Items where Author is "Asherson, P."

2013

Mota, N. R. and Bau, C. H. and Banaschewski, T. and Buitelaar, J. K. and Ebstein, R. P. and Franke, B. and Gill, M. and Kuntsi, J. and Manor, I. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. and Steinhausen, H. -C. and Faraone, S. V. and Asherson, P.. (2013) Association between DRD2/DRD4 interaction and conduct disorder : A potential developmental pathway to alcohol dependence. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 162, H. 6. pp. 546-549.

Bralten, J. and Franke, B. and Waldman, ID. and Rommelse, N. and Hartman, C. and Asherson, P. and Banaschewski, T. and Ebstein, RP. and Gill, M. and Miranda, A. and Oades, RD. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Osterlaan, J. and Sonuga-Barke, EJ. and Steinhausen, H. -C. and Faraone, SV. and Buitelaar, J. and Arias-Vásquez, A.. (2013) Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD. Journal of the American Academy of Child and Adolescent Psychiatry, Vol. 52, H. 11. pp. 1204-1212.

Kuntsi J., Frazier-Wood and A. C., Banaschewski and T., Gill and M., Miranda and A., Oades and R. D., Roeyers and H., Rothenberger and Steinhausen, H. -C. and van der Meere, J. J. and Faraone, S. V. and Asherson, P. and Rijsdijk. F., . (2013) Genetic analysis of reaction time variability : room for improvement? Psychological Medicine, Vol. 43, H. 6. pp. 1323-1333.

Hamshere, M. L. and Langley, K. and Martin, J. and Agha, S. S. and Stergiakouli, E. and Anney, R. J. and Buitelaar, J. and Faraone, S. V. and Lesch, K. P. and Neale, B. M. and Franke, B. and Sonuga-Barke, E. and Asherson, P. and Merwood, A. and Kuntsi, J. and Medland, S. E. and Ripke, S. and Steinhausen, H. -C. and Freitag, C. and Reif, A. and Renner, T. J. and Romanos, M. and Romanos, J. and Warnke, A. and Meyer, J. and Palmason, H. and Vasquez, A. A. and Lambregts-Rommelse, N. and Roeyers, H. and Biederman, J. and Doyle, A. E. and Hakonarson, H. and Rothenberger, A. and Banaschewski, T. and Oades, R. D. and McGough, J. J. and Kent, L. and Williams, N. and Owen, M. J. and Holmans, P. and O'Donovan, M. C. and Thapar, A.. (2013) High loading of polygenic risk for ADHD in children comorbid for aggression. American Journal of Psychiatry, Vol. 170, H. 8. pp. 909-916.

2010

Aebi, M. and Müller, U. C. and Asherson, P. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Eisenberg, J. and Gill, M. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Thompson, M. and Taylor, E. and Faraone, S. V. and Steinhausen, H.-C.. (2010) Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined type. Psychological Medicine, Vol. 40, H. 12. pp. 2089-2100.

Kuntsi, J. and Wood, A. C. and Rijsdijk, F. and Johnson, K. A. and Andreou, P. and Albrecht, B. and Arias-Vasquez, A. and Buitelaar, J. K. and Mcloughlin, G. and Rommelse, N. N. J. and Sergeant, J. A. and Sonuga-Barke E. J. S., Uebel and H., van der Meere and J. J, Banaschewski and T., Gill and M., Manor and I., Miranda and A., Mulas and F., Oades and R. D., Roeyers and H., Rothenberger and A., Steinhausen and H.-C., Faraone S. V. and Asherson, P.. (2010) Separation of cognitive impairments in attention deficit hyperactivity disorder into two familial factors. Archives of general psychiatry, Vol. 67, H. 11. pp. 1159-1167.

Wood, A. C. and Rijsdijk, F. and Johnson, K. A. and Andreou, P. and Albrecht, B. and Arias-Vasquez, A. and Buitelaar, J. K. and McLoughlin, G. and Rommelse, N. N. J. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Uebel, H. and van der Meere, J. J. and Banaschewski, T. and Gill, M. and Manor, I. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P. and Kuntsi, J.. (2010) The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ. Psychological Medicine, Vol. 41, H. 4. pp. 861-871.

2009

Hawi, Z. and Kent, L. and Hill, M. and Anney, R. J. L. and Brookes, K. J. and Barry, E. and Franke, B. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Faraone, S. V. and Asherson, P. and Gill, M.. (2009) ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 150B, H. 1. pp. 97-102.

2008

Asherson, P. and Zhou, K. and Anney, R. J. L. and Franke, B. and Buitelaar, J. and Ebstein, R. and Gill, M. and Altink, M. and Arnold, R. and Boer, F. and Brookes, K. and Buschgens, C. and Butler, L. and Cambell, D. and Chen, W. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Johansson, L. and Lubetzki, I. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Neale, B. and Rijsdijk, F. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Xu, X. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and 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, Vol. 13, H. 5. pp. 514-521.

Brookes, K. J. and Xu, X. and Anney, R. and Franke, B. and Zhou, K. and Chen, Wai and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Eisenberg, J. and Gill, M. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and 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, Neuropsychiatric genetics, Vol. 147B, H. 8. pp. 1519-1523.

Christiansen, H. and Chen, W. and Oades, R. D. and Asherson, P. and Taylor, E. A. and Lasky-Su, J. and Zhou, K. and Banaschewski, T. and Buschgens, C. and Franke, B. and Gabriels, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Psychogiou, L. and Rommelse, N. N. J. and Uebel, H. and Buitelaar, J. and Ebstein, R. P. and Eisenberg, J. and Gill, M. and Miranda, A. and Mulas, F. and Roeyers, H. and Rothenberger, A. and Sergeant, J. A. and Sonuga-Barke, E. J. S. and Steinhausen, H.-C. and Thompson, M. and Faraone, S. V.. (2008) Co-transmission of conduct problems with attention-deficit/hyperactivity disorder : familial evidence for a distinct disorder. Journal of neural transmission, Vol. 115, No. 2. pp. 163-175.

Brookes, K. J. and Neale, B. and Xu, X. and Thapar, A. and Gill, M. and Langley, K. and Hawi, Z. and Mill, J. and Taylor, E. and Franke, B. and Chen, W. and Ebstein, R. and Buitelaar, J. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Manor, I. and Miranda, A. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H. C. and Faraone, S. V. and Asherson, P.. (2008) Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 1. pp. 94-99.

Xu, X. and Duman, E. A. and Aysimi, E. and Anney, R. and Brookes, K. and Franke, B. and Zhou, K. and Buschgens, C. and Chen, W. and Christiansen, H. and Eisenberg, J. and Gabriëls, I. and Manor, I. and Marco, R. and Müller, U. C. and Mulligan, A. and Rommelse, N. and Thompson, M. and Uebel, H. and Banaschewski, T. and Buitelaar, J. and Ebstein, R. and Gill, M. and Miranda, A. and Mulas, F. and Oades, R. D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Steinhausen, H.-C. and Taylor, E. and Faraone, S. V. and Asherson, P.. (2008) No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1306-1309.

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

2006

Brookes, K. and Xu, X. and Chen, W. and Zhou, K. and Neale, B. and Lowe, N. and Anney, R. and Aneey, R. and Franke, B. and Gill, M. and Ebstein, R. and Buitelaar, J. and Sham, P. and Campbell, D. and Knight, J. and Andreou, P. and Altink, M. and Arnold, R. and Boer, F. and Buschgens, C. and Butler, L. and Christiansen, H. and Feldman, L. and Fleischman, K. and Fliers, E. and Howe-Forbes, R. and Goldfarb, A. and Heise, A. and Gabriëls, I. and Korn-Lubetzki, I. and Johansson, L. and Marco, R. and Medad, S. and Minderaa, R. and Mulas, F. and Müller, U. and Mulligan, A. and Rabin, K. and Rommelse, N. and Sethna, V. and Sorohan, J. and Uebel, H. and Psychogiou, L. and Weeks, A. and Barrett, R. and Craig, I. and Banaschewski, T. and Sonuga-Barke, E. and Eisenberg, J. and Kuntsi, J. and Manor, I. and McGuffin, P. and Miranda, A. and Oades, R. D. and Plomin, R. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Steinhausen, H.-C. and Taylor, E. and Thompson, M. and Faraone, S. V. and Asherson, P.. (2006) 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, Vol. 11, H. 10. pp. 934-953.