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Journal articles on the topic 'Interhemispheric processing'

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1

Banich, Marie T., and Joel I. Shenker. "Investigations of interhemispheric processing: Methodological considerations." Neuropsychology 8, no. 2 (1994): 263–77. http://dx.doi.org/10.1037/0894-4105.8.2.263.

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2

Catts, S. V., P. B. Ward, J. R. Garvey, and N. McConaghy. "SEPs and interhemispheric processing in schizophrenia." Electroencephalography and Clinical Neurophysiology 61, no. 3 (1985): S175. http://dx.doi.org/10.1016/0013-4694(85)90674-1.

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3

Soshi, Takahiro. "Neural Coupling between Interhemispheric and Frontoparietal Functional Connectivity during Semantic Processing." Brain Sciences 13, no. 11 (2023): 1601. http://dx.doi.org/10.3390/brainsci13111601.

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Interhemispheric and frontoparietal functional connectivity have been reported to increase during explicit information processing. However, it is unclear how and when interhemispheric and frontoparietal functional connectivity interact during explicit semantic processing. Here, we tested the neural coupling hypothesis that explicit semantic processing promotes neural activity in the nondominant right hemispheric areas, owing to synchronization with enhanced frontoparietal functional connectivity at later processing stages. We analyzed electroencephalogram data obtained using a semantic priming
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4

Banich, Marie T., Sara Goering, Neal Stolar, and Aysenil Belger. "Interhemispheric Processing in Left- and Right-Handers." International Journal of Neuroscience 54, no. 3-4 (1990): 197–208. http://dx.doi.org/10.3109/00207459008986636.

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5

Bocci, Tommaso, Davide Barloscio, Laura Parenti, et al. "O201 Interhemispheric processing in hyperkinetic movement disorders." Clinical Neurophysiology 128, no. 9 (2017): e242. http://dx.doi.org/10.1016/j.clinph.2017.07.209.

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6

Bayard, Sophie, Nadia Gosselin, Manon Robert, and Maryse Lassonde. "Inter- and Intra-hemispheric Processing of Visual Event-related Potentials in the Absence of the Corpus Callosum." Journal of Cognitive Neuroscience 16, no. 3 (2004): 401–14. http://dx.doi.org/10.1162/089892904322926746.

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Interhemispheric differences of the N100 latency in visual evoked potentials have been used to estimate interhemispheric transfer time (e.g., Saron & Davidson, 1989). Recent work has also suggested that the P300 component could reflect the efficacy of interhemispheric transmission (Polich & Hoffman, 1998). The purpose of the present study was to study the differential role of the corpus callosum (CC) and anterior commissure (AC) in the interhemispheric propagation of these two electrophysiological components. Thus, the amplitude and latency distribution of the N100 and P300 components
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7

Takeuchi, Naoyuki, Yutaka Oouchida, and Shin-Ichi Izumi. "Motor Control and Neural Plasticity through Interhemispheric Interactions." Neural Plasticity 2012 (2012): 1–13. http://dx.doi.org/10.1155/2012/823285.

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The corpus callosum, which is the largest white matter structure in the human brain, connects the 2 cerebral hemispheres. It plays a crucial role in maintaining the independent processing of the hemispheres and in integrating information between both hemispheres. The functional integrity of interhemispheric interactions can be tested electrophysiologically in humans by using transcranial magnetic stimulation, electroencephalography, and functional magnetic resonance imaging. As a brain structural imaging, diffusion tensor imaging has revealed the microstructural connectivity underlying interhe
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8

Christman, Stephen D., and Ruth E. Propper. "Superior episodic memory is associated with interhemispheric processing." Neuropsychology 15, no. 4 (2001): 607–16. http://dx.doi.org/10.1037/0894-4105.15.4.607.

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9

Putnam, Mary Colvin, Megan S. Steven, Karl W. Doron, Adam C. Riggall, and Michael S. Gazzaniga. "Cortical Projection Topography of the Human Splenium: Hemispheric Asymmetry and Individual Differences." Journal of Cognitive Neuroscience 22, no. 8 (2010): 1662–69. http://dx.doi.org/10.1162/jocn.2009.21290.

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The corpus callosum is the largest white matter pathway in the human brain. The most posterior portion, known as the splenium, is critical for interhemispheric communication between visual areas. The current study employed diffusion tensor imaging to delineate the complete cortical projection topography of the human splenium. Homotopic and heterotopic connections were revealed between the splenium and the posterior visual areas, including the occipital and the posterior parietal cortices. In nearly one third of participants, there were homotopic connections between the primary visual cortices,
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10

Kim, Sangyub, Joonwoo Kim, and Kichun Nam. "Electrophysiological Evidence Reveals the Asymmetric Transfer from the Right to Left Hemisphere as Key to Reading Proficiency." Brain Sciences 13, no. 4 (2023): 621. http://dx.doi.org/10.3390/brainsci13040621.

