Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

246 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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.
Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia.
Bah J, Quach H, Ebstein RP, Segman RH, Melke J, Jamain S, Rietschel M, Modai I, Kanas K, Karni O, Lerer B, Gourion D, Krebs MO, Etain B, Schürhoff F, Szöke A, Leboyer M, Bourgeron T. Bah J, et al. Among authors: bourgeron t. Neuroreport. 2004 Aug 26;15(12):1987-91. doi: 10.1097/00001756-200408260-00031. Neuroreport. 2004. PMID: 15305151
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