| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1037232742 |
| P356 | DOI | 10.1038/NRN2461 |
| P698 | PubMed publication ID | 19143051 |
| P5875 | ResearchGate publication ID | 23786508 |
| P50 | author | Marcus R. Munafò | Q21094872 |
| P2093 | author name string | Colin G DeYoung | |
| Jin Fan | |||
| Adam E Green | |||
| Jeremy R Gray | |||
| John A Fossella | |||
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| COMT genotype predicts BOLD signal and noise characteristics in prefrontal circuits | Q48456516 | ||
| Interactive effects of APOE and CHRNA4 on attention and white matter volume in healthy middle-aged and older adults | Q48462465 | ||
| Association between dopamine D4 receptor (DRD4) gene polymorphisms and novelty-elicited auditory event-related potentials in preschool children | Q48481522 | ||
| Impact of complex genetic variation in COMT on human brain function | Q48492697 | ||
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| Journals should publish all "null" results and should sparingly publish "positive" results | Q52998122 | ||
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| Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region | Q28297391 | ||
| Association of the NRG1 gene and schizophrenia: a meta-analysis | Q28300667 | ||
| Replicating genotype-phenotype associations | Q29614919 | ||
| Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia | Q29614929 | ||
| Replication validity of genetic association studies | Q29615456 | ||
| Serotonin transporter genetic variation and the response of the human amygdala | Q29617804 | ||
| 5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression | Q29618835 | ||
| Genes and the parsing of cognitive processes | Q30942053 | ||
| Evaluation of a structural polymorphism in the ankyrin repeat and kinase domain containing 1 (ANKK1) gene and the activation of executive attention networks | Q31049768 | ||
| The endophenotype concept in psychiatric genetics | Q33693915 | ||
| Beyond affect: a role for genetic variation of the serotonin transporter in neural activation during a cognitive attention task | Q33922872 | ||
| COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor | Q33964426 | ||
| Variant BDNF (Val66Met) impact on brain structure and function | Q33997931 | ||
| Integration of emotion and cognition in the lateral prefrontal cortex | Q34021863 | ||
| Training, maturation, and genetic influences on the development of executive attention. | Q34078516 | ||
| Working memory: looking back and looking forward | Q34267089 | ||
| Genetic and neurochemical modulation of prefrontal cognitive functions in children. | Q34287350 | ||
| A meta-analysis of the association between the serotonin transporter gene polymorphism (5-HTTLPR) and trait anxiety | Q34299070 | ||
| Beyond heritability: neurotransmitter genes differentially modulate visuospatial attention and working memory | Q34312485 | ||
| Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits | Q34316352 | ||
| Genes, dopamine and cortical signal-to-noise ratio in schizophrenia | Q34357471 | ||
| A susceptibility gene for affective disorders and the response of the human amygdala | Q34392171 | ||
| The A1 allele of the human D2 dopamine receptor gene is associated with increased activity of striatal L-amino acid decarboxylase in healthy subjects. | Q34419630 | ||
| Identification of a genetic cluster influencing memory performance and hippocampal activity in humans | Q34427183 | ||
| Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operations | Q34436816 | ||
| A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity | Q34437037 | ||
| Amygdala responsiveness is modulated by tryptophan hydroxylase-2 gene variation. | Q34462273 | ||
| Generalist genes: implications for the cognitive sciences | Q34507996 | ||
| Gene-environment interactions in psychiatry: joining forces with neuroscience | Q34540742 | ||
| Differential effects of 5-HTTLPR genotypes on the behavioral and neural responses to tryptophan depletion in patients with major depression and controls | Q34570594 | ||
| Common Kibra alleles are associated with human memory performance | Q34575472 | ||
| Tolcapone improves cognition and cortical information processing in normal human subjects | Q34576438 | ||
| Association of CHRM2 with IQ: converging evidence for a gene influencing intelligence | Q34589759 | ||
| Neural mechanisms of genetic risk for impulsivity and violence in humans | Q34597413 | ||
| Bridging psychology and biology. The analysis of individuals in groups | Q34651943 | ||
| Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme | Q34721779 | ||