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The present investigation aimed to explore the interhemispheric interactions that contribute to changes in reading proficiency by examining the processing of visual word recognition in relation to word familiarity. A lexical decision task was administered to 25 participants, and their electrophysiological activity was recorded. A behavioral analysis showed the faster and more accurate processing of highly familiar words compared to less familiar ones. An event-related potential analysis uncovered an asymmetric familiarity effect over the N100 and N400 components across the two hemispheres, ind
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11

Stracke, H., H. Okamoto, and C. Pantev. "Interhemispheric Support during Demanding Auditory Signal-in-Noise Processing." Cerebral Cortex 19, no. 6 (2008): 1440–47. http://dx.doi.org/10.1093/cercor/bhn183.

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12

Stephan, K. E., J. C. Marshall, W. D. Penny, K. J. Friston, and G. R. Fink. "Interhemispheric Integration of Visual Processing during Task-Driven Lateralization." Journal of Neuroscience 27, no. 13 (2007): 3512–22. http://dx.doi.org/10.1523/jneurosci.4766-06.2007.

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13

Steinmann, Saskia, and Christoph Mulert. "Functional relevance of interhemispheric fiber tracts in speech processing." Journal of Neurolinguistics 25, no. 1 (2012): 1–12. http://dx.doi.org/10.1016/j.jneuroling.2011.07.003.

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14

Eshel, N., CC Ruff, F. Blankenburg, and J. Driver. "Parietal TMS reveals excitatory interhemispheric interactions during somatosensory processing." NeuroImage 47 (July 2009): S131. http://dx.doi.org/10.1016/s1053-8119(09)71282-0.

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15

Mohr, Bettina, Anna Landgrebe, and Stefan R. Schweinberger. "Interhemispheric cooperation for familiar but not unfamiliar face processing." Neuropsychologia 40, no. 11 (2002): 1841–48. http://dx.doi.org/10.1016/s0028-3932(02)00040-4.

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16

Maertens, Marianne, and Stefan Pollmann. "Interhemispheric resource sharing: Decreasing benefits with increasing processing efficiency." Brain and Cognition 58, no. 2 (2005): 183–92. http://dx.doi.org/10.1016/j.bandc.2004.11.002.

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17

Brysbaert, Marc. "Interhemispheric transfer and the processing of foveally presented stimuli." Behavioural Brain Research 64, no. 1-2 (1994): 151–61. http://dx.doi.org/10.1016/0166-4328(94)90127-9.

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18

Leisman, Gerry, and Robert Melillo. "A call to arms: Somatosensory perception and action." Behavioral and Brain Sciences 30, no. 2 (2007): 214–15. http://dx.doi.org/10.1017/s0140525x07001537.

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AbstractSomatosensory processing for action guidance can be dissociated from perception and memory processing. The dorsal system has a global bias and the ventral system has a local processing bias. Autistics illustrate the point, showing a bias for part over wholes. Lateralized differences have also been noted in these modalities. The multi-modal dysfunction observed may suggest more an issue of interhemispheric communication.
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19

Chan, Russell W., Alex T. L. Leong, Leon C. Ho, et al. "Low-frequency hippocampal–cortical activity drives brain-wide resting-state functional MRI connectivity." Proceedings of the National Academy of Sciences 114, no. 33 (2017): E6972—E6981. http://dx.doi.org/10.1073/pnas.1703309114.

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The hippocampus, including the dorsal dentate gyrus (dDG), and cortex engage in bidirectional communication. We propose that low-frequency activity in hippocampal–cortical pathways contributes to brain-wide resting-state connectivity to integrate sensory information. Using optogenetic stimulation and brain-wide fMRI and resting-state fMRI (rsfMRI), we determined the large-scale effects of spatiotemporal-specific downstream propagation of hippocampal activity. Low-frequency (1 Hz), but not high-frequency (40 Hz), stimulation of dDG excitatory neurons evoked robust cortical and subcortical brain
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20

Sauerwein, H. "Intra- and interhemispheric processing of visual information in callosal agenesis." Neurocase 2, no. 3 (1996): 183af—202. http://dx.doi.org/10.1093/neucas/2.3.183-af.

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21

RATINCKX, E., H. NUERK, J. VANDIJCK, and K. WILLMES. "Effects of Interhemispheric Communication on Two-Digit Arabic Number Processing." Cortex 42, no. 8 (2006): 1128–37. http://dx.doi.org/10.1016/s0010-9452(08)70225-9.

