Cited by 127Posttraumatic Stress Disorder ResearchResilience and Mental HealthStress Responses and Cortisol

The DOI matches its Crossref record; 64 of the 65 references it cites were found in a registry or an index.

Resilience after 9/11: Multimodal neuroimaging evidence for stress-related change in the healthy adult brain

Open access

Ganzel, Barbara L., Kim, Pilyoung, Glover, Gary H., Temple, Elise·2008·NeuroImage

DOI 10.1016/j.neuroimage.2007.12.010PMC PMC2405811

Open this paper in CoChat — free account

Abstract

Exposure to psychological trauma is common and predicts long-term physical and mental health problems, even in those who initially appear resilient. Here, we used multimodal neuroimaging in healthy adults who were at different distances from the World Trade Center on 9/11/01 to examine the neural mechanisms that may underlie this association. More than 3 years after 9/11/01, adults with closer proximity to the disaster had lower gray matter volume in amygdala, hippocampus, insula, anterior cingulate, and medial prefrontal cortex, with control for age, gender, and total gray matter volume. Further analysis showed a nonlinear (first-order quadratic) association between total number of traumas in lifetime and amygdala gray matter volume and function in the whole group. Post hoc analysis of subgroups with higher versus lower levels of lifetime trauma exposure revealed systematic associations between amygdala gray matter volume, amygdala functional reactivity, and anxiety that suggest a nonlinear trajectory in the neural response to accumulated trauma in healthy adults.

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 · 10.1016/j.neuroimage.2007.12.010

Cites

64 of 64 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.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

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

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

Lifetime and 12-Month Prevalence of DSM-III-R Psychiatric Disorders in the United States: Results From the National Comorbidity Survey
Kessler, R. C. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950010008002 · Cited by 12,370
Posttraumatic Stress Disorder in the National Comorbidity Survey
Kessler, R. C. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950240066012 · Cited by 10,379
Statistical parametric maps in functional imaging: A general linear approach
Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688
Impact of Event Scale: A Measure of Subjective Stress
Horowitz, M., Wilner, N., & Alvarez, W. (1979) · Psychosomatic Medicine · doi:10.1097/00006842-197905000-00004 · Cited by 7,813
An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets
Maldjian, J. A., Laurienti, P. J., Kraft, R., & Burdette, J. H. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00169-1 · Cited by 5,066
A Voxel-Based Morphometric Study of Ageing in 465 Normal Adult Human Brains
Good, C. D., Johnsrude, I. S., Ashburner, J., Henson, R. N. A., Friston, K. J., & Frackowiak, R. S. J. (2001) · NeuroImage · doi:10.1006/nimg.2001.0786 · Cited by 4,561
Functional neuroanatomy of emotion: A meta-analysis of emotion activation studies in PET and fMRI
Phan, K. L., Wager, T., Taylor, S. F., & Liberzon, I. (2002) · NeuroImage · doi:10.1006/nimg.2002.1087 · Cited by 3,502
Trauma and Posttraumatic Stress Disorder in the Community: The 1996 Detroit Area Survey of Trauma
Breslau, N., Kessler, R. C., Chilcoat, H. D., Schultz, L. R., Davis, G. C., & Andreski, P. (1998) · Archives of General Psychiatry · doi:10.1001/archpsyc.55.7.626 · Cited by 2,407
For better or for worse: neural systems supporting the cognitive down- and up-regulation of negative emotion
Ochsner, K. N., Ray, R. D., Cooper, J. C., Robertson, E. R., Chopra, S., Gabrieli, J. D. E., & Gross, J. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.06.030 · Cited by 2,113
Psychological Sequelae of the September 11 Terrorist Attacks in New York City
Galea, S., Ahern, J., Resnick, H. S., Kilpatrick, D. G., Bucuvalas, M. J., Gold, J., & Vlahov, D. (2002) · New England Journal of Medicine · doi:10.1056/nejmsa013404 · Cited by 1,905

