ZFIN Person: Boisset, Gaëlle

ZFIN ID: ZDB-PERS-070723-3

Boisset, Gaëlle

Email:	gaelle.boisset@irovision.ch
URL:
Affiliation:
Address:	64, Av. du Gd-Champsec Case Postale 4168 Sion 4, CH-1950 Switzerland
Country:
Phone:
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

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

Boisset, G., and Schorderet, D.F. (2012) Zebrafish hmx1 promotes retinogenesis. Experimental Eye Research. 105:34-42

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

Boisset, G. (2009) The zebrafish as an animal model in ophthalmic diseases : Fleck corneal dystrophy and Schorderet-Munier syndrome. Thesis. :137p

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

NON-ZEBRAFISH PUBLICATIONS