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Results: 1 to 20 of 33

1.

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. 2014 Sep 30. pii: S0006-3223(14)00716-1. doi: 10.1016/j.biopsych.2014.09.017. [Epub ahead of print]

PMID:
25534755
[PubMed - as supplied by publisher]
2.

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.

PMID:
25010486
[PubMed - in process]
3.

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.

PMID:
24821083
[PubMed - in process]
4.

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.

PMID:
24768552
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

PMID:
24748103
[PubMed - in process]
Free PMC Article
6.

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.

PMID:
23746936
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

[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.

PMID:
23541918
[PubMed - indexed for MEDLINE]
8.

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

Chaste P, Leboyer M.

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

PMID:
23226953
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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.

PMID:
23067556
[PubMed]
Free PMC Article
10.

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.

PMID:
22760338
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
22738402
[PubMed]
Free PMC Article
12.

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.

PMID:
22346768
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
21615493
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
21394203
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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.

PMID:
20967277
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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.

PMID:
20695031
[PubMed - indexed for MEDLINE]
17.

Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population.

Chaste P, Clement N, Mercati O, Guillaume JL, Delorme R, Botros HG, Pagan C, Périvier S, Scheid I, Nygren G, Anckarsäter H, Rastam M, Ståhlberg O, Gillberg C, Serrano E, Lemière N, Launay JM, Mouren-Simeoni MC, Leboyer M, Gillberg C, Jockers R, Bourgeron T.

PLoS One. 2010 Jul 15;5(7):e11495. doi: 10.1371/journal.pone.0011495.

PMID:
20657642
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Key role for gene dosage and synaptic homeostasis in autism spectrum disorders.

Toro R, Konyukh M, Delorme R, Leblond C, Chaste P, Fauchereau F, Coleman M, Leboyer M, Gillberg C, Bourgeron T.

Trends Genet. 2010 Aug;26(8):363-72. doi: 10.1016/j.tig.2010.05.007. Epub 2010 Jul 6. Review.

PMID:
20609491
[PubMed - indexed for MEDLINE]
19.

Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.

Delorme R, Betancur C, Scheid I, Anckarsäter H, Chaste P, Jamain S, Schuroff F, Nygren G, Herbrecht E, Dumaine A, Mouren MC, Råstam M, Leboyer M, Gillberg C, Bourgeron T.

BMC Med Genet. 2010 Jul 5;11:108. doi: 10.1186/1471-2350-11-108.

PMID:
20602773
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.

Delorme R, Moreno-De-Luca D, Gennetier A, Maier W, Chaste P, Mössner R, Grabe HJ, Ruhrmann S, Falkai P, Mouren MC, Leboyer M, Wagner M, Betancur C.

BMC Med Genet. 2010 Jun 21;11:100. doi: 10.1186/1471-2350-11-100.

PMID:
20565924
[PubMed - indexed for MEDLINE]
Free PMC Article

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