Show all 65 references

Sorted by citations

Central role of the brain in stress and adaptation: Links to socioeconomic status, health, and disease
McEwen, B. S., & Gianaros, P. J. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05331.x · Cited by 1,715
Brain on stress: how the social environment gets under the skin
McEwen, B. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121254109 · Cited by 1,200
Stress- and Allostasis-Induced Brain Plasticity
McEwen, B. S., & Gianaros, P. J. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-052209-100430 · Cited by 1,171
The hippocampus in major depression: evidence for the convergence of the bench and bedside in psychiatric research?
MacQueen, G., & Frodl, T. (2011) · Molecular Psychiatry · doi:10.1038/mp.2010.80 · Cited by 665
The plasticity of human maternal brain: Longitudinal changes in brain anatomy during the early postpartum period
Kim, P., Leckman, J. F., Mayes, L. C., Feldman, R., Wang, X., & Swain, J. E. (2010) · Behavioral Neuroscience · doi:10.1037/a0020884 · Cited by 440
Self-citation
Allostasis and the human brain: Integrating models of stress from the social and life sciences.
Ganzel, B. L., Morris, P., & Wethington, E. (2010) · Psychological Review · doi:10.1037/a0017773 · Cited by 415
Self-citation
A systematic review and meta-analysis of magnetic resonance imaging measurement of structural volumes in posttraumatic stress disorder
O'Doherty, D. C. M., Chitty, K. M., Saddiqui, S., Bennett, M. R., & Lagopoulos, J. (2015) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2015.01.002 · Cited by 375
Cumulative adversity and smaller gray matter volume in medial prefrontal, anterior cingulate, and insula regions
Ansell, E. B., Rando, K., Tuit, K., Guarnaccia, J., & Sinha, R. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.022 · Cited by 354
Early-life stress is associated with impairment in cognitive control in adolescence: An fMRI study
Mueller, S. C., Maheu, F. S., Dozier, M., Peloso, E., Mandell, D., Leibenluft, E., Pine, D. S., & Ernst, M. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.06.013 · Cited by 297
Recognizing resilience: Learning from the effects of stress on the brain
McEwen, B. S., Gray, J. D., & Nasca, C. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.09.001 · Cited by 292
Amygdala Volume Changes in Posttraumatic Stress Disorder in a Large Case-Controlled Veterans Group
Morey, R. A., Gold, A. L., LaBar, K. S., Beall, S. K., Brown, V. M., Haswell, C. C., Nasser, J. D., Wagner, H. R., McCarthy, G., & Mid-Atlantic MIRECC Workgroup, F. T. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.50 · Cited by 289
The maternal brain and its plasticity in humans
Kim, P., Strathearn, L., & Swain, J. E. (2016) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.08.001 · Cited by 278
Self-citation
The impact of developmental timing for stress and recovery
Gee, D. G., & Casey, B. J. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2015.02.001 · Cited by 245
“Parallel findings of increased amygdala volume and functional reactivity, smaller hippocampal volume, and altered prefrontal function and connectivity have been observed in humans following stress (Ganzel et al., 2007, 2008; Liston et al., 2006; Liston et al., 2009; Sheridan et al., 2012a,b).”
Background
Traumatic Brain Injury in Intimate Partner Violence: A Critical Review of Outcomes and Mechanisms
Kwako, L. E., Glass, N. E., Campbell, J. C., Melvin, K. C., Barr, T. L., & Gill, J. (2011) · Trauma Violence & Abuse · doi:10.1177/1524838011404251 · Cited by 278
Stress-Induced Grey Matter Loss Determined by MRI Is Primarily Due to Loss of Dendrites and Their Synapses
Kassem, M. S., Lagopoulos, J., Stait‐Gardner, T., Price, W. S., Chohan, T. W., Arnold, J. C., Hatton, S. N., & Bennett, M. R. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8365-7 · Cited by 224
PTSD-related neuroimaging abnormalities in brain function, structure, and biochemistry
Harnett, N. G., Goodman, A. M., & Knight, D. C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113331 · Cited by 201
Neurophysiological and neurocognitive mechanisms underlying the effects of yoga-based practices: towards a comprehensive theoretical framework
