Cited by 326

The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.

Abnormal Medial Prefrontal Cortex Resting-State Connectivity in Bipolar Disorder and Schizophrenia

Open access

Chai, Xiaoqian J, Whitfield-Gabrieli, Susan, Shinn, Ann K, Gabrieli, John D E, Nieto Castañón, Alfonso, McCarthy, Julie M, Cohen, Bruce M, Öngür, Dost·2011·Neuropsychopharmacology

DOI 10.1038/npp.2011.88

Open this paper in CoChat — free account

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1038/npp.2011.88

Cites

65 of 65 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Self-check

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

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

Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets
Maldjian, J. A., Laurienti, P. J., Kraft, R. A., & Burdette, J. H. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00169-1 · Cited by 5,085
Conn : A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks
Whitfield-Gabrieli, S., & Nieto-Castanon, A. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0073 · Cited by 4,885
A component based noise correction method (CompCor) for BOLD and perfusion based fMRI
Behzadi, Y., Restom, K., Liau, J., & Liu, T. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.04.042 · Cited by 4,502
MANIC DEPRESSIVE ILLNESS
(1984) · The Lancet · doi:10.1016/s0140-6736(84)92810-1 · Cited by 2,925
A critical role for the right fronto-insular cortex in switching between central-executive and default-mode networks
Sridharan, D., Levitin, D. J., & Menon, V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800005105 · Cited by 2,892
The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627
Efficiency and Cost of Economical Brain Functional Networks
Achard, S., & Bullmore, E. (2007) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030017 · Cited by 2,553
Reciprocal Limbic-Cortical Function and Negative Mood: Converging PET Findings in Depression and Normal Sadness
Mayberg, H. S., Liotti, M., Brannan, S. K., McGinnis, S., Mahurin, R. K., Jerabek, P. A., Silva, J. A., Tekell, J. L., Martin, C. C., Lancaster, J. L., et al. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.5.675 · Cited by 2,416
The impact of global signal regression on resting state correlations: are anti-correlated networks introduced?
Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.036 · Cited by 2,387
Neurobiology of emotion perception I: the neural basis of normal emotion perception
Phillips, M. L., Drevets, W. C., Rauch, S. L., & Lane, R. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00168-9 · Cited by 2,173
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
Lichtenstein, P., Yip, B. H., Björk, C., Pawitan, Y., Cannon, T. D., Sullivan, P. F., & Hultman, C. M. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60072-6 · Cited by 2,125
Chlorpromazine Equivalent Doses for the Newer Atypical Antipsychotics
Woods, S. W. (2003) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v64n0607 · Cited by 2,050
Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia: I. Regional Cerebral Blood Flow Evidence
Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,019
Neurobiology of emotion perception II: implications for major psychiatric disorders
Phillips, M. L., Drevets, W. C., Rauch, S. L., & Lane, R. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00171-9 · Cited by 1,736
Hyperactivity and hyperconnectivity of the default network in schizophrenia and in first-degree relatives of persons with schizophrenia
Whitfield-Gabrieli, S., Thermenos, H. W., Milanovic, S., Tsuang, M. T., Faraone, S. V., McCarley, R. W., Shenton, M. E., Green, A. I., Nieto-Castanon, A., LaViolette, P., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809141106 · Cited by 1,435
Self-citation
Spontaneous low‐frequency BOLD signal fluctuations: An fMRI investigation of the resting‐state default mode of brain function hypothesis
Fransson, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20113 · Cited by 1,388
A neural model of voluntary and automatic emotion regulation: implications for understanding the pathophysiology and neurodevelopment of bipolar disorder
Phillips, M. L., Ladouceur, C. D., & Drevets, W. C. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.65 · Cited by 1,383 · cited 1×
“…including Brodmann areas 32, 24, 25, and 10, has extensive and reciprocal connections to the limbic circuit and surrounding prefrontal cortical regions (Öngür and Price 2000), and has been suggested to contribute to the emotional regulation impairment in bipolar disorder (Phillips et al, 2008).”
Background
Functional Connectivity and Brain Networks in Schizophrenia
Lynall, M.-E., Bassett, D. S., Kerwin, R., McKenna, P. J., Kitzbichler, M., Muller, U., & Bullmore, E. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0333-10.2010 · Cited by 1,363
Competition between functional brain networks mediates behavioral variability
Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.008 · Cited by 1,287
Hierarchical Organization of Human Cortical Networks in Health and Schizophrenia
