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The molecular genetic architecture of attention deficit hyperactivity disorder

Molecular psychiatry, 2015-03, Vol.20 (3), p.289-297

2015

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The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders

Molecular psychiatry, 2020-02, Vol.25 (2), p.368-378

2020

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Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

Molecular psychiatry, 2014-03, Vol.19 (3), p.294-301

2014

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Mapping susceptibility loci in attention deficit hyperactivity disorder : preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children

Molecular psychiatry, 1999-03, Vol.4 (2), p.192-196

1999

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Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study

Molecular psychiatry, 2017-04, Vol.22 (4), p.580-584

2017

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Dopamine transporter genotype predicts behavioural and neural measures of response inhibition

Molecular psychiatry, 2012-11, Vol.17 (11), p.1086-1092

2012

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Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD

Molecular psychiatry, 2005-10, Vol.10 (10), p.944-949

2005

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Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): evidence of linkage and association in the irish population

Molecular psychiatry, 2002-01, Vol.7 (8), p.913-917

2002

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Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time

Molecular psychiatry, 2014-09, Vol.19 (9), p.1031-1036

2014

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Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-12, Vol.147B (8), p.1531-1535

2008

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Trends in the Overlap of Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: Prevalence, Clinical Management, Language and Genetics

Current developmental disorders reports, 2018-03, Vol.5 (1), p.49-57

2018

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Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism

Molecular psychiatry, 1997-07, Vol.2 (4), p.311-313

1997

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Evidence that genetic variation in the oxytocin receptor ( OXTR) gene influences social cognition in ADHD

Progress in neuro-psychopharmacology & biological psychiatry, 2010-05, Vol.34 (4), p.697-702

2010

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Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD

Molecular psychiatry, 2016-11, Vol.21 (11), p.1589-1598

2016

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Human amygdala volume is predicted by common DNA variation in the stathmin and serotonin transporter genes

Translational psychiatry, 2013-07, Vol.3 (7), p.e283-e283

2013

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Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD

Molecular psychiatry, 2005-10, Vol.10 (10), p.939-943

2005

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Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-12, Vol.153B (8), p.1417-1424

2010

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Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci

Molecular psychiatry, 2003-03, Vol.8 (3), p.299-308

2003

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Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 273 nuclear families from a multi-centre sample

Molecular psychiatry, 2002-08, Vol.7 (7), p.718-725

2002

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Dopaminergic genotype biases spatial attention in healthy children

Molecular psychiatry, 2007-08, Vol.12 (8), p.786-792

2007

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Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis

Molecular psychiatry, 2002-01, Vol.7 (8), p.908-912

2002

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Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants

The pharmacogenomics journal, 2010-10, Vol.10 (5), p.442-447

2010

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ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-01, Vol.153B (1), p.97-102

2010

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Replication of a rare protective allele in the noradrenaline transporter gene and ADHD

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-12, Vol.147B (8), p.1564-1567

2008

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Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample

Irish journal of medical science, 2010-06, Vol.179 (2), p.269-272

2010

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The molecular genetic architecture of attention deficit hyperactivity disorder

The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

Mapping susceptibility loci in attention deficit hyperactivity disorder : preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study

Dopamine transporter genotype predicts behavioural and neural measures of response inhibition

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD

Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): evidence of linkage and association in the irish population

Alpha-2A adrenergic receptor gene variants are associated with increased intra-individual variability in response time

Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder

Trends in the Overlap of Autism Spectrum Disorder and Attention Deficit Hyperactivity Disorder: Prevalence, Clinical Management, Language and Genetics

Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism

Evidence that genetic variation in the oxytocin receptor ( OXTR) gene influences social cognition in ADHD

Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD

Human amygdala volume is predicted by common DNA variation in the stathmin and serotonin transporter genes

Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD

Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression

Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci

Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 273 nuclear families from a multi-centre sample

Dopaminergic genotype biases spatial attention in healthy children

Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis

Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants

ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD

Haplotype association of calpain 10 gene variants with type 2 diabetes mellitus in an Irish sample

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