ZFIN ID: ZDB-PERS-070723-2
Schorderet, Daniel
Email: daniel.schorderet@irovision.ch
Affiliation: Institut de Recherche en Ophtalmologie (IRO)
Address: 64, Av. du Gd-Champsec Case Postale 4168 Sion 4, CH-1950 Switzerland
Country: Switzerland


El Fersioui, Y., Pinton, G., Allaman-Pillet, N., Schorderet, D.F. (2021) Hmx1 regulates urfh1 expression in the craniofacial region in zebrafish. PLoS One. 16:e0245239
Aleström, P., D'Angelo, L., Midtlyng, P.J., Schorderet, D.F., Schulte-Merker, S., Sohm, F., Warner, S. (2019) Zebrafish: Housing and husbandry recommendations. Laboratory animals. 54(3):213-224
Crippa, S., Nemir, M., Ounzain, S., Ibberson, M., Berthonneche, C., Sarre, A., Boisset, G., Maison, D., Harshman, K., Xenarios, I., Diviani, D., Schorderet, D., Pedrazzini, T. (2016) Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways. Cardiovascular research. 110(1):73-84
Marcelli, F., Boisset, G., Schorderet, D.F. (2014) A Dimerized HMX1 Inhibits EPHA6/epha4b in Mouse and Zebrafish Retinas. PLoS One. 9:e100096
Page, L., Polok, B., Bustamante, M., and Schorderet, D.F. (2013) Bigh3 Is Upregulated in Regenerating Zebrafish Fin. Zebrafish. 10(1):36-42
Boisset, G., and Schorderet, D.F. (2012) Zebrafish hmx1 promotes retinogenesis. Experimental Eye Research. 105:34-42
Slavotinek, A.M., Chao, R., Vacik, T., Yahyavi, M., Vacik, T., Abouzeid, H., Bardakjian, T., Schneider, A., Shaw, G., Sherr, E.H., Lemke, G., Youssef, M., and Schorderet, D.F. (2012) VAX1 mutation associated with microphthalmia, corpus callosum agenesis and orofacial clefting-the first description of a VAX1 phenotype in humans. Human Mutation. 33(2):364-368
Abouzeid, H., Boisset, G., Favez, T., Youssef, M., Marzouk, I., Shakankiry, N., Bayoumi, N., Descombes, P., Agosti, C., Munier, F.L., and Schorderet, D.F. (2011) Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome. American journal of human genetics. 88(1):92-98
Polok, B., Escher, P., Ambresin, A., Chouery, E., Bolay, S., Meunier, I., Nan, F., Hamel, C., Munier, F.L., Thilo, B., Mégarbané, A., and Schorderet, D.F. (2009) Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta. American journal of human genetics. 84(2):259-265
Boisset, G., Polok, B.K., and Schorderet, D.F. (2008) Characterization of pip5k3 fleck corneal dystrophy-linked gene in zebrafish. Gene expression patterns : GEP. 8(6):404-410
Schorderet, D.F., Nichini, O., Boisset, G., Polok, B., Tiab, L., Mayeur, H., Raji, B., de la Houssaye, G., Abitbol, M.M., and Munier, F.L. (2008) Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome. American journal of human genetics. 82(5):1178-1184