Altered dynamic coupling of lateral occipital complex during visual perception in schizophrenia
There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional...
Saved in:
Published in | NeuroImage (Orlando, Fla.) Vol. 55; no. 3; pp. 1219 - 1226 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.04.2011
Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 1053-8119 1095-9572 1095-9572 |
DOI | 10.1016/j.neuroimage.2010.12.045 |
Cover
Loading…
Abstract | There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia.
Eighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented.
Eleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients.
The increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia.
► Schizophrenia patients and controls did not differ in overall coupling with LO. ► Controls showed changes in coupling between LO and higher-level regions. ► Patients showed altered coupling with LO in the precuneus, and inf. and sup. frontal gyri. |
---|---|
AbstractList | There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia.
Eighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented.
Eleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients.
The increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia. There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia.INTRODUCTIONThere is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia.Eighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented.MATERIALS AND METHODSEighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented.Eleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients.RESULTSEleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients.The increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia.DISCUSSIONThe increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia. There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia. Eighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented. Eleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients. The increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia. ► Schizophrenia patients and controls did not differ in overall coupling with LO. ► Controls showed changes in coupling between LO and higher-level regions. ► Patients showed altered coupling with LO in the precuneus, and inf. and sup. frontal gyri. Introduction There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia. Materials and methods Eighteen patients with schizophrenia and eighteen matched controls performed a backward masking task during functional magnetic resonance imaging (fMRI). Stimulus onset asynchronies were manipulated to change the level of target visibility. To examine connectivity with LO function we conducted psychophysiological interactions (PPI) analyses using: 1) a region of interest (ROI) approach and 2) a whole brain analysis. ROIs were defined based on a contrast of trials on which a target was presented versus null trials in which no stimuli were presented. Results Eleven ROIs were identified. Both groups showed similar strength of coupling between LO and the 11 ROIs when visibility was not taken into account. Healthy controls showed clear changes in coupling between LO and prefrontal and parietal regions as a function of target visibility (higher coupling with more visible targets). In comparison, patients showed reduced dynamic coupling with LO in the right superior frontal gyrus (significant after correcting for multiple comparisons) and a trend for reduced coupling in the left precuneus and left inferior frontal regions. Whole brain analysis identified additional regions that showed dynamic coupling with LO in healthy controls, but not in patients. Discussion The increased coupling between LO and higher-level parietal and prefrontal regions during visual awareness in healthy controls likely reflects visual reentrant processing. The lack of modulation of coupling between LO and key prefrontal and parietal regions found in schizophrenia may partly reflect abnormalities in LO tuning. The altered LO coupling may contribute to visual perception abnormalities in schizophrenia. There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO). We previously demonstrated that schizophrenia patients had broader topography and reduced magnitude of activity of LO. However, the functional connectivity of LO with other brain regions during visual perception has not been directly investigated in schizophrenia. |
Author | Engel, Stephen A. Glahn, David C. Nuechterlein, Keith H. Green, Michael F. Harvey, Philippe-Olivier Cohen, Mark S. Lee, Junghee Wynn, Jonathan K. |
AuthorAffiliation | 4 Olin Neuropsychiatry Research Center, Institute of Living, New Haven, Connecticut 1 Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles 2 VA Greater Los Angeles, Healthcare Center System, Los Angeles, California 5 Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut 3 Department of Psychology, University of Minnesota, Minneapolis 6 Department of Psychology, University of California, Los Angeles |
AuthorAffiliation_xml | – name: 4 Olin Neuropsychiatry Research Center, Institute of Living, New Haven, Connecticut – name: 2 VA Greater Los Angeles, Healthcare Center System, Los Angeles, California – name: 3 Department of Psychology, University of Minnesota, Minneapolis – name: 1 Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles – name: 6 Department of Psychology, University of California, Los Angeles – name: 5 Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut |
Author_xml | – sequence: 1 givenname: Philippe-Olivier surname: Harvey fullname: Harvey, Philippe-Olivier email: poharvey@ucla.edu organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA – sequence: 2 givenname: Junghee surname: Lee fullname: Lee, Junghee organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA – sequence: 3 givenname: Mark S. surname: Cohen fullname: Cohen, Mark S. organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA – sequence: 4 givenname: Stephen A. surname: Engel fullname: Engel, Stephen A. organization: Department of Psychology, University of Minnesota, Minneapolis, MN, USA – sequence: 5 givenname: David C. surname: Glahn fullname: Glahn, David C. organization: Olin Neuropsychiatry Research Center, Institute of Living, New Haven, CT, USA – sequence: 6 givenname: Keith H. surname: Nuechterlein fullname: Nuechterlein, Keith H. organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA – sequence: 7 givenname: Jonathan K. surname: Wynn fullname: Wynn, Jonathan K. organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA – sequence: 8 givenname: Michael F. surname: Green fullname: Green, Michael F. organization: Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21194569$$D View this record in MEDLINE/PubMed |