Schmalzl, L., Powers, C., & Henje Blom, E. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00235 · Cited by 170
Neural plasticity in fathers of human infants
Kim, P., Rigo, P., Mayes, L. C., Feldman, R., Leckman, J. F., & Swain, J. E. (2014) · Social Neuroscience · doi:10.1080/17470919.2014.933713 · Cited by 164
Self-citation
The Neurobiological Role of the Dorsolateral Prefrontal Cortex in Recovery From Trauma
Lyoo, I. K., Kim, J. E., Yoon, S. J., Hwang, J., Bae, S., & Kim, D. J. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.70 · Cited by 160
Perceived quality of maternal care in childhood and structure and function of mothers' brain
Kim, P., Leckman, J. F., Mayes, L. C., Newman, M., Feldman, R., & Swain, J. E. (2009) · Developmental Science · doi:10.1111/j.1467-7687.2009.00923.x · Cited by 152
Self-citation
Smaller amygdala volume and reduced anterior cingulate gray matter density associated with history of post-traumatic stress disorder
Rogers, M. A., Yamasue, H., Abe, O., Yamada, H., Ohtani, T., Iwanami, A., Aoki, S., Kato, N., & Kasai, K. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.06.001 · Cited by 142
Resilience: A psychobiological construct for psychiatric disorders
Shrivastava, A., & Desousa, A. (2016) · Indian Journal of Psychiatry · doi:10.4103/0019-5545.174365 · Cited by 127
Grey matter reduction associated with posttraumatic stress disorder and traumatic stress
Li, L., Wu, M. C., Liao, Y., Ouyang, L., Du, M., Lei, D., Chen, L., Yao, L., Huang, X., & Gong, Q. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.04.003 · Cited by 131
Effects of stressful life events on human brain structure: A longitudinal voxel-based morphometry study
Papagni, S. A., Benetti, S., Arulanantham, S., McCrory, E., McGuire, P., & Mechelli, A. (2011) · Stress · doi:10.3109/10253890.2010.522279 · Cited by 126
The neural development of empathy is sensitive to caregiving and early trauma
Lévy, J., Goldstein, A., & Feldman, R. (2019) · Nature Communications · doi:10.1038/s41467-019-09927-y · Cited by 125
Brain structural changes as vulnerability factors and acquired signs of post-earthquake stress
Sekiguchi, A., Sugiura, M., Taki, Y., Kotozaki, Y., Nouchi, R., Takeuchi, H., Araki, T., Hanawa, S., Nakagawa, S., Miyauchi, C. M., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.51 · Cited by 117
An ecological approach to understanding the developing brain: Examples linking poverty, parenting, neighborhoods, and the brain.
Hyde, L. W., Gard, A. M., Tomlinson, R. C., Burt, S. A., Mitchell, C. M., & Monk, C. S. (2020) · American Psychologist · doi:10.1037/amp0000741 · Cited by 128
Neuroimaging research in posttraumatic stress disorder – Focus on amygdala, hippocampus and prefrontal cortex
Henigsberg, N., Kalember, P., Petrović, Z. K., & Šečić, A. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.11.003 · Cited by 105
Resting state functional connectivity of the anterior cingulate cortex in veterans with and without post-traumatic stress disorder
Kennis, M., Rademaker, A. R., van Rooij, S. J. H., Kahn, R. S., & Geuze, E. (2014) · Human Brain Mapping · doi:10.1002/hbm.22615 · Cited by 109
Reduced hippocampal gray matter volume is a common feature of patients with major depression, bipolar disorder, and schizophrenia spectrum disorders
Brosch, K., Stein, F., Schmitt, S., Pfarr, J., Ringwald, K. G., Thomas‐Odenthal, F., Meller, T., Steinsträter, O., Waltemate, L., Lemke, H., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01687-4 · Cited by 113
Effect of leukocyte telomere length on total and regional brain volumes in a large population-based cohort
King, K. S., Kozlitina, J., Rosenberg, R. N., Peshock, R. M., McColl, R. W., & Garcia, C. K. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.1926 · Cited by 95
The impact of stress on epidermal barrier function: an evidence‐based review
Maarouf, M., Maarouf, C. L., Yosipovitch, G., & Shi, V. Y. (2019) · British Journal of Dermatology · doi:10.1111/bjd.17605 · Cited by 92
Scars in depression: is a conceptual shift necessary to solve the puzzle?
Wichers, M., Geschwind, N., van Os, J., & Peeters, F. P. M. L. (2009) · Psychological Medicine · doi:10.1017/s0033291709990420 · Cited by 91
