Results 1 to 10 of 10
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TypeTitleAuthor(s)YearViews
Copy number variations of chromosome 16p13.1 region associated with schizophreniaIngason, A; Rujescu, D; Cichon, S; Sigurdsson, E; Sigmundsson, T; Pietiläinen, OPH; BuizerVoskamp, JE; Strengman, E; Francks, C; Muglia, P; Gylfason, A; Gustafsson, O; Olason, PI; Steinberg, S; Hansen, T; Jakobsen, KD; Rasmussen, HB; Giegling, I; Möller, HJ; Hartmann, A; Crombie, C; Fraser, G; Walker, N; Lonnqvist, J; Suvisaari, J; TuulioHenriksson, A; Bramon, E; Kiemeney, LA; Franke, B; Murray, R; Vassos, E; Toulopoulou, T; Mühleisen, TW; Tosato, S; Ruggeri, M; Djurovic, S; Andreassen, OA; Zhang, Z; Werge, T; Ophoff, RA; Rietschel, M; Nöthen, MM; Petursson, H; Stefansson, H; Peltonen, L; Collier, D; Stefansson, K; Clair, DMS2011197
 
Disruption of the neurexin 1 gene is associated with schizophreniaRujescu, D; Ingason, A; Cichon, S; Pietiläinen, OPH; Barnes, MR; Toulopoulou, T; Picchioni, M; Vassos, E; Ettinger, U; Bramon, E; Murray, R; Ruggeri, M; Tosato, S; Bonetto, C; Steinberg, S; Sigurdsson, E; Sigmundsson, T; Petursson, H; Gylfason, A; Olason, PI; Hardarsson, G; Jonsdottir, GA; Gustafsson, O; Fossdal, R; Giegling, I; Möller, HJ; Hartmann, AM; Hoffmann, P; Crombie, C; Fraser, G; Walker, N; Lonnqvist, J; Suvisaari, J; TuulioHenriksson, A; Djurovic, S; Melle, I; Andreassen, OA; Hansen, T; Werge, T; Kiemeney, LA; Franke, B; Veltman, J; BuizerVoskamp, JE; Sabatti, C; Ophoff, RA; Rietschel, M; Nöthen, MM; Stefansson, K; Peltonen, L; St Clair, D; Stefansson, H; Collier, DA; Kahn, RS; Linszen, D; von Os, J; Wiersma, D; Bruggeman, R; Cahn, W; de Haan, L; Krabbendam, L; MyinGermeys, I2009220
 
Common variants conferring risk of schizophreniaStefansson, H; Ophoff, RA; Steinberg, S; Andreassen, OA; Cichon, S; Rujescu, D; Werge, T; Pietiläinen, OPH; Mors, O; Mortensen, PB; Sigurdsson, E; Gustafsson, O; Nyegaard, M; TuulioHenriksson, A; Ingason, A; Hansen, T; Suvisaari, J; Lonnqvist, J; Paunio, T; Børglum, AD; Hartmann, A; FinkJensen, A; Nordentoft, M; Hougaard, D; NorgaardPedersen, B; Böttcher, Y; Olesen, J; Breuer, R; Möller, HJ; Giegling, I; Rasmussen, HB; Timm, S; Mattheisen, M; Bitter, I; Réthelyi, JM; Magnusdottir, BB; Sigmundsson, T; Olason, P; Masson, G; Gulcher, JR; Haraldsson, M; Fossdal, R; Thorgeirsson, TE; Thorsteinsdottir, U; Ruggeri, M; Tosato, S; Franke, B; Strengman, E; Kiemeney, LA; Melle, I; Djurovic, S; Abramova, L; Kaleda, V; Sanjuan, J; De Frutos, R; Bramon, E; Vassos, E; Fraser, G; Ettinger, U; Picchioni, M; Walker, N; Toulopoulou, T; Need, AC; Ge, D; Lim Yoon, J; Shianna, KV; Freimer, NB; Cantor, RM; Murray, R; Kong, A; Golimbet, V; Carracedo, A; Arango, C; Costas, J; Jönsson, EG; Terenius, L; Agartz, I; Petursson, H; Nöthen, MM; Rietschel, M; Matthews, PM; Muglia, P; Peltonen, L; St Clair, D; Goldstein, DB; Stefansson, K; Collier, DA; Kahn, RS; Linszen, DH; Van Os, J; Wiersma, D; Bruggeman, R; Cahn, W; De Haan, L; Krabbendam, L; MyinGermeys, I2009190
 
Population differences in the International Multi-Centre ADHD Gene (IMAGE) project (Genetic Epidemiology DOI: 10.1002/gepi.20265)Neale, BM; Sham, PC; Purcell, S; Banaschewski, T; Buitelaar, J; Franke, B; SonugaBarke, E; Ebstein, R; Eisenberg, J; Mulligan, A; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Chen, W; Zhou, K; Asherson, P; Faraone, SV200865
 
DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkageChen, W; Zhou, K; Sham, P; Franke, B; Kuntsi, J; Campbell, D; Fleischman, K; Knight, J; Andreou, P; Arnold, R; Altink, M; Boer, F; Boholst, MJ; Buschgens, C; Butler, L; Christiansen, H; Fliers, E; HoweForbes, R; Gabriëls, I; Heise, A; KornLubetzki, I; Marco, R; Medad, S; Minderaa, R; Müller, UC; Mulligan, A; Psychogiou, L; Rommelse, N; Sethna, V; Uebel, H; McGuffin, P; Plomin, R; Banaschewski, T; Buitelaar, J; Ebstein, R; Eisenberg, J; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; SonugaBarke, E; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P2008238
 
Linkage to Chromosome 1p36 for Attention-Deficit/Hyperactivity Disorder Traits in School and Home SettingsZhou, K; Asherson, P; Sham, P; Franke, B; Anney, RJL; 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, BM; Rijsdijk, F; Rommelse, N; Uebel, H; Psychogiou, L; Xu, X; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Manor, I; Miranda, A; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV2008240
 
Large recurrent microdeletions associated with schizophreniaStefansson, H; Rujescu, D; Cichon, S; Pietiläinen, OPH; Ingason, A; Steinberg, S; Fossdal, R; Sigurdsson, E; Sigmundsson, T; BuizerVoskamp, JE; Hansen, T; Jakobsen, KD; Muglia, P; Francks, C; Matthews, PM; Gylfason, A; Halldorsson, BV; Gudbjartsson, D; Thorgeirsson, TE; Sigurdsson, A; Jonasdottir, A; Jonasdottir, A; Bjornsson, A; Mattiasdottir, S; Blondal, T; Haraldsson, M; Magnusdottir, BB; Giegling, I; Möller, HJ; Hartmann, A; Shianna, KV; Ge, D; Need, AC; Crombie, C; Fraser, G; Walker, N; Lonnqvist, J; Suvisaari, J; TuulioHenriksson, A; Paunio, T; Toulopoulou, T; Bramon, E; Di Forti, M; Murray, R; Ruggeri, M; Vassos, E; Tosato, S; Walshe, M; Li, T; Vasilescu, C; Mühleisen, TW; Wang, AG; Ullum, H; Djurovic, S; Melle, I; Olesen, J; Kiemeney, LA; Franke, B; Sabatti, C; Freimer, NB; Gulcher, JR; Thorsteinsdottir, U; Kong, A; Andreassen, OA; Ophoff, RA; Georgi, A; Rietschel, M; Werge, T; Petursson, H; Goldstein, DB; Nöthen, MM; Peltonen, L; Collier, DA; St Clair, D; Stefansson, K; Kahn, RS; Linszen, DH; Van Os, J; Wiersma, D; Bruggeman, R; Cahn, W; De Haan, L; Krabbendam, L; MyinGermeys, I2008204
 
Population differences in the international multi-centre ADHD gene projectNeale, BM; Sham, PC; Purcell, S; Banaschewski, T; Buitelaar, J; Franke, B; SonugaBarke, E; Ebstein, R; Eisenberg, J; Mulligan, A; Gill, M; Manor, I; Miranda, A; Mulas, F; Oades, RD; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Zhou, K; Asherson, P; Faraone, SV2008119
 
Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes (Molecular Psychiatry (2006) 11, (934-953) DOI: 10.1038/sj.mp.4001869)Brookes, K; Xu, X; Chen, W; Zhou, K; Neale, B; Lowe, N; Anney, R; Franke, B; Gill, M; Ebstein, R; Buitelaar, J; Sham, P; Campbell, D; Knight, J; Andreou, P; Altink, M; Arnold, R; Boer, F; Buschgens, C; Butler, L; Christiansen, H; Feldman, L; Fleischman, K; Fliers, E; HoweForbes, R; Goldfarb, A; Heise, A; Gabriëls, I; KornLubetzki, I; Johansson, L; Marco, R; Medad, S; Minderaa, R; Mulas, F; Müller, U; Mulligan, A; Rabin, K; Rommelse, N; Sethna, V; Sorohan, J; Uebel, H; Psychogiou, L; Weeks, A; Barrett, R; Craig, I; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Kuntsi, J; Manor, I; Mcguffin, P; Miranda, A; Oades, RD; Plomin, R; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P200677
 
The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genesBrookes, K; Xu, X; Chen, W; Zhou, K; Neale, B; Lowe, N; Aneey, R; Franke, B; Gill, M; Ebstein, R; Buitelaar, J; Sham, P; Campbell, D; Knight, J; Andreou, P; Altink, M; Arnold, R; Boer, F; Buschgens, C; Butler, L; Christiansen, H; Feldman, L; Fleischman, K; Fliers, E; HoweForbes, R; Goldfarb, A; Heise, A; Gabriëls, I; KornLubetzki, I; Marco, R; Medad, S; Minderaa, R; Mulas, F; Müller, U; Mulligan, A; Rabin, K; Rommelse, N; Sethna, V; Sorohan, J; Uebel, H; Psychogiou, L; Weeks, A; Barrett, R; Craig, I; Banaschewski, T; SonugaBarke, E; Eisenberg, J; Kuntsi, J; Manor, I; McGuffin, P; Miranda, A; Oades, RD; Plomin, R; Roeyers, H; Rothenberger, A; Sergeant, J; Steinhausen, HC; Taylor, E; Thompson, M; Faraone, SV; Asherson, P; Johansson, L2006165
 
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