BookMark | eNqNUk1v1DAQtVAR_YC_gCJx4JTFTuzEviDaihakSlzgbDmTya6XxA52smL59ThqS2Ev7MmjmTfPb2beOTlx3iEhGaMrRln1brtyOAdvB7PGVUGXdLGiXDwjZ4wqkStRFydLLMpcMqZOyXmMW0qpYly-IKdFynFRqTOiL_sJA7ZZu3dmsJCBn8feunXmu6w3qWb6zAPY0U4pAj-MPf7M2jksmJ2Nc8qOGADHyXqXWZdF2NhfftwEdNa8JM8700d89fBekG83H79ef8rvvtx-vr68y6FibMpr06haFo2SzKjGUKioqUEKIRrZ1mVtUHWcq87wqi2F5GC6jhmUZcEZQMvKC_L-nnecmwFbQDcl5XoMaUdhr72x-t-Ksxu99jtdUq6k4Ing7QNB8D9mjJMebATse-PQz1ErRqui4qz4LzKpVlQUsk7INwfIrZ-DS3vQrOK8rpWqVEK9_lv6H82PR3qaDYKPMWCnIR1jWXeaxPaaUb24Qm_1kyv04grNCp1ckQjkAcHjH0e0Xt23YjrezmLQESw6wNYGhEm33h5D8uGABJLFLJj-O-6Po_gNarHw1g |
CitedBy_id | crossref_primary_10_1016_j_neuropsychologia_2011_06_012 crossref_primary_10_1080_13803395_2017_1420142 crossref_primary_10_1016_j_schres_2020_03_020 crossref_primary_10_3758_s13415_013_0194_2 crossref_primary_10_1002_mpr_1818 crossref_primary_10_1371_journal_pone_0221409 crossref_primary_10_1016_j_pnpbp_2016_08_004 crossref_primary_10_1016_j_psyneuen_2015_08_012 crossref_primary_10_2147_NDT_S246163 crossref_primary_10_1134_S0362119720010119 crossref_primary_10_1016_j_schres_2025_03_003 crossref_primary_10_1016_j_neuropsychologia_2023_108603 crossref_primary_10_1016_j_neuropsychologia_2013_10_004 crossref_primary_10_1162_CPSY_a_00004 crossref_primary_10_1016_j_psychres_2012_05_014 crossref_primary_10_1016_j_neubiorev_2013_10_004 crossref_primary_10_1093_cercor_bhw151 crossref_primary_10_1038_s41598_022_14914_3 crossref_primary_10_1038_s41537_021_00147_2 crossref_primary_10_1111_bdi_70013 crossref_primary_10_2174_1573400515666190119163522 crossref_primary_10_1016_j_ijpsycho_2019_06_002 crossref_primary_10_1016_j_pnpbp_2023_110827 crossref_primary_10_1093_schbul_sbr051 crossref_primary_10_1016_j_neuropsychologia_2014_02_011 crossref_primary_10_1016_j_schres_2018_12_005 crossref_primary_10_1093_schbul_sbs041 crossref_primary_10_1016_j_schres_2016_04_020 crossref_primary_10_1093_cercor_bhs169 crossref_primary_10_1093_schbul_sbad042 crossref_primary_10_1016_j_nicl_2016_09_022 crossref_primary_10_1093_schizbullopen_sgaa018 crossref_primary_10_3389_fpsyt_2017_00109 crossref_primary_10_1016_j_scog_2015_04_001 crossref_primary_10_1016_j_pscychresns_2019_05_006 crossref_primary_10_1093_cercor_bhac421 |
Cites_doi | 10.1162/jocn.2007.19.9.1488 10.1155/2000/421719 10.1098/rstb.2007.2094 10.1093/cercor/bhn059 10.1038/77754 10.1001/archgenpsychiatry.2009.132 10.1016/j.neuron.2005.05.012 10.1016/S0006-3223(97)00316-8 10.1017/S0033291701004330 10.1098/rstb.2007.2093 10.1097/00001504-200503000-00008 10.1176/appi.ajp.2007.07081223 10.1176/appi.ajp.163.3.448 10.3758/BF03212157 10.1016/S0278-5846(00)00166-4 10.1006/nimg.1997.0291 10.1523/JNEUROSCI.12-11-04545.1992 10.1093/brain/awl004 10.1176/ajp.156.9.1367 10.1017/S003329170200716X 10.1523/JNEUROSCI.15-04-03215.1995 10.1038/89551 10.1073/pnas.92.18.8135 10.1523/JNEUROSCI.6158-09.2010 10.3389/neuro.09.017.2009 10.1016/j.biopsych.2008.03.023 10.1001/archpsyc.59.11.1011 10.1016/S0042-6989(01)00073-6 10.1016/j.neuroimage.2003.09.030 10.1038/77712 10.1016/S0920-9964(97)00140-0 10.1093/schbul/sbn176 10.1016/j.pscychresns.2008.01.005 10.1093/cercor/11.7.628 10.1016/S0920-9964(01)00341-3 10.1007/s11065-006-9002-x 10.1093/cercor/bhi069 10.1016/j.jpsychires.2009.09.003 10.1038/nrn1648 10.1006/nimg.1997.0290 10.1146/annurev.neuro.27.070203.144220 10.1038/375121a0 10.1016/S0959-4388(03)00040-0 10.1523/JNEUROSCI.20-09-03310.2000 10.1162/0898929052880011 10.1016/j.neuroimage.2006.03.006 10.1016/j.neuroimage.2003.09.031 |
ContentType | Journal Article |
Copyright | 2010 Elsevier Inc. Copyright © 2010 Elsevier Inc. All rights reserved. Copyright Elsevier Limited Apr 1, 2011 |
Copyright_xml | – notice: 2010 Elsevier Inc. – notice: Copyright © 2010 Elsevier Inc. All rights reserved. – notice: Copyright Elsevier Limited Apr 1, 2011 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7TK 7X7 7XB 88E 88G 8AO 8FD 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FR3 FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M2M M7P P64 PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS PSYQQ Q9U RC3 7X8 7QO 5PM |
DOI | 10.1016/j.neuroimage.2010.12.045 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Neurosciences Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Psychology Database (Alumni) ProQuest Pharma Collection Technology Research Database ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection ProQuest One ProQuest Central Korea Engineering Research Database Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) Biological Sciences Health & Medical Collection (Alumni) Medical Database Psychology Database Biological Science Database Biotechnology and BioEngineering Abstracts ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China ProQuest One Psychology ProQuest Central Basic Genetics Abstracts MEDLINE - Academic Biotechnology Research Abstracts PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest One Psychology ProQuest Central Student Technology Research Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Central ProQuest One Applied & Life Sciences ProQuest Health & Medical Research Collection Genetics Abstracts Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Biological Science Collection ProQuest Central Basic ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Psychology Journals (Alumni) Biological Science Database ProQuest SciTech Collection Neurosciences Abstracts ProQuest Hospital Collection (Alumni) Biotechnology and BioEngineering Abstracts ProQuest Health & Medical Complete ProQuest Medical Library ProQuest Psychology Journals ProQuest One Academic UKI Edition Engineering Research Database ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic Biotechnology Research Abstracts |
