RAFAELA
MARCO TAVERNER
TITULAR DE UNIVERSIDAD
Medical Research Council
Londres, Reino UnidoPublikationen in Zusammenarbeit mit Forschern von Medical Research Council (7)
2014
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Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 165, Núm. 8, pp. 691-704
2011
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A functional variant of the serotonin transporter gene ((SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings
Biological Psychiatry, Vol. 70, Núm. 3, pp. 230-236
2009
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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 (2008) 147B, (1306-1309))
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
2008
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Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: Familial evidence for a distinct disorder
Journal of Neural Transmission, Vol. 115, Núm. 2, pp. 163-175
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DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 147, Núm. 8, pp. 1450-1460
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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. 147, Núm. 7, pp. 1306-1309
2006
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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, Núm. 10, pp. 934-953