Cited by 155Attention Deficit Hyperactivity DisorderNeural and Behavioral Psychology StudiesDevelopmental and Educational Neuropsychology

Functional Magnetic Resonance Imaging Evidence for Abnormalities in Response Selection in Attention Deficit Hyperactivity Disorder: Differences in Activation Associated with Response Inhibition but Not Habitual Motor Response

Open access
Suskauer, Stacy J., Simmonds, Daniel J., Fotedar, Sunaina, Blankner, Joanna G., Pekar, James J., Denckla, Martha B., Mostofsky, Stewart H.·2008·Journal of Cognitive Neuroscience

Abstract

Impaired response inhibition is thought to be a core deficit in attention deficit hyperactivity disorder (ADHD). Prior imaging studies investigating response inhibition in children with ADHD have used tasks involving different cognitive resources, thereby complicating the interpretation of their findings. In this study, a classical go/no-go task with a well-ingrained stimulus-response association (green = go; red = no-go) was used in order to minimize extraneous cognitive demands. Twenty-five children with ADHD and 25 typically developing (TD) children between the ages of 8 and 13 years and group-matched for IQ and performance on the go/no-go task were studied using event-related functional magnetic resonance imaging (fMRI). Analyses were used to examine differences in activation between the ADHD and TD groups for "go" (habitual motor response) and "no-go" (requiring inhibition of the motor response) events. Region-of-interest analyses revealed no between-group difference in activation in association with "go" events. For "no-go" events, the children with ADHD demonstrated significantly less activation than did TD controls within a network important for inhibiting a motor response to a visual stimulus, with frontal differences localized to the pre-supplementary motor area. Although blood oxygenation level-dependent fMRI data show no differences between children with ADHD and TD children in association with a habituated motor "go" response, during "no-go" events, which require selecting not to respond, children with ADHD show diminished recruitment of networks important for response inhibition. The findings suggest that abnormalities in circuits important for motor response selection contribute to deficits in response inhibition in children with ADHD and lend support to the growing awareness of ADHD-associated anomalies in medial frontal regions important for the control of voluntary actions.

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1162/jocn.2008.20032

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.

A few free checks a day · papers already verified open instantly · results are public