DatabaseTitleList | MEDLINE MEDLINE - Academic ProQuest One Psychology Engineering Research Database |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Education |
EISSN | 1095-9572 |
EndPage | 1226 |
ExternalDocumentID | PMC3049854 3556011121 21194569 10_1016_j_neuroimage_2010_12_045 S1053811910016319 |
Genre | Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: NIMH NIH HHS grantid: R01 MH043292 – fundername: NIMH NIH HHS grantid: MH043292 – fundername: NIMH NIH HHS grantid: R29 MH043292 – fundername: CIHR |
GroupedDBID | --- --K --M .~1 0R~ 123 1B1 1RT 1~. 1~5 4.4 457 4G. 5RE 5VS 7-5 71M 7X7 88E 8AO 8FE 8FH 8FI 8FJ 8P~ 9JM AABNK AAEDT AAEDW AAIKJ AAKOC AALRI AAOAW AAQFI AATTM AAXKI AAXLA AAXUO AAYWO ABBQC ABCQJ ABFNM ABFRF ABIVO ABJNI ABMAC ABUWG ABXDB ACDAQ ACGFO ACGFS ACIEU ACPRK ACRLP ACRPL ACVFH ADBBV ADCNI ADEZE ADFRT ADMUD ADNMO AEBSH AEFWE AEIPS AEKER AENEX AEUPX AFJKZ AFKRA AFPUW AFTJW AFXIZ AGCQF AGUBO AGWIK AGYEJ AHHHB AHMBA AIEXJ AIIUN AIKHN AITUG AJRQY AKBMS AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ANZVX AXJTR AZQEC BBNVY BENPR BHPHI BKOJK BLXMC BNPGV BPHCQ BVXVI CCPQU CS3 DM4 DU5 DWQXO EBS EFBJH EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FIRID FNPLU FYGXN FYUFA G-Q GBLVA GNUQQ GROUPED_DOAJ HCIFZ HMCUK HZ~ IHE J1W KOM LG5 LK8 LX8 M1P M29 M2M M2V M41 M7P MO0 MOBAO N9A O-L O9- OAUVE OVD OZT P-8 P-9 P2P PC. PHGZM PHGZT PJZUB PPXIY PQGLB PQQKQ PROAC PSQYO PSYQQ PUEGO Q38 ROL RPZ SAE SCC SDF SDG SDP SES SSH SSN SSZ T5K TEORI UKHRP UV1 YK3 ZU3 ~G- 3V. AACTN AADPK AAIAV ABLVK ABYKQ AFKWA AJBFU AJOXV AMFUW C45 EFLBG HMQ LCYCR RIG SNS ZA5 .1- .FO 29N 53G AAFWJ AAQXK AAYXX ABMZM ADFGL ADVLN ADXHL AFPKN AFRHN AGHFR AGQPQ AGRNS AIGII AJUYK AKRLJ ALIPV APXCP ASPBG AVWKF AZFZN CAG CITATION COF FEDTE FGOYB G-2 HDW HEI HMK HMO HVGLF OK1 R2- SEW WUQ XPP Z5R ZMT CGR CUY CVF ECM EIF NPM 7TK 7XB 8FD 8FK FR3 K9. P64 PKEHL PQEST PQUKI PRINS Q9U RC3 7X8 7QO 5PM |
ID | FETCH-LOGICAL-c611t-7ab9782b981a9ba0c60a7c8555b8d737ae9f449fa46d3584caff1ae83241ccd13 |
IEDL.DBID | 7X7 |
ISSN | 1053-8119 1095-9572 |
IngestDate | Thu Aug 21 13:52:13 EDT 2025 Thu Sep 04 15:52:45 EDT 2025 Thu Sep 04 22:44:10 EDT 2025 Wed Aug 13 04:19:32 EDT 2025 Mon Jul 21 06:06:55 EDT 2025 Tue Jul 01 02:14:40 EDT 2025 Thu Apr 24 22:57:57 EDT 2025 Fri Feb 23 02:20:27 EST 2024 Tue Aug 26 16:36:35 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Keywords | Schizophrenia fMRI Lateral occipital complex Functional connectivity/ Dynamic coupling Backward visual masking |
Language | English |
License | https://www.elsevier.com/tdm/userlicense/1.0 Copyright © 2010 Elsevier Inc. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c611t-7ab9782b981a9ba0c60a7c8555b8d737ae9f449fa46d3584caff1ae83241ccd13 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
PMID | 21194569 |
PQID | 1644779969 |
PQPubID | 2031077 |
PageCount | 8 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3049854 proquest_miscellaneous_910626412 proquest_miscellaneous_855905287 proquest_journals_1644779969 pubmed_primary_21194569 crossref_citationtrail_10_1016_j_neuroimage_2010_12_045 crossref_primary_10_1016_j_neuroimage_2010_12_045 elsevier_sciencedirect_doi_10_1016_j_neuroimage_2010_12_045 elsevier_clinicalkey_doi_10_1016_j_neuroimage_2010_12_045 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2011-04-01 |
PublicationDateYYYYMMDD | 2011-04-01 |
PublicationDate_xml | – month: 04 year: 2011 text: 2011-04-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Amsterdam |
PublicationTitle | NeuroImage (Orlando, Fla.) |
PublicationTitleAlternate | Neuroimage |
PublicationYear | 2011 |
Publisher | Elsevier Inc Elsevier Limited |
Publisher_xml | – name: Elsevier Inc – name: Elsevier Limited |
References | Haynes, Driver, Rees (bb0150) 2005; 46 Green, Nuechterlein, Breitmeyer, Mintz (bb0115) 1999; 156 Yoon, Maddock, Rokem, Silver, Minzenberg, Ragland, Carter (bb0255) 2010; 30 Crick, Koch (bb0055) 1995; 375 Grill-Spector, Kourtzi, Kanwisher (bb0135) 2001; 41 Green, Glahn, Engel, Nuechterlein, Sabb, Strojwas, Cohen (bb0105) 2005; 17 Butler, DeSanti, Maddox, Harkavy-Friedman, Amador, Goetz, Javitt, Gorman (bb0020) 2003; 59 Rees (bb0190) 2007; 362 Dehaene, Naccache, Cohen, Bihan, Mangin, Poline, Riviere (bb0060) 2001; 4 Calhoun, Eichele, Pearlson (bb0040) 2009; 3 Green, Lee, Cohen, Engel, Korb, Nuechterlein, Wynn, Glahn (bb0110) 2009; 66 Liu (bb0170) 2004; 21 Kouider, Dehaene (bb0160) 2007; 362 Lewis, Hashimoto, Volk (bb0245) 2005; 6 Sergi, Rassovsky, Nuechterlein, Green (bb0205) 2006; 163 Grill-Spector (bb0130) 2003; 13 Grill-Spector, Malach (bb0145) 2004; 27 Friston (bb0095) 1998; 30 Ventura, Lukoff, Nuechterlein, Liberman, Green, Shaner (bb0225) 1993; 3 Greicius, Supekar, Menon, Dougherty (bb0125) 2009; 19 Fahrenfort, Scholte, Lamme (bb0075) 2007; 19 Kourtzi, Kanwisher (bb0165) 2000; 20 Breitmeyer, Ogmen (bb0015) 2000; 62 Alvarez, Emory (bb0005) 2006; 16 Camchong, Macdonald, Bell, Mueller, Lim (bb0045) 2009 Deneux, Faugeras (bb0065) 2006; 32 Green, Nuechterlein, Breitmeyer, Tsuang, Mintz (bb0120) 2003; 33 Cavanna, Trimble (bb0050) 2006; 129 Grill-Spector, Kushnir, Hendler, Malach (bb0140) 2000; 3 Friston, Buechel, Fink, Morris, Rolls, Dolan (bb0100) 1997; 6 Butler, Javitt (bb0025) 2005; 18 Tootell, Reppas, Kwong, Malach, Born, Brady, Rosen, Belliveau (bb0220) 1995; 15 First, Spitzer, Gibbon, Williams (bb0085) 1997 Wynn, Green, Engel, Korb, Lee, Glahn, Nuechterlein, Cohen (bb0230) 2008; 164 Butler, Silverstein, Dakin (bb0030) 2008; 64 Hashimoto, Bazmi, Mirnics, Wu, Sampson, Lewis (bb0235) 2008; 165 Kritzer, Cowey, Somogyi (bb0240) 1992; 12 Ashburner, Friston (bb0010) 1997; 6 McClure (bb0185) 2001; 25 Rorden, Brett (bb0200) 2000; 12 Henseler, Falkai, Gruber (bb0155) 2010; 44 Foxe, Murray, Javitt (bb0090) 2005; 15 Stephan, Friston, Frith (bb0210) 2009; 35 Liu, Frank (bb0175) 2004; 21 Doniger, Foxe, Murray, Higgins, Javitt (bb0070) 2002; 59 Wang, Fujita, Murayama (bb0250) 2000; 3 Robertson, Tormos, Maeda, Pascual-Leone (bb0195) 2001; 11 Malach, Reppas, Benson, Kwong, Jiang, Kennedy, Ledden, Brady, Rosen, Tootell (bb0180) 1995; 92 Stephan, Magnotta, White, Arndt, Flaum, O'Leary, Andreasen (bb0215) 2001; 31 Cadenhead, Serper, Braff (bb0035) 1998; 43 First, Gibbon, Spitzer, Williams, Benjamin (bb0080) 1996 Liu (10.1016/j.neuroimage.2010.12.045_bb0170) 2004; 21 Alvarez (10.1016/j.neuroimage.2010.12.045_bb0005) 2006; 16 Butler (10.1016/j.neuroimage.2010.12.045_bb0025) 2005; 18 Green (10.1016/j.neuroimage.2010.12.045_bb0115) 1999; 156 First (10.1016/j.neuroimage.2010.12.045_bb0085) 1997 Camchong (10.1016/j.neuroimage.2010.12.045_bb0045) 2009 Crick (10.1016/j.neuroimage.2010.12.045_bb0055) 1995; 375 Deneux (10.1016/j.neuroimage.2010.12.045_bb0065) 2006; 32 McClure (10.1016/j.neuroimage.2010.12.045_bb0185) 2001; 25 Hashimoto (10.1016/j.neuroimage.2010.12.045_bb0235) 2008; 165 Stephan (10.1016/j.neuroimage.2010.12.045_bb0210) 2009; 35 Grill-Spector (10.1016/j.neuroimage.2010.12.045_bb0135) 2001; 41 Haynes (10.1016/j.neuroimage.2010.12.045_bb0150) 2005; 46 Grill-Spector (10.1016/j.neuroimage.2010.12.045_bb0140) 2000; 3 Breitmeyer (10.1016/j.neuroimage.2010.12.045_bb0015) 2000; 62 Lewis (10.1016/j.neuroimage.2010.12.045_bb0245) 2005; 6 Green (10.1016/j.neuroimage.2010.12.045_bb0110) 2009; 66 Tootell (10.1016/j.neuroimage.2010.12.045_bb0220) 1995; 15 Fahrenfort (10.1016/j.neuroimage.2010.12.045_bb0075) 2007; 19 Wynn (10.1016/j.neuroimage.2010.12.045_bb0230) 2008; 164 Wang (10.1016/j.neuroimage.2010.12.045_bb0250) 2000; 3 Yoon (10.1016/j.neuroimage.2010.12.045_bb0255) 2010; 30 Kouider (10.1016/j.neuroimage.2010.12.045_bb0160) 2007; 362 Greicius (10.1016/j.neuroimage.2010.12.045_bb0125) 2009; 19 Doniger (10.1016/j.neuroimage.2010.12.045_bb0070) 2002; 59 Butler (10.1016/j.neuroimage.2010.12.045_bb0020) 2003; 59 Malach (10.1016/j.neuroimage.2010.12.045_bb0180) 1995; 92 Robertson (10.1016/j.neuroimage.2010.12.045_bb0195) 2001; 11 First (10.1016/j.neuroimage.2010.12.045_bb0080) 1996 Ventura (10.1016/j.neuroimage.2010.12.045_bb0225) 1993; 3 Friston (10.1016/j.neuroimage.2010.12.045_bb0100) 1997; 6 Calhoun (10.1016/j.neuroimage.2010.12.045_bb0040) 2009; 3 Liu (10.1016/j.neuroimage.2010.12.045_bb0175) 2004; 21 Grill-Spector (10.1016/j.neuroimage.2010.12.045_bb0145) 2004; 27 Friston (10.1016/j.neuroimage.2010.12.045_bb0095) 1998; 30 Rorden (10.1016/j.neuroimage.2010.12.045_bb0200) 2000; 12 Butler (10.1016/j.neuroimage.2010.12.045_bb0030) 2008; 64 Stephan (10.1016/j.neuroimage.2010.12.045_bb0215) 2001; 31 Foxe (10.1016/j.neuroimage.2010.12.045_bb0090) 2005; 15 Cavanna (10.1016/j.neuroimage.2010.12.045_bb0050) 2006; 129 Grill-Spector (10.1016/j.neuroimage.2010.12.045_bb0130) 2003; 13 Kourtzi (10.1016/j.neuroimage.2010.12.045_bb0165) 2000; 20 Ashburner (10.1016/j.neuroimage.2010.12.045_bb0010) 1997; 6 Dehaene (10.1016/j.neuroimage.2010.12.045_bb0060) 2001; 4 Green (10.1016/j.neuroimage.2010.12.045_bb0105) 2005; 17 Green (10.1016/j.neuroimage.2010.12.045_bb0120) 2003; 33 Cadenhead (10.1016/j.neuroimage.2010.12.045_bb0035) 1998; 43 Rees (10.1016/j.neuroimage.2010.12.045_bb0190) 2007; 362 Henseler (10.1016/j.neuroimage.2010.12.045_bb0155) 2010; 44 Kritzer (10.1016/j.neuroimage.2010.12.045_bb0240) 1992; 12 Sergi (10.1016/j.neuroimage.2010.12.045_bb0205) 2006; 163 |
References_xml | – volume: 18 start-page: 151 year: 2005 end-page: 157 ident: bb0025 article-title: Early-stage visual processing deficits in schizophrenia publication-title: Curr. Opin. Psychiatry – volume: 19 start-page: 1488 year: 2007 end-page: 1497 ident: bb0075 article-title: Masking disrupts reentrant processing in human visual cortex publication-title: J. Cogn. Neurosci. – volume: 21 start-page: 387 year: 2004 end-page: 400 ident: bb0175 article-title: Efficiency, power, and entropy in event-related FMRI with multiple trial types. Part I: theory publication-title: Neuroimage – volume: 27 start-page: 649 year: 2004 end-page: 677 ident: bb0145 article-title: The human visual cortex publication-title: Annu. Rev. Neurosci. – volume: 64 start-page: 40 year: 2008 end-page: 47 ident: bb0030 article-title: Visual perception and its impairment in schizophrenia publication-title: Biol. Psychiatry – volume: 362 start-page: 877 year: 2007 end-page: 886 ident: bb0190 article-title: Neural correlates of the contents of visual awareness in humans publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci. – volume: 25 start-page: 301 year: 2001 end-page: 311 ident: bb0185 article-title: The visual backward masking deficit in schizophrenia publication-title: Prog. Neuropsychopharmacol. Biol. Psychiatry – volume: 3 start-page: 227 year: 1993 end-page: 243 ident: bb0225 article-title: Brief Psychiatric Rating Scale (BPRS) expanded version: scales, anchor points, and administration manual publication-title: Int. J. Meth. Psychiatr. Res. – volume: 32 start-page: 1669 year: 2006 end-page: 1689 ident: bb0065 article-title: Using nonlinear models in fMRI data analysis: model selection and activation detection publication-title: Neuroimage – volume: 59 start-page: 199 year: 2003 end-page: 209 ident: bb0020 article-title: Visual backward-masking deficits in schizophrenia: relationship to visual pathway function and symptomatology publication-title: Schizophr. Res. – volume: 59 start-page: 1011 year: 2002 end-page: 1020 ident: bb0070 article-title: Impaired visual object recognition and dorsal/ventral stream interaction in schizophrenia publication-title: Arch. Gen. Psychiatry – volume: 46 start-page: 811 year: 2005 end-page: 821 ident: bb0150 article-title: Visibility reflects dynamic changes of effective connectivity between V1 and fusiform cortex publication-title: Neuron – volume: 31 start-page: 1065 year: 2001 end-page: 1078 ident: bb0215 article-title: Effects of olanzapine on cerebellar functional connectivity in schizophrenia measured by fMRI during a simple motor task publication-title: Psychol. Med. – volume: 20 start-page: 3310 year: 2000 end-page: 3318 ident: bb0165 article-title: Cortical regions involved in perceiving object shape publication-title: J. Neurosci. – year: 1997 ident: bb0085 article-title: Structured Clinical Interview for DSM-IV Axis I Disorders – volume: 163 start-page: 448 year: 2006 end-page: 454 ident: bb0205 article-title: Social perception as a mediator of the influence of early visual processing on functional status in schizophrenia publication-title: Am. J. Psychiatry – volume: 66 start-page: 1295 year: 2009 end-page: 1303 ident: bb0110 article-title: Functional