The Resilient Emotional Brain: A Scoping Review of the Medial Prefrontal Cortex and Limbic Structure and Function in Resilient Adults With a History of Childhood Maltreatment
Moreno-López, L., Ioannidis, K., Askelund, A. D., Smith, A., Schueler, K., & van Harmelen, A. (2019) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.12.008 · Cited by 98
Allostasis and the developing human brain: Explicit consideration of implicit models
Ganzel, B. L., & Morris, P. (2011) · Development and Psychopathology · doi:10.1017/s0954579411000447 · Cited by 93
Self-citation
Cognitive reappraisal in trauma-exposed women with borderline personality disorder
Lang, S., Kotchoubey, B., Frick, C., Spitzer, C., Grabe, H. J., & Barnow, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.061 · Cited by 108
Ventral striatum and amygdala activity as convergence sites for early adversity and conduct disorder
Holz, N. E., Boecker-Schlier, R., Buchmann, A. F., Blomeyer, D., Jennen-Steinmetz, C., Baumeister, S., Plichta, M. M., Cattrell, A., Schumann, G., Esser, G., et al. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw120 · Cited by 70
Lower anterior cingulate volume in seriously violent men with antisocial personality disorder or schizophrenia and a history of childhood abuse
Kumari, V., Uddin, S., Premkumar, P., Young, S., Gudjonsson, G. H., Raghuvanshi, S., Barkataki, I., Sumich, A. L., Taylor, P. J., & Das, M. (2013) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867413512690 · Cited by 73
Trauma-Informed Hospice and Palliative Care
Ganzel, B. L. (2016) · The Gerontologist · doi:10.1093/geront/gnw146 · Cited by 69
Self-citation
Stress and the healthy adolescent brain: Evidence for the neural embedding of life events
Ganzel, B. L., Kim, P., Gilmore, H. M., Tottenham, N., & Temple, E. (2013) · Development and Psychopathology · doi:10.1017/s0954579413000242 · Cited by 66
Self-citation
Neuroimaging-based biomarker discovery and validation
Woo, C., & Wager, T. D. (2015) · Pain · doi:10.1097/j.pain.0000000000000223 · Cited by 59
Different Regional Gray Matter Loss in Recent Onset PTSD and Non PTSD after a Single Prolonged Trauma Exposure
Chen, Y., Fu, K., Chen, F., Tang, L., Zhang, J., Huan, Y., Cui, J., Mu, Y., Qi, S., Xiong, L., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048298 · Cited by 59
Mismatch or allostatic load? Timing of life adversity differentially shapes gray matter volume and anxious temperament
Kuhn, M., Scharfenort, R., Schümann, D., Schiele, M. A., Klahn, A. L., Deckert, J., Domschke, K., Haaker, J., Kalisch, R., Pauli, P., et al. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv137 · Cited by 56
A Biobehavioral Approach to Understanding Obesity and the Development of Obesogenic Illnesses Among Latino Immigrants in the United States
D’Alonzo, K. T., Johnson, S., & Fanfan, D. (2012) · Biological Research For Nursing · doi:10.1177/1099800412457017 · Cited by 57
Takotsubo Syndrome – Predictable from brain imaging data
Klein, C., Hiestand, T., Ghadri, J. R., Templin, C., Jäncke, L., & Hänggi, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-05592-7 · Cited by 55
Negative life stress and longitudinal hippocampal volume changes in older adults with and without depression
Zannas, A. S., McQuoid, D. R., Payne, M. E., Steffens, D. C., MacFall, J. R., Ashley-Koch, A., & Taylor, W. D. (2013) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2013.02.008 · Cited by 53
Morphological brain measures of cortico‐limbic inhibition related to resilience
Gupta, A., Love, A., Kilpatrick, L. A., Labus, J. S., Bhatt, R., Chang, L., Tillisch, K., Naliboff, B., & Mayer, E. A. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24007 · Cited by 54
Positive coping styles and perigenual ACC volume: two related mechanisms for conferring resilience?
Holz, N. E., Boecker, R., Jennen-Steinmetz, C., Buchmann, A. F., Blomeyer, D., Baumeister, S., Plichta, M. M., Esser, G., Schmidt, M. H., Meyer‐Lindenberg, A., et al. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw005 · Cited by 54
Cognitive impairment and World Trade Centre-related exposures
Clouston, S., Hall, C. B., Kritikos, M., Bennett, D. A., DeKosky, S. T., Edwards, J. D., Finch, C. E., Kreisl, W. C., Mielke, M. M., Peskind, E. R., et al. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-021-00576-8 · Cited by 54
