Torthaí cuardaigh - Karayiorgou, M

Selection for retroviral insertions into regulated genes. de réir Gogos, J A, Lowry, W, Karayiorgou, M

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Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome de réir Sobin, C, Kiley-Brabeck, K, Karayiorgou, M

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Detection of single base mismatches of thymine and cytosine residues by potassium permanganate and hydroxylamine in the presence of tetralkylammonium salts. de réir Gogos, J A, Karayiorgou, M, Aburatani, H, Kafatos, F C

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A Disc1 mutation differentially affects neurites and spines in hippocampal and cortical neurons de réir Lepagnol-Bestel, AM, Kvajo, M, Karayiorgou, M, Simonneau, M, Gogos, JA

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Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-suscepti... de réir Bennett, R L, Karayiorgou, M, Sobin, C A, Norwood, T H, Kay, M A

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Homozygosity mapping of the Achromatopsia locus in the Pingelapese. de réir Winick, J D, Blundell, M L, Galke, B L, Salam, A A, Leal, S M, Karayiorgou, M

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Importance of membrane-bound catechol-O-methyltransferase in L-DOPA metabolism: a pharmacokinetic study in two types of Comt gene modified mice de réir Käenmäki, M, Tammimäki, A, Garcia-Horsman, JA, Myöhänen, T, Schendzielorz, N, Karayiorgou, M, Gogos, JA, Männistö, PT

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System-based proteomic and metabonomic analysis of the Df(16)A(+/−) mouse identifies potential miR-185 targets and molecular pathway alterations de réir Wesseling, H, Xu, B, Want, E J, Holmes, E, Guest, P C, Karayiorgou, M, Gogos, J A, Bahn, S

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Deletion of Rapgef6, a candidate schizophrenia susceptibility gene, disrupts amygdala function in mice de réir Levy, R J, Kvajo, M, Li, Y, Tsvetkov, E, Dong, W, Yoshikawa, Y, Kataoka, T, Bolshakov, V Y, Karayiorgou, M, Gogos, J A

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. de réir Karayiorgou, M, Morris, M A, Morrow, B, Shprintzen, R J, Goldberg, R, Borrow, J, Gos, A, Nestadt, G, Wolyniec, P S, Lasseter, V K

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Neuroanatomical Phenotypes in a Mouse Model of the 22q11.2 Microdeletion de réir Ellegood, J., Markx, S., Lerch, J.P., Steadman, P.E., Genç, C., Provenzano, F, Kushner, S.A., Henkelman, R.M., Karayiorgou, M., Gogos, J.A.

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Homozygous deletions within human chromosome band 9p21 in melanoma. de réir Fountain, J W, Karayiorgou, M, Ernstoff, M S, Kirkwood, J M, Vlock, D R, Titus-Ernstoff, L, Bouchard, B, Vijayasaradhi, S, Houghton, A N, Lahti, J

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Cntnap4/Caspr4 Differentially Contributes to GABAergic and Dopaminergic Synaptic Transmission de réir 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.

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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia de réir Francks, C, Maegawa, S, Laurén, J, Abrahams, BS, Velayos-Baeza, A, Medland, SE, Colella, S, Groszer, M, McAuley, EZ, Caffrey, TM, Timmusk, T, Pruunsild, P, Koppel, I, Lind, PA, Matsumoto-Itaba, N, Nicod, J, Xiong, L, Joober, R, Enard, W, Krinsky, B, Nanba, E, Richardson, AJ, Riley, BP, Martin, NG, Strittmatter, SM, Möller, H-J, Rujescu, D, St Clair, D, Muglia, P, Roos, JL, Fisher, SE, Wade-Martins, R, Rouleau, GA, Stein, JF, Karayiorgou, M, Geschwind, DH, Ragoussis, J, Kendler, KS, Airaksinen, MS, Oshimura, M, DeLisi, LE, Monaco, AP

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia de réir Ng, MYM, Levinson, DF, Faraone, SV, Suarez, BK, DeLisi, LE, Arinami, T, Riley, B, Paunio, T, Pulver, AE, Irmansyah, Holmans, PA, Escamilla, M, Wildenauer, DB, Williams, NM, Laurent, C, Mowry, BJ, Brzustowicz, LM, Maziade, M, Sklar, P, Garver, DL, Abecasis, GR, Lerer, B, Fallin, MD, Gurling, HMD, Gejman, PV, Lindholm, E, Moises, HW, Byerley, W, Wijsman, EM, Forabosco, P, Tsuang, MT, Hwu, H-G, Okazaki, Y, Kendler, KS, Wormley, B, Fanous, A, Walsh, D, O’Neill, FA, Peltonen, L, Nestadt, G, Lasseter, VK, Liang, KY, Papadimitriou, GM, Dikeos, DG, Schwab, SG, Owen, MJ, O’Donovan, MC, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, VL, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, RR, Silverman, JM, Bassett, AS, Roy, M-A, Mérette, C, Pato, CN, Pato, MT, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, AR, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M, Lewis, CM

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