouzidi, Nassima, Dias, Miguel Miranda De Sousa, Pugliese, Thomas, Michiels, Christelle, Robert, Camille, Desrosiers, Melissa, Sahel, José-Alain, Audo, Isabelle, Dalkara, Deniz, Zeitz, Christina

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Shedding light on myopia by studying complete congenital stationary night blindness von Zeitz, Christina, Roger, Jérome E., Audo, Isabelle, Michiels, Christelle, Sánchez-Farías, Nuria, Varin, Juliette, Frederiksen, Helen, Wilmet, Baptiste, Callebert, Jacques, Gimenez, Marie-Laure, Bouzidi, Nassima, Blond, Frederic, Guilllonneau, Xavier, Fouquet, Stéphane, Léveillard, Thierry, Smirnov, Vasily, Vincent, Ajoy, Héon, Elise, Sahel, José-Alain, Kloeckener-Gruissem, Barbara, Sennlaub, Florian, Morgans, Catherine W., Duvoisin, Robert M., Tkatchenko, Andrei V., Picaud, Serge

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