World Trade Center Health Program: First Decade of Research
Santiago-Colón, A., Daniels, R., Reissman, D. B., Anderson, K. R., Calvert, G., Caplan, A., Carreón, T., Katruska, A., Kubale, T., Liu, R.-L., et al. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17197290 · Cited by 44
Brain volumetric changes in the general population following the COVID-19 outbreak and lockdown
Salomon, T., Cohen, A., Barazany, D., Ben-Zvi, G., Botvinik‐Nezer, R., Gera, R., Oren, S., Roll, D., Rozic, G., Saliy, A., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118311 · Cited by 51
Neural Network Modulation by Trauma as a Marker of Resilience
James, L. M., Engdahl, B. E., Leuthold, A., Lewis, S. M., Kampen, E. V., & Georgopoulos, A. P. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.878 · Cited by 44
Neuroendocrine mechanisms for parental sensitivity: overview, recent advances and future directions
Swain, J., & Ho, S. (2017) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2017.02.027 · Cited by 39
Association of Fatigue and Stress With Gray Matter Volume
Kokubun, K., Nemoto, K., Oka, H., Fukuda, H., Yamakawa, Y., & Watanabe, Y. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00154 · Cited by 41
Cortical inhibition deficits in recent onset PTSD after a single prolonged trauma exposure
Qi, S., Mu, Y.-F., Liu, K., Zhang, J., Huan, Y., Tan, Q.-R., Shi, M., Wang, Q., Chen, Y.-C., Wang, H.-H., et al. (2013) · NeuroImage: Clinical · doi:10.1016/j.nicl.2013.08.013 · Cited by 44
Heterogeneity of non-conscious fear perception in posttraumatic stress disorder as a function of physiological arousal: An fMRI study
Kemp, A. H., Felmingham, K. L., Falconer, E. M., Liddell, B. J., Bryant, R. A., & Williams, L. M. (2009) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2009.04.012 · Cited by 40
Impact of acute stress on human brain microstructure: An MR diffusion study of earthquake survivors
Chen, L., Lui, S., Wu, Q., Zhang, W., Zhou, D., Chen, H., Huang, X., Kuang, W., Chan, R. C. K., Mechelli, A., et al. (2011) · Human Brain Mapping · doi:10.1002/hbm.21438 · Cited by 40
Regional cerebral changes and functional connectivity during the observation of negative emotional stimuli in subjects with post-traumatic stress disorder
Mazza, M., Tempesta, D., Pino, M. C., Catalucci, A., Gallucci, M., & Ferrara, M. (2013) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-013-0394-3 · Cited by 40
Victims' Time Discounting 2.5 Years after the Wenchuan Earthquake: An ERP Study
Li, J.-Z., Gui, D.-Y., Feng, C.-L., Wang, W.-Z., Du, B.-Q., Gan, T., & Luo, Y.-J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040316 · Cited by 37
Altered functional connectivity in the brain default-mode network of earthquake survivors persists after 2 years despite recovery from anxiety symptoms
Du, M., Liao, W., Lui, S., Huang, X., Li, F. Y., Kuang, W., Li, J., Chen, H.-F., Kendrick, K. M., & Gong, Q. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv040 · Cited by 38
Perinatal stress and human hippocampal volume: Findings from typically developing young adults
Marečková, K., Mareček, R., Bencúrová, P., Klánová, J., Dušek, L., & Brázdil, M. (2018) · Scientific Reports · doi:10.1038/s41598-018-23046-6 · Cited by 37
Long-Term Effects of Acute Stress on the Prefrontal-Limbic System in the Healthy Adult
Li, Y., Hou, X., Wei, D., Du, X., Zhang, Q., Liu, G., & Qiu, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0168315 · Cited by 37
The Neural Basis of Empathy and Empathic Behavior in the Context of Chronic Trauma
Lévy, J., Yirmiya, K., Goldstein, A., & Feldman, R. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00562 · Cited by 37
Expedition Cognition: A Review and Prospective of Subterranean Neuroscience With Spaceflight Applications
Mogilever, N. B., Zuccarelli, L., Burles, F., Iaria, G., Strapazzon, G., Bessone, L., & Coffey, E. B. J. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00407 · Cited by 30
Smaller amygdala volume and increased neuroticism predict anxiety symptoms in healthy subjects: A volumetric approach using manual tracing
Hu, Y., Moore, M., Bertels, Z., Phan, K. L., Dolcos, F., & Dolcos, S. M. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.11.008 · Cited by 34
