Historical Overfishing and the Recent Collapse of Coastal Ecosystems
Jeremy B. C. Jackson, Kirby, Michael X., Berger, Wolfgang H., Bjorndal, Karen A., Botsford, Louis W., Bourque, Bruce J., Bradbury, Roger H., Cooke, Richard, Erlandson, Jon, Estes, James A., Hughes, Terence P., Kidwell, Susan, Lange, Carina B., Lenihan, Hunter S., Pandolfi, John M., Peterson, Charles H., Steneck, Robert S., Tegner, Mia J., Warner, Robert R.
Published in Science (American Association for the Advancement of Science) (27.07.2001)
Published in Science (American Association for the Advancement of Science) (27.07.2001)
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Genotype–phenotype spectrum in isolated and syndromic nanophthalmos
Lang, Elena, Koller, Samuel, Atac, David, Pfäffli, Oliver A., Hanson, James V.M., Feil, Silke, Bähr, Luzy, Bahr, Angela, Kottke, Raimund, Joset, Pascal, Fasler, Katrin, Barthelmes, Daniel, Steindl, Katharina, Konrad, Daniel, Wille, David‐Alexander, Berger, Wolfgang, Gerth‐Kahlert, Christina
Published in Acta ophthalmologica (Oxford, England) (01.06.2021)
Published in Acta ophthalmologica (Oxford, England) (01.06.2021)
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Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and Limitations
Tiwari, Amit, Lemke, Johannes, Altmueller, Janine, Thiele, Holger, Glaus, Esther, Fleischhauer, Johannes, Nürnberg, Peter, Neidhardt, John, Berger, Wolfgang
Published in PloS one (08.07.2016)
Published in PloS one (08.07.2016)
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Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
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
Published in American journal of human genetics (10.02.2012)
Published in American journal of human genetics (10.02.2012)
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Functional Analysis of a Novel, Non-Canonical RPGR Splice Variant Causing X-Linked Retinitis Pigmentosa
Koller, Samuel, Beltraminelli, Tim, Maggi, Jordi, Wlodarczyk, Agnès, Feil, Silke, Baehr, Luzy, Gerth-Kahlert, Christina, Menghini, Moreno, Berger, Wolfgang
Published in Genes (18.04.2023)
Published in Genes (18.04.2023)
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Journal Article
De Novo Assembly-Based Analysis of RPGR Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline
Maggi, Jordi, Roberts, Lisa, Koller, Samuel, Rebello, George, Berger, Wolfgang, Ramesar, Rajkumar
Published in Genes (15.07.2020)
Published in Genes (15.07.2020)
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Journal Article
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development
Atac, David, Maggi, Kevin, Feil, Silke, Maggi, Jordi, Cuevas, Elisa, Sowden, Jane C., Koller, Samuel, Berger, Wolfgang
Published in Cells (Basel, Switzerland) (03.07.2024)
Published in Cells (Basel, Switzerland) (03.07.2024)
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The cataract and glucosuria associated monocarboxylate transporter MCT12 is a new creatine transporter
Abplanalp, Jeannette, Laczko, Endre, Philp, Nancy J, Neidhardt, John, Zuercher, Jurian, Braun, Philipp, Schorderet, Daniel F, Munier, Francis L, Verrey, François, Berger, Wolfgang, Camargo, Simone M R, Kloeckener-Gruissem, Barbara
Published in Human molecular genetics (15.08.2013)
Published in Human molecular genetics (15.08.2013)
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Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes
Haug, Patricia, Koller, Samuel, Maggi, Jordi, Lang, Elena, Feil, Silke, Wlodarczyk, Agnès, Bähr, Luzy, Steindl, Katharina, Rohrbach, Marianne, Gerth-Kahlert, Christina, Berger, Wolfgang
Published in Genes (06.01.2021)
Published in Genes (06.01.2021)
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Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans
