RNA-seq analysis of amygdala tissue reveals characteristic expression profiles in schizophrenia

por Chang, X, Liu, Y, Hahn, C-G, Gur, R E, Sleiman, P M A, Hakonarson, H
Publicado 2017

Association between polygenic risk for schizophrenia, neurocognition and social cognition across development

por Germine, L, Robinson, E B, Smoller, J W, Calkins, M E, Moore, T M, Hakonarson, H, Daly, M J, Lee, P H, Holmes, A J, Buckner, R L, Gur, R C, Gur, R E
Publicado 2016

Rare structural variation of synapse and neurotransmission genes in autism

por Gai, X, Xie, H M, Perin, J C, Takahashi, N, Murphy, K, Wenocur, A S, D'arcy, M, O'Hara, R J, Goldmuntz, E, Grice, D E, Shaikh, T H, Hakonarson, H, Buxbaum, J D, Elia, J, White, P S
Publicado 2012

Psychiatric gene discoveries shape evidence on ADHD's biology

por Thapar, A, Martin, J, Mick, E, Arias Vásquez, A, Langley, K, Scherer, S W, Schachar, R, Crosbie, J, Williams, N, Franke, B, Elia, J, Glessner, J, Hakonarson, H, Owen, M J, Faraone, S V, O'Donovan, M C, Holmans, P
Publicado 2016

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

por Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Publicado 2009

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

por Elia, J, Gai, X, Xie, H M, Perin, J C, Geiger, E, Glessner, J T, D'arcy, M, deBerardinis, R, Frackelton, E, Kim, C, Lantieri, F, Muganga, B M, Wang, L, Takeda, T, Rappaport, E F, Grant, S F A, Berrettini, W, Devoto, M, Shaikh, T H, Hakonarson, H, White, P S
Publicado 2010

Cntnap4/Caspr4 Differentially Contributes to GABAergic and Dopaminergic Synaptic Transmission

por Karayannis, T., Au, E., Patel, J.C., Kruglikov, I., Markx, S., Delorme, R., Héron, D., Salomon, D., Glessner, J., Restituito, S., Gordon, A., Rodriguez-Murillo, L., Roy, N.C., Gogos, J., Rudy, B., Rice, M.E., Karayiorgou, M., Hakonarson, H., Keren, B., Huguet, G., Bourgeron, T., Hoeffer, C., Tsien, R.W., Peles, E., Fishell, G.
Publicado 2014

NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases

por Perea-Romero, I., Blanco-Kelly, F., Sanchez-Navarro, I., Lorda-Sanchez, I., Tahsin-Swafiri, S., Avila-Fernandez, A., Martin-Merida, I., Trujillo-Tiebas, M. J., Lopez-Rodriguez, R., Rodriguez de Alba, M., Iancu, I. F., Romero, R., Quinodoz, M., Hakonarson, H., Garcia-Sandova, Blanca, Minguez, P., Corton, M., Rivolta, C., Ayuso, C.
Publicado 2021

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD

por Jain, M, Vélez, J I, Acosta, M T, Palacio, L G, Balog, J, Roessler, E, Pineda, D, Londoño, A C, Palacio, J D, Arbelaez, A, Lopera, F, Elia, J, Hakonarson, H, Seitz, C, Freitag, C M, Palmason, H, Meyer, J, Romanos, M, Walitza, S, Hemminger, U, Warnke, A, Romanos, J, Renner, T, Jacob, C, Lesch, K-P, Swanson, J, Castellanos, F X, Bailey-Wilson, J E, Arcos-Burgos, M, Muenke, M
Publicado 2012

Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network

por Bush, WS, Crosslin, DR, Owusu‐Obeng, A, Wallace, J, Almoguera, B, Basford, MA, Bielinski, SJ, Carrell, DS, Connolly, JJ, Crawford, D, Doheny, KF, Gallego, CJ, Gordon, AS, Keating, B, Kirby, J, Kitchner, T, Manzi, S, Mejia, AR, Pan, V, Perry, CL, Peterson, JF, Prows, CA, Ralston, J, Scott, SA, Scrol, A, Smith, M, Stallings, SC, Veldhuizen, T, Wolf, W, Volpi, S, Wiley, K, Li, R, Manolio, T, Bottinger, E, Brilliant, MH, Carey, D, Chisholm, RL, Chute, CG, Haines, JL, Hakonarson, H, Harley, JB, Holm, IA, Kullo, IJ, Jarvik, GP, Larson, EB, McCarty, CA, Williams, MS, Denny, JC, Rasmussen‐Torvik, LJ, Roden, DM, Ritchie, MD
Publicado 2016