An event related potential study of inhibitory and attentional control in Williams syndrome adults
Open accessAbstract
The primary aim of the current study was to employ event-related potentials (ERPs) methodology to disentangle the mechanisms related to inhibitory control in older adults with Williams syndrome (WS). Eleven older adults with WS (mean age 42), 16 typically developing adults (mean age 42) and 13 typically developing children (mean age 12) participated in the study. ERPs were recorded during a three-stimulus visual oddball task, during which participants were required to make a response to a rare target stimulus embedded in a train of frequent non-target stimuli. A task-irrelevant infrequent stimulus was also present at randomised intervals during the session. The P3a latency data response related to task-irrelevant stimulus processing was delayed in WS. In addition, the early perceptual N2 amplitude was attenuated. These data are indicative of compromised early monitoring of perceptual input, accompanied by appropriate orientation of responses to task-irrelevant stimuli. However, the P3a delay suggests inefficient evaluation of the task-irrelevant stimuli. These data are discussed in terms of deficits in the disengagement of attentional processes, and the regulation of monitoring processes required for successful inhibition.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Attentional issues are widely reported in WS.
“which is unsurprising given the attentional issues widely reported in WS (Breckenridge et al., 2013; Greer et al., 2017; Leyfer et al., 2006).”
From NIH Toolbox Cognition Battery Feasibility in Individuals With Williams Syndrome (2022) · cites this paper as Greer et al., 2017
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Nieuwenhuis, S., Yeung, N., van den Wildenberg, W., & Ridderinkhof, K. R. (2003) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.3.1.17 · Cited by 1,250 · see citing works
Simmonds, D. J., Pekar, J. J., & Mostofsky, S. H. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.07.015 · Cited by 1,015 · see citing works
The power of statistical tests in meta-analysis
Hedges, L. V., & Pigott, T. D. (2001) · Psychological Methods · doi:10.1037/1082-989x.6.3.203 · Cited by 716 · see citing works
Meyer-Lindenberg, A., Mervis, C. B., & Faith Berman, K. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1906 · Cited by 411 · see citing works
Viewing it differently: social scene perception in Williams syndrome and autism
Riby, D. M., & Hancock, P. J. B. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.05.003 · Cited by 374 · see citing works
Self-citationNeural correlates of genetically abnormal social cognition in Williams syndrome
Meyer-Lindenberg, A., Hariri, A. R., Munoz, K. E., Mervis, C. B., Mattay, V. S., Morris, C. A., & Berman, K. F. (2005) · Nature Neuroscience · doi:10.1038/nn1494 · Cited by 357 · see citing works
Flagged first, then by citations
Research works printed but not linked: 81
- [1]Morris CA, Mervis CB. Williams Syndrome and Related Disorders. Annu Rev Genomics Hum Genet. 2000; 1: 461– 84. 10.1146/annurev.genom.1.1.461 11701637 · DOI
- [2]Osborne LR, Mervis CB. Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development. Expert reviews in molecular medicine. 2007; 9(15): 1– 16. 10.1017/S146239940700035X 17565757 PMC2893216 · DOI
- [4]Porter M, Coltheart M. Cognitive Heterogeneity in Williams Syndrome. Developmental neuropsychology. 2005; 27(2): 275– 306. 10.1207/s15326942dn2702_5 15753050 · DOI
- [5]Searcy YM, Lincoln AJ, Rose FE, Klima ES, Bavar N, Korenberg JR, et al The relationship between age and IQ in adults with Williams syndrome. American Journal on Mental Retardation. 2004; 109(3): 231– 6. 10.1352/0895-8017(2004)109<231:TRBAAI>2.0.CO;2 15072519 · DOI
- [6]Jarrold C, Baddeley AD, Phillips C. Long-Term Memory for Verbal and Visual Information in Down Syndrome and Williams Syndrome: Performance on the Doors and People Test. Cortex. 2007; 43(2): 233– 47. 17405669