neuroanatomy of visual masking deficits in schizophrenia publication-title: Arch. Gen. Psychiatry – volume: 13 start-page: 159 year: 2003 end-page: 166 ident: bb0130 article-title: The neural basis of object perception publication-title: Curr. Opin. Neurobiol. – volume: 3 start-page: 17 year: 2009 ident: bb0040 article-title: Functional brain networks in schizophrenia: a review publication-title: Front. Hum. Neurosci. – volume: 129 start-page: 564 year: 2006 end-page: 583 ident: bb0050 article-title: The precuneus: a review of its functional anatomy and behavioural correlates publication-title: Brain – volume: 11 start-page: 628 year: 2001 end-page: 635 ident: bb0195 article-title: The role of the dorsolateral prefrontal cortex during sequence learning is specific for spatial information publication-title: Cereb. Cortex – year: 1996 ident: bb0080 article-title: Structured Clinical Interview for DSM-IV Axis II Personality Disorders – volume: 6 start-page: 218 year: 1997 end-page: 229 ident: bb0100 article-title: Psychophysiological and modulatory interactions in neuroimaging publication-title: Neuroimage – volume: 33 start-page: 887 year: 2003 end-page: 895 ident: bb0120 article-title: Forward and backward visual masking in schizophrenia: influence of age publication-title: Psychol. Med. – volume: 92 start-page: 8135 year: 1995 end-page: 8139 ident: bb0180 article-title: Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex publication-title: Proc. Natl Acad. Sci. USA – volume: 16 start-page: 17 year: 2006 end-page: 42 ident: bb0005 article-title: Executive function and the frontal lobes: a meta-analytic review publication-title: Neuropsychol. Rev. – volume: 156 start-page: 1367 year: 1999 end-page: 1373 ident: bb0115 article-title: Backward masking in unmedicated schizophrenic patients in psychotic remission: possible reflection of aberrant cortical oscillation publication-title: Am. J. Psychiatry – volume: 43 start-page: 132 year: 1998 end-page: 138 ident: bb0035 article-title: Transient versus sustained visual channels in the visual backward masking deficits of schizophrenia patients publication-title: Biol. Psychiatry – volume: 62 start-page: 1572 year: 2000 end-page: 1595 ident: bb0015 article-title: Recent models and findings in visual backward masking: a comparison, review, and update publication-title: Percept. Psychophys. – volume: 30 start-page: 3777 year: 2010 end-page: 3781 ident: bb0255 article-title: GABA concentration is reduced in visual cortex in schizophrenia and correlates with orientation-specific surround suppression publication-title: J. Neurosci. – volume: 375 start-page: 121 year: 1995 end-page: 123 ident: bb0055 article-title: Are we aware of neural activity in primary visual cortex? publication-title: Nature – volume: 15 start-page: 3215 year: 1995 end-page: 3230 ident: bb0220 article-title: Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging publication-title: J. Neurosci. – volume: 164 start-page: 97 year: 2008 end-page: 105 ident: bb0230 article-title: Increased extent of object-selective cortex in schizophrenia publication-title: Psychiatry Res. – volume: 6 start-page: 209 year: 1997 end-page: 217 ident: bb0010 article-title: Multimodal image coregistration and partitioning—a unified framework publication-title: Neuroimage – volume: 30 start-page: 115 year: 1998 end-page: 125 ident: bb0095 article-title: The disconnection hypothesis publication-title: Schizophr. Res. – volume: 4 start-page: 752 year: 2001 end-page: 758 ident: bb0060 article-title: Cerebral mechanisms of word masking and unconscious repetition priming publication-title: Nat. Neurosci. – volume: 362 start-page: 857 year: 2007 end-page: 875 ident: bb0160 article-title: Levels of processing during non-conscious perception: a critical review of visual masking publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci. – volume: 41 start-page: 1409 year: 2001 end-page: 1422 ident: bb0135 article-title: The lateral occipital complex and its role in object recognition publication-title: Vis. Res. – volume: 165 start-page: 479 year: 2008 end-page: 489 ident: bb0235 article-title: Conserved regional patterns of GABA-related transcript expression in the neocortex of subjects with schizophrenia publication-title: Am. J. Psychiatry – volume: 6 start-page: 312 year: 2005 end-page: 324 ident: bb0245 article-title: Cortical inhibitory neurons and schizophrenia publication-title: Nat. Rev. Neurosci. – volume: 19 start-page: 72 year: 2009 end-page: 78 ident: bb0125 article-title: Resting-state functional connectivity reflects structural connectivity in the default mode network publication-title: Cereb. Cortex – volume: 12 start-page: 4545 year: 1992 end-page: 4564 ident: bb0240 article-title: Patterns of inter- and intralaminar GABAergic connections distinguish striate (V1) and extrastriate (V2, V4) visual cortices and their functionally specialized subdivisions in the rhesus monkey publication-title: J. Neurosci. – volume: 21 start-page: 401 year: 2004 end-page: 413 ident: bb0170 article-title: Efficiency, power, and entropy in event-related fMRI with multiple trial types. Part II: design of experiments publication-title: Neuroimage – year: 2009 ident: bb0045 article-title: Altered functional and anatomical connectivity in schizophrenia publication-title: Schizophr. Bull. – volume: 17 start-page: 13 year: 2005 end-page: 23 ident: bb0105 article-title: Regional brain activity associated with visual backward masking publication-title: J. Cogn. Neurosci. – volume: 3 start-page: 837 year: 2000 end-page: 843 ident: bb0140 article-title: The dynamics of object-selective activation correlate with recognition performance in humans publication-title: Nat. Neurosci. – volume: 3 start-page: 807 year: 2000 end-page: 813 ident: bb0250 article-title: Neuronal mechanisms of selectivity for object features revealed by blocking inhibition in inferotemporal cortex publication-title: Nat. Neurosci. – volume: 15 start-page: 1914 year: 2005 end-page: 1927 ident: bb0090 article-title: Filling-in in schizophrenia: a high-density electrical mapping and source-analysis investigation of illusory contour processing publication-title: Cereb. Cortex – volume: 12 start-page: 