White matter hemisphere asymmetries in healthy subjects and in schizophrenia: a diffusion tensor MRI study.
Open accessAbstract
Hemisphere asymmetry was explored in normal healthy subjects and in patients with schizophrenia using a novel voxel-based tensor analysis applied to fractional anisotropy (FA) of the diffusion tensor. Our voxel-based approach, which requires precise spatial normalization to remove the misalignment of fiber tracts, includes generating a symmetrical group average template of the diffusion tensor by applying nonlinear elastic warping of the demons algorithm. We then normalized all 32 diffusion tensor MRIs from healthy subjects and 23 from schizophrenic subjects to the symmetrical average template. For each brain, six channels of tensor component images and one T2-weighted image were used for registration to match tensor orientation and shape between images. A statistical evaluation of white matter asymmetry was then conducted on the normalized FA images and their flipped images. In controls, we found left-higher-than-right anisotropic asymmetry in the anterior part of the corpus callosum, cingulum bundle, the optic radiation, and the superior cerebellar peduncle, and right-higher-than-left anisotropic asymmetry in the anterior limb of the internal capsule and the anterior limb's prefrontal regions, in the uncinate fasciculus, and in the superior longitudinal fasciculus. In patients, the asymmetry was lower, although still present, in the cingulum bundle and the anterior corpus callosum, and not found in the anterior limb of the internal capsule, the uncinate fasciculus, and the superior cerebellar peduncle compared to healthy subjects. These findings of anisotropic asymmetry pattern differences between healthy controls and patients with schizophrenia are likely related to neurodevelopmental abnormalities in schizophrenia.
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?
Hemispheric asymmetry in the UF has been observed for both volume and diffusion metrics, but there are inconsistencies in the directionality of such asymmetry.
“Hemispheric asymmetry in the UF has been observed for both volume and diffusion metrics but there are inconsistencies in the directionality of such asymmetry of the UF.”
From Cortical Terminations of the Inferior Fronto-Occipital and Uncinate Fasciculi: Anatomical Stem-Based Virtual Dissection (2016) · cites this paper as Park et al., 2004
The Discussion (page unavailable) reports differing left–right patterns of uncinate fasciculus fractional anisotropy and concludes that its asymmetry remains controversial. It also cites a postmortem finding for cross-sectional area and fiber number, but does not report an uncinate fasciculus volume measurement; that specific part of the claim is not established by our copy. (LLM, conf=0.85)
Experimental — accuracy not yet measured
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 72 · Cited by 295
Research works printed but not linked: 67
- Aboitiz F, Scheibel AB, Fisher RS, Zaidel E. Fiber composition of the human corpus callosum. Brain Res. 1992;598 (1–2):143–153. doi: 10.1016/0006-8993(92)90178-c. [DOI] [PubMed] [Google Scholar] · DOI
- Akbarian S, Kim JJ, Potkin SG, Hetrick WP, Bunney WE, Jr, Jones EG. Maldistribution of interstitial neurons in prefrontal white matter of the brains of schizophrenic patients. Arch Gen Psychiatry. 1996;53 (5):425–436. doi: 10.1001/archpsyc.1996.01830050061010. [DOI] [PubMed] [Google Scholar] · DOI