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

The citation lists haven’t been fetched yet

References 105 · Cited by 155

Research works printed but not linked: 72

  1. Aron AR, Robbins TW, Poldrack RA. Inhibition and the right inferior frontal cortex. Trends in Cognitive Sciences. 2004;8:170–177. doi: 10.1016/j.tics.2004.02.010. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  2. Asahi S, Okamoto Y, Okada G, Yamawaki S, Yokota N. Negative correlation between right prefrontal activity during response inhibition and impulsiveness: A fMRI study. European Archives of Psychiatry and Clinical Neuroscience. 2004;254:245–251. doi: 10.1007/s00406-004-0488-z. [DOI] [PubMed] [Google Scholar] · DOI
  3. Astafiev SV, Shulman GL, Corbetta M. Visuospatial reorienting signals in the human temporo-parietal junction are independent of response selection. European Journal of Neuroscience. 2006;23:591–596. doi: 10.1111/j.1460-9568.2005.04573.x. [DOI] [PubMed] [Google Scholar] · DOI
  4. Bellgrove MA, Hester R, Garavan H. The functional neuroanatomical correlates of response variability: Evidence from a response inhibition task. Neuropsychologia. 2004;42:1910–1916. doi: 10.1016/j.neuropsychologia.2004.05.007. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  5. Berlin L, Bohlin G, Nyberg L, Janols LO. How well do measures of inhibition and other executive functions discriminate between children with ADHD and controls? Child Neuropsychology. 2004;10:1–13. doi: 10.1076/chin.10.1.1.26243. [DOI] [PubMed] [Google Scholar] · DOI
  6. Booth JR, Burman DD, Meyer JR, Lei Z, Trommer BL, Davenport ND, et al. Larger deficits in brain networks for response inhibition than for visual selective attention in attention deficit hyperactivity disorder (ADHD) Journal of Child Psychology and Psychiatry. 2005;46:94–111. doi: 10.1111/j.1469-7610.2004.00337.x. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  7. Booth JR, Burman DD, Meyer JR, Trommer BL, Davenport ND, Parrish TB, et al. Brain–behavior correlation in children depends on the neurocognitive network. Human Brain Mapping. 2004;23:99–108. doi: 10.1002/hbm.20051. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  8. Brett M, Leff AP, Rorden C, Ashburner J. Spatial normalization of brain images with focal lesions using cost function masking. Neuroimage. 2001;14:486–500. doi: 10.1006/nimg.2001.0845. [DOI] [PubMed] [Google Scholar] · DOI
  9. Calhoun V, Adali T, Kraut M, Pearlson G. A weighted least-squares algorithm for estimation and visualization of relative latencies in event-related functional MRI. Magnetic Resonance in Medicine. 2000;44:947–954. doi: 10.1002/1522-2594(200012)44:6<947::aid-mrm17>3.0.co;2-5. [DOI] [PubMed] [Google Scholar] · DOI
  10. Carmona S, Vilarroya O, Bielsa A, Tremols V, Soliva JC, Rovira M, et al. Global and regional gray matter reductions in ADHD: A voxel-based morphometric study. Neuroscience Letters. 2005;389:88–93. doi: 10.1016/j.neulet.2005.07.020. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  11. Castellanos FX, Giedd JN, Berquin PC, Walter JM, Sharp W, Tran T, et al. Quantitative brain magnetic resonance imaging in girls with attention-deficit/hyperactivity disorder. Archives of General Psychiatry. 2001;58:289–295. doi: 10.1001/archpsyc.58.3.289. [DOI] [PubMed] [Google Scholar] · DOI
  12. Conners CK. Conners Rating Scales—revised. North Tonawanda, NY: Multiheath Systems; 1997. [Google Scholar]
  13. Connolly JD, Goodale MA, Desouza JF, Menon RS, Vilis T. A comparison of frontoparietal fMRI activation during anti-saccades and anti-pointing. Journal of Neurophysiology. 2000;84:1645–1655. doi: 10.1152/jn.2000.84.3.1645. [DOI] [PubMed] [Google Scholar] · DOI
  14. Denckla MB, Rudel RG. Anomalies of motor development in hyperactive boys. Annals of Neurology. 1978;3:231–233. doi: 10.1002/ana.410030308. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  15. Downar J, Crawley AP, Mikulis DJ, Davis KD. A cortical network sensitive to stimulus salience in a neutral behavioral context across multiple sensory modalities. Journal of Neurophysiology. 2002;87:615–620. doi: 10.1152/jn.00636.2001. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  16. Dum RP, Strick PL. The origin of corticospinal projections from the premotor areas in the frontal lobe. Journal of Neuroscience. 1991;11:667–689. doi: 10.1523/JNEUROSCI.11-03-00667.1991. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  17. Durston S, Mulder M, Casey BJ, Ziermans T, van Engeland H. Activation in ventral prefrontal cortex is sensitive to genetic vulnerability for attention-deficit hyperactivity disorder. Biological Psychiatry. 2006;60:1062–1070. doi: 10.1016/j.biopsych.2005.12.020. [DOI] [PubMed] [Google Scholar] · DOI
