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Results: 1 to 20 of 91

1.

Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission.

Karayannis T, Au E, Patel C, Kruglikov I, Markx S, Delorme R, Héron D, Salomon D, Glessner J, Restituito S, Gordon A, Rodriguez-Murillo L, Roy NC, Gogos JA, Rudy B, Rice ME, Karayiorgou M, Hakonarson H, Keren B, Huguet G, Bourgeron T, Hoeffer C, Tsien RW, Peles E, Fishell G.

Nature. 2014 Jul 10;511(7508):236-40.

PMID:
24870235
[PubMed - in process]
2.

Attention-deficit/hyperactivity disorder symptom expression: a comparison of individual age at onset using item response theory.

Peyre H, Hoertel N, Cortese S, Acquaviva E, De Maricourt P, Limosin F, Delorme R.

J Clin Psychiatry. 2014 Apr;75(4):386-92. doi: 10.4088/JCP.13m08638.

PMID:
24813406
[PubMed - indexed for MEDLINE]
3.

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 Article
4.

Adulthood self-reported cardiovascular risk and ADHD medications: results from the 2004-2005 National Epidemiologic Survey on Alcohol and Related Conditions.

Peyre H, Hoertel N, Hatteea H, Limosin F, Dubuc C, Delorme R.

J Clin Psychiatry. 2014 Feb;75(2):181-2. doi: 10.4088/JCP.13l08736. No abstract available.

PMID:
24602253
[PubMed - indexed for MEDLINE]
5.

Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders.

Huguet G, Nava C, Lemière N, Patin E, Laval G, Ey E, Brice A, Leboyer M, Szepetowski P, Gillberg C, Depienne C, Delorme R, Bourgeron T.

PLoS One. 2014 Mar 3;9(3):e88600. doi: 10.1371/journal.pone.0088600. eCollection 2014.

PMID:
24594579
[PubMed - in process]
Free PMC Article
6.

Long-term effects of ADHD medication on adult height: results from the NESARC.

Peyre H, Hoertel N, Cortese S, Acquaviva E, Limosin F, Delorme R.

J Clin Psychiatry. 2013 Nov;74(11):1123-4. doi: 10.4088/JCP.13l08580. No abstract available.

PMID:
24330902
[PubMed - indexed for MEDLINE]
7.

[Cardiovascular risks and management during Attention Deficit Hyperactivity Disorder treatment with methylphenidate].

Bange F, Le Heuzey MF, Acquaviva E, Delorme R, Mouren MC.

Arch Pediatr. 2014 Jan;21(1):108-12. doi: 10.1016/j.arcped.2013.11.001. Epub 2013 Dec 3. French.

PMID:
24309201
[PubMed - in process]
8.

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.

PMID:
24299421
[PubMed - indexed for MEDLINE]
Free Article
9.

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.

Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, Bloch MH, Blom RM, Bruun RD, Budman CL, Camarena B, Campbell D, Cappi C, Cardona Silgado JC, Cath DC, Cavallini MC, Chavira DA, Chouinard S, Conti DV, Cook EH, Coric V, Cullen BA, Deforce D, Delorme R, Dion Y, Edlund CK, Egberts K, Falkai P, Fernandez TV, Gallagher PJ, Garrido H, Geller D, Girard SL, Grabe HJ, Grados MA, Greenberg BD, Gross-Tsur V, Haddad S, Heiman GA, Hemmings SM, Hounie AG, Illmann C, Jankovic J, Jenike MA, Kennedy JL, King RA, Kremeyer B, Kurlan R, Lanzagorta N, Leboyer M, Leckman JF, Lennertz L, Liu C, Lochner C, Lowe TL, Macciardi F, McCracken JT, McGrath LM, Mesa Restrepo SC, Moessner R, Morgan J, Muller H, Murphy DL, Naarden AL, Ochoa WC, Ophoff RA, Osiecki L, Pakstis AJ, Pato MT, Pato CN, Piacentini J, Pittenger C, Pollak Y, Rauch SL, Renner TJ, Reus VI, Richter MA, Riddle MA, Robertson MM, Romero R, Rosàrio MC, Rosenberg D, Rouleau GA, Ruhrmann S, Ruiz-Linares A, Sampaio AS, Samuels J, Sandor P, Sheppard B, Singer HS, Smit JH, Stein DJ, Strengman E, Tischfield JA, Valencia Duarte AV, Vallada H, Van Nieuwerburgh F, Veenstra-Vanderweele J, Walitza S, Wang Y, Wendland JR, Westenberg HG, Shugart YY, Miguel EC, McMahon W, Wagner M, Nicolini H, Posthuma D, Hanna GL, Heutink P, Denys D, Arnold PD, Oostra BA, Nestadt G, Freimer NB, Pauls DL, Wray NR, Stewart SE, Mathews CA, Knowles JA, Cox NJ, Scharf JM.

PLoS Genet. 2013 Oct;9(10):e1003864. doi: 10.1371/journal.pgen.1003864. Epub 2013 Oct 24.

PMID:
24204291
[PubMed - in process]
Free PMC Article
10.

The emerging role of SHANK genes in neuropsychiatric disorders.

Guilmatre A, Huguet G, Delorme R, Bourgeron T.

Dev Neurobiol. 2014 Feb;74(2):113-22. doi: 10.1002/dneu.22128. Epub 2013 Oct 7.

PMID:
24124131
[PubMed - in process]
11.