- [7]Vicari S, Bellucci S, Carlesimo GA. Visual and spatial long-term memory: differential pattern of impairments in Williams and Down syndromes. Developmental Medicine & Child Neurology. 2005; 47(05): 305– 11. 15892372
- [8]Brock J. Language abilities in Williams syndrome: A critical review. Development and psychopathology. 2007; 19(01): 97– 127. 17241486
- [9]Little K, Riby DM, Janes E, Clark F, Fleck R, Rodgers J. Heterogeneity of social approach behaviour in Williams syndrome: the role of response inhibition. Research in developmental disabilities. 2013; 34(3): 959– 67. 10.1016/j.ridd.2012.11.020 23291513 · DOI
- [10]Mervis CB, Klein-Tasman BP. Williams syndrome: cognition, personality, and adaptive behavior. Mental retardation and developmental disabilities research reviews. 2000; 6(2): 148– 58. 10.1002/1098-2779(2000)6:2<148::AID-MRDD10>3.0.CO;2-T 10899809 · DOI
- [11]Riby D, Kirk H, Hanley M, Riby L. Stranger danger awareness in Williams syndrome. Journal of Intellectual Disability Research. 2014; 58(6): 572– 82. 10.1111/jir.12055 23718278 · DOI
- [12]Jones W, Bellugi U, Lai Z, Chiles M, Reilly J, Lincoln A, et al II. Hypersociability in Williams syndrome. Cognitive Neuroscience, Journal of. 2000; 12(Supplement 1): 30– 46. 10953232
- [14]Frigerio E, Burt DM, Gagliardi C, Cioffi G, Martelli S, Perrett DI, et al Is everybody always my friend? Perception of approachability in Williams syndrome. Neuropsychologia. 2006; 44(2): 254– 9. 10.1016/j.neuropsychologia.2005.05.008 16005478 · DOI
- [15]Jarvinen-Pasley A, Vines BW, Hill KJ, Yam A, Grichanik M, Mills D, et al Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome. Neuropsychologia. 2010; 48(2): 456– 66. 10.1016/j.neuropsychologia.2009.10.003 19822162 PMC4096156 · DOI
- [16]Riby DM, Jones N, Brown PH, Robinson LJ, Langton SR, Bruce V, et al Attention to faces in Williams syndrome. Journal of autism and developmental disorders. 2011; 41(9): 1228– 39. 10.1007/s10803-010-1141-5 21125323 · DOI
- [17]Costanzo F, Varuzza C, Menghini D, Addona F, Gianesini T, Vicari S. Executive functions in intellectual disabilities: a comparison between Williams syndrome and Down syndrome. Research in developmental disabilities. 2013; 34(5): 1770– 80. 10.1016/j.ridd.2013.01.024 23501586 · DOI · Paper page
- [18]Osorio A, Cruz R, Sampaio A, Garayzabal E, Martinez-Regueiro R, Goncalves OF, et al How executive functions are related to intelligence in Williams syndrome. Research in developmental disabilities. 2012; 33(4): 1169– 75. 10.1016/j.ridd.2012.02.003 22502842 · DOI
- [19]Menghini D, Addona F, Costanzo F, Vicari S. Executive functions in individuals with Williams syndrome. Journal of intellectual disability research: JIDR. 2010; 54(5): 418– 32. 10.1111/j.1365-2788.2010.01287.x 20537048 · DOI
- [20]Hocking DR, Thomas D, Menant JC, Porter MA, Smith S, Lord SR, et al The interplay between executive control and motor functioning in Williams syndrome. Developmental science. 2013; 16(3): 428– 42. 10.1111/desc.12042 23587040 · DOI
- [21]Porter MA, Coltheart M, Langdon R. The neuropsychological basis of hypersociability in Williams and Down syndrome. Neuropsychologia. 2007; 45(12): 2839– 49. 10.1016/j.neuropsychologia.2007.05.006 17597166 · DOI · Paper page
- [22]Greer J, Riby DM, Hamiliton C, Riby LM. Attentional lapse and inhibition control in adults with Williams Syndrome. Research in developmental disabilities. 2013; 34(11): 4170– 7. 10.1016/j.ridd.2013.08.041 24076981 · DOI
- [23]Atkinson J, Braddick O. From genes to brain development to phenotypic behavior:" dorsal-stream vulnerability" in relation to spatial cognition, attention, and planning of actions in Williams syndrome (WS) and other developmental disorders. Progress in brain research. 2010; 189: 261– 83. 21489394
- [24]Scerif G, Cornish K, Wilding J, Driver J, Karmiloff‐Smith A. Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome. Developmental science. 2004; 7(1): 116– 30. 15323123
