All publications

Disclaimer: on the specification of authors in ZORA

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.

ZORA Publikationsliste

Download-Optionen

Format für Download Link

Download alsCSV Download alsRIS Download alsBIBTEX

Publikationen

Junge, S., Kloeckener-Gruissem, B., Zufferey, R., Keisker, A., Salgo, B., Fauchere, J. C., Scherer, F., Shalaby, T., Grotzer, M., Siler, U., Seger, R., & Güngör, T. (2007). Correlation between recent thymic emigrants and CD31+ (PECAM-1) CD4+ T cells in normal individuals during aging and in lymphopenic children European Journal of Immunology, 37, 3270–3280. https://doi.org/10.1002/eji.200636976
Banin, E., Mizrahi-Meissonnier, L., Neis, R., Silverstein, S., Magyar, I., Abeliovich, D., Roepman, R., Berger, W., Rosenberg, T., & Sharon, D. (2007). A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa American Journal of Medical Genetics. Part A, 143A, 1150–1158. https://doi.org/10.1002/ajmg.a.31642
Bahadori, R., Biehlmaier, O., Zeitz, C., Labhart, T., Makhankov, Y. V., Forster, U., Gesemann, M., Berger, W., & Neuhauss, S. (2006). Nyctalopin is essential for synaptic transmission in the cone dominated zebrafish retina European Journal of Neuroscience, 24, 1664–1674. https://doi.org/10.1111/j.1460-9568.2006.05053.x
Biebinger, R., Arnold, M., Koss, M., Kloeckener-Gruissem, B., Langhans, W., Hurrell, R. F., & Zimmermann, M. B. (2006). Effect of concurrent vitamin A and iodine deficiencies on the thyroid-pituitary axis in rats Thyroid, 16, 961–965. https://doi.org/10.1089/thy.2006.16.961
Kurz, D. J., Kloeckener-Gruissem, B., Akhmedov, A., Eberli, F. R., Bühler, I., Berger, W., Bertel, O., & Lüscher, T. F. (2006). Degenerative aortic valve stenosis, but not coronary disease, is associated with shorter telomere length in the elderly Arteriosclerosis, Thrombosis, and Vascular Biology, 26, e114–e117. https://doi.org/10.1161/01.ATV.0000222961.24912.69
Neidhardt, J., Barthelmes, D., Farahmand, F., Fleischhauer, J. C., & Berger, W. (2006). Different amino acid substitutions at the same position in rhodopsin lead to distinct phenotypes Investigative Ophthalmology & Visual Science, 47, 1630–1635. https://doi.org/10.1167/iovs.05-1317
Imboden, M., Nicod, L., Nieters, A., Glaus, E., Matyas, G., Bircher, A. J., Ackermann-Liebrich, U., Berger, W., & Probst-Hensch, N. M. (2006). The common G-allele of interleukin-18 single-nucleotide polymorphism is a genetic risk factor for atopic asthma. The SAPALDIA Cohort Study Clinical and Experimental Allergy, 36, 211–218. https://doi.org/10.1111/j.1365-2222.2006.02424.x
Wycisk, K. A., Budde, B., Feil, S., et al, Buzzi, F., Neidhardt, J., Glaus, E., Nürnberg, P., & Berger, W. (2006). Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation Investigative Ophthalmology & Visual Science, 47, 3523–3530. https://doi.org/10.1167/iovs.06-0271
Zeitz, C., et al, & Berger, W. (2006). Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness American Journal of Human Genetics, 79, 657–667. https://doi.org/10.1086/508067
Bartholdi, D., Klein, A., Weissert, M., Koenig, N., Baumer, A., Boltshauser, E., Schinzel, A., Berger, W., & Mátyás, G. (2006). Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene Clinical Genetics, 69, 319–326. https://doi.org/10.1111/j.1399-0004.2006.00604.x