Cingulate subregions in posttraumatic stress disorder, chronic stress, and treatment
Hinojosa, C. A., Kaur, N., VanElzakker, M. B., & Shin, L. M. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00020-0 · Cited by 26
Neuroendocrine mechanisms underlying behavioral stability: implications for the evolutionary origin of personality
Duckworth, R. A. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12797 · Cited by 25
White Matter Microstructural Changes as Vulnerability Factors and Acquired Signs of Post-Earthquake Distress
Sekiguchi, A., Sugiura, M., Taki, Y., Kotozaki, Y., Nouchi, R., Takeuchi, H., Araki, T., Hanawa, S., Nakagawa, S., Miyauchi, C. M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0083967 · Cited by 26
Brain structural plasticity in survivors of a major earthquake
Lui, S., Chen, L., Yao, L., Xiao, Y., Wu, Q. Z., Zhang, J. R., Huang, X. Q., Zhang, W., Wang, Y. Q., Chen, H. F., et al. (2013) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.120244 · Cited by 22
Right temporal cortical hypertrophy in resilience to trauma: an MRI study
Nilsen, A. S., Hilland, E., Kogstad, N., Heir, T., Hauff, E., Lien, L., & Endestad, T. (2016) · European Journal of Psychotraumatology · doi:10.3402/ejpt.v7.31314 · Cited by 25
Remote and adjacent psychological predictors of early-adulthood resilience: Role of early-life trauma, extraversion, life-events, depression, and social-support
Shen, S., Chen, Z., Qin, X., Mengjia, Z., & Dai, Q. (2021) · PLoS ONE · doi:10.1371/journal.pone.0251859 · Cited by 24
Transdiagnostic findings across major depressive disorder, bipolar disorder and schizophrenia: A qualitative review
Stein, F., & Kircher, T. T. J. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.119464 · Cited by 23
Thalamic volume and fear extinction interact to predict acute posttraumatic stress severity
Steuber, E. R., Seligowski, A. V., Roeckner, A. R., Reda, M., Lebois, L. A. M., van Rooij, S. J. H., Murty, V. P., Ely, T. D., Bruce, S. E., House, S. L., et al. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.07.023 · Cited by 18
Low-grade inflammation disrupts structural plasticity in the human brain
Szabó, C., Kelemen, O., & Kéri, S. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.002 · Cited by 18
Diffusion tensor imaging brain structural clustering patterns in major depressive disorder
Xu, D., Xu, G., Zhao, Z., Sublette, M. E., Miller, J. M., & Mann, J. J. (2021) · Human Brain Mapping · doi:10.1002/hbm.25597 · Cited by 15
Earthquake experience interference effects in a modified Stroop task: An ERP study
Wei, D., Qiu, J., Tu, S., Tian, F., Su, Y., & Luo, Y. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.03.005 · Cited by 16
Sociodemographic disparities in corticolimbic structures
Shaked, D., Millman, Z. B., Moody, D. L. B., Rosenberger, W. F., Shao, H., Katzel, L. I., Davatzikos, C. A., Gullapalli, R. P., Seliger, S. L., Erus, G., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216338 · Cited by 17
Neuroanatomical correlates of perceived stress controllability in adolescents and emerging adults
Fassett-Carman, A. N., Smolker, H., Hankin, B. L., Snyder, H. R., & Banich, M. T. (2022) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-022-00985-2 · Cited by 14
A Workshop on Cognitive Aging and Impairment in the 9/11-Exposed Population
Daniels, R. D., Clouston, S., Hall, C. B., Anderson, K. R., Bennett, D. A., Bromet, E. J., Calvert, G. M., Carreón, T., DeKosky, S. T., Diminich, E. D., et al. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18020681 · Cited by 14
Cannabidiol and the corticoraphe circuit in post-traumatic stress disorder
Alexander, C., & Vasefi, M. (2021) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2021.08.001 · Cited by 12
How personal earthquake experience impacts on the Stroop interference effect: An event-related potential study
Qiu, J., Su, Y., Li, H., Wei, D., Tu, S., & Zhang, Q. (2010) · Psychophysiology · doi:10.1111/j.1469-8986.2010.01017.x · Cited by 11
Resilience as a Psychopathological Construct for Psychiatric Disorders
Shrivastava, A., Sousa, A. D., & Lodha, P. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9721-0_23 · Cited by 11
