Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 37


Telepsychiatry for Children and Adolescents: A Review of the PROMETTED Project.

Doyen CM, Oreve MJ, Desailly E, Goupil V, Zarca K, L'Hermitte Y, Chaste P, Bau MO, Beaujard D, Haddadi S, Bibay A, Contejean Y, Coutrot MT, Crespin L, Frioux I, Speranza M, Francois N, Kaye K.

Telemed J E Health. 2018 Jan;24(1):3-10. doi: 10.1089/tmj.2017.0041. Epub 2017 Dec 11.


Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.

Pagan C, Goubran-Botros H, Delorme R, Benabou M, Lemière N, Murray K, Amsellem F, Callebert J, Chaste P, Jamain S, Fauchereau F, Huguet G, Maronde E, Leboyer M, Launay JM, Bourgeron T.

Sci Rep. 2017 May 18;7(1):2096. doi: 10.1038/s41598-017-02152-x.


The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability.

Chaste P, Roeder K, Devlin B.

Annu Rev Genomics Hum Genet. 2017 Aug 31;18:167-187. doi: 10.1146/annurev-genom-083115-022647. Epub 2017 Apr 19. Review.


Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.

Addis L, Ahn JW, Dobson R, Dixit A, Ogilvie CM, Pinto D, Vaags AK, Coon H, Chaste P, Wilson S, Parr JR, Andrieux J, Lenne B, Tumer Z, Leuzzi V, Aubell K, Koillinen H, Curran S, Marshall CR, Scherer SW, Strug LJ, Collier DA, Pal DK.

Hum Mutat. 2015 Sep;36(9):842-50. doi: 10.1002/humu.22816. Epub 2015 Jun 30.


A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?

Chaste P, Klei L, Sanders SJ, Hus V, Murtha MT, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Mane SM, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, Lese Martin C, Beaudet AL, Lord C, State MW, Cook EH Jr, Devlin B.

Biol Psychiatry. 2015 May 1;77(9):775-84. doi: 10.1016/j.biopsych.2014.09.017. Epub 2014 Sep 30.


Feelings of regret and disappointment in adults with high-functioning autism.

Zalla T, Sirigu A, Robic S, Chaste P, Leboyer M, Coricelli G.

Cortex. 2014 Sep;58:112-22. doi: 10.1016/j.cortex.2014.05.008. Epub 2014 Jun 9.


Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

Chaste P, Sanders SJ, Mohan KN, Klei L, Song Y, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Martin CL, Devlin B, Beaudet AL, Cook EH Jr, Kim SJ.

Autism Res. 2014 Jun;7(3):355-62. doi: 10.1002/aur.1378. Epub 2014 May 12.


Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.

Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, Conceição IC, Chiocchetti AG, Casey JP, Cai G, Cabrol C, Bolshakova N, Bacchelli E, Anney R, Gallinger S, Cotterchio M, Casey G, Zwaigenbaum L, Wittemeyer K, Wing K, Wallace S, van Engeland H, Tryfon A, Thomson S, Soorya L, Rogé B, Roberts W, Poustka F, Mouga S, Minshew N, McInnes LA, McGrew SG, Lord C, Leboyer M, Le Couteur AS, Kolevzon A, Jiménez González P, Jacob S, Holt R, Guter S, Green J, Green A, Gillberg C, Fernandez BA, Duque F, Delorme R, Dawson G, Chaste P, Café C, Brennan S, Bourgeron T, Bolton PF, Bölte S, Bernier R, Baird G, Bailey AJ, Anagnostou E, Almeida J, Wijsman EM, Vieland VJ, Vicente AM, Schellenberg GD, Pericak-Vance M, Paterson AD, Parr JR, Oliveira G, Nurnberger JI, Monaco AP, Maestrini E, Klauck SM, Hakonarson H, Haines JL, Geschwind DH, Freitag CM, Folstein SE, Ennis S, Coon H, Battaglia A, Szatmari P, Sutcliffe JS, Hallmayer J, Gill M, Cook EH, Buxbaum JD, Devlin B, Gallagher L, Betancur C, Scherer SW.