Baumgartner, C., Mátyás, G., Steinmann, B., Eberle, M., Stein, J. I., & Baumgartner, D. (2006). A bioinformatics framework for genotype-phenotype correlation in humans with Marfan syndrome caused by FBN1 gene mutations Journal of Biomedical Informatics, 39, 171–183. https://doi.org/10.1016/j.jbi.2005.06.001
Kloeckener-Gruissem, B., Bartholdi, D., Abdou, M. T., Zimmermann, D. R., & Berger, W. (2006). Identification of the genetic defect in the original Wagner syndrome family Molecular Vision, 350–355. http://www.molvis.org/molvis/v12/a39/
Matyas, G., Arnold, E., Carrel, T., Baumgartner, D., Boileau, C., Berger, W., & Steinmann, B. (2006). Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders Human Mutation, 27, 760–769. https://doi.org/10.1002/humu.20353
Wycisk, K. A., Zeitz, C., Feil, S., Wittmer, M., Forster, U., Neidhardt, J., Wissinger, B., Zrenner, E., Wilke, R., Kohl, S., & Berger, W. (2006). Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy American Journal of Human Genetics, 79, 973–977. https://doi.org/10.1086/508944
Baumgartner, D., Baumgartner, C., Schermer, E., Engl, G., Schweigmann, U., Matyas, G., Steinmann, B., & Stein, J. I. (2006). Different patterns of aortic wall elasticity in patients with Marfan syndrome: a noninvasive follow-up study Journal of Thoracic and Cardiovascular Surgery, 132, 811–819. https://doi.org/10.1016/j.jtcvs.2006.07.001
Imboden, M., Nieters, A., Bircher, A. J., Brutsche, M., Becker, N., Wjst, M., Ackermann-Liebrich, U., Berger, W., Probst-Hensch, N. M., & SAPALDIA Team. (2006). Cytokine gene polymorphisms and atopic disease in two European cohorts (ECRHS-Basel and SAPALDIA) Clinical and Molecular Allergy, 4, 9. https://doi.org/10.1186/1476-7961-4-9
Wollmann, G., et al, & Berger, W. (2006). Voltage-dependent ion channels in the mouse RPE: comparison with Norrie disease mice Vision Research, 46, 688–698. https://doi.org/10.1016/j.visres.2005.08.030
Hsieh, M., Boerboom, D., Shimada, M., Lo, Y., Parlow, A. F., Luhmann, U. F. O., Berger, W., & Richards, J. S. (2005). Mice Null for Frizzled4 (Fzd4−/−) Are Infertile and Exhibit Impaired Corpora Lutea Formation and Function1 Biology of Reproduction, 73, 1135–1146. https://doi.org/10.1095/biolreprod.105.042739
Zeitz, C., van Genderen, M., Neidhardt, J., Luhmann, U. F. O., Hoeben, F., Forster, U., Wycisk, K. A., Matyas, G., Hoyng, C. B., Riemslag, F., Meire, F., Cremers, F. P. M., & Berger, W. (2005). Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram Investigative Ophthalmology & Visual Science, 46, 4328–4335. https://doi.org/10.1167/iovs.05-0526
Luhmann, U. F. O., Lin, J., Acar, N., Lammel, S., Feil, S., Grimm, C., Seeliger, M. W., Hammes, H.-P., & Berger, W. (2005). Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature Investigative Ophthalmology & Visual Science, 46, 3372–3382. https://doi.org/10.1167/iovs.05-0174

Seitennummerierung

Disclaimer

This website has been archived and will not receive further updates. Accordingly, all content is provided “as is” and may be incorrect, incomplete, or outdated. We apologize for any inconvenience.

Diese Website wurde archiviert und wird nicht mehr aktualisiert. Sämtliche Inhalte werden ohne Gewähr und „wie besehen“ bereitgestellt und können unrichtig, unvollständig oder veraltet sein. Wir entschuldigen uns für etwaige Unannehmlichkeiten.

15/01/2026 ~BK

Quicklinks

Hauptnavigation