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Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder.Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder.Pharmacogenetics of methylphenidate response and tolerability in attention-deficit/hyperactivity disorder.Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder.Effect of CYP2D6, CYP2C9 and ABCB1 genotypes on fluoxetine plasma concentrations and clinical improvement in children and adolescent patients.Role of GAD2 and HTR1B genes in early-onset obsessive-compulsive disorder: results from transmission disequilibrium study.The effect of age on DNA concentration from whole saliva: Implications for the standard isolation methodAttention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causalityEpigenetic signature for attention-deficit/hyperactivity disorder: identification of miR-26b-5p, miR-185-5p, and miR-191-5p as potential biomarkers in peripheral blood mononuclear cells
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P50
description
researcher ORCID ID = 0000-0003-0856-6247
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wetenschapper
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name
Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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type
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Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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Pagerols M
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Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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Mireia Pagerols
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P108
P106
P108
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P496
0000-0003-0856-6247