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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 (2016). Psychiatric gene discoveries shape evidence on ADHD's biology. Molecular Psychiatry, 21(9):1202-1207.

Elia, J; Glessner, J T; Wang, K; Takahashi, N; Shtir, C J; Hadley, D; Sleiman, P M A; Zhang, H; Kim, C E; Robison, R; Lyon, G J; Flory, J H; Bradfield, J P; Imielinski, M; Hou, C; Frackelton, E C; Chiavacci, R M; Sakurai, T; Rabin, C; Middleton, F A; Thomas, K A; Garris, M; Mentch, F; Freitag, C M; Steinhausen, H C; Todorov, A A; Reif, A; Rothenberger, A; Franke, B; Mick, E O; Roeyers, H; Buitelaar, J; Lesch, K P; Banaschewski, T; Ebstein, R P; Mulas, F; Oades, R D; Sergeant, J; Sonuga-Barke, E; Renner, T J; Romanos, M; Romanos, J; Warnke, A; Walitza, S; Meyer, J; Pálmason, H; Seitz, C; Loo, S K; Smalley, S L; Biederman, J; Kent, L; Asherson, P; Anney, R J L; Gaynor, J W; Shaw, P; Devoto, M; White, P S; Grant, S F A; Buxbaum, J D; Rapoport, J L; Williams, N M; Nelson, S F; Faraone, S V; Hakonarson, H (2011). Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics, 44(1):78-84.

Arcos-Burgos, M; Jain, M; Acosta, M T; Shively, S; Stanescu, H; Wallis, D; Domené, S; Vélez, J I; Karkera, J D; Balog, J; Berg, K; Kleta, R; Gahl, W A; Roessler, E; Long, R; Lie, J; Pineda, D; Londoño, A C; Palacio, J D; Arbelaez, A; Lopera, F; Elia, J; Hakonarson, H; Johansson, S; Knappskog, P M; Haavik, J; Ribases, M; Cormand, B; Bayes, M; Casas, M; Ramos-Quiroga, J A; Hervas, A; Maher, B S; Faraone, S V; 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; Vortmeyer, A; Bailey-Wilson, J E; Castellanos, F X; Muenke, M (2010). A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. Molecular Psychiatry, 15(11):1053-1066.

Van Deerlin, V M; Sleiman, P M A; Martinez-Lage, M; Chen-Plotkin, A; Wang, L S; Graff-Radford, N R; Dickson, D W; Rademakers, R; Boeve, B F; Grossman, M; Arnold, S E; Mann, D M A; Pickering-Brown, S M; Seelaar, H; Heutink, P; van Swieten, J C; Murrell, J R; Ghetti, B; Spina, S; Grafman, J; Hodges, J; Spillantini, M G; Gilman, S; Lieberman, A P; Kaye, J A; Woltjer, R L; Bigio, E H; Mesulam, M; Al-Sarraj, S; Troakes, C; Rosenberg, R N; White, C L; Ferrer, I; Lladó, A; Neumann, M; Kretzschmar, H A; Hulette, C M; Welsh-Bohmer, K A; Miller, B L; Alzualde, A; Lopez de Munain, A; McKee, A C; Gearing, M; Levey, A I; Lah, J J; Hardy, J; Rohrer, J D; Lashley, T; Mackenzie, I R A; Feldman, H H; Hamilton, R L; Dekosky, S T; van der Zee, J; Kumar-Singh, S; Van Broeckhoven, C; Mayeux, R; Vonsattel, J P G; Troncoso, J C; Kril, J J; Kwok, J B J; Halliday, G M; Bird, T D; Ince, P G; Shaw, P J; Cairns, N J; Morris, J C; McLean, C A; DeCarli, C; Ellis, W G; Freeman, S H; Frosch, M P; Growdon, J H; Perl, D P; Sano, M; Bennett, D A; Schneider, J A; Beach, T G; Reiman, E M; Woodruff, B K; Cummings, J; Vinters, H V; Miller, C A; Chui, H C; Alafuzoff, I; Hartikainen, P; Seilhean, D; Galasko, D; Masliah, E; Cotman, C W; Tuñón, M T; Martínez, M C C; Munoz, D G; Carroll, S L; Marson, D; Riederer, P F; Bogdanovic, N; Schellenberg, G D; Hakonarson, H; Trojanowski, J Q; Lee, V M Y (2010). Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics, 42(3):234-239.

Franke, A; McGovern, D P; Barrett, J C; Wang, K; Radford-Smith, G L; Ahmad, T; Lees, C W; Balschun, T; Lee, J; Roberts, R; Anderson, C A; Bis, J C; Bumpstead, S; Ellinghaus, D; Festen, E M; Georges, M; Green, T; Haritunians, T; Jostins, L; Latiano, A; Mathew, C G; Montgomery, G W; Prescott, N J; Raychaudhuri, S; Rotter, J I; Schumm, P; Sharma, Y; Simms, L A; Taylor, K D; Whiteman, D; Wijmenga, C; Baldassano, R N; Barclay, M; Bayless, T M; Brand, S; Büning, C; Cohen, A; Colombel, J F; Cottone, M; Stronati, L; Denson, T; De Vos, M; D'Inca, R; Dubinsky, M; Edwards, C; Florin, T; Franchimont, D; Gearry, R; Glas, J; Van Gossum, A; Guthery, S L; Halfvarson, J; Verspaget, H W; Hugot, J P; Karban, A; Laukens, D; Lawrance, I; Lemann, M; Levine, A; Libioulle, C; Louis, E; Mowat, C; Newman, W; Panés, J; Phillips, A; Proctor, D D; Regueiro, M; Russell, R; Rutgeerts, P; Sanderson, J; Sans, M; Seibold, F; Steinhart, A H; Stokkers, P C; Torkvist, L; Kullak-Ublick, G; Wilson, D; Walters, T; Targan, S R; Brant, S R; Rioux, J D; D'Amato, M; Weersma, R K; Kugathasan, S; Griffiths, A M; Mansfield, J C; Vermeire, S; Duerr, R H; Silverberg, M S; Satsangi, J; Schreiber, S; Cho, J H; Annese, V; Hakonarson, H; Daly, M J; Parkes, M (2010). Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nature Genetics, 42(12):1118-1125.

This list was generated on Thu Jul 27 10:58:16 2017 CEST.