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22

Müller-Oehring, Eva M., Tilman Schulte, Erich Kasten, et al. "Parallel interhemispheric processing in hemineglect: Relation to visual field defects." Neuropsychologia 47, no. 12 (2009): 2397–408. http://dx.doi.org/10.1016/j.neuropsychologia.2009.04.014.

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23

Brown, Warren S., and Malcolm A. Jeeves. "Bilateral visual field processing and evoked potential interhemispheric transmission time." Neuropsychologia 31, no. 12 (1993): 1267–81. http://dx.doi.org/10.1016/0028-3932(93)90097-j.

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24

Phillips, Kimberley A., Cheryl D. Stimpson, Jeroen B. Smaers, et al. "The corpus callosum in primates: processing speed of axons and the evolution of hemispheric asymmetry." Proceedings of the Royal Society B: Biological Sciences 282, no. 1818 (2015): 20151535. http://dx.doi.org/10.1098/rspb.2015.1535.

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Interhemispheric communication may be constrained as brain size increases because of transmission delays in action potentials over the length of axons. Although one might expect larger brains to have progressively thicker axons to compensate, spatial packing is a limiting factor. Axon size distributions within the primate corpus callosum (CC) may provide insights into how these demands affect conduction velocity. We used electron microscopy to explore phylogenetic variation in myelinated axon density and diameter of the CC from 14 different anthropoid primate species, including humans. The maj
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25

Van der Haegen, Lise, Qing Cai, Michaël A. Stevens, and Marc Brysbaert. "Interhemispheric Communication Influences Reading Behavior." Journal of Cognitive Neuroscience 25, no. 9 (2013): 1442–52. http://dx.doi.org/10.1162/jocn_a_00412.

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We can read words at an amazing speed, with the left hemisphere taking the burden of the processing in most readers (i.e., over 95% of right-handers and about 75% of left-handers). Yet, it is a long-standing question whether word reading in central vision is possible without information transfer between the left and right hemispheres (LH/RH). Here we show that such communication is required by comparing word naming latencies and eye movement data of people with LH language dominance and a unique sample of healthy RH dominant people. The results reveal that individuals with LH speech dominance
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26

Biondi, Massimo, Pasquale Parise, Piero Venturi, Lucilla Riccio, Giacobba Brunetti, and Paolo Pancheri. "Frontal Hemisphere Lateralization and Depressive Personality Traits." Perceptual and Motor Skills 77, no. 3 (1993): 1035–42. http://dx.doi.org/10.2466/pms.1993.77.3.1035.

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To assess the relationship between hemispheric differences in information processing and interhemispheric asymmetries in terms of brain bioelectrical activity, we correlated scores on the MMPI Depression scale with interhemispheric asymmetry, measured as peak amplitude and latency of the P3 component of somatosensory evoked potentials (SEPs) at the frontocortical region of 14 healthy unselected volunteers (8 men and 6 women) who were about to start a course in autogenic training. The sample was subdivided into two groups on the basis of the median score on the MMPI Depression scale. Subjects s
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27

Hunter, Zoë R., Marc Brysbaert, and Stefan Knecht. "Foveal Word Reading Requires Interhemispheric Communication." Journal of Cognitive Neuroscience 19, no. 8 (2007): 1373–87. http://dx.doi.org/10.1162/jocn.2007.19.8.1373.

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The left cerebral hemisphere is dominant for language processing in most individuals. It has been suggested that this asymmetric language representation can influence behavioral performance in foveal word-naming tasks. We carried out two experiments in which we obtained laterality indices by means of functional imaging during a mental word-generation task, using functional transcranial Doppler sonography and functional magnetic resonance imaging, respectively. Subsequently, we administered a behavioral word-naming task, where participants had to name foveally presented words of different lengt
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28

Savage, Cary R., and David G. Thomas. "Information Processing and Interhemispheric Transfer in Left- and Right-Handed Adults." International Journal of Neuroscience 71, no. 1-4 (1993): 201–19. http://dx.doi.org/10.3109/00207459309000605.

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29

Todorow, Michelle, Joseph F. DeSouza, Brenda L. Banwell, and Christine Till. "Interhemispheric cooperation in global–local visual processing in pediatric multiple sclerosis." Journal of Clinical and Experimental Neuropsychology 36, no. 2 (2014): 111–26. http://dx.doi.org/10.1080/13803395.2013.867013.

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30

Mohr, B., F. Pulvermüller, R. Cohen, and B. Rockstroh. "Cerebral laterality and interhemispheric cooperation during word processing in schizophrenic patients." Schizophrenia Research 41, no. 1 (2000): 17. http://dx.doi.org/10.1016/s0920-9964(00)90341-4.