191 year: 2000 end-page: 200 ident: bb0200 article-title: Stereotaxic display of brain lesions publication-title: Behav. Neurol. – volume: 44 start-page: 364 year: 2010 end-page: 372 ident: bb0155 article-title: Disturbed functional connectivity within brain networks subserving domain-specific subcomponents of working memory in schizophrenia: relation to performance and clinical symptoms publication-title: J. Psychiatr. Res. – volume: 35 start-page: 509 year: 2009 end-page: 527 ident: bb0210 article-title: Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring publication-title: Schizophr. Bull. – volume: 19 start-page: 1488 year: 2007 ident: 10.1016/j.neuroimage.2010.12.045_bb0075 article-title: Masking disrupts reentrant processing in human visual cortex publication-title: J. Cogn. Neurosci. doi: 10.1162/jocn.2007.19.9.1488 – volume: 12 start-page: 191 year: 2000 ident: 10.1016/j.neuroimage.2010.12.045_bb0200 article-title: Stereotaxic display of brain lesions publication-title: Behav. Neurol. doi: 10.1155/2000/421719 – volume: 362 start-page: 877 year: 2007 ident: 10.1016/j.neuroimage.2010.12.045_bb0190 article-title: Neural correlates of the contents of visual awareness in humans publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci. doi: 10.1098/rstb.2007.2094 – volume: 19 start-page: 72 year: 2009 ident: 10.1016/j.neuroimage.2010.12.045_bb0125 article-title: Resting-state functional connectivity reflects structural connectivity in the default mode network publication-title: Cereb. Cortex doi: 10.1093/cercor/bhn059 – volume: 3 start-page: 837 year: 2000 ident: 10.1016/j.neuroimage.2010.12.045_bb0140 article-title: The dynamics of object-selective activation correlate with recognition performance in humans publication-title: Nat. Neurosci. doi: 10.1038/77754 – volume: 66 start-page: 1295 year: 2009 ident: 10.1016/j.neuroimage.2010.12.045_bb0110 article-title: Functional neuroanatomy of visual masking deficits in schizophrenia publication-title: Arch. Gen. Psychiatry doi: 10.1001/archgenpsychiatry.2009.132 – volume: 46 start-page: 811 year: 2005 ident: 10.1016/j.neuroimage.2010.12.045_bb0150 article-title: Visibility reflects dynamic changes of effective connectivity between V1 and fusiform cortex publication-title: Neuron doi: 10.1016/j.neuron.2005.05.012 – volume: 43 start-page: 132 year: 1998 ident: 10.1016/j.neuroimage.2010.12.045_bb0035 article-title: Transient versus sustained visual channels in the visual backward masking deficits of schizophrenia patients publication-title: Biol. Psychiatry doi: 10.1016/S0006-3223(97)00316-8 – volume: 31 start-page: 1065 year: 2001 ident: 10.1016/j.neuroimage.2010.12.045_bb0215 article-title: Effects of olanzapine on cerebellar functional connectivity in schizophrenia measured by fMRI during a simple motor task publication-title: Psychol. Med. doi: 10.1017/S0033291701004330 – volume: 362 start-page: 857 year: 2007 ident: 10.1016/j.neuroimage.2010.12.045_bb0160 article-title: Levels of processing during non-conscious perception: a critical review of visual masking publication-title: Philos. Trans. R. Soc. Lond. B Biol. Sci. doi: 10.1098/rstb.2007.2093 – volume: 18 start-page: 151 year: 2005 ident: 10.1016/j.neuroimage.2010.12.045_bb0025 article-title: Early-stage visual processing deficits in schizophrenia publication-title: Curr. Opin. Psychiatry doi: 10.1097/00001504-200503000-00008 – volume: 165 start-page: 479 issue: 4 year: 2008 ident: 10.1016/j.neuroimage.2010.12.045_bb0235 article-title: Conserved regional patterns of GABA-related transcript expression in the neocortex of subjects with schizophrenia publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.2007.07081223 – volume: 163 start-page: 448 year: 2006 ident: 10.1016/j.neuroimage.2010.12.045_bb0205 article-title: Social perception as a mediator of the influence of early visual processing on functional status in schizophrenia publication-title: Am. J. Psychiatry doi: 10.1176/appi.ajp.163.3.448 – volume: 62 start-page: 1572 year: 2000 ident: 10.1016/j.neuroimage.2010.12.045_bb0015 article-title: Recent models and findings in visual backward masking: a comparison, review, and update publication-title: Percept. Psychophys. doi: 10.3758/BF03212157 – volume: 25 start-page: 301 year: 2001 ident: 10.1016/j.neuroimage.2010.12.045_bb0185 article-title: The visual backward masking deficit in schizophrenia publication-title: Prog. Neuropsychopharmacol. Biol. Psychiatry doi: 10.1016/S0278-5846(00)00166-4 – year: 1997 ident: 10.1016/j.neuroimage.2010.12.045_bb0085 – volume: 6 start-page: 218 year: 1997 ident: 10.1016/j.neuroimage.2010.12.045_bb0100 article-title: Psychophysiological and modulatory interactions in neuroimaging publication-title: Neuroimage doi: 10.1006/nimg.1997.0291 – volume: 12 start-page: 4545 issue: 11 year: 1992 ident: 10.1016/j.neuroimage.2010.12.045_bb0240 article-title: Patterns of inter- and intralaminar GABAergic connections distinguish striate (V1) and extrastriate (V2, V4) visual cortices and their functionally specialized subdivisions in the rhesus monkey publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.12-11-04545.1992 – volume: 129 start-page: 564 year: 2006 ident: 10.1016/j.neuroimage.2010.12.045_bb0050 article-title: The precuneus: a review of its functional anatomy and behavioural correlates publication-title: Brain doi: 10.1093/brain/awl004 – volume: 156 start-page: 1367 year: 1999 ident: 10.1016/j.neuroimage.2010.12.045_bb0115 article-title: Backward masking in unmedicated schizophrenic patients in psychotic remission: possible reflection of aberrant cortical oscillation publication-title: Am. J. Psychiatry doi: 10.1176/ajp.156.9.1367 – volume: 33 start-page: 887 year: 2003 ident: 10.1016/j.neuroimage.2010.12.045_bb0120 article-title: Forward and backward visual masking in schizophrenia: influence of age publication-title: Psychol. Med. doi: 10.1017/S003329170200716X – volume: 15 start-page: 3215 year: 1995 ident: 10.1016/j.neuroimage.2010.12.045_bb0220 article-title: Functional analysis of human MT and related visual cortical areas using magnetic resonance imaging publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.15-04-03215.1995 – volume: 4 start-page: 752 year: 2001 ident: 