  18. Durston S, Tottenham NT, Thomas KM, Davidson MC, Eigsti IM, Yang YH, et al. Differential patterns of striatal activation in young children with and without ADHD. Biological Psychiatry. 2003;53:871–878. doi: 10.1016/s0006-3223(02)01904-2. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  19. Feifel D, Farber RH, Clementz BA, Perry W, Anllo-Vento L. Inhibitory deficits in ocular motor behavior in adults with attention-deficit/hyperactivity disorder. Biological Psychiatry. 2004;56:333–339. doi: 10.1016/j.biopsych.2004.06.019. [DOI] [PubMed] [Google Scholar] · DOI
  20. Friston KJ, Holmes AP, Worsley KJ, Poline JP, Frith CD, Frackowiak RSJ. Statistical parametric maps in functional imaging: A general linear approach. Human Brain Mapping. 1995;2:189–210. [Google Scholar]
  21. Garavan H, Hester R, Murphy K, Fassbender C, Kelly C. Individual differences in the functional neuroanatomy of inhibitory control. Brain Research. 2006;1105:130–142. doi: 10.1016/j.brainres.2006.03.029. [DOI] [PubMed] [Google Scholar] · DOI
  22. Garavan H, Ross TJ, Stein EA. Right hemispheric dominance of inhibitory control: An event-related functional MRI study. Proceedings of the National Academy of Sciences, USA. 1999;96:8301–8306. doi: 10.1073/pnas.96.14.8301. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  23. Hanisch C, Radach R, Holtkamp K, Herpertz-Dahlmann B, Konrad K. Oculomotor inhibition in children with and without attention-deficit hyperactivity disorder (ADHD) Journal of Neural Transmission. 2006;113:671–684. doi: 10.1007/s00702-005-0344-y. [DOI] [PubMed] [Google Scholar] · DOI
  24. Hester RL, Murphy K, Foxe JJ, Foxe DM, Javitt DC, Garavan H. Predicting success: Patterns of cortical activation and deactivation prior to response inhibition. Journal of Cognitive Neuroscience. 2004;16:776–785. doi: 10.1162/089892904970726. [DOI] [PubMed] [Google Scholar] · DOI
  25. Holmes AP, Friston KJ. Generalisability, random effects and population inference. Neuroimage. 1998;7:S754. [Google Scholar]
  26. Hoshi E, Tanji J. Differential roles of neuronal activity in the supplementary and presupplementary motor areas: From information retrieval to motor planning and execution. Journal of Neurophysiology. 2004;92:3482–3499. doi: 10.1152/jn.00547.2004. [DOI] [PubMed] [Google Scholar] · DOI
  27. Humberstone M, Sawle GV, Clare S, Hykin J, Coxon R, Bowtell R, et al. Functional magnetic resonance imaging of single motor events reveals human presupplementary motor area. Annals of Neurology. 1997;42:632–637. doi: 10.1002/ana.410420414. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  28. Hurks PP, Adam JJ, Hendriksen JG, Vles JS, Feron FJ, Kalff AC, et al. Controlled visuomotor preparation deficits in attention-deficit/hyperactivity disorder. Neuropsychology. 2005;19:66–76. doi: 10.1037/0894-4105.19.1.66. [DOI] [PubMed] [Google Scholar] · DOI
  29. Isoda M, Hikosaka O. Switching from automatic to controlled action by monkey medial frontal cortex. Nature Neuroscience. 2007;10:240–248. doi: 10.1038/nn1830. [DOI] [PubMed] [Google Scholar] · DOI
  30. Klein C, Wendling K, Huettner P, Ruder H, Peper M. Intra-subject variability in attention-deficit hyperactivity disorder. Biological Psychiatry. 2006;60:1088–1097. doi: 10.1016/j.biopsych.2006.04.003. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  31. Klimkeit EI, Mattingley JB, Sheppard DM, Lee P, Bradshaw JL. Motor preparation, motor execution, attention, and executive functions in attention deficit/hyperactivity disorder (ADHD) Child Neuropsychology. 2005;11:153–173. doi: 10.1080/092970490911298. [DOI] [PubMed] [Google Scholar] · DOI
  32. Konishi S, Nakajima K, Uchida I, Kikyo H, Kameyama M, Miyashita Y. Common inhibitory mechanism in human inferior prefrontal cortex revealed by event-related functional MRI. Brain. 1999;122:981–991. doi: 10.1093/brain/122.5.981. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  33. Kuntsi J, McLoughlin G, Asherson P. Attention deficit hyperactivity disorder. Neuromolecular Medicine. 2006;8:461–484. doi: 10.1385/NMM:8:4:461. [DOI] [PubMed] [Google Scholar] · DOI
  34. Lehericy S, Ducros M, Krainik A, Francois C, Van de Moortele PF, Ugurbil K, et al. 3-D diffusion tensor axonal tracking shows distinct SMA and pre-SMA projections to the human striatum. Cerebral Cortex. 2004;14:1302–1309. doi: 10.1093/cercor/bhh091. [DOI] [PubMed] [Google Scholar] · DOI
  35. Leth-Steensen C, Elbaz ZK, Douglas VI. Mean response times, variability, and skew in the responding of ADHD children: A response time distributional approach. Acta Psychologica (Amsterdam) 2000;104:167–190. doi: 10.1016/s0001-6918(00)00019-6. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  36. Lu MT, Preston JB, Strick PL. Interconnections between the prefrontal cortex and the premotor areas in the frontal lobe. Journal of Comparative Neurology. 1994;341:375–392. doi: 10.1002/cne.903410308. [DOI] [PubMed] [Google Scholar] · DOI
