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Plos One|December 24, 2010
Genetic variants in toll-like receptors are not associated with rheumatoid arthritis susceptibility or anti-tumour necrosis factor treatment outcomeMarieke J H Coenen, Christian Enevold, Pilar Barrera, et al.
Autism Research : Official Journal of the International Society for Autism Research|July 16, 2016
Lack of replication of previous autism spectrum disorder GWAS hits in European populationsBàrbara Torrico, Andreas G Chiocchetti, Elena Bacchelli, et al.
Molecular Psychiatry|January 18, 2021
Structural brain imaging studies offer clues about the effects of the shared genetic etiology among neuropsychiatric disordersNevena V Radonjić, Jonathan L Hess, Paula Rovira, et al.
Neuroscience and Biobehavioral Reviews|November 10, 2021
Non-mental diseases associated with ADHD across the lifespan: Fidgety Philipp and Pippi Longstocking at risk of multimorbidity?Sarah Kittel-Schneider, Gara Arteaga-Henriquez, Alejandro Arias Vasquez, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 28, 2020
Executive functioning and emotion recognition in youth with oppositional defiant disorder and/or conduct disorderRenee Kleine Deters, Jilly Naaijen, Mireia Rosa, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 30, 2016
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorderErlend J Brevik, Marjolein M J van Donkelaar, Heike Weber, et al.
World Psychiatry : Official Journal of the World Psychiatric Association (WPA)|September 15, 2025
Attention-deficit/hyperactivity disorder (ADHD) in adults: evidence base, uncertainties and controversiesSamuele Cortese, Mark A Bellgrove, Isabell Brikell, et al.
Frontiers in Behavioral Neuroscience|July 25, 2022
Toward Precision Medicine in ADHDJan Buitelaar, Sven Bölte, Daniel Brandeis, et al.
International Journal of Molecular Sciences|October 14, 2022
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple SclerosisJulia Horjus, Tineke van Mourik-Banda, Marco A P Heerings, et al.
Biological Psychiatry|April 19, 2011
A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblingsEdmund J S Sonuga-Barke, Robert Kumsta, Wolff Schlotz, et al.
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