10.1016/j.neuroimage.2010.12.045_bb0060 article-title: Cerebral mechanisms of word masking and unconscious repetition priming publication-title: Nat. Neurosci. doi: 10.1038/89551 – volume: 92 start-page: 8135 year: 1995 ident: 10.1016/j.neuroimage.2010.12.045_bb0180 article-title: Object-related activity revealed by functional magnetic resonance imaging in human occipital cortex publication-title: Proc. Natl Acad. Sci. USA doi: 10.1073/pnas.92.18.8135 – volume: 30 start-page: 3777 issue: 10 year: 2010 ident: 10.1016/j.neuroimage.2010.12.045_bb0255 article-title: GABA concentration is reduced in visual cortex in schizophrenia and correlates with orientation-specific surround suppression publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.6158-09.2010 – volume: 3 start-page: 17 year: 2009 ident: 10.1016/j.neuroimage.2010.12.045_bb0040 article-title: Functional brain networks in schizophrenia: a review publication-title: Front. Hum. Neurosci. doi: 10.3389/neuro.09.017.2009 – volume: 64 start-page: 40 year: 2008 ident: 10.1016/j.neuroimage.2010.12.045_bb0030 article-title: Visual perception and its impairment in schizophrenia publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2008.03.023 – volume: 59 start-page: 1011 year: 2002 ident: 10.1016/j.neuroimage.2010.12.045_bb0070 article-title: Impaired visual object recognition and dorsal/ventral stream interaction in schizophrenia publication-title: Arch. Gen. Psychiatry doi: 10.1001/archpsyc.59.11.1011 – volume: 41 start-page: 1409 year: 2001 ident: 10.1016/j.neuroimage.2010.12.045_bb0135 article-title: The lateral occipital complex and its role in object recognition publication-title: Vis. Res. doi: 10.1016/S0042-6989(01)00073-6 – volume: 21 start-page: 387 year: 2004 ident: 10.1016/j.neuroimage.2010.12.045_bb0175 article-title: Efficiency, power, and entropy in event-related FMRI with multiple trial types. Part I: theory publication-title: Neuroimage doi: 10.1016/j.neuroimage.2003.09.030 – volume: 3 start-page: 807 issue: 8 year: 2000 ident: 10.1016/j.neuroimage.2010.12.045_bb0250 article-title: Neuronal mechanisms of selectivity for object features revealed by blocking inhibition in inferotemporal cortex publication-title: Nat. Neurosci. doi: 10.1038/77712 – volume: 30 start-page: 115 year: 1998 ident: 10.1016/j.neuroimage.2010.12.045_bb0095 article-title: The disconnection hypothesis publication-title: Schizophr. Res. doi: 10.1016/S0920-9964(97)00140-0 – volume: 35 start-page: 509 year: 2009 ident: 10.1016/j.neuroimage.2010.12.045_bb0210 article-title: Dysconnection in schizophrenia: from abnormal synaptic plasticity to failures of self-monitoring publication-title: Schizophr. Bull. doi: 10.1093/schbul/sbn176 – volume: 164 start-page: 97 year: 2008 ident: 10.1016/j.neuroimage.2010.12.045_bb0230 article-title: Increased extent of object-selective cortex in schizophrenia publication-title: Psychiatry Res. doi: 10.1016/j.pscychresns.2008.01.005 – year: 2009 ident: 10.1016/j.neuroimage.2010.12.045_bb0045 article-title: Altered functional and anatomical connectivity in schizophrenia publication-title: Schizophr. Bull. – volume: 11 start-page: 628 year: 2001 ident: 10.1016/j.neuroimage.2010.12.045_bb0195 article-title: The role of the dorsolateral prefrontal cortex during sequence learning is specific for spatial information publication-title: Cereb. Cortex doi: 10.1093/cercor/11.7.628 – volume: 59 start-page: 199 year: 2003 ident: 10.1016/j.neuroimage.2010.12.045_bb0020 article-title: Visual backward-masking deficits in schizophrenia: relationship to visual pathway function and symptomatology publication-title: Schizophr. Res. doi: 10.1016/S0920-9964(01)00341-3 – volume: 16 start-page: 17 year: 2006 ident: 10.1016/j.neuroimage.2010.12.045_bb0005 article-title: Executive function and the frontal lobes: a meta-analytic review publication-title: Neuropsychol. Rev. doi: 10.1007/s11065-006-9002-x – volume: 15 start-page: 1914 year: 2005 ident: 10.1016/j.neuroimage.2010.12.045_bb0090 article-title: Filling-in in schizophrenia: a high-density electrical mapping and source-analysis investigation of illusory contour processing publication-title: Cereb. Cortex doi: 10.1093/cercor/bhi069 – volume: 44 start-page: 364 issue: 6 year: 2010 ident: 10.1016/j.neuroimage.2010.12.045_bb0155 article-title: Disturbed functional connectivity within brain networks subserving domain-specific subcomponents of working memory in schizophrenia: relation to performance and clinical symptoms publication-title: J. Psychiatr. Res. doi: 10.1016/j.jpsychires.2009.09.003 – volume: 6 start-page: 312 issue: 4 year: 2005 ident: 10.1016/j.neuroimage.2010.12.045_bb0245 article-title: Cortical inhibitory neurons and schizophrenia publication-title: Nat. Rev. Neurosci. doi: 10.1038/nrn1648 – volume: 6 start-page: 209 year: 1997 ident: 10.1016/j.neuroimage.2010.12.045_bb0010 article-title: Multimodal image coregistration and partitioning—a unified framework publication-title: Neuroimage doi: 10.1006/nimg.1997.0290 – volume: 27 start-page: 649 year: 2004 ident: 10.1016/j.neuroimage.2010.12.045_bb0145 article-title: The human visual cortex publication-title: Annu. Rev. Neurosci. doi: 10.1146/annurev.neuro.27.070203.144220 – volume: 375 start-page: 121 year: 1995 ident: 10.1016/j.neuroimage.2010.12.045_bb0055 article-title: Are we aware of neural activity in primary visual cortex? publication-title: Nature doi: 10.1038/375121a0 – year: 1996 ident: 10.1016/j.neuroimage.2010.12.045_bb0080 – volume: 13 start-page: 159 year: 2003 ident: 10.1016/j.neuroimage.2010.12.045_bb0130 article-title: The neural basis of object perception publication-title: Curr. Opin. Neurobiol. doi: 10.1016/S0959-4388(03)00040-0 – volume: 3 start-page: 227 year: 1993 ident: 10.1016/j.neuroimage.2010.12.045_bb0225 article-title: Brief Psychiatric Rating Scale (BPRS) expanded version: scales, anchor points, and administration manual publication-title: Int. J. Meth. Psychiatr. Res. – volume: 20 start-page: 3310 year: 2000 ident: 10.1016/j.neuroimage.2010.12.045_bb0165 article-title: Cortical regions involved in perceiving object shape publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.20-09-03310.2000 – volume: 17 start-page: 13 year: 2005 ident: 10.1016/j.neuroimage.2010.12.045_bb0105 article-title: Regional brain activity associated with visual backward masking publication-title: J. Cogn. Neurosci. doi: 10.1162/0898929052880011 – volume: 32 start-page: 1669 year: 2006 ident: 10.1016/j.neuroimage.2010.12.045_bb0065 article-title: Using nonlinear models in fMRI data analysis: model selection and activation detection publication-title: Neuroimage doi: 10.1016/j.neuroimage.2006.03.006 – volume: 21 start-page: 401 year: 2004 ident: 10.1016/j.neuroimage.2010.12.045_bb0170 article-title: Efficiency, power, and entropy in event-related fMRI with multiple trial types. Part II: design of experiments publication-title: Neuroimage doi: 10.1016/j.neuroimage.2003.09.031 |
