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Items: 22

1.

Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome.

Tabet AC, Rolland T, Ducloy M, Lévy J, Buratti J, Mathieu A, Haye D, Perrin L, Dupont C, Passemard S, Capri Y, Verloes A, Drunat S, Keren B, Mignot C, Marey I, Jacquette A, Whalen S, Pipiras E, Benzacken B, Chantot-Bastaraud S, Afenjar A, Héron D, Le Caignec C, Beneteau C, Pichon O, Isidor B, David A, El Khattabi L, Kemeny S, Gouas L, Vago P, Mosca-Boidron AL, Faivre L, Missirian C, Philip N, Sanlaville D, Edery P, Satre V, Coutton C, Devillard F, Dieterich K, Vuillaume ML, Rooryck C, Lacombe D, Pinson L, Gatinois V, Puechberty J, Chiesa J, Lespinasse J, Dubourg C, Quelin C, Fradin M, Journel H, Toutain A, Martin D, Benmansour A, Leblond CS, Toro R, Amsellem F, Delorme R, Bourgeron T.

NPJ Genom Med. 2019 Jul 1;4:16. doi: 10.1038/s41525-019-0090-y. eCollection 2019.

2.

Morning Plasma Melatonin Differences in Autism: Beyond the Impact of Pineal Gland Volume.

Maruani A, Dumas G, Beggiato A, Traut N, Peyre H, Cohen-Freoua A, Amsellem F, Elmaleh M, Germanaud D, Launay JM, Bourgeron T, Toro R, Delorme R.

Front Psychiatry. 2019 Feb 6;10:11. doi: 10.3389/fpsyt.2019.00011. eCollection 2019.

3.

Synesthesia & autistic features in a large family: Evidence for spatial imagery as a common factor.

Bouvet L, Amsellem F, Maruani A, Tonus-Vic Dupont A, Mathieu A, Bourgeron T, Delorme R, Mottron L.

Behav Brain Res. 2019 Apr 19;362:266-272. doi: 10.1016/j.bbr.2019.01.014. Epub 2019 Jan 9.

PMID:
30639511
4.

Author Correction: Distinct effects of social motivation on face evaluations in adolescents with and without autism.

Safra L, Ioannou C, Amsellem F, Delorme R, Chevallier C.

Sci Rep. 2018 Dec 21;8(1):18077. doi: 10.1038/s41598-018-37593-5.

5.

Alpha Waves as a Neuromarker of Autism Spectrum Disorder: The Challenge of Reproducibility and Heterogeneity.

Lefebvre A, Delorme R, Delanoë C, Amsellem F, Beggiato A, Germanaud D, Bourgeron T, Toro R, Dumas G.

Front Neurosci. 2018 Oct 1;12:662. doi: 10.3389/fnins.2018.00662. eCollection 2018.

6.

Increased risk of ADHD in families with ASD.

Septier M, Peyre H, Amsellem F, Beggiato A, Maruani A, Poumeyreau M, Amestoy A, Scheid I, Gaman A, Bolognani F, Honey G, Bouquet C, Ly-Le Moal M, Bouvard M, Leboyer M, Bourgeron T, Delorme R.

Eur Child Adolesc Psychiatry. 2019 Feb;28(2):281-288. doi: 10.1007/s00787-018-1206-0. Epub 2018 Sep 28.

PMID:
30267210
7.

Distinct effects of social motivation on face evaluations in adolescents with and without autism.

Safra L, Ioannou C, Amsellem F, Delorme R, Chevallier C.

Sci Rep. 2018 Jul 13;8(1):10648. doi: 10.1038/s41598-018-28514-7. Erratum in: Sci Rep. 2018 Dec 21;8(1):18077.

8.

A framework to identify contributing genes in patients with Phelan-McDermid syndrome.

Tabet AC, Rolland T, Ducloy M, Lévy J, Buratti J, Mathieu A, Haye D, Perrin L, Dupont C, Passemard S, Capri Y, Verloes A, Drunat S, Keren B, Mignot C, Marey I, Jacquette A, Whalen S, Pipiras E, Benzacken B, Chantot-Bastaraud S, Afenjar A, Héron D, Le Caignec C, Beneteau C, Pichon O, Isidor B, David A, El Khattabi L, Kemeny S, Gouas L, Vago P, Mosca-Boidron AL, Faivre L, Missirian C, Philip N, Sanlaville D, Edery P, Satre V, Coutton C, Devillard F, Dieterich K, Vuillaume ML, Rooryck C, Lacombe D, Pinson L, Gatinois V, Puechberty J, Chiesa J, Lespinasse J, Dubourg C, Quelin C, Fradin M, Journel H, Toutain A, Martin D, Benmansour A, Leblond CS, Toro R, Amsellem F, Delorme R, Bourgeron T.