Bassett, D. S., Bullmore, E., Verchinski, B. A., Mattay, V. S., Weinberger, D. R., & Meyer-Lindenberg, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1929-08.2008 · Cited by 1,229
Meta-analysis of 41 functional neuroimaging studies of executive function in schizophrenia
Minzenberg, M. J., Laird, A. R., Thelen, S., Carter, C. S., & Glahn, D. C. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.91 · Cited by 1,158
Anticorrelations in resting state networks without global signal regression
Chai, X. J., Castañón, A. N., Öngür, D., & Whitfield-Gabrieli, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.048 · Cited by 1,144
Self-citation
Functional connectivity of default mode network components: correlation, anticorrelation, and causality
Uddin, L. Q., Clare Kelly, A. M., Biswal, B. B., Xavier Castellanos, F., & Milham, M. P. (2009) · Human Brain Mapping · doi:10.1002/hbm.20531 · Cited by 1,135
A Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging
McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321593117 · Cited by 1,080
Disrupted small-world networks in schizophrenia
Liu, Y., Liang, M., Zhou, Y., He, Y., Hao, Y., Song, M., Yu, C., Liu, H., Liu, Z., & Jiang, T. (2008) · Brain · doi:10.1093/brain/awn018 · Cited by 1,033
The functional neuroanatomy of bipolar disorder: a review of neuroimaging findings
Strakowski, S. M., DelBello, M. P., & Adler, C. M. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001585 · Cited by 818
Functional Specialization within Rostral Prefrontal Cortex (Area 10): A Meta-analysis
Gilbert, S. J., Spengler, S., Simons, J. S., Steele, J. D., Lawrie, S. M., Frith, C. D., & Burgess, P. W. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.6.932 · Cited by 683
Relation of Prefrontal Cortex Dysfunction to Working Memory and Symptoms in Schizophrenia
Perlstein, W. M., Carter, C. S., Noll, D. C., & Cohen, J. D. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.7.1105 · Cited by 645
Selective Deficits in Prefrontal Cortex Function in Medication-Naive Patients With Schizophrenia
Barch, D. M., Carter, C. S., Braver, T. S., Sabb, F. W., MacDonald, A., Noll, D. C., & Cohen, J. D. (2001) · Archives of General Psychiatry · doi:10.1001/archpsyc.58.3.280 · Cited by 614
How default is the default mode of brain function?
Fransson, P. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.06.017 · Cited by 611
Development of Anterior Cingulate Functional Connectivity from Late Childhood to Early Adulthood
Kelly, A. M. C., Di Martino, A., Uddin, L. Q., Shehzad, Z., Gee, D. G., Reiss, P. T., Margulies, D. S., Castellanos, F. X., & Milham, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn117 · Cited by 572 · cited 1×
“Dorsal executive control regions including the DLPFC are anticorrelated with the MPFC in healthy subjects during rest (Fox et al, 2005; Fransson, 2005; Kelly et al, 2009; Uddin et al, 2009).”
Background
Spontaneous Low-Frequency Fluctuations in the BOLD Signal in Schizophrenic Patients: Anomalies in the Default Network
Bluhm, R. L., Miller, J., Lanius, R. A., Osuch, E. A., Boksman, K., Neufeld, R., Theberge, J., Schaefer, B., & Williamson, P. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm052 · Cited by 568
Subcortical and ventral prefrontal cortical neural responses to facial expressions distinguish patients with bipolar disorder and major depression
Lawrence, N. S., Williams, A. M., Surguladze, S., Giampietro, V., Brammer, M. J., Andrew, C., Frangou, S., Ecker, C., & Phillips, M. L. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.11.017 · Cited by 548
Functional disintegration in paranoid schizophrenia using resting-state fMRI
Zhou, Y., Liang, M., Tian, L., Wang, K., Hao, Y., Liu, H., Liu, Z., & Jiang, T. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.05.029 · Cited by 437
Default mode network abnormalities in bipolar disorder and schizophrenia
Öngür, D., Lundy, M., Greenhouse, I., Shinn, A. K., Menon, V., Cohen, B. M., & Renshaw, P. F. (2010) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2010.04.008 · Cited by 407
Self-citation
Anxiety Dissociates Dorsal and Ventral Medial Prefrontal Cortex Functional Connectivity with the Amygdala at Rest
Kim, M. J., Gee, D. G., Loucks, R. A., Davis, F. C., & Whalen, P. J. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq237 · Cited by 388
Short-term Effects of Antipsychotic Treatment on Cerebral Function in Drug-Naive First-Episode Schizophrenia Revealed by “Resting State” Functional Magnetic Resonance Imaging
Lui, S., Li, T., Deng, W., Jiang, L., Wu, Q., Tang, H., Yue, Q., Huang, X., Chan, R. C., Collier, D. A., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.84 · Cited by 365
Resting state corticolimbic connectivity abnormalities in unmedicated bipolar disorder and unipolar depression
Anand, A., Li, Y., Wang, Y., Lowe, M. J., & Dzemidzic, M. (2009) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2008.03.012 · Cited by 353
Evolution of neuropsychological dysfunction during the course of schizophrenia and bipolar disorder
Lewandowski, K. E., Cohen, B. M., & Öngur, D. (2011) · Psychological Medicine · doi:10.1017/s0033291710001042 · Cited by 336
Self-citation