  37. Luppino G, Matelli M, Camarda R, Rizzolatti G. Corticocortical connections of area F3 (SMA-proper) and area F6 (pre-SMA) in the macaque monkey. Journal of Comparative Neurology. 1993;338:114–140. doi: 10.1002/cne.903380109. [DOI] [PubMed] [Google Scholar] · DOI
  38. Mahone EM, Koth CW, Cutting L, Singer HS, Denckla MB. Executive function in fluency and recall measures among children with Tourette syndrome or ADHD. Journal of the International Neuropsychological Society. 2001;7:102–111. doi: 10.1017/s1355617701711101. [DOI] [PubMed] [Google Scholar] · DOI
  39. Middleton FA, Strick PL. Cerebellar output channels. In: Schmahmann JD, editor. The cerebellum in cognition. San Diego: Academic Press; 1997. pp. 61–107. [Google Scholar]
  40. Mostofsky SH, Lasker AG, Cutting LE, Denckla MB, Zee DS. Oculomotor abnormalities in attention deficit hyperactivity disorder: A preliminary study. Neurology. 2001;57:423–430. doi: 10.1212/wnl.57.3.423. [DOI] [PubMed] [Google Scholar] · DOI
  41. Mostofsky SH, Newschaffer CJ, Denckla MB. Overflow movements predict impaired response inhibition in children with ADHD. Perceptual and Motor Skills. 2003;97:1315–1331. doi: 10.2466/pms.2003.97.3f.1315. [DOI] [PubMed] [Google Scholar] · DOI
  42. Mostofsky SH, Rimrodt SL, Schafer JG, Boyce A, Goldberg MC, Pekar JJ, et al. Atypical motor and sensory cortex activation in attention-deficit/hyperactivity disorder: A functional magnetic resonance imaging study of simple sequential finger tapping. Biological Psychiatry. 2006;59:48–56. doi: 10.1016/j.biopsych.2005.06.011. [DOI] [PubMed] [Google Scholar] · DOI
  43. Mostofsky SH, Schafer JG, Abrams MT, Goldberg MC, Flower AA, Boyce A, et al. fMRI evidence that the neural basis of response inhibition is task-dependent. Brain Research, Cognitive Brain Research. 2003;17:419–430. doi: 10.1016/s0926-6410(03)00144-7. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  44. Nigg JT. The ADHD response-inhibition deficit as measured by the stop task: Replication with DSM-IV combined type, extension, and qualification. Journal of Abnormal Child Psychology. 1999;27:393–402. doi: 10.1023/a:1021980002473. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  45. Nigg JT. Is ADHD a disinhibitory disorder? Psychological Bulletin. 2001;127:571–598. doi: 10.1037/0033-2909.127.5.571. [DOI] [PubMed] [Google Scholar] · DOI
  46. Picard N, Strick PL. Motor areas of the medial wall: A review of their location and functional activation. Cerebral Cortex. 1996;6:342–353. doi: 10.1093/cercor/6.3.342. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  47. Picton TW, Stuss DT, Alexander MP, Shallice T, Binns MA, Gillingham S. Effects of focal frontal lesions on response inhibition. Cerebral Cortex. 2006;17:826–838. doi: 10.1093/cercor/bhk031. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  48. Pitcher TM, Piek JP, Hay DA. Fine and gross motor ability in males with ADHD. Developmental Medicine and Child Neurology. 2003;45:525–535. doi: 10.1017/s0012162203000975. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  49. Reader MJ, Harris EL, Scheuerholz LJ, Denckla MB. Attention deficit hyperactivity disorder and executive dysfunction. Developmental Neuropsychology. 1994;10:493–512. [Google Scholar]
  50. Reich W. Diagnostic interview for children and adolescents (DICA) Journal of the American Academy of Child and Adolescent Psychiatry. 2000;39:59–66. doi: 10.1097/00004583-200001000-00017. [DOI] [PubMed] [Google Scholar] · DOI
  51. Rubia K, Overmeyer S, Taylor E, Brammer M, Williams SCR, Simmons A, et al. Hypofrontality in attention deficit hyperactivity disorder during higher-order motor control: A study with functional MRI. American Journal of Psychiatry. 1999;156:891–896. doi: 10.1176/ajp.156.6.891. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  52. Rubia K, Russell T, Overmeyer S, Brammer MJ, Bullmore ET, Sharma T, et al. Mapping motor inhibition: Conjunctive brain activations across different versions of go/no-go and stop tasks. Neuroimage. 2001;13:250–261. doi: 10.1006/nimg.2000.0685. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  53. Rubia K, Smith AB, Brammer MJ, Toone B, Taylor E. Abnormal brain activation during inhibition and error detection in medication-naive adolescents with ADHD. American Journal of Psychiatry. 2005;162:1067–1075. doi: 10.1176/appi.ajp.162.6.1067. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  54. Rubia K, Taylor A, Taylor E, Sergeant JA. Synchronization, anticipation, and consistency in motor timing of children with dimensionally defined attention deficit hyperactivity behavior. Perceptual and Motor Skills. 1999;89:1237–1258. doi: 10.2466/pms.1999.89.3f.1237. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  55. Schachar R, Tannock R, Marriott M, Logan G. Deficient inhibitory control in attention deficit hyperactivity disorder. Journal of Abnormal Child Psychology. 1995;23:411–437. doi: 10.1007/BF01447206. [DOI] [PubMed] [Google Scholar] · DOI