Lifetime PTSD and geriatric depression symptomatology relate to altered dorsomedial frontal and amygdala morphometry
Knight, L. K., Naaz, F., Stoica, T., & Depue, B. E. (2017) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2017.07.003 · Cited by 12
Long-term tract-specific white matter microstructural changes after acute stress
Meng, L., Tong, S., Li, K., & Gong, Q. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00380-w · Cited by 10
Neurological disease in the aftermath of terrorism: a review
Cauwer, H. D., & Somville, F. J. M. P. (2018) · Acta Neurologica Belgica · doi:10.1007/s13760-018-0924-x · Cited by 10
Neuromodulation as a therapeutic approach for post-traumatic stress disorder: the evidence to date
Manocchio, F., Enepekides, J., Nestor, S. M., Giacobbe, P., Rabin, J. S., Burke, M. J., Lanctôt, K. L., Goubran, M., Meng, Y., Lipsman, N., et al. (2024) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2024.2442658 · Cited by 8
Preventing the Long-term Effects of General Anesthesia on the Developing Brain: How Translational Research can Contribute
Salaün, J., Poirel, N., Dahmani, S., Chagnot, A., Gakuba, C., Ali, C., Gérard, J., Hanouz, J., ORLIAGUET, G. A., & Vivien, D. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.02.029 · Cited by 8
Aftermath of 3/11: Earthquakes and involuntary attentional orienting to sudden ambient sounds
Kimura, M., Ueda, M., Takeda, Y., Sugimoto, F., & Katayama, J. (2013) · Biological Psychology · doi:10.1016/j.biopsycho.2013.08.008 · Cited by 8
Adolescent earthquake survivors' show increased prefrontal cortex activation to masked earthquake images as adults
Du, X., Wei, D., Ganzel, B. L., Kim, P., Zhang, Q., & Qiu, J. (2014) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2014.12.001 · Cited by 7
Self-citation
Major gender differences in relations between life stressor frequency and gray matter in adolescence and emerging adulthood.
Fassett-Carman, A. N., Smolker, H. R., Hankin, B. L., Snyder, H. R., & Banich, M. T. (2022) · Developmental Psychology · doi:10.1037/dev0001489 · Cited by 6
A Public Health Framework for Preventing Mental Disorders in the Context of Pandemics
Litz, B. T., Cummings, M. H., Grunthal, B., & McLean, C. L. (2021) · Cognitive and Behavioral Practice · doi:10.1016/j.cbpra.2020.11.004 · Cited by 8
The Brain on Stress: The Good and the Bad
McEwen, B. S. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_1 · Cited by 5
Stress-Sensitive Parental Brain Systems Regulate Emotion Response and Motivate Sensitive Child Care
Swain, J. E. (2017) · Springer eBooks · doi:10.1007/978-3-319-65077-7_14 · Cited by 5
Reorienting resilience: adapting resilience for post-disaster research
Johnson, J., & Galea, S. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511994791.016 · Cited by 5
The social dimensions of the preventive efficient stress situation model (PRESS) questionnaire in light of the general self-efficacy, health belief model, the theory of care-seeking behavior, and symbolic interactionism in healthcare
St.Hilaire, C. (2016) · Cogent Social Sciences · doi:10.1080/23311886.2016.1234669 · Cited by 7
Ripple Effect of a Pandemic: Analysis of the Psychological Stress Landscape during COVID19Preprint
Agarwal, A. K. (2020) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/nat49 · Cited by 3
The Role of Sleep in Emotional Processing
Tempesta, D., Socci, V., Gennaro, L. D., & Ferrara, M. (2019) · Springer eBooks · doi:10.1007/978-981-13-2814-5_6 · Cited by 5
Sex-based differences in brain morphometry under chronic stress: A pilot MRI study
Shang, Z., Liu, N., Ouyang, H., Cai, X., Yan, W., Wang, J., Zhan, J., Jia, Y., Xing, C., Huang, L., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e30354 · Cited by 3
Traumatic Experiences Disrupt Amygdala – Prefrontal Connectivity
Hoon, D. (2012) · InTech eBooks · doi:10.5772/48691 · Cited by 3
Subliminal trauma reminders impact neural processing of cognitive control in adults with developmental earthquake trauma: a preliminary report
Du, X., Li, Y., Ran, Q., Kim, P., Ganzel, B. L., Liang, G., Lei, H. C., Zhang, Q., Meng, H., & Qiu, J. (2015) · Experimental Brain Research · doi:10.1007/s00221-015-4502-7 · Cited by 3
Self-citation

