ZFIN Person: Ernest, Sylvain

ZFIN ID: ZDB-PERS-980604-2

Ernest, Sylvain

Email:	sylvain.ernest@inserm.fr
URL:
Affiliation:	Groupe Danio
Address:	Embryology and Genetics of Malformations, Labo 408, bureau 402b2 INSERM UMR 1163, Institut Imagine, 24 Boulevard du Montparnasse, 75015 Paris, France.
Country:	France
Phone:	33-1-42-75-43-47
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Morel, G., Ernest, S., Serey-Gaut, M., Jonard, L., Balogoun, A.R., Parodi, M., Loundon, N., Achard, S., Marlin, S. (2023) RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models. Clinical genetics. 104(6):669-673

Bouasker, S., Patel, N., Greenlees, R., Wellesley, D., Fares Taie, L., Almontashiri, N.A., Baptista, J., Alghamdi, M.A., Boissel, S., Martinovic, J., Prokudin, I., Holden, S., Mudhar, H.S., Riley, L.G., Nassif, C., Attie-Bitach, T., Miguet, M., Delous, M., Ernest, S., Plaisancié, J., Calvas, P., Rozet, J.M., Khan, A.O., Hamdan, F.F., Jamieson, R.V., Alkuraya, F.S., Michaud, J.L., Chassaing, N. (2022) Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans. Journal of Medical Genetics. 60(3):294-300

Bonnet, A., Lambert, G., Ernest, S., Dutrieux, F.X., Coulpier, F., Lemoine, S., Lobbardi, R., Rosa, F.M. (2017) Quaking RNA-Binding Proteins Control Early Myofibril Formation by Modulating Tropomyosin. Developmental Cell. 42(5):527-541.e4

Ernest, S., Rosa, F.M. (2015) A genomic region encompassing a newly identified exon provides enhancing activity sufficient for normal myo7aa expression in zebrafish sensory hair cells. Developmental Neurobiology. 75(9):961-83

Boyer, B., Ernest, S., and Rosa, F. (2013) Egr-1 induction provides a genetic response to food aversion in zebrafish. Frontiers in behavioral neuroscience. 7:51

Kapsimali, M., Kaushik, A.L., Gibon, G., Dirian, L., Ernest, S., and Rosa, F.M. (2011) Fgf signaling controls pharyngeal taste bud formation through miR-200 and Delta-Notch activity. Development (Cambridge, England). 138(16):3473-3484

Khatib, A.M., Lahlil, R., Scamuffa, N., Akimenko, M.A., Ernest, S., Lomri, A., Lalou, C., Seidah, N.G., Villoutreix, B.O., Calvo, F., and Siegfried, G. (2010) Zebrafish ProVEGF-C Expression, Proteolytic Processing and Inhibitory Effect of Unprocessed ProVEGF-C during Fin Regeneration. PLoS One. 5(7):e11438

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

Ernest, S., Guadagnini, S., Prevost, M.C., and Soussi-Yanicostas, N. (2007) Localization of anosmin-1a and anosmin-1b in the inner ear and neuromasts of zebrafish. Gene expression patterns : GEP. 7(3):274-281

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

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

NON-ZEBRAFISH PUBLICATIONS