- Amunts K, Jancke L, Mohlberg H, Steinmetz H, Zilles K. Interhemispheric asymmetry of the human motor cortex related to handedness and gender. Neuropsychologia. 2000;38 (3):304–312. doi: 10.1016/s0028-3932(99)00075-5. [DOI] [PubMed] [Google Scholar] · DOI
- Anderson B, Southern BD, Powers RE. Anatomic asymmetries of the posterior superior temporal lobes: a postmortem study. Neuropsychiatry Neuropsychol Behav Neurol. 1999;12 (4):247–254. [PubMed] [Google Scholar]
- Barnea-Goraly N, Eliez S, Hedeus M, Menon V, White CD, Moseley M, Reiss AL. White matter tract alterations in fragile X syndrome: preliminary evidence from diffusion tensor imaging. Am J Med Genet. 2003;118B (1):81–88. doi: 10.1002/ajmg.b.10035. [DOI] [PubMed] [Google Scholar] · DOI
- Basser PJ. Inferring microstructural features and the physiological state of tissues from diffusion-weighted images. NMR Biomed. 1995;8 (7–8):333–344. doi: 10.1002/nbm.1940080707. [DOI] [PubMed] [Google Scholar] · DOI
- Basser PJ, Mattiello J, LeBihan D. MR diffusion tensor spectroscopy and imaging. Biophys J. 1994;66 (1):259–267. doi: 10.1016/S0006-3495(94)80775-1. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- Beaton AA. The relation of planum temporale asymmetry and morphology of the corpus callosum to handedness, gender, and dyslexia: a review of the evidence. Brain Lang. 1997;60 (2):255–322. doi: 10.1006/brln.1997.1825. [DOI] [PubMed] [Google Scholar] · DOI
- Buchsbaum MS, Tang CY, Peled S, Gudbjartsson H, Lu D, Hazlett EA, Downhill J, Haznedar M, Fallon JH, Atlas SW. MRI white matter diffusion anisotropy and PET metabolic rate in schizophrenia. NeuroReport. 1998;9 (3):425–430. doi: 10.1097/00001756-199802160-00013. [DOI] [PubMed] [Google Scholar] · DOI
- Burns J, Job D, Bastin ME, Whalley H, Macgillivray T, Johnstone EC, Lawrie SM. Structural disconnectivity in schizophrenia: a diffusion tensor magnetic resonance imaging study. Br J Psychiatry. 2003;182:439–443. [PubMed] [Google Scholar]
- Cao Y, Whalen S, Huang J, Berger KL, DeLano MC. Asymmetry of subinsular anisotropy by in vivo diffusion tensor imaging. Hum Brain Mapp. 2003;20:82–90. doi: 10.1002/hbm.10130. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- Deakin JF, Simpson MD. A two-process theory of schizophrenia: evidence from studies in post-mortem brain. J Psychiatr Res. 1997;31 (2):277–295. doi: 10.1016/s0022-3956(96)00042-8. [DOI] [PubMed] [Google Scholar] · DOI
- Di Virgilio G, Clarke S. Direct interhemispheric visual input to human speech areas. Hum Brain Mapp. 1997;5 (5):347–354. doi: 10.1002/(SICI)1097-0193(1997)5:5<347::AID-HBM3>3.0.CO;2-3. [DOI] [PubMed] [Google Scholar] · DOI
- Ebeling U, von Cramon D. Topography of the uncinate fascicle and adjacent temporal fiber tracts. Acta Neurochir (Wien) 1992;115 (3–4):143–148. doi: 10.1007/BF01406373. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- Eriksson SH, Rugg-Gunn FJ, Symms MR, Barker GJ, Duncan JS. Diffusion tensor imaging in patients with epilepsy and malformations of cortical development. Brain. 2001;124 (Pt 3):617–626. doi: 10.1093/brain/124.3.617. [DOI] [PubMed] [Google Scholar] · DOI
- Foong J, Symms MR, Barker GJ, Maier M, Miller DH, Ron MA. Investigating regional white matter in schizophrenia using diffusion tensor imaging. NeuroReport. 2002;13 (3):333–336. doi: 10.1097/00001756-200203040-00017. [DOI] [PubMed] [Google Scholar] · DOI
- Galaburda AM, LeMay M, Kemper TL, Geschwind N. Right–left asymmetrics in the brain. Science. 1978a;199 (4331):852–856. doi: 10.1126/science.341314. [DOI] [PubMed] [Google Scholar] · DOI