| Cognitive and magnetic resonance imaging brain morphometric correlates of brain-derived neurotrophic factor Val66Met gene polymorphism in patients with schizophrenia and healthy volunteers | Q34726039 | ||
| Allelic association of human dopamine D2 receptor gene in alcoholism | Q34998499 | ||
| Catechol O -methyltransferase val 158 -met genotype and individual variation in the brain response to amphetamine | Q35023131 | ||
| Mapping the genetic variation of executive attention onto brain activity | Q35163847 | ||
| Modulatory role of serotonin in neural information processing: implications for human psychopathology | Q35555835 | ||
| The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes | Q35860569 | ||
| Epistasis between catechol-O-methyltransferase and type II metabotropic glutamate receptor 3 genes on working memory brain function | Q35894585 | ||
| Chemistry of the adaptive mind | Q35946389 | ||
| Does measurement instrument moderate the association between the serotonin transporter gene and anxiety-related personality traits? A meta-analysis | Q35984302 | ||
| Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder | Q36139662 | ||
| Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory. | Q36300098 | ||
| Genetics of emotional regulation: the role of the serotonin transporter in neural function | Q36418581 | ||
| Genetics of human brain oscillations | Q36422389 | ||
| The molecular genetics of cognition: dopamine, COMT and BDNF. | Q36485001 | ||
| Typologies of attentional networks | Q36500187 | ||
| Tangled webs: tracing the connections between genes and cognition | Q36501821 | ||
| Attention genes | Q36689286 | ||
| Neuregulin 1 genotype and schizophrenia | Q37076200 | ||
| Serotonin transporter (5-HTTLPR) genotype and amygdala activation: a meta-analysis | Q37370760 | ||
| Deficits on subject-ordered tasks after frontal- and temporal-lobe lesions in man. | Q38499946 | ||
| Establishment of genetic associations for complex diseases is independent of early study findings | Q39218509 | ||
| Stability of amygdala BOLD response to fearful faces over multiple scan sessions. | Q40428342 | ||
| Subjective ordering, short-term memory, and the frontal lobes | Q41225786 | ||
| A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition | Q43941587 | ||
| Human attentional networks | Q44203217 | ||
| Association study of a functional catechol-O-methyltransferase-gene polymorphism and cognitive function in healthy females | Q44301951 | ||
| Genetic origins of anxiety in women: a role for a functional catechol-O-methyltransferase polymorphism | Q44327740 | ||
| Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia | Q44578270 | ||
| Human choline transporter gene variation is associated with corticolimbic reactivity and autonomic-cholinergic function. | Q44922180 | ||
| Allelic variation of serotonin transporter function modulates the brain electrical response for error processing | Q44929734 | ||
| Amygdala-prefrontal coupling depends on a genetic variation of the serotonin transporter | Q45183612 | ||
| Bias in genetic association studies: effects of research location and resources | Q45205755 | ||
| Differential effects of DRD4 and DAT1 genotype on fronto-striatal gray matter volumes in a sample of subjects with attention deficit hyperactivity disorder, their unaffected siblings, and controls. | Q45277253 | ||
| Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype | Q46430940 | ||
| Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health | Q46495963 | ||
| Effect of catechol-O-methyltransferase val158met genotype on attentional control. | Q46497177 | ||
| Individual differences in extraversion and dopamine genetics predict neural reward responses | Q46618137 | ||
| Role of functional genetic variation in the dopamine D2 receptor (DRD2) in response to bupropion and nicotine replacement therapy for tobacco dependence: results of two randomized clinical trials | Q46670494 | ||
| Monoamine oxidase-a genetic variations influence brain activity associated with inhibitory control: new insight into the neural correlates of impulsivity. | Q46733825 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neuroscience | Q207011 |
| cognitive neuroscience | Q1138951 | ||
| P304 | page(s) | 710-720 | |
| P577 | publication date | 2008-09-01 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | Nature Reviews Neuroscience | Q2108225 |
| P1476 | title | Using genetic data in cognitive neuroscience: from growing pains to genuine insights | |
| P478 | volume | 9 |
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| Q37065276 | Brain white matter structure and COMT gene are linked to second-language learning in adults |
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