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In the below list, publications with fewer than 30 authors are transferred 1:1 to ZORA. No author names are deleted. --> Reason: complete metadata per publication, also for further use (e.g. in Swisscovery).
For publications with more (>30) authors, the authors are automatically truncated to the number 30 during import. An "et al" is created in the same step. If UZH authors are omitted as a result, they are added at the end, after "et al".
For the complete list of authors in order of publication, please use the text file on this website or the original publication on ZORA.

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Publikationen

Luhmann, U. F. O., Meunier, D., Shi, W., Lüttges, A., Pfarrer, C., Fundele, R., & Berger, W. (2005). Fetal loss in homozygous mutant Norrie disease mice: A new role of Norrin in reproduction Genesis, 42, 253–262. https://doi.org/10.1002/gene.20141
Kloeckener-Gruissem, B., Betts, D. R., Zankl, A., Berger, W., & Güngör, T. (2005). A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9 American Journal of Medical Genetics. Part A, 136A, 31–37. https://doi.org/10.1002/ajmg.a.30767
Zeitz, C., Minotti, R., Feil, S., Matyas, G., Cremers, F. P. M., Hoyng, C. B., & Berger, W. (2005). Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness Molecular Vision, 11, 179–183. http://www.molvis.org/molvis/v11/a20/
Ohlmann, A., Scholz, M., Goldwich, A., Chauhan, B. K., Hudl, K., Ohlmann, A. V., Zrenner, E., Berger, W., Cvekl, A., Seeliger, M. W., & Tamm, E. R. (2005). Ectopic Norrin Induces Growth of Ocular Capillaries and Restores Normal Retinal Angiogenesis in Norrie Disease Mutant Mice Journal of Neuroscience, 25, 1701–1710. https://doi.org/10.1523/jneurosci.4756-04.2005
Zeitz, C., Scherthan, H., Freier, S., Feil, S., Suckow, V., Schweiger, S., & Berger, W. (2003). NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein Investigative Ophthalmology & Visual Science, 44, 4184–4191. https://doi.org/10.1167/iovs.03-0251
Collod-Béroud, G., Le Bourdelles, S., Adès, L. C., Ala-Kokko, L., Booms, P., Boxer, M., Child, A., Comeglio, P., De Paepe, A., Hyland, J. C., Holman, K., Kaitila, I., Loeys, B., Matyas, G., Nuytinck, L., Peltonen, L., Rantamaki, T., Robinson, P. N., Steinmann, B., … Boileau, C. (2003). Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database Human Mutation, 22, 199–208. https://doi.org/10.1002/humu.10249
Berger, W. (2003). Genetische Ursachen degenerativer Netzhauterkrankungen des Menschen Therapeutische Umschau : Monatsschrift für praktische Medizin, 60, 473–476. https://doi.org/10.1024/0040-5930.60.8.473
Finkeldey, R., & Matyas, G. (2003). Genetic variation of oaks (Quercus spp.) in Switzerland. 3. Lack of impact of postglacial recolonization history on nuclear gene loci TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik, 106, 346–352. https://doi.org/10.1007/s00122-002-1002-5

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