Qubit entanglement between ring-resonator photon-pair sources on a silicon chip

por Silverstone, J. W., Santagati, R., Bonneau, D., Strain, M. J., Sorel, M., O'Brien, J. L., Thompson, M. G.
Publicado 2015

Prognostic molecular markers with no impact on decision-making: the paradox of gliomas based on a prospective study

por Wager, M, Menei, P, Guilhot, J, Levillain, P, Michalak, S, Bataille, B, Blanc, J-L, Lapierre, F, Rigoard, P, Milin, S, Duthe, F, Bonneau, D, Larsen, C-J, Karayan-Tapon, L
Publicado 2008

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

por Mercati, O, Huguet, G, Danckaert, A, André-Leroux, G, Maruani, A, Bellinzoni, M, Rolland, T, Gouder, L, Mathieu, A, Buratti, J, Amsellem, F, Benabou, M, Van-Gils, J, Beggiato, A, Konyukh, M, Bourgeois, J-P, Gazzellone, M J, Yuen, R K C, Walker, S, Delépine, M, Boland, A, Régnault, B, Francois, M, Van Den Abbeele, T, Mosca-Boidron, A L, Faivre, L, Shimoda, Y, Watanabe, K, Bonneau, D, Rastam, M, Leboyer, M, Scherer, S W, Gillberg, C, Delorme, R, Cloëz-Tayarani, I, Bourgeron, T
Publicado 2017

Multi-system neurological disease is common in patients with OPA1 mutations

por Yu-Wai-Man, P., Griffiths, P.G., Gorman, G.S., Lourenco, C.M., Wright, A.F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M.L., Caporali, L., Lamperti, C., Tallaksen, C.M., Duffey, P., Miller, J., Whittaker, R.G., Baker, M.R., Jackson, M.J., Clarke, M.P., Dhillon, B., Czermin, B., Stewart, J.D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R.W., Turnbull, D.M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L.A., Horvath, R., Amati-Bonneau, P., Chinnery, P.F.
Publicado 2010