Creatine and guanidinoacetate reference values in a French population.

Joncquel-Chevalier Curt M, Cheillan D, Briand G, Salomons GS, Mention-Mulliez K, Dobbelaere D, Cuisset JM, Lion-François L, Des Portes V, Chabli A, Valayannopoulos V, Benoist JF, Pinard JM, Simard G, Douay O, Deiva K, Tardieu M, Afenjar A, Héron D, Rivier F, Chabrol B, Prieur F, Cartault F, Pitelet G, Goldenberg A, Bekri S, Gerard M, Delorme R, Porchet N, Vianey-Saban C, Vamecq J.

Mol Genet Metab. 2013 Nov;110(3):263-7. doi: 10.1016/j.ymgme.2013.09.005. Epub 2013 Sep 16.

PMID:
24090707
[PubMed - indexed for MEDLINE]
12.

Adolescents and young adults who are not in employment, education, or training.

Scott J, Fowler D, McGorry P, Birchwood M, Killackey E, Christensen H, Glozier N, Yung A, Power P, Nordentoft M, Singh S, Brietzke E, Davidson S, Conus P, Bellivier F, Delorme R, Macmillan I, Buchanan J, Colom F, Vieta E, Bauer M, McGuire P, Merikangas K, Hickie I.

BMJ. 2013 Sep 18;347:f5270. doi: 10.1136/bmj.f5270. No abstract available.

PMID:
24048295
[PubMed - indexed for MEDLINE]
13.

Characterization of SLITRK1 variation in obsessive-compulsive disorder.

Ozomaro U, Cai G, Kajiwara Y, Yoon S, Makarov V, Delorme R, Betancur C, Ruhrmann S, Falkai P, Grabe HJ, Maier W, Wagner M, Lennertz L, Moessner R, Murphy DL, Buxbaum JD, Züchner S, Grice DE.

PLoS One. 2013 Aug 21;8(8):e70376. doi: 10.1371/journal.pone.0070376. eCollection 2013.

PMID:
23990902
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Differentiation from human pluripotent stem cells of cortical neurons of the superficial layers amenable to psychiatric disease modeling and high-throughput drug screening.

Boissart C, Poulet A, Georges P, Darville H, Julita E, Delorme R, Bourgeron T, Peschanski M, Benchoua A.

Transl Psychiatry. 2013 Aug 20;3:e294. doi: 10.1038/tp.2013.71.

PMID:
23962924
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Progress toward treatments for synaptic defects in autism.

Delorme R, Ey E, Toro R, Leboyer M, Gillberg C, Bourgeron T.

Nat Med. 2013 Jun;19(6):685-94. doi: 10.1038/nm.3193. Epub 2013 Jun 6. Review.

PMID:
23744158
[PubMed - indexed for MEDLINE]
16.

Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.

Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA, Yu D, Scharf JM, Chan E, Kassam F, Moya PR, Wendland JR, Delorme R, Richter MA, Kennedy JL, Veenstra-VanderWeele J, Samuels J, Greenberg BD, McCracken JT, Knowles JA, Fyer AJ, Rauch SL, Riddle MA, Grados MA, Bienvenu OJ, Cullen B, Wang Y, Shugart YY, Piacentini J, Rasmussen S, Nestadt G, Murphy DL, Jenike MA, Cook EH, Pauls DL, Hanna GL, Mathews CA.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jun;162B(4):367-79. doi: 10.1002/ajmg.b.32137. Epub 2013 Apr 18.

PMID:
23606572
[PubMed - indexed for MEDLINE]
17.

Dose point kernels in liquid water: an intra-comparison between GEANT4-DNA and a variety of Monte Carlo codes.

Champion C, Incerti S, Perrot Y, Delorme R, Bordage MC, Bardiès M, Mascialino B, Tran HN, Ivanchenko V, Bernal M, Francis Z, Groetz JE, Fromm M, Campos L.

Appl Radiat Isot. 2014 Jan;83 Pt B:137-41. doi: 10.1016/j.apradiso.2013.01.037. Epub 2013 Feb 14.

PMID:
23478094
[PubMed - in process]
18.

Memory for past events: movement and action chains in high-functioning autism spectrum disorders.

Daprati E, Nico D, Delorme R, Leboyer M, Zalla T.

Exp Brain Res. 2013 May;226(3):325-34. doi: 10.1007/s00221-013-3436-1. Epub 2013 Feb 16.

PMID:
23417648
[PubMed - indexed for MEDLINE]
19.

Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms.

Cheillan D, Joncquel-Chevalier Curt M, Briand G, Salomons GS, Mention-Mulliez K, Dobbelaere D, Cuisset JM, Lion-François L, Portes VD, Chabli A, Valayannopoulos V, Benoist JF, Pinard JM, Simard G, Douay O, Deiva K, Afenjar A, Héron D, Rivier F, Chabrol B, Prieur F, Cartault F, Pitelet G, Goldenberg A, Bekri S, Gerard M, Delorme R, Tardieu M, Porchet N, Vianey-Saban C, Vamecq J.

Orphanet J Rare Dis. 2012 Dec 13;7:96. doi: 10.1186/1750-1172-7-96.

PMID:
23234264
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

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.

Transl Psychiatry. 2012 Oct 23;2:e179. doi: 10.1038/tp.2012.102.

PMID:
23092983
[PubMed - indexed for MEDLINE]
Free PMC Article

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