ZFIN Person: Petit, Christine

ZFIN ID: ZDB-PERS-011219-1

Petit, Christine

Email:	cpetit@pasteur.fr
URL:
Affiliation:
Address:	Unité de Génétique des Déficits Sensoriels CNRS URA 1968 Institut Pasteur 25 rue du Dr Roux Paris , F-75724 France
Country:
Phone:	33-1-45-68-88-91
Fax:	33-1-45-67-69-78
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

1. Development and physiology of the acoustico-lateralis system.
2. Human hereditary deafness.

PUBLICATIONS

Delmaghani, S., Aghaie, A., Bouyacoub, Y., El Hachmi, H., Bonnet, C., Riahi, Z., Chardenoux, S., Perfettini, I., Hardelin, J.P., Houmeida, A., Herbomel, P., Petit, C. (2016) Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. American journal of human genetics. 98:1266-1270

Zhao, Y., Zhao, F., Zong, L., Zhang, P., Guan, L., Zhang, J., Wang, D., Wang, J., Chai, W., Lan, L., Li, Q., Han, B., Yang, L., Jin, X., Yang, W., Hu, X., Wang, X., Li, N., Li, Y., Petit, C., Wang, J., Wang, H.Y., and Wang, Q. (2013) Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss. PLoS One. 8(7):e69549

Yanicostas, C., Ernest, S., Dayraud, C., Petit, C., and Soussi-Yanicostas, N. (2008) Essential requirement for zebrafish anosmin-1a in the migration of the posterior lateral line primordium. Developmental Biology. 320(2):469-479

Coimbra, R.S., Weil, D., Brottier, P., Blanchard, S., Levi, M., Hardelin, J.-P., Weissenbach, J., and Petit, C. (2002) A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear. Genome research. 12(6):1007-1011

Ernest, S., Rauch, G.J., Haffter, P., Geisler, R., Petit, C., and Nicolson, T. (2000) Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Human molecular genetics. 9(14):2189-2196

Ardouin, O., Legouis, R., Fasano, L., David-Watine, B., Korn, H., Hardelin, J.P., and Petit, C. (2000) Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndrome. Mechanisms of Development. 90(1):89-94

Nicolson, T., Ernest, S., Rauch, J., Petit, C., Söllner, C., Seiler, C., and Busch, E. (2000) Isolation of the genes responsible for hearing disorders in zebrafish. The European journal of neuroscience. 12:316

Sahly, I., Andermann, P., and Petit, C. (1999) The zebrafish eya1 gene and its expression pattern during embryogenesis. Development genes and evolution. 209(7):399-410

NON-ZEBRAFISH PUBLICATIONS