  56. Schlaggar BL, Brown TT, Lugar HM, Visscher KM, Miezin FM, Petersen SE. Functional neuroanatomical differences between adults and school-age children in the processing of single words. Science. 2002;296:1476–1479. doi: 10.1126/science.1069464. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  57. Schulz KP, Fan J, Tang CY, Newcorn JH, Buchsbaum MS, Cheung AM, et al. Response inhibition in adolescents diagnosed with attention deficit hyperactivity disorder during childhood: An event-related fMRI study. American Journal of Psychiatry. 2004;161:1650–1657. doi: 10.1176/appi.ajp.161.9.1650. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  58. Shaw P, Lerch J, Greenstein D, Sharp W, Clasen L, Evans A, et al. Longitudinal mapping of cortical thickness and clinical outcome in children and adolescents with attention-deficit/hyperactivity disorder. Archives of General Psychiatry. 2006;63:540–549. doi: 10.1001/archpsyc.63.5.540. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  59. Simmonds DJ, Fotedar SG, Suskauer SJ, Pekar JJ, Denckla MB, Mostofsky SH. Functional brain correlates of response time variability in children. Neuropsychologia. 2007;45:2147–2157. doi: 10.1016/j.neuropsychologia.2007.01.013. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  60. Smith AB, Taylor E, Brammer M, Toone B, Rubia K. Task-specific hypoactivation in prefrontal and temporoparietal brain regions during motor inhibition and task switching in medication-naive children and adolescents with attention deficit hyperactivity disorder. American Journal of Psychiatry. 2006;163:1044–1051. doi: 10.1176/ajp.2006.163.6.1044. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  61. Steger J, Imhof K, Coutts E, Gundelfinger R, Steinhausen HC, Brandeis D. Attentional and neuromotor deficits in ADHD. Developmental Medicine and Child Neurology. 2001;43:172–179. [PubMed] [Google Scholar]
  62. Stevens J, Quittner AL, Zuckerman JB, Moore S. Behavioral inhibition, self-regulation of motivation, and working memory in children with attention deficit hyperactivity disorder. Developmental Neuropsychology. 2002;21:117–139. doi: 10.1207/S15326942DN2102_1. [DOI] [PubMed] [Google Scholar] · DOI
  63. Tamm L, Menon V, Reiss AL. Parietal attentional system aberrations during target detection in adolescents with attention deficit hyperactivity disorder: Event-related fMRI evidence. American Journal of Psychiatry. 2006;163:1033–1043. doi: 10.1176/ajp.2006.163.6.1033. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  64. Toma K, Honda M, Hanakawa T, Okada T, Fukuyama H, Ikeda A, et al. Activities of the primary and supplementary motor areas increase in preparation and execution of voluntary muscle relaxation: An event-related fMRI study. Journal of Neuroscience. 1999;19:3527–3534. doi: 10.1523/JNEUROSCI.19-09-03527.1999. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  65. Toplak ME, Tannock R. Tapping and anticipation performance in attention deficit hyperactivity disorder. Perceptual and Motor Skills. 2005;100:659–675. doi: 10.2466/pms.100.3.659-675. [DOI] [PubMed] [Google Scholar] · DOI
  66. Vaidya CJ, Bunge SA, Dudukovic NM, Zalecki CA, Elliott GR, Gabrieli JD. Altered neural substrates of cognitive control in childhood ADHD: Evidence from functional magnetic resonance imaging. American Journal of Psychiatry. 2005;162:1605–1613. doi: 10.1176/appi.ajp.162.9.1605. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
  67. Wager TD, Sylvester CY, Lacey SC, Nee DE, Franklin M, Jonides J. Common and unique components of response inhibition revealed by fMRI. Neuroimage. 2005;27:323–340. doi: 10.1016/j.neuroimage.2005.01.054. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
  68. Wechsler DL. Wechsler Intelligence Scale for Children—III. San Antonio, TX: The Psychological Corporation; 1991. [Google Scholar]
  69. Wechsler DL. Wechsler Individual Achievement Test. San Antonio, TX: The Psychological Corporation; 1992. [Google Scholar]
  70. Wechsler DL. Weschsler Individual Achievement Test—II. San Antonio, TX: The Psychological Corporation; 2002. [Google Scholar]
  71. Wechsler DL. Wechsler Intelligence Scale for Children—IV. San Antonio, TX: The Psychological Corporation; 2003. [Google Scholar]
  72. Wellington TM, Semrud-Clikeman M, Gregory AL, Murphy JM, Lancaster JL. Magnetic resonance imaging volumetric analysis of the putamen in children with ADHD: Combined type versus control. Journal of Attention Disorders. 2006;10:171–180. doi: 10.1177/1087054705284242. [DOI] [PubMed] [Google Scholar] · DOI

