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Convergence of Genes and Cellular Pathways Dysregulated in ..:

Pinto, Dalila ; Delaby, Elsa ; Merico, Daniele...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2014.03.018. , 2014

Link: https://inserm.hal.science/inserm-00986225

RT Journal
T1 <Title>Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsorbonneuniv:oai:HAL:inserm-00986225v1&Exemplar=1&LAN=DE
				
A1 Pinto, Dalila
A1 Delaby, Elsa
A1 Merico, Daniele
A1 Barbosa, Mafalda
A1 Merikangas, Alison
A1 Klei, Lambertus
A1 Thiruvahindrapuram, Bhooma
A1 Xu, Xiao
A1 Ziman, Robert
A1 Wang, Zhuozhi
A1 Vorstman, Jacob, A. S
A1 Thompson, Ann
A1 Regan, Regina
A1 Pilorge, Marion
A1 Pellecchia, Giovanna
A1 Pagnamenta, Alistair, T
A1 Oliveira, Bárbara
A1 Marshall, Christian, R
A1 Magalhaes, Tiago, R
A1 Lowe, Jennifer, K
A1 Howe, Jennifer, L
A1 Griswold, Anthony, J
A1 Gilbert, John
A1 Duketis, Eftichia
A1 Dombroski, Beth, A
A1 de Jonge, Maretha, V
A1 Cuccaro, Michael
A1 Crawford, Emily, L
A1 Correia, Catarina, T
A1 Conroy, Judith
A1 Conceição, Inês, C
A1 Chiocchetti, Andreas, G
A1 Casey, Jillian, P
A1 Cai, Guiqing
A1 Cabrol, Christelle
A1 Bolshakova, Nadia
A1 Bacchelli, Elena
A1 Anney, Richard
A1 Gallinger, Steven
A1 Cotterchio, Michelle
A1 Casey, Graham
A1 Zwaigenbaum, Lonnie
A1 Wittemeyer, Kerstin
A1 Wing, Kirsty
A1 Wallace, Simon
A1 van Engeland, Herman
A1 Tryfon, Ana
A1 Thomson, Susanne
A1 Soorya, Latha
A1 Rogé, Bernadette
A1 Roberts, Wendy
A1 Poustka, Fritz
A1 Mouga, Susana
A1 Minshew, Nancy
A1 Mcinnes, Alison, L
A1 Mcgrew, Susan, G
A1 Lord, Catherine
A1 Leboyer, Marion
A1 Le Couteur, Ann, S
A1 Kolevzon, Alexander
A1 Jiménez González, Patricia
A1 Jacob, Suma
A1 Holt, Richard
A1 Guter, Stephen
A1 Green, Jonathan
A1 Green, Andrew
A1 Gillberg, Christopher
A1 Fernandez, Bridget, A
A1 Duque, Frederico
A1 Delorme, Richard
A1 Dawson, Geraldine
A1 Chaste, Pauline
A1 Café, Cátia
A1 Brennan, Sean
A1 Bourgeron, Thomas
A1 Bolton, Patrick, F
A1 Bölte, Sven
A1 Bernier, Raphael
A1 Baird, Gillian
A1 Bailey, Anthony, J
A1 Anagnostou, Evdokia
A1 Almeida, Joana
A1 Wijsman, Ellen, M
A1 Vieland, Veronica, J
A1 Vicente, Astrid, M
A1 Schellenberg, Gerard, D
A1 Pericak-Vance, Margaret
A1 Paterson, Andrew, D
A1 Parr, Jeremy, R
A1 Oliveira, Guiomar
A1 Nurnberger, John, I
A1 Monaco, Anthony, P
A1 Maestrini, Elena
A1 Klauck, Sabine, M
A1 Hakonarson, Hakon
A1 Haines, Jonathan, L
A1 Geschwind, Daniel, H
A1 Freitag, Christine, M
A1 Folstein, Susan, E
A1 Ennis, Sean
A1 Coon, Hilary
A1 Battaglia, Agatino
A1 Szatmari, Peter
A1 Sutcliffe, James, S
A1 Hallmayer, Joachim
A1 Gill, Michael
A1 Cook, Edwin, H
A1 Buxbaum, Joseph, D
A1 Devlin, Bernie
A1 Gallagher, Louise
A1 Betancur, Catalina
A1 Scherer, Stephen, W
PB HAL CCSD; Elsevier (Cell Press)
YR 2014
K1 de novo
K1 inherited
K1 gene networks
K1 pathways
K1 Copy Number Variation
K1 CHD2
K1 HDAC4
K1 GDI1
K1 autism
K1 rare CNV
K1 SETD5
K1 [SDV.GEN]Life Sciences [q-bio]/Genetics
JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2014.03.018
LK http://dx.doi.org/https://inserm.hal.science/inserm-00986225
DO https://inserm.hal.science/inserm-00986225
SF ELIB - SuUB Bremen

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