NPJ Genom Med. 2017 Oct 23;2:32. doi: 10.1038/s41525-017-0035-2. eCollection 2017. Erratum in: NPJ Genom Med. 2019 Jul 1;4:16.

9.

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.

10.

Shared mechanism for emotion processing in adolescents with and without autism.

Ioannou C, Zein ME, Wyart V, Scheid I, Amsellem F, Delorme R, Chevallier C, Grèzes J.

Sci Rep. 2017 Feb 20;7:42696. doi: 10.1038/srep42696.

11.

Gender differences in autism spectrum disorders: Divergence among specific core symptoms.

Beggiato A, Peyre H, Maruani A, Scheid I, Rastam M, Amsellem F, Gillberg CI, Leboyer M, Bourgeron T, Gillberg C, Delorme R.

Autism Res. 2017 Apr;10(4):680-689. doi: 10.1002/aur.1715. Epub 2016 Nov 3.

PMID:
27809408
12.

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.

Mol Psychiatry. 2017 Apr;22(4):625-633. doi: 10.1038/mp.2016.61. Epub 2016 May 10.

13.

Gaze direction detection in autism spectrum disorder.

Forgeot d'Arc B, Delorme R, Zalla T, Lefebvre A, Amsellem F, Moukawane S, Letellier L, Leboyer M, Mouren MC, Ramus F.

Autism. 2017 Jan;21(1):100-107. Epub 2016 Apr 30.

PMID:
27132008
14.

[Early detection of autism spectrum disorders: emerging symptoms and biomarkers].

Goussé V, Amsellem F, Delorme R.

Bull Acad Natl Med. 2016 Mar;200(3):415-22. Review. French.

PMID:
28627160
15.

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

Maruani A, Huguet G, Beggiato A, ElMaleh M, Toro R, Leblond CS, Mathieu A, Amsellem F, Lemière N, Verloes A, Leboyer M, Gillberg C, Bourgeron T, Delorme R.

Am J Med Genet A. 2015 Dec;167A(12):3019-30. doi: 10.1002/ajmg.a.37345. Epub 2015 Sep 3.

16.

The serotonin-N-acetylserotonin-melatonin pathway as a biomarker for autism spectrum disorders.

Pagan C, Delorme R, Callebert J, Goubran-Botros H, Amsellem F, Drouot X, Boudebesse C, Le Dudal K, Ngo-Nguyen N, Laouamri H, Gillberg C, Leboyer M, Bourgeron T, Launay JM.

Transl Psychiatry. 2014 Nov 11;4:e479. doi: 10.1038/tp.2014.120.

17.

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.

Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T.

PLoS Genet. 2014 Sep 4;10(9):e1004580. doi: 10.1371/journal.pgen.1004580. eCollection 2014 Sep.

18.

Atypical Social Judgment and Sensitivity to Perceptual Cues in Autism Spectrum Disorders.

Forgeot d'Arc B, Ramus F, Lefebvre A, Brottier D, Zalla T, Moukawane S, Amsellem F, Letellier L, Peyre H, Mouren MC, Leboyer M, Delorme R.

J Autism Dev Disord. 2016 May;46(5):1574-81. doi: 10.1007/s10803-014-2208-5.

PMID:
25149177
19.

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.

20.

Heterozygous FA2H mutations in autism spectrum disorders.

Scheid I, Maruani A, Huguet G, Leblond CS, Nygren G, Anckarsäter H, Beggiato A, Rastam M, Amsellem F, Gillberg IC, Elmaleh M, Leboyer M, Gillberg C, Betancur C, Coleman M, Hama H, Cook EH, Bourgeron T, Delorme R.

BMC Med Genet. 2013 Dec 3;14:124. doi: 10.1186/1471-2350-14-124.

21.

Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.

Tabet AC, Pilorge M, Delorme R, Amsellem F, Pinard JM, Leboyer M, Verloes A, Benzacken B, Betancur C.

Eur J Hum Genet. 2012 May;20(5):540-6. doi: 10.1038/ejhg.2011.244. Epub 2012 Jan 11. Erratum in: Eur J Hum Genet. 2012 May;20(5):594.

22.

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.

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