- Galaburda AM, Sanides F, Geschwind N. Human brain. Cytoarchitectonic left-right asymmetries in the temporal speech region. Arch Neurol. 1978b;35 (12):812–817. doi: 10.1001/archneur.1978.00500360036007. [DOI] [PubMed] [Google Scholar] · DOI
- Gazzaniga MS. Cerebral specialization and interhemispheric communication: does the corpus callosum enable the human condition? Brain. 2000;123 (Pt 7):1293–1326. doi: 10.1093/brain/123.7.1293. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- Geschwind N. Cerebral dominance and anatomic asymmetry. N Engl J Med. 1972;287 (4):194–195. doi: 10.1056/NEJM197207272870416. [DOI] [PubMed] [Google Scholar] · DOI
- Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: I A hypothesis and a program for research. Arch Neurol. 1985a;42 (5):428–459. doi: 10.1001/archneur.1985.04060050026008. [DOI] [PubMed] [Google Scholar] · DOI
- Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: II A hypothesis and a program for research. Arch Neurol. 1985b;42 (6):521–552. doi: 10.1001/archneur.1985.04060060019009. [DOI] [PubMed] [Google Scholar] · DOI
- Geschwind N, Galaburda AM. Cerebral lateralization. Biological mechanisms, associations, and pathology: III A hypothesis and a program for research. Arch Neurol. 1985c;42 (7):634–654. doi: 10.1001/archneur.1985.04060070024012. [DOI] [PubMed] [Google Scholar] · DOI
- Good CD, Johnsrude I, Ashburner J, Henson RN, Friston KJ, Frackowiak RS. Cerebral asymmetry and the effects of sex and handedness on brain structure: a voxel-based morphometric analysis of 465 normal adult human brains. NeuroImage. 2001;14 (3):685–700. doi: 10.1006/nimg.2001.0857. [DOI] [PubMed] [Google Scholar] · DOI
- Gudbjartsson H, Maier SE, Mulkern RV, Morocz IA, Patz S, Jolesz FA. Line scan diffusion imaging. Magn Reson Med. 1996;36 (4):509–519. doi: 10.1002/mrm.1910360403. [DOI] [PubMed] [Google Scholar] · DOI
- Guimond A, Meunier J, Thirion JP. Average brain models: a convergence study. Comput Vis Image Underst. 2000;77:192–210. [Google Scholar]
- Guimond A, Roche A, Ayache N, Meunier J. Three-dimensional multimodal brain warping using the demons algorithm and adaptive intensity corrections. IEEE Trans Med Imag. 2001;20 (1):58–69. doi: 10.1109/42.906425. [DOI] [PubMed] [Google Scholar] · DOI
- Guimond A, Guttmann CRG, Warfield SK, Westin C-F. Deformable registration of DT-MRI data based on transformation invariant tensor characteristics. Proceedings of the IEEE International Symposium on Biomedical Imaging (ISBI’02); Washington (DC), USA. 2002. [Google Scholar]
- Highley JR, Esiri MM, McDonald B, Cooper SJ, Crow TJ. Temporal-lobe length is reduced, and gyral folding is increased in schizophrenia: a post-mortem study. Schizophr Res. 1998a;34 (1–2):1–12. doi: 10.1016/s0920-9964(98)00078-4. [DOI] [PubMed] [Google Scholar] · DOI
- Highley JR, Esiri MM, McDonald B, Cortina-Borja M, Cooper SJ, Herron BM, Crow TJ. Anomalies of cerebral asymmetry in schizophrenia interact with gender and age of onset: a post-mortem study. Schizophr Res. 1998b;34 (1–2):13–25. doi: 10.1016/s0920-9964(98)00077-2. [DOI] [PubMed] [Google Scholar] · DOI
- Highley JR, McDonald B, Walker MA, Esiri MM, Crow TJ. Schizophrenia and temporal lobe asymmetry. A post-mortem stereological study of tissue volume. Br J Psychiatry. 1999;175:127–134. doi: 10.1192/bjp.175.2.127. [DOI] [PubMed] [Google Scholar] · DOI