Authors: Ganzel, B. L., Kim, P., Glover, G. H., & Temple, E.
Affiliations: Cornell University (US)
Stanford University (US)
Dartmouth College (US)
Corresponding author: Ganzel, Barbara L.
ORCID: Kim, Pilyoung
Glover, Gary H.
Venue: NeuroImage
Publisher: Elsevier BV
Published: 2008-04
Volume: 40
Issue: 2
Pages: 788-795
ISSN: 1053-8119 (ISSN-L)
DOI: 10.1016/j.neuroimage.2007.12.010
PMC: PMC2405811
OpenAlex: W1969289932
Cited by: 127
References: 65
Citations by year: 2026: 1 · 2025: 2 · 2024: 6 · 2023: 2 · 2022: 3 · 2021: 11 · 2020: 6 · 2019: 10 · 2018: 6 · 2017: 6 · 2016: 10 · 2015: 10 · 2014: 11 · 2013: 9 · 2012: 11
FWCI: 5.46
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: NeuroImage (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institutes of Health
National Institute of Mental Health (F32MH068139, MH68139)
Topics: Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
Social Sciences › Psychology › Clinical Psychology › Resilience and Mental Health
Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Keywords: September 11 attacks, psychological trauma, resilience, gray matter volume, amygdala, hippocampus, insula, anterior cingulate cortex, medial prefrontal cortex, anxiety, lifetime trauma exposure, healthy adults
MeSH terms: Adaptation, Psychological, Adult, Amygdala, Female, Humans, Magnetic Resonance Imaging, Male, Organ Size, Stress, Psychological, September 11 Terrorist Attacks

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

Resilience after 9/11: Multimodal neuroimaging evidence for stress-related change in the healthy adult brain

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks