about
Parent of origin effects in attention/deficit hyperactivity disorder (ADHD): analysis of data from the international multicenter ADHD genetics (IMAGE) program.Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples.Investigation of the serotonin 2C receptor gene in attention deficit hyperactivity disorder in UK samples.The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interactionThe analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes.Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settingsReplication of a rare protective allele in the noradrenaline transporter gene and ADHD.Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease.The DRD4 receptor Exon 3 VNTR and 5' SNP variants and mRNA expression in human post-mortem brain tissue.5HTT genotype moderates the influence of early institutional deprivation on emotional problems in adolescence: evidence from the English and Romanian Adoptee (ERA) study.Dopamine transporter gene polymorphism moderates the effects of severe deprivation on ADHD symptoms: developmental continuities in gene-environment interplay.A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association.Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder.Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity.Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD.No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.Family-based association study of serotonin transporter gene polymorphisms in attention deficit hyperactivity disorder: no evidence for association in UK and Taiwanese samples.DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters.A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy.Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder.Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies.Relationship between VNTR polymorphisms of the human dopamine transporter gene and expression in post-mortem midbrain tissue.Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD.Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples.Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth.Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD.Association of fatty acid desaturase genes with attention-deficit/hyperactivity disorder.Partial Replication of a DRD4 Association in ADHD Individuals Using a Statistically Derived Quantitative Trait for ADHD in a Family-Based Association TestIncreased cerebral perfusion in adult attention deficit hyperactivity disorder is normalised by stimulant treatment: A non-invasive MRI pilot studyAlzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairmentCorrection: Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Keeley Brookes
@ast
Keeley Brookes
@en
Keeley Brookes
@es
Keeley Brookes
@nl
Keeley Brookes
@sl
type
label
Keeley Brookes
@ast
Keeley Brookes
@en
Keeley Brookes
@es
Keeley Brookes
@nl
Keeley Brookes
@sl
altLabel
Brookes K
@en
Brookes KJ
@en
KJ Brookes
@en
Keeley-Joanne Brookes
@en
prefLabel
Keeley Brookes
@ast
Keeley Brookes
@en
Keeley Brookes
@es
Keeley Brookes
@nl
Keeley Brookes
@sl
P108
P106
P31
P496
0000-0003-2427-2513
P569
2000-01-01T00:00:00Z