- Highley JR, Walker MA, Esiri MM, Crow TJ, Harrison PJ. Asymmetry of the uncinate fasciculus: a post-mortem study of normal subjects and patients with schizophrenia. Cereb Cortex. 2002;12 (11):1218–1224. doi: 10.1093/cercor/12.11.1218. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- Holinger DP, Galaburda AM, Harrison PJ. Cerebral asymmetry. In: Harrison PJ, Roberts GW, editors. The Neuropathology of Schizophrenia. Progress and Interpretation. Oxford Univ. Press; Oxford: 2000. pp. 151–172. [Google Scholar]
- Kennedy DN, O’Craven KM, Ticho BS, Goldstein AM, Makris N, Henson JW. Structural and functional brain asymmetries in human situs inversus totalis. Neurology. 1999;53 (6):1260–1265. doi: 10.1212/wnl.53.6.1260. [DOI] [PubMed] [Google Scholar] · DOI
- Kimura D. The asymmetry of the human brain. Sci Am. 1973;228 (3):70–78. doi: 10.1038/scientificamerican0373-70. [DOI] [PubMed] [Google Scholar] · DOI
- Kubicki M, Westin CF, Maier SE, Frumin M, Nestor PG, Salisbury DF, Kikinis R, Jolesz FA, McCarley RW, Shenton ME. Uncinate fasciculus findings in schizophrenia: a magnetic resonance diffusion tensor imaging study. Am J Psychiatry. 2002;159 (5):813–820. doi: 10.1176/appi.ajp.159.5.813. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- Kubicki M, Westin CF, Nestor PG, Wible CG, Frumin M, Maier SE, Kikinis R, Jolesz FA, McCarley RW, Shenton ME. Cingulate fasciculus integrity disruption in schizophrenia: a magnetic resonance diffusion tensor imaging study. Biol Psychiatry. 2003;54 (11):1171–1180. doi: 10.1016/s0006-3223(03)00419-0. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- Lancaster JL, Kochunov PV, Thompson PM, Toga AW, Fox PT. Asymmetry of the brain surface from deformation field analysis. Hum Brain Mapp. 2003;19 (2):79–89. doi: 10.1002/hbm.10105. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- Lim KO, Hedehus M, Moseley M, de Crespigny A, Sullivan EV, Pfefferbaum A. Compromised white matter tract integrity in schizophrenia inferred from diffusion tensor imaging. Arch Gen Psychiatry. 1999;56 (4):367–374. doi: 10.1001/archpsyc.56.4.367. [DOI] [PubMed] [Google Scholar] · DOI
- Lin CC, Mudholkar GS. A simple test for normality against asymmetric alternatives. Biometrika. 1980;67:455–461. [Google Scholar]
- Maier SE, Gudbjartsson H, Patz S, Hsu L, Lovblad KO, Edelman RR, Warach S, Jolesz FA. Line scan diffusion imaging: characterization in healthy subjects and stroke patients. AJR Am J Roentgenol. 1998;171 (1):85–93. doi: 10.2214/ajr.171.1.9648769. [DOI] [PubMed] [Google Scholar] · DOI
- Makris N, Meyer JW, Bates JF, Yeterian EH, Kennedy DN, Caviness VS. MRI-Based topographic parcellation of human cerebral white matter and nuclei II. Rationale and applications with systematics of cerebral connectivity. NeuroImage. 1999;9 (1):18–45. doi: 10.1006/nimg.1998.0384. [DOI] [PubMed] [Google Scholar] · DOI
- Mamata H, Mamata Y, Westin CF, Shenton ME, Kikinis R, Jolesz FA, Maier SE. High-resolution line scan diffusion tensor MR imaging of white matter fiber tract anatomy. AJNR Am J Neuroradiol. 2002;23 (1):67–75. [PMC free article] [PubMed] [Google Scholar]
- McDonald B, Highley JR, Walker MA, Herron BM, Cooper SJ, Esiri MM, Crow TJ. Anomalous asymmetry of fusiform and parahippocampal gyrus gray matter in schizophrenia: a postmortem study. Am J Psychiatry. 2000;157 (1):40–47. doi: 10.1176/ajp.157.1.40. [DOI] [PubMed] [Google Scholar] · DOI
- Moffat SD, Hampson E, Lee DH. Morphology of the planum temporale and corpus callosum in left handers with evidence of left and right hemisphere speech representation. Brain. 1998;121 (Pt 12):2369–2379. doi: 10.1093/brain/121.12.2369. [DOI] [PubMed] [Google Scholar] · DOI