Am J Hum Genet. 2014 May 1;94(5):677-94. doi: 10.1016/j.ajhg.2014.03.018. Epub 2014 Apr 24.


Individuals with autism spectrum disorders do not use social stereotypes in irony comprehension.

Zalla T, Amsellem F, Chaste P, Ervas F, Leboyer M, Champagne-Lavau M.

PLoS One. 2014 Apr 18;9(4):e95568. doi: 10.1371/journal.pone.0095568. eCollection 2014.


Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.

Chaste P, Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Lese Martin C, Martin DM, Morrow EM, Walsh CA, Sutcliffe JS, State MW, Devlin B, Cook EH Jr, Kim SJ.

Biol Psychiatry. 2013 Oct 15;74(8):576-84. doi: 10.1016/j.biopsych.2013.04.018. Epub 2013 Jun 6.


[Anorexia nervosa in the light of neurocognitive functioning: New theoretical and therapeutic perspectives].

Martinez G, Cook-Darzens S, Chaste P, Mouren MC, Doyen C.

Encephale. 2014 Apr;40(2):160-7. doi: 10.1016/j.encep.2012.06.004. Epub 2013 Mar 28. Review. French.


Autism risk factors: genes, environment, and gene-environment interactions.

Chaste P, Leboyer M.

Dialogues Clin Neurosci. 2012 Sep;14(3):281-92. Review.


Common genetic variants, acting additively, are a major source of risk for autism.

Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin CL, Martin DM, Morrow EM, Walsh CA, Melhem NM, Chaste P, Sutcliffe JS, State MW, Cook EH Jr, Roeder K, Devlin B.

Mol Autism. 2012 Oct 15;3(1):9. doi: 10.1186/2040-2392-3-9.


The role of causal and intentional judgments in moral reasoning in individuals with high functioning autism.

Buon M, Dupoux E, Jacob P, Chaste P, Leboyer M, Zalla T.

J Autism Dev Disord. 2013 Feb;43(2):458-70. doi: 10.1007/s10803-012-1588-7.


High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.

Chaste P, Betancur C, Gérard-Blanluet M, Bargiacchi A, Kuzbari S, Drunat S, Leboyer M, Bourgeron T, Delorme R.

Mol Autism. 2012 Jun 27;3(1):5. doi: 10.1186/2040-2392-3-5.


Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

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.

PLoS Genet. 2012 Feb;8(2):e1002521. doi: 10.1371/journal.pgen.1002521. Epub 2012 Feb 9.


Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.

Chaste P, Clement N, Botros HG, Guillaume JL, Konyukh M, Pagan C, Scheid I, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Gillberg IC, Melke J, Delorme R, Leblond C, Toro R, Huguet G, Fauchereau F, Durand C, Boudarene L, Serrano E, Lemière N, Launay JM, Leboyer M, Jockers R, Gillberg C, Bourgeron T.

J Pineal Res. 2011 Nov;51(4):394-9. doi: 10.1111/j.1600-079X.2011.00902.x. Epub 2011 May 26.


Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.

Konyukh M, Delorme R, Chaste P, Leblond C, Lemière N, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Amsellem F, Gillberg IC, Mouren-Simeoni MC, Herbrecht E, Fauchereau F, Toro R, Gillberg C, Leboyer M, Bourgeron T.

PLoS One. 2011 Mar 4;6(3):e17289. doi: 10.1371/journal.pone.0017289.


Memory for self-performed actions in individuals with Asperger syndrome.

Zalla T, Daprati E, Sav AM, Chaste P, Nico D, Leboyer M.

PLoS One. 2010 Oct 12;5(10):e13370. doi: 10.1371/journal.pone.0013370.


Using videotaped vignettes to improve the teaching quality in child and adolescent psychiatry.

Delorme R, Chaste P, Scheid I, Cortese S, Mouren MC.

Med Teach. 2010;32(8):703-4. No abstract available.


Supplemental Content

Loading ...
Support Center