SSID | ssj0009148 |
Score | 2.200384 |
Snippet | There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital complex (LO).... Introduction There is mounting evidence that visual perception abnormalities in schizophrenia are partly explained by a dysfunction of the lateral occipital... |
SourceID | pubmedcentral proquest pubmed crossref elsevier |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1219 |
SubjectTerms | Adolescent Adult Backward visual masking Brain Charitable foundations Diagnostic and Statistical Manual of Mental Disorders Education Excitatory Postsynaptic Potentials Female fMRI Functional connectivity/ Dynamic coupling Humans Lateral occipital complex Magnetic Resonance Imaging Male Medical imaging Medical research Middle Aged Neural Pathways - physiology Occipital Lobe - physiology Perceptual Masking Photic Stimulation Psychiatric Status Rating Scales Psychomotor Performance - physiology Schizophrenia Schizophrenia - physiopathology Schizophrenic Psychology Studies Visual Perception - physiology Young Adult |
SummonAdditionalLinks | – databaseName: Elsevier SD Freedom Collection Journals [SCFCJ] dbid: AIKHN link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lj9MwELZWXQlxQbwpLMgHrlXjxI5j7alasSog9gIr7c3yKxBUkmrbIn7-zsROdstDqsQ1yVSpPc_MN58JeZs7yFM52DcHBcE2YwF-MBQzyY1UNvPIf4Joi4tyeck_XImrI3I2zMIgrDL5_ujTe2-drszTas7XTTP_DJkBhBuoNzBtKZD68zgvVCkm5Hjx_uPy4pZ7l_E4ESfgRUAgAXoizKunjWx-gPFGnBd-G8TZpr9HqT-z0N_BlHei0_lD8iCllXQR3_wROQrtY3LvU2qcPyF6gV3x4KmPJ9BT1-1wFvcr7Wq6MjiGvKKdc01_iAjtgebhF41DjPRns9nB1fUIgqFNSzd34XpPyeX5uy9ny1k6W2HmSsa2M2ks1I-5VRUzyprMlZmRrhJC2MrLQpqgas5VbXjpC0hSnKlrZgLYP2fOeVY8I5O2a8MLQjMrQmYg7EsDoc57VVZWmNza3AhvmZwSOayldol4HM-_WOkBYfZd3-6Cxl3QLNewC1PCRsl1JN84QEYN26WH4VJwhxoixAGyp6PsnhIeKH0yaIdOjmCjoRrlUkJRqaaEjrfBhLEvY9rQ7TYaVl1lAkrXfz8CSg6VJ2f5lDyP6jYuCFL0QRYMvy_3FHF8AAnE9--0zbeeSBxbrJXgL__rb78i9-N3dkQznZDJ9noXXkOitrVvkiHeALwcQCQ priority: 102 providerName: Elsevier |
Title | Altered dynamic coupling of lateral occipital complex during visual perception in schizophrenia |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S1053811910016319 https://dx.doi.org/10.1016/j.neuroimage.2010.12.045 https://www.ncbi.nlm.nih.gov/pubmed/21194569 https://www.proquest.com/docview/1644779969 https://www.proquest.com/docview/855905287 https://www.proquest.com/docview/910626412 https://pubmed.ncbi.nlm.nih.gov/PMC3049854 |
Volume | 55 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9swDBbWFhh2Gbp3ti7QYVdvli1ZNnYY0qJF9gqKYgVyE_Ty5iGz0zoZdupvL2XJTrsXcjIQi4EhkdQn8SOJ0KtEA06lYN8UFMSFGVPwgzaNOJW8ULFx9U8c22KWTc_phzmbhwu3NtAqe5_YOWrTaHdH_gZgPeUc0HnxbnkRua5RLroaWmjsoL2udBnoM5_zTdFdQn0qHIMvgAGByeP5XV29yOoHWK0neLlLQZfU9Pft6U_4-TuL8sa2dLKP7gc8iSdeAR6gO7Z-iO5-DhHzR0hMXDjcGmx863msm7VLwv2KmxIvpMs_XuBG66rrHoI7hrn9hX32Iv5ZtWv4dTmwX3BV4_YmT-8xOj85_nI0jUJThUhnhKwiLhUcHBNV5EQWSsY6iyXXOWNM5YanXNqipLQoJc1MCuhEy7Ik0oLhU6K1IekTtFs3tX2GcKyYjSXs91zCHmdMkeWKyUSpRDKjCB8h3s-l0KHiuGt8sRA9tey72KyCcKsgSCJgFUaIDJJLX3VjC5miXy7RZ5WCHxSwNWwh-3aQDcjDI4otpQ967RDBA7Rio68jhIfXYLsuICNr26xbAbNexAzOrP8eAmgOjpyUJCP01KvbMCGuNh_AX_h_fksRhwGucvjtN3X1rasg7mKrOaPP___hL9A9f4PueEoHaHd1ubYvAYKt1BjtvL4i487axmhvcnT26dQ933-czuB5eDw7PbsGGFw5Wg |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELbKVgIuiDcLBXyAY0Sc2HEshFCBVlvarhBqpd6MX4GgJVnILo8_xW9kHCfZlpf20muSiRLPePzZ880MQo8SAziVwvymYCA-zJiCH3RpxKniQsfW1z_xbItpNjmmr0_YyQb62efCeFpl7xNbR21r48_InwCsp5wDOhfP558j3zXKR1f7FhrBLPbdj2-wZWue7b0C_T5Okt2do5eTqOsqEJmMkEXElYadU6JFTpTQKjZZrLjJGWM6tzzlyomCUlEomtkUlmejioIoB5ZPiTGWpPDeC2iT-ozWEdp8sTN983ZV5pfQkHzH4J8JER13KDDK2gqV5SfwE4FS5o8hfRrV3xfEPwHv77zNUwvh7lV0pUOweDuY3DW04arr6OJhF6O_geS2D8A7i21odo9NvfRpv-9xXeCZ8hnPM1wbU7b9SnDLaXffcciXxF_LZglX5wPfBpcVbk4zA2-i43MZ8FtoVNWVu4NwrJmLFSAMrmBVtVZkuWYq0TpRzGrCx4j3YylNV-Pct9qYyZ7M9lGutCC9FiRJJGhhjMggOQ91PtaQEb26ZJ_HCp5XwmK0huzTQbbDOgHDrCm91VuH7HxOI1czZIzwcBu8hQ8BqcrVy0bCqIuYwS75348AfoRNLiXJGN0O5jYMiK8GCIAb3s_PGOLwgK9VfvZOVX5oa5b7aG7O6N3_f_hDdGlydHggD_am-_fQ5XB-71lSW2i0-LJ09wEALvSDbtZh9O68J_ov-Dtyhg |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELZKkSouFW-WFvABjlHjxI5jVRWqKKuWQsWBSnszfqUELcmW7FL4a_w6xnGSbXlpL70mmSixZ8afPd_MIPQ8MYBTKdg3BQXxYcYU_KBLI04VFzq2vv6JZ1ucZIen9M2ETdbQzz4XxtMqe5_YOmpbG39GvgOwnnIO6FzsFB0t4v3B-OXsPPIdpHyktW-nEVTk2P24gO1bs3d0AHP9IknGrz-8Ooy6DgORyQiZR1xp2EUlWuRECa1ik8WKm5wxpnPLU66cKCgVhaKZTWGpNqooiHJgBZQYY0kK772BbvIUUBXYEp_wZcFfQkMaHoO_J0R0LKLALWtrVZZfwGMEcpk_kPQJVX9fGv-Evr8zOC8tiePbaLPDsng_KN8dtOaqu2jjXRetv4fkvg_FO4ttaHuPTb3wCcBnuC7wVPnc5ymujSnbziW4Zbe77zhkTuJvZbOAq7OBeYPLCjeXOYL30em1DPcDtF7VlXuEcKyZixVgDa5gfbVWZLlmKtE6UcxqwkeI92MpTVft3DfdmMqe1vZZLmdB-lmQJJEwCyNEBslZqPixgozop0v2Ga3ggyUsSyvI7g6yHeoJaGZF6e1eO2TnfRq5tJURwsNt8Bs-GKQqVy8aCaMuYgb75X8_AkgStruUJCP0MKjbMCC-LiBAb3g_v6KIwwO-avnVO1X5qa1e7uO6OaOP___hz9AGmLd8e3RyvIVuhYN8T5faRuvzrwv3BJDgXD9tTQ6jj9dt478AoxB1TQ |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Altered+dynamic+coupling+of+lateral+occipital+complex+during+visual+perception+in+schizophrenia&rft.jtitle=NeuroImage+%28Orlando%2C+Fla.%29&rft.au=Harvey%2C+Philippe-Olivier&rft.au=Lee%2C+Junghee&rft.au=Cohen%2C+Mark+S&rft.au=Engel%2C+Stephen+A&rft.date=2011-04-01&rft.pub=Elsevier+Limited&rft.issn=1053-8119&rft.eissn=1095-9572&rft.volume=55&rft.issue=3&rft.spage=1219&rft_id=info:doi/10.1016%2Fj.neuroimage.2010.12.045&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=3556011121 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1053-8119&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1053-8119&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1053-8119&client=summon |