- [25]Rhodes SM, Riby DM, Park J, Fraser E, Campbell LE. Executive neuropsychological functioning in individuals with Williams syndrome. Neuropsychologia. 2010; 48(5): 1216– 26. 10.1016/j.neuropsychologia.2009.12.021 20026085 · DOI
- [27]Mobbs D, Eckert MA, Mills D, Korenberg J, Bellugi U, Galaburda AM, et al Frontostriatal dysfunction during response inhibition in Williams syndrome. Biological psychiatry. 2007; 62(3): 256– 61. 10.1016/j.biopsych.2006.05.041 16996488 · DOI
- [28]Rhodes SM, Riby DM, Matthews K, Coghill DR. Attention-deficit/hyperactivity disorder and Williams syndrome: Shared behavioral and neuropsychological profiles. Journal of clinical and experimental neuropsychology. 2011; 33(1): 147– 56. 10.1080/13803395.2010.495057 20700845 · DOI
- [29]Robertson IH, Manly T, Andrade J, Baddeley BT, Yiend J. Oops!': performance correlates of everyday attentional failures in traumatic brain injured and normal subjects. Neuropsychologia. 1997; 35(6): 747– 58. 9204482
- [30]Smith AD, Gilchrist ID, Hood B, Tassabehji M, Karmiloff-Smith A. Inefficient search of large-scale space in Williams syndrome: further insights on the role of LIMK1 deletion in deficits of spatial cognition. Perception. 2009; 38(5): 694– 701. 19662944
- [31]Jones W, Bellugi U, Lai Z, Chiles M, Reilly J, Lincoln A, et al II. Hypersociability in Williams syndrome. Journal of Cognitive Neuroscience. 2000; 12(Supplement 1): 30– 46. 10953232
- [32]Sergeant J. The cognitive-energetic model: an empirical approach to attention-deficit hyperactivity disorder. Neuroscience & Biobehavioral Reviews. 2000; 24(1): 7– 12. 10654654
- [33]Mills DL, Alvarez TD, St George M, Applebaum LG III. Electrophysiological Studies of face processing in adults with Williams syndrome. Journal of Cognitive Neuroscience. 2000; 12(Suplement1); 47– 67. 10953233
- [34]Key AP, Dykens EM. Face repetition detection and social interest: An ERP study in adults with and without Williams syndrome. Social neuroscience. 2015. PMC5266528 26667404
- [36]Polich J. Updating P300: an integrative theory of P3a and P3b. Clinical neurophysiology: official journal of the International Federation of Clinical Neurophysiology. 2007; 118(10): 2128– 48. 17573239 PMC2715154
- [37]Bachiller A, Romero S, Molina V, Alonso JF, Mañanas MA, Poza J, et al Auditory P3a and P3b neural generators in schizophrenia: An adaptive sLORETA P300 localization approach. Schizophrenia research. 2015; 169(1): 318– 25. 26481687
- [38]Smith JL, Johnstone SJ, Barry RJ. Movement-related potentials in the Go/NoGo task: The P3 reflects both cognitive and motor inhibition. Clinical neurophysiology. 2008; 119(3): 704– 14. 10.1016/j.clinph.2007.11.042 18164657 · DOI
- [39]Goldstein A, Spencer KM, Donchin E. The influence of stimulus deviance and novelty on the P300 and novelty P3. Psychophysiology. 2002; 39(06): 781– 90. 12462506
- [40]Barron E, Riby LM, Greer J, Smallwood J. Absorbed in thought the effect of mind wandering on the processing of relevant and irrelevant events. Psychological science. 2011. 21460338
- [41]Riby LM, Orme E. A familiar pattern? Semantic memory contributes to the enhancement of visuo-spatial memories. Brain and cognition. 2013; 81(2): 215– 22. 10.1016/j.bandc.2012.10.011 23262176 · DOI
- [42]Daffner KR, Alperin BR, Mott KK, Tusch E, Holcomb PJ. Age-related differences in early novelty processing: Using PCA to parse the overlapping anterior P2 and N2 components. Biological psychology. 2015. PMC4374636 25596483
- [43]Folstein JR, Van Petten C. Influence of cognitive control and mismatch on the N2 component of the ERP: a review. Psychophysiology. 2008; 45(1): 152– 70. 10.1111/j.1469-8986.2007.00602.x 17850238 PMC2365910 · DOI · Paper page
- [44]Picton TW, Alain C, Otten L, Ritter W, Achim A, eacute. Mismatch negativity: different water in the same river. Audiology and Neurotology. 2000; 5(3–4): 111– 39 10859408
- [45]Polich J. Theoretical overview of P3a and P3b: Springer; 2003.
