Ghent University Academic Bibliography

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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, S Newhouse, S Ripke, BM Neale, SM Purcell, D Posthuma, et al.

(2015) NATURE NEUROSCIENCE. 18(2). p.199-209
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Stimulant treatment for ADHD Reply

AP Groenman, J Oosteriaan, NNJ Rommelse, B Franke, CU Greven, PJ Hoekstra, CA Hartman, M Luman, Herbert Roeyers (UGent) , RD Oades, et al.

(2014) BRITISH JOURNAL OF PSYCHIATRY. 204(6). p.490-491
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Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity

TF Smith, AD Anastopoulos, ME Garrett, A Arias-Vasquez, B Franke, RD Oades, Edmund Barke (UGent) , P Asherson, M Gill, JK Buitelaar, et al.

(2014) AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 165(8). p.691-704
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- Journal Article
- A1
- open access
Substance use disorders in adolescents with attention deficit hyperactivity disorder: a 4-year follow-up study

AP Groenman, J Oosterlaan, N Rommelse, B Franke, Herbert Roeyers (UGent) , RD Oades, JA Sergeant, JK Buitelaar and SV Faraone

(2013) ADDICTION. 108(8). p.1503-1511
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- Journal Article
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Stimulant treatment for attention-deficit hyperactivity disorder and risk of developing substance use disorder

AP Groenman, J Oosterlaan, NNJ Rommelse, B Franke, CU Greven, PJ Hoekstra, CA Hartman, M Luman, Herbert Roeyers (UGent) , RD Oades, et al.

(2013) BRITISH JOURNAL OF PSYCHIATRY. 203(2). p.112-119
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Association between DRD2/DRD4 interaction and conduct disorder: a potential developmental pathway to alcohol dependence

NR Mota, CHD Bau, T Banaschewski, JK Buitelaar, RP Ebstein, B Franke, M Gill, J Kuntsi, I Manor, A Miranda, et al.

(2013) AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 162(6). p.546-549
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Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD

J Bralten, B Franke, I Waldman, N Rommelse, C Hartman, P Asherson, T Banaschewski, RP Ebstein, M Gill, A Miranda, et al.

(2013) JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY. 52(11). p.1204-1212
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High loading of polygenic risk for ADHD in children with comorbid aggression

ML Hamshere, K Langley, J Martin, SS Agha, E Stergiakouli, RJL Anney, J Buitelaar, SV Faraone, KP Lesch, BM Neale, et al.

(2013) AMERICAN JOURNAL OF PSYCHIATRY. 170(8). p.909-916
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, BJ Mowry, A Thapar, ME Goddard, JS Witte, et al.

(2013) NATURE GENETICS. 45(9). p.984-996
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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3

NM Williams, B Franke, E Mick, RJL Anney, CM Freitag, M Gill, A Thapar, MC O'Donovan, MJ Owen, P Holmans, et al.

(2012) AMERICAN JOURNAL OF PSYCHIATRY. 169(2). p.195-204

Academic Bibliography

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Stimulant treatment for ADHD Reply

Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity

Substance use disorders in adolescents with attention deficit hyperactivity disorder: a 4-year follow-up study

Stimulant treatment for attention-deficit hyperactivity disorder and risk of developing substance use disorder

Association between DRD2/DRD4 interaction and conduct disorder: a potential developmental pathway to alcohol dependence

Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD

High loading of polygenic risk for ADHD in children with comorbid aggression

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3

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