- Mohr B, Heim S, Pulvermuller F, Rockstroh B. Functional asymmetry in schizophrenic patients during auditory speech processing. Schizophr Res. 2001;52 (1–2):69–78. doi: 10.1016/s0920-9964(00)00183-3. [DOI] [PubMed] [Google Scholar] · DOI
- Nestor PG, Shenton ME, Wible C, Hokama H, O’Donnell BF, Law S, McCarley RW. A neuropsychological analysis of schizophrenic thought disorder. Schizophr Res. 1998;29 (3):217–225. doi: 10.1016/s0920-9964(97)00101-1. [DOI] [PubMed] [Google Scholar] · DOI
- Park HJ, Kubicki M, Shenton ME, Guimond A, McCarley RW, Maier M, Kikinis R, Jolesz FA, Westin CF. Spatial normalization of diffusion tensor MRI using multiple channels. Neuro-Image. 2003a;20 (4):1995–2009. doi: 10.1016/j.neuroimage.2003.08.008. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
- Park HJ, Westin C-F, Brun A, Kubicki M, McCarley RW, Shenton ME. A method for hemispheric asymmetry of white matters using diffusion tensor MRI. Proceedings of Human Brain Mapping 2003; New York, USA. 2003b. Neuroimage S(918) [Google Scholar]
- Peled S, Gudbjartsson H, Westin CF, Kikinis R, Jolesz FA. Magnetic resonance imaging shows orientation and asymmetry of white matter fiber tracts. Brain Res. 1998;780 (1):27–33. doi: 10.1016/s0006-8993(97)00635-5. [DOI] [PubMed] [Google Scholar] · DOI
- Pujol J, Lopez-Sala A, Deus J, Cardoner N, Sebastian-Galles N, Conesa G, Capdevila A. The lateral asymmetry of the human brain studied by volumetric magnetic resonance imaging. NeuroImage. 2002;17 (2):670–679. [PubMed] [Google Scholar]
- Rockstroh B, Kissler J, Mohr B, Eulitz C, Lommen U, Wienbruch C, Cohen R, Elbert T. Altered hemispheric asymmetry of auditory magnetic fields to tones and syllables in schizophrenia. Biol Psychiatry. 2001;49 (8):694–703. doi: 10.1016/s0006-3223(00)01023-4. [DOI] [PubMed] [Google Scholar] · DOI
- Rosen GD, Sherman GF, Galaburda AM. Neuronal subtypes and anatomic asymmetry: changes in neuronal number and cell-packing density. Neuroscience. 1993;56 (4):833–839. doi: 10.1016/0306-4522(93)90131-x. [DOI] [PubMed] [Google Scholar] · DOI
- Rugg-Gunn FJ, Eriksson SH, Symms MR, Barker GJ, Duncan JS. Diffusion tensor imaging of cryptogenic and acquired partial epilepsies. Brain. 2001;124 (Pt 3):627–636. doi: 10.1093/brain/124.3.627. [DOI] [PubMed] [Google Scholar] · DOI
- Sommer IE, Ramsey NF, Kahn RS. Language lateralization in schizophrenia, an fMRI study. Schizophr Res. 2001;52 (1–2):57–67. doi: 10.1016/s0920-9964(00)00180-8. [DOI] [PubMed] [Google Scholar] · DOI
- Springer SP, Deutsch G. Left Brain, Right Brain: Perspectives From Cognitive Neuroscience Freeman and Co. Worth Publishers; USA: 1998. [Google Scholar]
- Takahashi T, Kawasaki Y, Kurokawa K, Hagino H, Nohara S, Yamashita I, Nakamura K, Murata M, Matsui M, Suzuki M, Seto H, Kurachi M. Lack of normal structural asymmetry of the anterior cingulate gyrus in female patients with schizophrenia: a volumetric magnetic resonance imaging study. Schizophr Res. 2002;55 (1–2):69–81. doi: 10.1016/s0920-9964(01)00200-6. [DOI] [PubMed] [Google Scholar] · DOI
- Toga AW, Thompson PM. Maps of the brain. Anat Rec. 2001;265 (2):37–53. doi: 10.1002/ar.1057. [DOI] [PubMed] [Google Scholar] · DOI
- Toga AW, Thompson PM. Mapping brain asymmetry. Nat Rev Neurosci. 2003;4 (1):37–48. doi: 10.1038/nrn1009. [DOI] [PubMed] [Google Scholar] · DOI
- Turetsky B, Cowell PE, Gur RC, Grossman RI, Shtasel DL, Gur RE. Frontal and temporal lobe brain volumes in schizophrenia. Relationship to symptoms and clinical subtype. Arch Gen Psychiatry. 1995;52 (12):1061–1070. doi: 10.1001/archpsyc.1995.03950240079013. [DOI] [PubMed] [Google Scholar] · DOI