- [46]Kähkönen S, Ahveninen J, Pekkonen E, Kaakkola S, Huttunen J, Ilmoniemi RJ, et al Dopamine modulates involuntary attention shifting and reorienting: an electromagnetic study. Clinical Neurophysiology. 2002; 113(12): 1894– 902. 12464326
- [47]Riby LM. The joys of spring. Experimental psychology. 2013. 22851380
- [48]Conroy MA, Polich J. Normative variation of P3a and P3b from a large sample: Gender, topography, and response time. Journal of Psychophysiology. 2007; 21(1): 22– 32.
- [49]del Re EC, Spencer KM, Oribe N, Mesholam-Gately RI, Goldstein J, Shenton ME, et al Clinical high risk and first episode schizophrenia: auditory event-related potentials. Psychiatry Research: Neuroimaging. 2015; 231(2): 126– 33. 10.1016/j.pscychresns.2014.11.012 25557063 PMC4314407 · DOI
- [50]Osborne A, Riby LM. The Effect of Predisposing Risk Factors of an Eating Disorder on Response Inhibition and Working Memory: An Event-Related Potentials Study. Research in Psychology and Behavioral Sciences. 2016; 4(1): 1– 6.
- [51]Cléry H, Bonnet-Brilhault F, Lenoir P, Barthelemy C, Bruneau N, Gomot M. Atypical visual change processing in children with autism: an electrophysiological study. Psychophysiology. 2013; 50(3): 240– 52. 10.1111/psyp.12006 23316882 · DOI
- [52]Grice S, Spratling MW, Karmiloff-Smith A, Halit H, Csibra G, de Haan M, et al Disordered visual processing and oscillatory brain activity in autism and Williams Syndrome. Neuroreport. 2001; 12(12): 2697– 700. 11522950
- [53]Haas BW, Mills D, Yam A, Hoeft F, Bellugi U, Reiss A. Genetic influences on sociability: heightened amygdala reactivity and event-related responses to positive social stimuli in Williams syndrome. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2009; 29(4): 1132– 9. 19176822 PMC2754840
- [54]Key AP, Dykens EM. Electrophysiological study of local/global processing in Williams syndrome. Journal of neurodevelopmental disorders. 2011; 3(1): 28– 38. 10.1007/s11689-010-9064-1 21484595 PMC3163994 · DOI
- [55]Segalowitz SJ, Davies PL. Charting the maturation of the frontal lobe: An electrophysiological strategy. Brain and cognition. 2004; 55(1): 116– 33. 10.1016/S0278-2626(03)00283-5 15134847 · DOI
- [56]Stige S, Fjell AM, Smith L, Lindgren M, Walhovd KB. The development of visual P3a and P3b. Developmental neuropsychology. 2007; 32(1): 563– 84. 10.1080/87565640701361096 17650994 · DOI
- [57]Barry RJ, Clarke AR, McCarthy R, Selikowitz M, Brown CR, Heaven PC. Event-related potentials in adults with Attention-Deficit/Hyperactivity Disorder: an investigation using an inter-modal auditory/visual oddball task. International Journal of Psychophysiology. 2009; 71(2): 124– 31. 10.1016/j.ijpsycho.2008.09.009 19022305 · DOI
- [58]Sokhadze E, Baruth J, Tasman A, Sears L, Mathai G, El-Baz A, et al Event-related potential study of novelty processing abnormalities in autism. Applied Psychophysiology and Biofeedback. 2009; 34(1): 37– 51. 10.1007/s10484-009-9074-5 19199028 · DOI
- [59]Karmiloff-Smith A. Challenging the use of adult neuropsychological models for explaining neurodevelopmental disorders: Develop ed versus develop ing brains. The Quarterly Journal of Experimental Psychology. 2013; 66(1): 1– 14. 10.1080/17470218.2012.744424 23173948 · DOI
- [61]Oldfield RC. The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia. 1971; 9(1): 97– 113. 5146491
