Thomas Bourgeron - Selected Publications#
February 2016 ISI Web of science
Results found: 157; Sum of the Times Cited: 8944; Citing Articles: 5967; Average Citations per Item: 56.97; h-index: 41
Toro R., Poline JB, Huguet G., Loth E, Frouin V, Banaschewski T., Barker GJ, Bokde A, Buchel C., Carvalho FM, Conrod P, FauthBuhler M., Flor H, Gallinat J, Garavan H, Gowland P., Heinz A, Ittermann B, Lawrence C, Lemaitre H, Mann K, Nees F, Paus T, Pausova Z, Rietschel M, Robbins T, Smolka MN, Strohle A, Schumann G, and Bourgeron T Genomic architecture of human neuroanatomical diversity Molecular Psychiatry (2014) doi: 10.103 (0 citation)
Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T. Meta-analysis of SHANK mutations in Autism Spectrum Disorders: A gradient of severity in cognitive impairments. PLOS Genetics. (2014) 10, e1004580. (1 citation)
Karayannis T, E. Au, J. Patel, I. Kruglikov, S. Mark, R. Delorme, D. Héron, J. Glessner, S. Restituito, A. Gordon, L. Rodriguez-Murillo, N.C. Roy, J. Gogos, B. Rudy, M.E. Rice, M. Karayiorgou, H. Hakonarson, B. Keren, G. Huguet, Bourgeron T, C. Hoeffer, R.W. Tsien, E. Peles, G. Fishell. Cntnap4 Differentially Contributes to GABAergic and Dopaminergic Synaptic Transmission Nature (2014) May 25. doi: 10.1038 (4 citations)
Delorme R, Ey E, Toro R, Leboyer M, Gillberg C, and Bourgeron T. Progress towards treatments for synaptic defects in autism. Nature Medicine (2013) 19:685-94. (38 citations)
Schmeisser MJ, Ey E, Kuebler A, Bockmann J, Wegener S, Stempel AV, Kuebler A, Janssen AL, Udvardi PT, Shiban E, Spilker C, Balschun D, Skryabin BV, tom Dieck S, Smalla KH, Montag D, Leblond CS, Faure P, Torquet N, Le Sourd AM, Toro R, Grabrucker AM, Shoichet SA, Schmitz D, Kreutz MR, Bourgeron T, Gundelfinger ED and Boeckers TM. (2012) Hyperactivity and autistic-like behaviours in mice lacking ProSAP1/Shank2. Nature (2012) 486 : 256-60. (83 citations)
Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, Klauck SM, Poustka F, Freitag CM, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira AF, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer SW, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren MC, Leboyer M, Gillberg C, Boeckers TM, Bourgeron T. Genetic and functional analyses of SHANK2 mutations provide evidence for a multiple hit model of autism spectrum disorders. PLoS Genetics (2012) 8(2):e1002521. (92 citations)
Pinto D, Pagnamenta A, Klei L Merico D, Anney R , Merico D, Regan R, Conroy J, Magalhaes T, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T et al. Functional impact of global rare copy number variation in autism Nature (2010) 466 : 368-72. (682 citations)
Melke J, Goubran-Botros H, Chaste P, Betancur C, Nygren G, AnckarsäterH, Rastam M, Ståhlberg O, Gillberg IC, Delorme R, Chabane N, Mouren-Simeoni MC, Fauchereau F, Durand CM, Chevalier F, Drouot X, Collet C, Launay JM, Leboyer M, Gillberg C, and Bourgeron T Abnormal Melatonin Synthesis in Autism Spectrum Disorders Molecular Psychiatry (2008) 13:90-98. (129 citations)
Durand C, Betancur C, Boeckers TM, Bockmann J, Chaste P, Fauchereau F, Nygren G, Rastam M, Gillberg IC, Anckarsäter H, Sponheim E, Goubran-Botros H, Delorme R, Chabane N, Mouren-Simeoni MC, de Mas P, Bieth E, Rogé B, Héron D, Burglen L, Gillberg C, Leboyer M, Bourgeron T Mutations of the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nature Genetics (2007) 39:25-7. (546 citations)
Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T and the Paris study. Mutations of the X-linked neuroligins NLGN3 and NLGN4 are associated with autism Nature Genetics (2003) 34, 27-29. (801 citations)
