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Number of items: 8.

Chen, Y; Wang, H; Yoon, S O; Xu, X; Hottiger, M O; Svaren, J; Nave, K A; Kim, H A; Olson, E N; Lu, Q R (2011). HDAC-mediated deacetylation of NF-κB is critical for Schwann cell myelination. Nature Neuroscience, 14(4):437-441.

Zhou, K; Chen, W; Buitelaar, J; Banaschewski, T; Oades, R D; Franke, B; Sonuga-Barke, E; Ebstein, R; Eisenberg, J; Gill, M; Manor, I; Miranda, A; Mulas, F; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, H C; Lasky-Su, J; Taylor, E; Brookes, K J; Xu, X; Neale, B M; Rijsdijk, F; Thompson, M; Asherson, P; Faraone, S V (2008). Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD. American Journal of Medical Genetics. Part B, 147B(8):1481-1487.

Xu, X; Hawi, Z; Brookes, K J; Anney, R; Bellgrove, M; Franke, B; Barry, E; Chen, W; Kuntsi, J; Banaschewski, T; Buitelaar, J; Ebstein, R; Fitzgerald, M; Miranda, A; Oades, R D; Roeyers, H; Rothenberger, A; Sergeant, J; Sonuga-Barke, E; Steinhausen, H C; Faraone, S V; Gill, M; Asherson, P (2008). Replication of a rare protective allele in the noradrenaline transporter gene and ADHD. American Journal of Medical Genetics. Part B, 147B(8):1564-1567.

Anney, R J L; Hawi, Z; Sheehan, K; Mulligan, A; Pinto, C; Brookes, K J; Xu, X; Zhou, K; Franke, B; Buitelaar, J; Vermeulen, S H; Banaschewski, T; Sonuga-Barke, E; Ebstein, R; Manor, I; Miranda, A; Mulas, F; Oades, R D; Roeyers, H; Rommelse, N; Rothenberger, A; Sergeant, J; Steinhausen, H C; Taylor, E; Thompson, M; Asherson, P; Faraone, S V; Gill, M (2008). Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): Analysis of data from the international multicenter ADHD genetics (IMAGE) program. American Journal of Medical Genetics. Part B, 147B(8):1495-1500.

Xu, X; Duman, E A; Anney, R; Brookes, K; Franke, B; Zhou, K; Buschgens, C; Chen, W; Christiansen, H; Eisenberg, J; Gabriëls, I; Manor, I; Marco, R; Müller, U C; Mulligan, A; Rommelse, N; Thompson, M; Uebel, H; Banaschewski, T; Buitelaar, J; Ebstein, R; Gill, M; Miranda, A; Mulas, F; Oades, R D; Roeyers, H; Rothenberger, A; Sergeant, J; Sonuga-Barke, E; Steinhausen, H C; Taylor, E; Faraone, S V; Asherson, P (2008). Erratum: "No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder". American Journal of Medical Genetics. Part B, 150B(1):154.

Zhou, K; Asherson, P; Sham, P; Franke, B; Anney, R J L; Buitelaar, J; Ebstein, R; Gill, M; Brookes, K; Buschgens, C; Campbell, D; Chen, W; Christiansen, H; Fliers, E; Gabriëls, I; Johansson, L; Marco, R; Mulas, F; Müller, U; Mulligan, A; Neale, B M; Rijsdijk, F; Rommelse, N; Uebel, H; Psychogiou, L; Xu, X; Banaschewski, T; Sonuga-Barke, E; Eisenberg, J; Manor, I; Miranda, A; Oades, R D; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, H C; Taylor, E; Thompson, M; Faraone, S V (2008). Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological Psychiatry, 64(7):571-576.

Brookes, K J; Xu, X; Anney, R; Franke, B; Zhou, K; Chen, W; Banaschewski, T; Buitelaar, J; Ebstein, R; Eisenberg, J; Gill, M; Miranda, A; Oades, R D; Roeyers, H; Rothenberger, A; Sergeant, J; Sonuga-Barke, E; Steinhausen, H C; Taylor, E; Faraone, S V; Asherson, P (2008). Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: Evidence for allelic heterogeneity. American Journal of Medical Genetics. Part B, 147B(8):1519-1523.

Asherson, P; Zhou, K; Anney, R J L; Franke, B; Buitelaar, J; Ebstein, R; Gill, M; Altink, M; Arnold, R; Boer, F; Brookes, K; Buschgens, C; Butler, L; Cambell, D; Chen, W; Christiansen, H; Feldman, L; Fleischman, K; Fliers, E; Howe-Forbes, R; Goldfarb, A; Heise, A; Gabriëls, I; Johansson, L; Lubetzki, I; Marco, R; Medad, S; Minderaa, R; Mulas, F; Müller, U; Mulligan, A; Neale, B; Rijsdijk, F; Rabin, K; Rommelse, N; Sethna, V; Sorohan, J; Uebel, H; Psychogiou, L; Weeks, A; Barrett, R; Xu, X; Banaschewski, T; Sonuga-Barke, E; Eisenberg, J; Manor, I; Miranda, A; Oades, R D; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, H C; Taylor, E; Thompson, M; Faraone, S V (2008). A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry, 13(5):514-521.

This list was generated on Thu Nov 23 01:59:01 2017 CET.