Lista de obras -

A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD.

artículo científico publicado en 2012

Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children

artículo científico publicado en 2005

Association between dopamine transporter (DAT1) genotype, left-sided inattention, and an enhanced response to methylphenidate in attention-deficit hyperactivity disorder

artículo científico publicado en 2005

Association of DRD4 in children with ADHD and comorbid conduct problems

artículo científico publicado en 2002

DRD4 gene variants and sustained attention in attention deficit hyperactivity disorder (ADHD): effects of associated alleles at the VNTR and -521 SNP.

artículo científico publicado en 2005

Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype

artículo científico publicado en 2005

Dissociation in response to methylphenidate on response variability in a group of medication naïve children with ADHD.

artículo científico publicado en 2008

Dopaminergic system genes in ADHD: toward a biological hypothesis

artículo científico publicado en 2002

Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder.

artículo científico publicado en 2006

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes

artículo científico publicado en 2004

Methylphenidate improves some but not all measures of attention, as measured by the TEA-Ch in medication-naïve children with ADHD.

artículo científico publicado en 2013

Methylphenidate side effect profile is influenced by genetic variation in the attention-deficit/hyperactivity disorder-associated CES1 gene.

artículo científico publicado en 2013

Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: evidence of linkage and association with the SNP -616.

artículo científico publicado en 2004

Phenotype studies of the DRD4 gene polymorphisms in ADHD: association with oppositional defiant disorder and positive family history

artículo científico publicado en 2004

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder

artículo científico publicado en 2005

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

artículo científico publicado en 2009

Spatial attentional bias as a marker of genetic risk, symptom severity, and stimulant response in ADHD.

artículo científico publicado en 2007

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.

artículo científico publicado en 2005

Lista de obras de

A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD.

Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children

Association between dopamine transporter (DAT1) genotype, left-sided inattention, and an enhanced response to methylphenidate in attention-deficit hyperactivity disorder

Association of DRD4 in children with ADHD and comorbid conduct problems

DRD4 gene variants and sustained attention in attention deficit hyperactivity disorder (ADHD): effects of associated alleles at the VNTR and -521 SNP.

Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype

Dissociation in response to methylphenidate on response variability in a group of medication naïve children with ADHD.

Dopaminergic system genes in ADHD: toward a biological hypothesis

Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder.

Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes

Methylphenidate improves some but not all measures of attention, as measured by the TEA-Ch in medication-naïve children with ADHD.

Methylphenidate side effect profile is influenced by genetic variation in the attention-deficit/hyperactivity disorder-associated CES1 gene.

Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: evidence of linkage and association with the SNP -616.

Phenotype studies of the DRD4 gene polymorphisms in ADHD: association with oppositional defiant disorder and positive family history

Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

Spatial attentional bias as a marker of genetic risk, symptom severity, and stimulant response in ADHD.

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.