The DOI matches its Crossref record; 15 of the 16 references it cites were found in a registry or an index.
Auditory evoked magnetic fields in adults with fragile X syndrome.
Abstract
Hyper-reactivity and anxiety to sensory stimuli have been described in patients with fragile X syndrome (FXS), and may be related to abnormal processing in afferent sensory pathways. We used magnetoencephalography (MEG) to measure auditory responses to pure tones in 11 adults with FXS and 11 non-FXS subjects. The amplitude for the N100m auditory evoked field component was significantly higher for patients with FXS than for subjects. FXS subjects also had less lateralized N100m anterior-posterior dipole locations. These data may suggest that more neurons are activated by acoustic stimuli in FXS, consistent with subjective experience of increased stimulus intensity. Anomalous cerebral lateralization may suggest an early critical window for effects on neocortical development of the fragile X mental retardation protein (FMRP) produced by the FMR1 gene in individuals with FXS.
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“Auditory hypersensitivity is common in humans with FXS as measured by increased sound evoked responses, reduced habituation and expansion of brain regions activated by auditory stimuli (Rojas et al., 2001; Castrén et al., 2003; Van der Molen et al., 2012; Ethridge et al., 2016).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Rojas et al., 2001
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Cites
An Algorithm for Least-Squares Estimation of Nonlinear Parameters
Marquardt, D. W. (1963) · Journal of the Society for Industrial and Applied Mathematics · doi:10.1137/0111030 · Cited by 30,728
Basic mathematical and electromagnetic concepts of the biomagnetic inverse problem.
Sarvas, J. (1987) · Physics in Medicine and Biology · doi:10.1088/0031-9155/32/1/004 · Cited by 1,945
Fmr1 knockout mice: A model to study fragile X mental retardation
THEDUTCHBELGIANFRAGILEXCONSOR (1994) · Cell · doi:10.1016/0092-8674(94)90569-x · Cited by 1,108
Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
Comery, T. A., Harris, J. B., Willems, P. J., Oostra, B. A., Irwin, S. A., Weiler, I. J., & Greenough, W. T. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5401 · Cited by 1,046
LEFT HEMISPHERE SPECIALIZATION FOR LANGUAGE IN THE NEWBORN
Witelson, S. F., & Pallie, W. (1973) · Brain · doi:10.1093/brain/96.3.641 · Cited by 752
Neuroanatomy of fragile X syndrome
Reiss, A. L., Lee, J., & Freund, L. S. (1994) · Neurology · doi:10.1212/wnl.44.7.1317 · Cited by 191
Auditory M100 component 1: relationship to Heschl's gyri
Reite, M. L., Adams, M., Simon, J. H., Teale, P. D., Sheeder, J. L., Richardson, D., & Grabbe, R. (1994) · Cognitive Brain Research · doi:10.1016/0926-6410(94)90016-7 · Cited by 119
Nakasato, N., Fujita, S., Seki, K., Kawamura, T., Matani, A., Tamura, I., Fujiwara, S., & Yoshimoto, T. (1995) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(94)00280-x · Cited by 117
Magnetic Source Imaging Evidence of Sex Differences in Cerebral Lateralization in Schizophrenia
Reite, M. (1997) · Archives of General Psychiatry · doi:10.1001/archpsyc.1997.01830170059009 · Cited by 98
Late Auditory Magnetic Sources May Differ in the Left Hemisphere of Schizophrenic Patients
Reite, M. L. (1989) · Archives of General Psychiatry · doi:10.1001/archpsyc.1989.01810060087013 · Cited by 78
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1 of the 16 references couldn’t be matched to a known paper.
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- Bakker, 1994, Cell, 78, 23
- Weiler, 1999, Am J Med Genet, 83, 248, 10.1002/(SICI)1096-8628(19990402)83:4<248::AID-AJMG3>3.0.CO;2-1 · DOI
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Gibson, J. R., Bartley, A. F., Hays, S. A., & Huber, K. M. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90752.2008 · Cited by 529
Modeling fragile X syndrome in the Fmr1 knockout mouse
Kazdoba, T. M., Leach, P. T., Silverman, J. L., & Crawley, J. N. (2014) · Intractable & Rare Diseases Research · doi:10.5582/irdr.2014.01024 · Cited by 241
A phenotypic and molecular characterization of the fmr1‐tm1Cgr Fragile X mouse
Yan, Q. J., Asafo‐Adjei, P. K., Arnold, H. M., Brown, R. E., & Bauchwitz, R. P. (2004) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2004.00087.x · Cited by 213
Sinclair, D., Oranje, B., Razak, K. A., Siegel, S. J., & Schmid, S. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.029 · Cited by 198
Wang, J., Ethridge, L. E., Mosconi, M. W., White, S. P., Binder, D. K., Pedapati, E. V., Erickson, C. A., Byerly, M. J., & Sweeney, J. A. (2017) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-017-9191-z · Cited by 176
Metadata
- Authors
- Rojas, D. C., Benkers, T. L., Rogers, S. J., Teale, P. D., Reite, M. L., & Hagerman, R. J.
- Affiliations
- University of Colorado Health (US)
- Venue
- Neuroreport
- Published
- 2001-08
- Volume
- 12
- Issue
- 11
- Pages
- 2573-2576
- ISSN
- 0959-4965 (ISSN-L)
- OpenAlex
- W1981309718
- Cited by
- 73
- References
- 16
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 3 · 2023: 4 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 7 · 2018: 2 · 2017: 3 · 2016: 3 · 2015: 2 · 2014: 6 · 2013: 2 · 2012: 5
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroreport (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD 35468, HD 36071, R01HD036071)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
- Keywords
- fragile X syndrome, auditory evoked magnetic fields, N100m, hemispheric lateralization, FMRP, FMR1 gene, neocortex development
- MeSH terms
- Adult, Evoked Potentials, Auditory, Female, Fragile X Syndrome, Humans, Functional Laterality, Male, Intellectual Disability, Magnetoencephalography
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