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31

Rutherford, Barbara J., Andrej Brygin, and Michelina M. Ludovici. "Interhemispheric interaction: Word-distractor congruency and processing resources, in lexical decision." Brain and Cognition 67 (June 2008): 38. http://dx.doi.org/10.1016/j.bandc.2008.02.078.

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32

Banich, Marie T. "The Missing Link: The Role of Interhemispheric Interaction in Attentional Processing." Brain and Cognition 36, no. 2 (1998): 128–57. http://dx.doi.org/10.1006/brcg.1997.0950.

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33

Gavrilescu, M., S. Rossell, G. W. Stuart, et al. "Reduced connectivity of the auditory cortex in patients with auditory hallucinations: a resting state functional magnetic resonance imaging study." Psychological Medicine 40, no. 7 (2009): 1149–58. http://dx.doi.org/10.1017/s0033291709991632.

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BackgroundPrevious research has reported auditory processing deficits that are specific to schizophrenia patients with a history of auditory hallucinations (AH). One explanation for these findings is that there are abnormalities in the interhemispheric connectivity of auditory cortex pathways in AH patients; as yet this explanation has not been experimentally investigated. We assessed the interhemispheric connectivity of both primary (A1) and secondary (A2) auditory cortices in n=13 AH patients, n=13 schizophrenia patients without auditory hallucinations (non-AH) and n=16 healthy controls usin
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34

Braun, Achim, Gauvin, Desjardins, Roberge, and Suffren. "New Variations of Intrahemispheric and Interhemispheric Processing Indexed by the Dimond Paradigm." American Journal of Psychology 124, no. 2 (2011): 163. http://dx.doi.org/10.5406/amerjpsyc.124.2.0163.

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35

Robertson, Lynn C., Marvin R. Lamb, and Eran Zaidel. "Interhemispheric relations in processing hierarchical patterns: Evidence from normal and commissurotomized subjects." Neuropsychology 7, no. 3 (1993): 325–42. http://dx.doi.org/10.1037/0894-4105.7.3.325.

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36

Schulte, T., E. V. Sullivan, E. M. Müller-Oehring, E. Adalsteinsson, and A. Pfefferbaum. "Corpus Callosal Microstructural Integrity Influences Interhemispheric Processing: A Diffusion Tensor Imaging Study." Cerebral Cortex 15, no. 9 (2005): 1384–92. http://dx.doi.org/10.1093/cercor/bhi020.

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37

Joly, Olivier, Franck Ramus, Daniel Pressnitzer, Wim Vanduffel, and Guy A. Orban. "Interhemispheric Differences in Auditory Processing Revealed by fMRI in Awake Rhesus Monkeys." Cerebral Cortex 22, no. 4 (2011): 838–53. http://dx.doi.org/10.1093/cercor/bhr150.

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38

Jeeves, Malcom, Thomas Ludwig, Paul Moes, and Wayne Norman. "The Stability of Compromised Interhemispheric Processing in Callosal Dysgenesis and Partial Commissurotomy." Cortex 37, no. 5 (2001): 643–64. http://dx.doi.org/10.1016/s0010-9452(08)70611-7.

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39

Yoshizaki, Kazuhito. "Effects of visual familiarity for words on interhemispheric cooperation for lexical processing." Cognitive Brain Research 12, no. 3 (2001): 409–14. http://dx.doi.org/10.1016/s0926-6410(01)00079-9.

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40

Bocci, Tommaso, Martinus J. M. Hensghens, Andrea Di Rollo, et al. "Impaired interhemispheric processing in early Huntington’s Disease: A transcranial magnetic stimulation study." Clinical Neurophysiology 127, no. 2 (2016): 1750–52. http://dx.doi.org/10.1016/j.clinph.2015.10.036.

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41

Hatta, Takeshi, Ayako Kawakami, Terumasa Kogure, and Yasuhiro Itoh. "Effects of type of cognitive demand on bilateral advantage in interhemispheric processing." Psychological Research 66, no. 2 (2002): 133–42. http://dx.doi.org/10.1007/s004260100077.

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42

Schulte, T. "Parallel interhemispheric processing in aging and alcoholism: relation to corpus callosum size." Neuropsychologia 42, no. 2 (2004): 257–71. http://dx.doi.org/10.1016/s0028-3932(03)00155-6.

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43

Merriam, Arnold E., and Elizabeth B. Gardner. "Corpus callosum function in schizophrenia: A neuropsychological assessment of interhemispheric information processing." Neuropsychologia 25, no. 1 (1987): 185–93. http://dx.doi.org/10.1016/0028-3932(87)90130-8.