Knöpfel, Emilia Boiadjieva, Vilches, Clara, Camargo, Simone M R, Errasti-Murugarren, Ekaitz, Stäubli, Andrina, Mayayo, Clara, Munier, Francis L, Miroshnikova, Nataliya, Poncet, Nadège, Junza, Alexandra, Bhattacharya, Shomi S, Prat, Esther, Berry, Vanita, Berger, Wolfgang, Heon, Elise, Moore, Anthony T, Yanes, Óscar, Nunes, Virginia, Palacín, Manuel, Verrey, Francois, Kloeckener-Gruissem, Barbara
Published in Frontiers in physiology (04.06.2019)
Published in Frontiers in physiology (04.06.2019)
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RPGR mutations might cause reduced orientation of respiratory cilia
Bukowy-Bieryłło, Zuzanna, Ziętkiewicz, Ewa, Loges, Niki Tomas, Wittmer, Mariana, Geremek, Maciej, Olbrich, Heike, Fliegauf, Manfred, Voelkel, Katarzyna, Rutkiewicz, Ewa, Rutland, Jonathan, Morgan, Lucy, Pogorzelski, Andrzej, Martin, James, Haan, Eric, Berger, Wolfgang, Omran, Heymut, Witt, Michał
Published in Pediatric pulmonology (01.04.2013)
Published in Pediatric pulmonology (01.04.2013)
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Long-term consequences of developmental vascular defects on retinal vessel homeostasis and function in a mouse model of Norrie disease
Beck, Susanne C, Feng, Yuxi, Sothilingam, Vithiyanjali, Garcia Garrido, Marina, Tanimoto, Naoyuki, Acar, Niyazi, Shan, Shenliang, Seebauer, Britta, Berger, Wolfgang, Hammes, Hans-Peter, Seeliger, Mathias W
Published in PloS one (02.06.2017)
Published in PloS one (02.06.2017)
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U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation
Schmid, Fabian, Glaus, Esther, Barthelmes, Daniel, Fliegauf, Manfred, Gaspar, Harald, Nürnberg, Gudrun, Nürnberg, Peter, Omran, Heymut, Berger, Wolfgang, Neidhardt, John
Published in Human mutation (01.07.2011)
Published in Human mutation (01.07.2011)
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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness
ZEITZ, Christina, KLOECKENER-GRUISSEM, Barbara, MUNIER, Francis L, BERGER, Wolfgang, FORSTER, Ursula, KOHL, Susanne, MAGYAR, Istvan, WISSINGER, Bernd, MATYAS, Gabor, BORRUAT, Francois-Xavier, SCHORDERET, Daniel F, ZRENNER, Eberhart
Published in American journal of human genetics (01.10.2006)
Published in American journal of human genetics (01.10.2006)
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SwissGenVar: A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland
Kraemer, Dennis, Terumalai, Dillenn, Famiglietti, Maria Livia, Filges, Isabel, Joset, Pascal, Koller, Samuel, Maurer, Fabienne, Meier, Stéphanie, Nouspikel, Thierry, Sanz, Javier, Zweier, Christiane, Abramowicz, Marc, Berger, Wolfgang, Cichon, Sven, Schaller, André, Superti-Furga, Andrea, Barbié, Valérie, Rauch, Anita
Published in Journal of personalized medicine (01.06.2024)
Published in Journal of personalized medicine (01.06.2024)
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Impact of loading phase, initial response and CFH genotype on the long-term outcome of treatment for neovascular age-related macular degeneration
Menghini, Moreno, Kloeckener-Gruissem, Barbara, Fleischhauer, Johannes, Kurz-Levin, Malaika M, Sutter, Florian K P, Berger, Wolfgang, Barthelmes, Daniel
Published in PloS one (25.07.2012)
Published in PloS one (25.07.2012)
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Journal Article
Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy
Wycisk, Katharina Agnes, Zeitz, Christina, Feil, Silke, Wittmer, Mariana, Forster, Ursula, Neidhardt, John, Wissinger, Bernd, Zrenner, Eberhart, Wilke, Robert, Kohl, Susanne, Berger, Wolfgang
Published in American journal of human genetics (01.11.2006)
Published in American journal of human genetics (01.11.2006)
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