- [62]Van der Molen M, Van der Molen M, Ridderinkhof K, Hamel B, Curfs L, Ramakers G. Auditory and visual cortical activity during selective attention in fragile X syndrome: a cascade of processing deficiencies. Clinical Neurophysiology. 2012; 123(4): 720– 9. 10.1016/j.clinph.2011.08.023 21958658 · DOI · Paper page
- [63]Brinkman MJ, Stauder JE. Development and gender in the P50 paradigm. Clinical Neurophysiology. 2007; 118(7): 1517– 24. 10.1016/j.clinph.2007.04.002 17509936 · DOI
- [64]Klem GH, Lüders HO, Jasper H, Elger C. The ten-twenty electrode system of the International Federation. Electroencephalogr Clin Neurophysiol. 1999; 52(suppl.): 3. 10590970
- [65]St-Louis-Deschênes M, Moore R, Ellemberg D. The Selective Effect of Acute Aerobic Exercise on Neuroelectric Indices of Attention during Development. Pediat Therapeut. 2015; 5(238):2161–0665.1000238.
- [66]Steiner GZ, Brennan ML, Gonsalvez CJ, Barry RJ. Comparing P300 modulations: Target-to-target interval versus infrequent nontarget-to-nontarget interval in a three-stimulus task. Psychophysiology. 2013; 50(2): 187– 94. 10.1111/j.1469-8986.2012.01491.x 23153378 · DOI
- [67]Johnson R. On the neural generators of the P300 component of the event-related potential. Psychophysiology. 1993; 30: 90- 8416066
- [70]Wetzel N, Schröger E, Widmann A. The dissociation between the P3a event-related potential and behavioral distraction. Psychophysiology. 2013; 50(9): 920– 30. 10.1111/psyp.12072 23763292 · DOI
- [71]Comerchero MD, Polich J. P3a and P3b from typical auditory and visual stimuli. Clinical Neurophysiology. 1999; 110(1): 24– 30. 10348317
- [72]Escera C, Yago E, Alho K. Electrical responses reveal the temporal dynamics of brain events during involuntary attention switching. European Journal of Neuroscience. 2001; 14(5): 877– 83. 11576192
- [73]Lincoln A, Lai Z, Jones W. Shifting attention and joint attention dissociation in Williams syndrome: implications for the cerebellum and social deficits in autism. Neurocase. 2002; 8(2): 226– 32. 12119319
- [74]Brown JH, Johnson MH, Paterson SJ, Gilmore R, Longhi E, Karmiloff-Smith A. Spatial representation and attention in toddlers with Williams syndrome and Down syndrome. Neuropsychologia. 2003; 41(8): 1037– 46. 12667539
- [75]Thomas KM, Nelson CA. Age-related changes in the electrophysiological response to visual stimulus novelty: A topographical approach. Electroencephalography and clinical Neurophysiology. 1996; 98(4): 294– 308. 8641151
- [76]Kopp B, Lange F, Howe J, Wessel K. Age-related changes in neural recruitment for cognitive control. Brain and cognition. 2014; 85: 209– 19. 10.1016/j.bandc.2013.12.008 24434022 · DOI
- [77]Smit DJ, Posthuma D, Boomsma DI, de Geus EJ. Genetic contribution to the P3 in young and middle-aged adults. Twin Research and Human Genetics. 2007; 10(02): 335– 47. 17564523
- [78]Velanova K, Lustig C, Jacoby LL, Buckner RL. Evidence for frontally mediated controlled processing differences in older adults. Cerebral cortex. 2007; 17(5): 1033– 46. 10.1093/cercor/bhl013 16774962 · DOI
- [79]Reiss AL, Eckert MA, Rose FE, Karchemskiy A, Kesler S, Chang M, et al An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome. The Journal of neuroscience: the official journal of the Society for Neuroscience. 2004; 24(21): 5009– 15. 15163693 PMC3061615
- [80]Chiang M-C, Reiss AL, Lee AD, Bellugi U, Galaburda AM, Korenberg JR, et al 3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry. NeuroImage. 2007; 36(4): 1096– 109. 10.1016/j.neuroimage.2007.04.024 17512756 PMC2713103 · DOI
