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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Durand CM, 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. Durand CM, et al. Among authors: bourgeron t. Nat Genet. 2007 Jan;39(1):25-7. doi: 10.1038/ng1933. Epub 2006 Dec 17. Nat Genet. 2007. PMID: 17173049 Free PMC article.
Y chromosome haplogroups in autistic subjects.
Jamain S, Quach H, Quintana-Murci L, Betancur C, Philippe A, Gillberg C, Sponheim E, Skjeldal OH, Fellous M, Leboyer M, Bourgeron T. Jamain S, et al. Among authors: bourgeron t. Mol Psychiatry. 2002;7(2):217-9. doi: 10.1038/sj.mp.4000968. Mol Psychiatry. 2002. PMID: 11840316 Free PMC article.
Linkage and association of the glutamate receptor 6 gene with autism.
Jamain S, Betancur C, Quach H, Philippe A, Fellous M, Giros B, Gillberg C, Leboyer M, Bourgeron T; Paris Autism Research International Sibpair (PARIS) Study. Jamain S, et al. Among authors: bourgeron t. Mol Psychiatry. 2002;7(3):302-10. doi: 10.1038/sj.mp.4000979. Mol Psychiatry. 2002. PMID: 11920157 Free PMC article.
[Genetics of autism: from genome scans to candidate genes].
Jamain S, Betancur C, Giros B, Leboyer M, Bourgeron T. Jamain S, et al. Among authors: bourgeron t. Med Sci (Paris). 2003 Nov;19(11):1081-90. doi: 10.1051/medsci/200319111081. Med Sci (Paris). 2003. PMID: 14648479 Free article. Review. French.
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.
Delorme R, Betancur C, Wagner M, Krebs MO, Gorwood P, Pearl P, Nygren G, Durand CM, Buhtz F, Pickering P, Melke J, Ruhrmann S, Anckarsäter H, Chabane N, Kipman A, Reck C, Millet B, Roy I, Mouren-Simeoni MC, Maier W, Råstam M, Gillberg C, Leboyer M, Bourgeron T. Delorme R, et al. Among authors: bourgeron t. Mol Psychiatry. 2005 Dec;10(12):1059-61. doi: 10.1038/sj.mp.4001728. Mol Psychiatry. 2005. PMID: 16088327 Free PMC article. Clinical Trial. No abstract available.
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.
Durand CM, Kappeler C, Betancur C, Delorme R, Quach H, Goubran-Botros H, Melke J, Nygren G, Chabane N, Bellivier F, Szoke A, Schurhoff F, Rastam M, Anckarsäter H, Gillberg C, Leboyer M, Bourgeron T. Durand CM, et al. Among authors: bourgeron t. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):67-70. doi: 10.1002/ajmg.b.30229. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16331680 Free PMC article.
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.
Delorme R, Durand CM, Betancur C, Wagner M, Ruhrmann S, Grabe HJ, Nygren G, Gillberg C, Leboyer M, Bourgeron T, Courtet P, Jollant F, Buresi C, Aubry JM, Baud P, Bondolfi G, Bertschy G, Perroud N, Malafosse A. Delorme R, et al. Among authors: bourgeron t. Biol Psychiatry. 2006 Jul 15;60(2):202-3. doi: 10.1016/j.biopsych.2005.12.014. Epub 2006 Apr 11. Biol Psychiatry. 2006. PMID: 16581035
246 results