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44

Compton, Rebecca J., Keith Feigenson, and Page Widick. "Take it to the bridge: an interhemispheric processing advantage for emotional faces." Cognitive Brain Research 24, no. 1 (2005): 66–72. http://dx.doi.org/10.1016/j.cogbrainres.2004.12.002.

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45

Taylor, Kirsten I., and Marianne Regard. "Language in the Right Cerebral Hemisphere: Contributions from Reading Studies." Physiology 18, no. 6 (2003): 257–61. http://dx.doi.org/10.1152/nips.01454.2003.

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Evidence for a right hemispheric involvement in language processing, in particular at the level of word meaning, has emerged within the last half century. Hemispheric functional specializations are dynamic; right hemispheric language participation significantly increases under certain conditions, such as during an epileptic seizure and during recovery from stroke. Interhemispheric connections via the corpus callosum critically mediate these and other higher cortical functions.
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46

Yoshizaki, Kazuhito, and Yayoi Tsuji. "Benefits of Interhemispheric Integration on the Japanese Kana Script-Matching Tasks." Perceptual and Motor Skills 90, no. 1 (2000): 153–65. http://dx.doi.org/10.2466/pms.2000.90.1.153.

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We tested Banich's hypothesis that the benefits of bihemispheric processing were enhanced as task complexity increased, when some procedural shortcomings in the previous studies were overcome by using Japanese Kana script-matching tasks. In Exp. 1, the 20 right-handed subjects were given the Physical-Identity task (Katakana-Katakana scripts matching) and the Name-Identity task (Katakana-Hiragana scripts matching). On both tasks, a pair of Kana scripts was tachistoscopically presented in the left, right, and bilateral visual fields. Distractor stimuli were also presented with target Kana script
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47

Jordan, Jake T., Yi Tong, and Carolyn L. Pytte. "Transection of the ventral hippocampal commissure impairs spatial reference but not contextual or spatial working memory." Learning & Memory 29, no. 1 (2021): 29–37. http://dx.doi.org/10.1101/lm.053483.121.

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Plasticity is a neural phenomenon in which experience induces long-lasting changes to neuronal circuits and is at the center of most neurobiological theories of learning and memory. However, too much plasticity is maladaptive and must be balanced with substrate stability. Area CA3 of the hippocampus provides such a balance via hemispheric lateralization, with the left hemisphere dominant in providing plasticity and the right specialized for stability. Left and right CA3 project bilaterally to CA1; however, it is not known whether this downstream merging of lateralized plasticity and stability
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48

WEISSMAN, DANIEL H., MARIE T. BANICH, and EDDIE I. PUENTE. "An unbalanced distribution of inputs across the hemispheres facilitates interhemispheric interaction." Journal of the International Neuropsychological Society 6, no. 3 (2000): 313–21. http://dx.doi.org/10.1017/s1355617700633064.

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In this study, we investigated 2 possible mechanisms by which interhemispheric interaction (IHI) might facilitate performance. Twenty university students performed 3- and 4-item versions of a less complex physical identity (PI) task in which they decided whether 2 letters were perceptually identical (e.g., ‘A’ and ‘A’) and a more complex name identity (NI) task in which they decided whether 2 letters had the same name (e.g., ‘A’ and ‘a’). Consistent with prior work, IHI facilitated performance more for the relatively complex NI task than for the simpler PI task regardless of how many items wer
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49

Siman-Tov, Tali, David Papo, Natan Gadoth, et al. "Mind Your Left: Spatial Bias in Subcortical Fear Processing." Journal of Cognitive Neuroscience 21, no. 9 (2009): 1782–89. http://dx.doi.org/10.1162/jocn.2009.21120.

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Hemispheric lateralization of emotional processing has long been suggested, but its underlying neural mechanisms have not yet been defined. In this functional magnetic resonance imaging study, facial expressions were presented to 10 right-handed healthy adult females in an event-related visual half-field presentation paradigm. Differential activations to fearful versus neutral faces were observed in the amygdala, pulvinar, and superior colliculus only for faces presented in the left hemifield. Interestingly, the left hemifield advantage for fear processing was observed in both hemispheres. The
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50

Mohr, Bettina, Friedemann Pulvermüller, Rudolf Cohen, and Brigitte Rockstroh. "Interhemispheric cooperation during word processing: evidence for callosal transfer dysfunction in schizophrenic patients." Schizophrenia Research 46, no. 2-3 (2000): 231–39. http://dx.doi.org/10.1016/s0920-9964(00)00020-7.

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