Abnormal Amygdala-Prefrontal Effective Connectivity to Happy Faces Differentiates Bipolar from Major Depression
Almeida, J. R. C. D., Versace, A., Mechelli, A., Hassel, S., Quevedo, K., Kupfer, D. J., & Phillips, M. L. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.03.024 · Cited by 305
Manic-Depressive Illness
Fernandes, P. P., Ramaswamy, S., Marcil, W., & Petty, F. (2007) · xPharm: The Comprehensive Pharmacology Reference · doi:10.1016/b978-008055232-3.60649-x · Cited by 294
Heritability of “small‐world” networks in the brain: A graph theoretical analysis of resting‐state EEG functional connectivity
Smit, D. J. A., Stam, C. J., Posthuma, D., Boomsma, D. I., & de Geus, E. J. C. (2008) · Human Brain Mapping · doi:10.1002/hbm.20468 · Cited by 275
Abnormal ventral frontal response during performance of an affective go/no go task in patients with mania
Elliott, R., Ogilvie, A., Rubinsztein, J. S., Calderon, G., Dolan, R. J., & Sahakian, B. J. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.03.007 · Cited by 223
Abnormal Left and Right Amygdala-Orbitofrontal Cortical Functional Connectivity to Emotional Faces: State Versus Trait Vulnerability Markers of Depression in Bipolar Disorder
Versace, A., Thompson, W. K., Zhou, D., Almeida, J. R. C., Hassel, S., Klein, C. R., Kupfer, D. J., & Phillips, M. L. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.11.025 · Cited by 194
Functional connectivity between ventral prefrontal cortex and amygdala at low frequency in the resting state in bipolar disorder
Chepenik, L. G., Raffo, M., Hampson, M., Lacadie, C., Wang, F., Jones, M. M., Pittman, B., Skudlarski, P., & Blumberg, H. P. (2010) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2010.04.002 · Cited by 175
A functional MRI study of working memory task in euthymic bipolar disorder: evidence for task‐specific dysfunction
Monks, P. J., Thompson, J. M., Bullmore, E. T., Suckling, J., Brammer, M. J., Williams, S. C., Simmons, A., Giles, N., Lloyd, A. J., Louise Harrison, C., et al. (2004) · Bipolar Disorders · doi:10.1111/j.1399-5618.2004.00147.x · Cited by 174
fMRI Study of Maintenance and Manipulation Processes Within Working Memory in First-Episode Schizophrenia
Tan, H.-Y., Choo, W.-C., Fones, C. S. L., & Chee, M. W. L. (2005) · American Journal of Psychiatry · doi:10.1176/appi.ajp.162.10.1849 · Cited by 161
Amygdalofrontal Functional Disconnectivity and Aggression in Schizophrenia
Hoptman, M. J., D’Angelo, D., Catalano, D., Mauro, C. J., Shehzad, Z. E., Kelly, C. A. M., Castellanos, F. X., Javitt, D. C., & Milham, M. P. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp012 · Cited by 159
Neuroimaging of cognitive disability in schizophrenia: Search for a pathophysiological mechanism
Ragland, J. D., Yoon, J. H., Minzenberg, M., & Carter, C. S. (2007) · International Review of Psychiatry · doi:10.1080/09540260701486365 · Cited by 152
fMRI abnormalities in dorsolateral prefrontal cortex during a working memory task in manic, euthymic and depressed bipolar subjects
Townsend, J. D., Bookheimer, S. Y., Foland‐Ross, L. C., Sugar, C. A., & Altshuler, L. L. (2010) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.11.010 · Cited by 148
Deficit in a Neural Correlate of Reality Monitoring in Schizophrenia Patients
Vinogradov, S., Luks, T. L., Schulman, B. J., & Simpson, G. V. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn028 · Cited by 126
Impulsivity and neural correlates of response inhibition in schizophrenia
Kaladjian, A., Jeanningros, R., Azorin, J., Anton, J., & Mazzola‐Pomietto, P. (2010) · Psychological Medicine · doi:10.1017/s0033291710000796 · Cited by 98
An event-related functional MRI study of working memory in euthymic bipolar disorder
Lagopoulos, J., Ivanovski, B., & Malhi, G. S. (2007) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0717 · Cited by 97
Blunted activation in right ventrolateral prefrontal cortex during motor response inhibition in schizophrenia
Kaladjian, A., Jeanningros, R., Azorin, J., Grimault, S., Anton, J., & Mazzola‐Pomietto, P. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.07.033 · Cited by 83
Brain structural changes associated with chronicity and antipsychotic treatment in schizophrenia
Tomelleri, L., Jogia, J., Perlini, C., Bellani, M., Ferro, A., Rambaldelli, G., Tansella, M., Frangou, S., & Brambilla, P. (2009) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2009.07.007 · Cited by 67
Medial Frontal Hyperactivity in Reality Distortion
Taylor, S. F., Welsh, R. C., Chen, A. C., Velander, A. J., & Liberzon, I. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.11.029 · Cited by 59
A longitudinal fMRI study of the manic and euthymic states of bipolar disorder
Chen, C., Suckling, J., Ooi, C., Jacob, R., Lupson, V. C., Bullmore, E. T., & Lennox, B. (2010) · Bipolar Disorders · doi:10.1111/j.1399-5618.2010.00801.x · Cited by 51
Intact hemispheric specialization for spatial and shape working memory in schizophrenia
Manoach, D. S., White, N. S., Lindgren, K. A., Heckers, S., Coleman, M. J., Dubal, S., GOFF, D. C., & Holzman, P. S. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.06.017 · Cited by 14