Authors
Suskauer, S. J., Simmonds, D. J., Fotedar, S., Blankner, J. G., Pekar, J. J., Denckla, M. B., & Mostofsky, S. H.
Affiliations
  • Kennedy Krieger Institute (US)
  • 3USM Business Systems, Chantilly, VA
  • 4University of Tennessee College of Medicine
Venue
Journal of Cognitive Neuroscience
Published
2008-03-01
Volume
20
Issue
3
Pages
478-493
ISSN
  • 0898-929X (ISSN-L)
  • 1530-8898
OpenAlex
W2081722843
Cited by
155
References
105
Citations by year
2026: 1 · 2025: 6 · 2024: 3 · 2023: 6 · 2022: 1 · 2021: 6 · 2020: 12 · 2019: 5 · 2018: 7 · 2017: 11 · 2016: 11 · 2015: 8 · 2014: 4 · 2013: 11 · 2012: 11
FWCI
7.85
Type
journal article
Language
en
Open access
Locations
  • Journal of Cognitive Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institute of Mental Health (R01MH085328, R01MH078160)
  • National Institute of Neurological Disorders and Stroke (K02NS044850, R01NS047781)
  • National Center for Research Resources (M01RR000052)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Social Sciences › Psychology › Neuropsychology and Physiological Psychology › Developmental and Educational Neuropsychology
Keywords
attention deficit hyperactivity disorder, response inhibition, response selection, go/no-go task, pre-supplementary motor area, medial frontal cortex, children
MeSH terms
Adolescent, Attention Deficit Disorder with Hyperactivity, Brain Mapping, Cerebral Cortex, Child, Decision Making, Female, Humans, Image Processing, Computer-Assisted, Inhibition, Psychological, Magnetic Resonance Imaging, Male, Neuropsychological Tests, Oxygen, Reaction Time, Case-Control Studies

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