- [81]Kim H. Involvement of the dorsal and ventral attention networks in oddball stimulus processing: a meta-analysis. Human brain mapping. 2014; 35(5): 2265– 84. 10.1002/hbm.22326 23900833 PMC6868981 · DOI
- [82]Cornish K, Scerif G, Karmiloff-Smith A. Tracing syndrome-specific trajectories of attention across the lifespan. Cortex. 2007; 43(6): 672– 85. 17710820
- [83]Mills DL, Alvarez TD, George MS, Appelbaum LG, Bellugi U, Neville H. Linking Cognitive Neuroscience and Molecular Genetics: New Perspectives from Williams Syndrome-III. Electrophysiological Studies of Face Processing in Williams Syndrome. Journal of Cognitive Neuroscience. 2000; 12(1): 47– 64. 10953233
- [84]Mills DL, Dai L, Fishman I, Yam A, Appelbaum LG, St George M, et al Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing. Developmental neuropsychology. 2013; 38(8): 613– 42. 10.1080/87565641.2013.825617 24219698 PMC3992981 · DOI
- [86]Bruin K, Wijers A. Inhibition, response mode, and stimulus probability: a comparative event-related potential study. Clinical Neurophysiology. 2002; 113(7): 1172– 82. 12088714
- [87]Courchesne E, Hillyard SA, Galambos R. Stimulus novelty, task relevance and the visual evoked potential in man. Electroencephalography and clinical neurophysiology. 1975; 39(2): 131– 43. 50210
- [88]Polich J, Comerchero MD. P3a from visual stimuli: typicality, task, and topography. Brain topography. 2003; 15(3): 141– 52. 12705810
- [89]Landau B, Hoffman JE, Kurz N. Object recognition with severe spatial deficits in Williams syndrome: sparing and breakdown. Cognition. 2006; 100(3): 483– 510. 10.1016/j.cognition.2005.06.005 16185678 · DOI
Cited by
Sorted by citations
NIH Toolbox Cognition Battery Feasibility in Individuals With Williams Syndrome
Condy, E. E., Becker, L., Farmer, C., Kaat, A. J., Chlebowski, C., Kozel, B. A., & Thurm, A. (2022) · American Journal on Intellectual and Developmental Disabilities · doi:10.1352/1944-7558-127.6.473 · Cited by 6 · see citing works
- Authors
- Greer, J. M. H., Hamilton, C., McMullon, M. E. G., Riby, D. M., & Riby, L. M.
- Affiliations
- Northumbria University (GB)
- Durham University (GB)
- Corresponding author
- Riby, Leigh M.
- Venue
- PLOS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2017-02-10
- Volume
- 12
- Issue
- 2
- Pages
- e0170180
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC5302371
- OpenAlex
- W2586984223
- Cited by
- 13
- References
- 6
- Citations by year
- 2026: 2 · 2025: 1 · 2022: 1 · 2021: 3 · 2020: 1 · 2018: 3 · 2017: 2
- FWCI
- 0.69
- Type
- journal article
- Language
- en
- Update notices
- correction (2017-05-08)
- Open access
- gold
- doi.org
- Licence
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Northumbria Research Link (Northumbria University) (acceptedVersion)
- Durham Research Online (Durham University) (acceptedVersion, other-oa)
- Durham Research Online (Durham University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Northumbria University
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Social Sciences › Psychology › Neuropsychology and Physiological Psychology › Developmental and Educational Neuropsychology
- Keywords
- Williams syndrome, inhibitory control, attentional control, P3a, N2, visual oddball task, task-irrelevant stimuli, attentional disengagement, older adults, children
- MeSH terms
- Adolescent, Adult, Attention, Child, Evoked Potentials, Female, Humans, Male, Middle Aged, Neural Inhibition, Reaction Time, Case-Control Studies, Williams Syndrome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review