- Watkins KE, Paus T, Lerch JP, Zijdenbos A, Collins DL, Neelin P, Taylor J, Worsley KJ, Evans AC. Structural asymmetries in the human brain: a voxel-based statistical analysis of 142 MRI scans. Cereb Cortex. 2001;11 (9):868–877. doi: 10.1093/cercor/11.9.868. [DOI] [PubMed] [Google Scholar] · DOI
- Wechsler D. Wechsler Adult Intelligence Scale Psychological Corp. San Antonio, TX (Harcourt): 1997a. [Google Scholar]
- Wechsler D. The Wechsler Memory Scale Psychological Corp. San Antonio, TX (Harcourt): 1997b. [Google Scholar]
- Westbury CF, Zatorre RJ, Evans AC. Quantifying variability in the planum temporale: a probability map. Cereb Cortex. 1999;9 (4):392–405. doi: 10.1093/cercor/9.4.392. [DOI] [PubMed] [Google Scholar] · DOI
- Westin CF, Maier SE, Mamata H, Nabavi A, Jolesz FA, Kikinis R. Processing and visualization for diffusion tensor MRI. Med Image Anal. 2002;6 (2):93–108. doi: 10.1016/s1361-8415(02)00053-1. [DOI] [PubMed] [Google Scholar] · DOI
- Youn T, Park HJ, Kim JJ, Kim MS, Kwon JS. Altered hemispheric asymmetry and positive symptoms in schizophrenia: equivalent current dipole of auditory mismatch negativity. Schizophr Res. 2003;59 (2–3):253–260. doi: 10.1016/s0920-9964(02)00154-8. [DOI] [PubMed] [Google Scholar] · DOI
- Zhou SY, Suzuki M, Hagino H, Takahashi T, Kawasaki Y, Nohara I, Yamashita I, Seto H, Kurachi M. Decreased volume and increased asymmetry of the anterior limb of the internal capsule in patients with schizophrenia. Biol Psychiatry. 2003;54 (4):427–436. doi: 10.1016/s0006-3223(03)00007-6. [DOI] [PubMed] [Google Scholar] · DOI
- Authors
- Park, H.-J., Westin, C.-F., Kubicki, M., Maier, S. E., Niznikiewicz, M., Baer, A., Frumin, M., Kikinis, R., Jolesz, F. A., McCarley, R. W., & Shenton, M. E.
- Affiliations
- Brigham and Women's Hospital (US)
- Harvard University (US)
- Corresponding author
- Shenton, Martha E.
- ORCID
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2004-09
- Volume
- 23
- Issue
- 1
- Pages
- 213-223
- ISSN
- 1053-8119 (ISSN-L)
- PMC
- PMC2794419
- OpenAlex
- W2162632094
- Cited by
- 295
- References
- 72
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 7 · 2023: 5 · 2022: 6 · 2021: 11 · 2020: 9 · 2019: 12 · 2018: 17 · 2017: 14 · 2016: 11 · 2015: 14 · 2014: 10 · 2013: 9 · 2012: 19
- FWCI
- 15.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Funders
- Korea Science and Engineering Foundation
- National Institutes of Health (K02 MH 01110, R01 MH 40799, R01 MH 50747, R01 NS 39335, RO3 MH068464-01)
- National Center for Research Resources (11747, P41-RR13218)
- U.S. Department of Veterans Affairs
- National Alliance for Research on Schizophrenia and Depression
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Hemispheric Asymmetry in Neuroscience
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- schizophrenia, hemispheric lateralization, white matter, fractional anisotropy, corpus callosum, cingulum, optic radiation, superior cerebellar peduncle, internal capsule, uncinate fasciculus, superior longitudinal fasciculus, Demons algorithm, spatial normalization, neurodevelopmental abnormalities
- MeSH terms
- Adult, Algorithms, Brain, Cerebellum, Corpus Callosum, Dominance, Cerebral, Gyrus Cinguli, Humans, Image Processing, Computer-Assisted, Male, Middle Aged, Nerve Fibers, Optic Nerve, Reference Values, Schizophrenia, Artifacts, Anisotropy, Prefrontal Cortex, Perforant Pathway, Internal Capsule, Diffusion Magnetic Resonance Imaging
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