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Synaptic, transcriptional and chromatin genes disrupted in autism

dc.contributor.authorCarracedo Álvarez, Ángel
dc.date.accessioned2017-06-07T07:31:20Z
dc.date.available2017-06-07T07:31:20Z
dc.date.issued2014
dc.identifier.issn0028-0836
dc.identifier.urihttp://hdl.handle.net/20.500.11940/7504
dc.language.isoeng
dc.titleSynaptic, transcriptional and chromatin genes disrupted in autism
dc.typeArtigoes
dc.authorsophosDe Rubeis, S
dc.authorsophosHe, X
dc.authorsophosGoldberg, AP
dc.authorsophosPoultney, CS
dc.authorsophosSamocha, K
dc.authorsophosCicek, AE
dc.authorsophosKou, Y
dc.authorsophosLiu, L
dc.authorsophosFromer, M
dc.authorsophosWalker, S
dc.authorsophosSingh, T
dc.authorsophosKlei, L
dc.authorsophosKosmicki, J
dc.authorsophosFu, SC
dc.authorsophosAleksic, B
dc.authorsophosBiscaldi, M
dc.authorsophosBolton, PF
dc.authorsophosBrownfeld, JM
dc.authorsophosCai, JL
dc.authorsophosCampbell, NG
dc.authorsophosCarracedo, A
dc.authorsophosChahrour, MH
dc.authorsophosChiocchetti, AG
dc.authorsophosCoon, H
dc.authorsophosCrawford, EL
dc.authorsophosCrooks, L
dc.authorsophosCurran, SR
dc.authorsophosDawson, G
dc.authorsophosDuketis, E
dc.authorsophosFernandez, BA
dc.authorsophosGallagher, L
dc.authorsophosGeller, E
dc.authorsophosGuter, SJ
dc.authorsophosHill, RS
dc.authorsophosIonita-Laza, I
dc.authorsophosGonzalez, PJ
dc.authorsophosKilpinen, H
dc.authorsophosKlauck, SM
dc.authorsophosKolevzon, A
dc.authorsophosLee, I
dc.authorsophosLei, J
dc.authorsophosLehtimaki, T
dc.authorsophosLin, CF
dc.authorsophosMa'ayan, A
dc.authorsophosMarshall, CR
dc.authorsophosMcInnes, AL
dc.authorsophosNeale, B
dc.authorsophosOwen, MJ
dc.authorsophosOzaki, N
dc.authorsophosParellada, M
dc.authorsophosParr, JR
dc.authorsophosPurcell, S
dc.authorsophosPuura, K
dc.authorsophosRajagopalan, D
dc.authorsophosRehnstrom, K
dc.authorsophosReichenberg, A
dc.authorsophosSabo, A
dc.authorsophosSachse, M
dc.authorsophosSanders, SJ
dc.authorsophosSchafer, C
dc.authorsophosSchulte-Ruther, M
dc.authorsophosSkuse, D
dc.authorsophosStevens, C
dc.authorsophosSzatmari, P
dc.authorsophosTammimies, K
dc.authorsophosValladares, O
dc.authorsophosVoran, A
dc.authorsophosWang, LS
dc.authorsophosWeiss, LA
dc.authorsophosWillsey, AJ
dc.authorsophosYu, TW
dc.authorsophosYuen, RKC
dc.authorsophosCook, EH
dc.authorsophosFreitag, CM
dc.authorsophosGill, M
dc.authorsophosHultman, CM
dc.authorsophosLehner, T
dc.authorsophosPalotie, A
dc.authorsophosSchellenberg, GD
dc.authorsophosSkiar, P
dc.authorsophosState, MW
dc.authorsophosSutcliffe, JS
dc.authorsophosWalsh, CA
dc.authorsophosScherer, SW
dc.authorsophosZwick, ME
dc.authorsophosBarrett, JC
dc.authorsophosCutler, DJ
dc.authorsophosRoeder, K
dc.authorsophosDevlin, B
dc.authorsophosDaly, MJ
dc.authorsophosBuxbaum, JD
dc.authorsophosStudy, DDD
dc.authorsophosCollaborative, Homozygosity Mapping
dc.authorsophosConsortium, UK10K
dc.authorsophosConsortium, Autism Sequencing
dc.identifier.doi10.1038/nature13772
dc.identifier.isi344631400038
dc.identifier.pmid25363760
dc.identifier.sophos16238
dc.issue.number7526
dc.journal.titleNATURE
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.page.initial209
dc.page.finalU119
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number515


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