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772 results

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Page 1
Abnormal melatonin synthesis in autism spectrum disorders.
Melke J, Goubran Botros H, Chaste P, Betancur C, Nygren G, Anckarsäter H, 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, Bourgeron T. Melke J, et al. Among authors: gillberg c, gillberg ic. Mol Psychiatry. 2008 Jan;13(1):90-8. doi: 10.1038/sj.mp.4002016. Epub 2007 May 15. Mol Psychiatry. 2008. PMID: 17505466 Free PMC article.
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism.
Pilorge M, Fassier C, Le Corronc H, Potey A, Bai J, De Gois S, Delaby E, Assouline B, Guinchat V, Devillard F, Delorme R, Nygren G, Råstam M, Meier JC, Otani S, Cheval H, James VM, Topf M, Dear TN, Gillberg C, Leboyer M, Giros B, Gautron S, Hazan J, Harvey RJ, Legendre P, Betancur C. Pilorge M, et al. Among authors: gillberg c. Mol Psychiatry. 2016 Jul;21(7):936-45. doi: 10.1038/mp.2015.139. Epub 2015 Sep 15. Mol Psychiatry. 2016. PMID: 26370147 Free PMC article.
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
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 JP, Gazzellone MJ, Yuen RK, Walker S, Delépine M, Boland A, Régnault B, Francois M, Van Den Abbeele T, Mosca-Boidron AL, Faivre L, Shimoda Y, Watanabe K, Bonneau D, Rastam M, Leboyer M, Scherer SW, Gillberg C, Delorme R, Cloëz-Tayarani I, Bourgeron T. Mercati O, et al. Among authors: gillberg c. Mol Psychiatry. 2017 Apr;22(4):625-633. doi: 10.1038/mp.2016.61. Epub 2016 May 10. Mol Psychiatry. 2017. PMID: 27166760 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: gillberg c. 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: gillberg c. Mol Psychiatry. 2002;7(3):302-10. doi: 10.1038/sj.mp.4000979. Mol Psychiatry. 2002. PMID: 11920157 Free PMC article.
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: gillberg c. 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.
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE.
Nava C, Lamari F, Héron D, Mignot C, Rastetter A, Keren B, Cohen D, Faudet A, Bouteiller D, Gilleron M, Jacquette A, Whalen S, Afenjar A, Périsse D, Laurent C, Dupuits C, Gautier C, Gérard M, Huguet G, Caillet S, Leheup B, Leboyer M, Gillberg C, Delorme R, Bourgeron T, Brice A, Depienne C. Nava C, et al. Among authors: gillberg c. Transl Psychiatry. 2012 Oct 23;2(10):e179. doi: 10.1038/tp.2012.102. Transl Psychiatry. 2012. PMID: 23092983 Free PMC article.
Hypothyroidism and autism spectrum disorders.
Gillberg IC, Gillberg C, Kopp S. Gillberg IC, et al. Among authors: gillberg c. J Child Psychol Psychiatry. 1992 Mar;33(3):531-42. doi: 10.1111/j.1469-7610.1992.tb00889.x. J Child Psychol Psychiatry. 1992. PMID: 1577897
772 results