An improved framework for confound regression and filtering for control of motion artifact in the preprocessing of resting-state functional connectivity data
Satterthwaite, T. D., Elliott, M. A., Gerraty, R. T., Ruparel, K., Loughead, J., Calkins, M. E., Eickhoff, S. B., Hakonarson, H., Gur, R. C., Gur, R. E., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.052 · Cited by 1,881
Default Mode Network Activity and Connectivity in Psychopathology
Whitfield-Gabrieli, S., & Ford, J. M. (2012) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-032511-143049 · Cited by 1,465
A Critical Appraisal of Neuroimaging Studies of Bipolar Disorder: Toward a New Conceptualization of Underlying Neural Circuitry and a Road Map for Future Research
Phillips, M. L., & Swartz, H. A. (2014) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2014.13081008 · Cited by 636
Dysfunction of Large-Scale Brain Networks in Schizophrenia: A Meta-analysis of Resting-State Functional Connectivity
Dong, D., Wang, Y., Chang, X., Luo, C., & Yao, D. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx034 · Cited by 486
A Review of the Functional and Anatomical Default Mode Network in Schizophrenia
Hu, M.-L., Zong, X.-F., Mann, J. J., Zheng, J.-J., Liao, Y.-H., Li, Z.-C., He, Y., Chen, X.-G., & Tang, J.-S. (2017) · Neuroscience Bulletin · doi:10.1007/s12264-016-0090-1 · Cited by 331

See all 326

Authors: Chai, X. J., Whitfield-Gabrieli, S., Shinn, A. K., Gabrieli, J. D. E., Nieto Castañón, A., McCarthy, J. M., Cohen, B. M., & Öngür, D.
Venue: Neuropsychopharmacology
Publisher: Springer Science and Business Media LLC
Published: 2011-06-08
Volume: 36
Issue: 10
Pages: 2009-2017
ISSN: 0893-133X (ISSN-L)
1740-634X
DOI: 10.1038/npp.2011.88
OpenAlex: W2045844145
Cited by: 326
References: 65
FWCI: 11.31
Type: journal article
Language: en
Open access: bronze

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.

Abnormal Medial Prefrontal Cortex Resting-State Connectivity in Bipolar Disorder and Schizophrenia

Overview

Integrity signals

Verification

Claims the paper makes

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks

Data sources