A generalized form of context-dependent psychophysiological interactions (gPPI): A comparison to standard approaches

A new look at the statistical model identification

Akaike, H. (1974) · IEEE Transactions on Automatic Control · doi:10.1109/tac.1974.1100705 · Cited by 51,879

Model selection and multimodel inference: a practical information-theoretic approach.

Guthery, F. S., Burnham, K. P., & Anderson, D. R. (2003) · The Journal of Wildlife Management · doi:10.2307/3802723 · Cited by 41,495

ANew Look at the Statistical Model Identification

AKAlKE, H. (2011) · Cited by 4,177

Psychophysiological and Modulatory Interactions in Neuroimaging

Friston, K. J., Buechel, C., Fink, G. R., Morris, J., Rolls, E., & Dolan, R. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0291 · Cited by 3,097

Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1

Boynton, G., Engel, S., Glover, G., & Heeger, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04207.1996 · Cited by 2,522

Analysis of fMRI Time-Series Revisited

Friston, K. J., Holmes, A. P., Poline, J., Grasby, P. M., Williams, S., Frackowiak, R. S. J., & Turner, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1007 · Cited by 2,504

A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex

Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151

Erroneous analyses of interactions in neuroscience: A problem of significance

Nieuwenhuis, S., Forstmann, B. U., & Wagenmakers, E.-J. (2011) · Nature Neuroscience · doi:10.1038/nn.2886 · Cited by 864

Modeling regional and psychophysiologic interactions in fMRI: the importance of hemodynamic deconvolution

Gitelman, D. R., Penny, W. D., Ashburner, J., & Friston, K. J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00058-2 · Cited by 799

Characterizing evoked hemodynamics with fMRI.

Friston, K. J., Frith, C., Turner, R., & Frackowiak, R. (1995) · NeuroImage · doi:10.1006/nimg.1995.1018 · Cited by 711

Noradrenergic correlates of chronic cocaine craving: neuromelanin and functional brain imaging

Wang, W., Zhornitsky, S., Zhang, S., & Li, C. R. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-00937-9 · Cited by 26

Neural function during emotion regulation and future depressive symptoms in youth at risk for affective disorders

Fournier, J. C. J., Bertocci, M. A., Ladouceur, C. D., Bonar, L. K., Monk, K., Abdul‐waalee, H., Versace, A., Santos, J. P. L., Iyengar, S., Birmaher, B. B., et al. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01001-w · Cited by 27

On the functional brain networks involved in tool-related action understanding

Federico, G., Osiurak, F., Ciccarelli, G., Ilardi, C. R., Cavaliere, C., Tramontano, L., Alfano, V., Migliaccio, M., Cecca, A. D., Salvatore, M., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05518-2 · Cited by 25

Cognitive emotion regulation enhances aversive prediction error activity while reducing emotional responses

Bratec, S. M., Xie, X., Schmid, G., Doll, A., Schilbach, L., Zimmer, C., Wohlschläger, A. M., Riedl, V., & Sorg, C. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.038 · Cited by 30

Influencing Food Choices by Training: Evidence for Modulation of Frontoparietal Control Signals

Schönberg, T., Bakkour, A., Hover, A. M., Mumford, J. A., & Poldrack, R. A. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00495 · Cited by 25

Alterations in neural Theory of Mind processing in euthymic patients with bipolar disorder and unaffected relatives

Willert, A., Mohnke, S., Erk, S., Schnell, K., Romanczuk‐Seiferth, N., Quinlivan, E., Schreiter, S., Spengler, S., Herold, D., Wackerhagen, C., et al. (2015) · Bipolar Disorders · doi:10.1111/bdi.12352 · Cited by 26

Responses in early visual areas to contour integration are context dependent

Qiu, C., Burton, P. C., Kersten, D., & Olman, C. A. (2016) · Journal of Vision · doi:10.1167/16.8.19 · Cited by 25

Neurodevelopmental changes across adolescence in viewing and labeling dynamic peer emotions

Flannery, J., Giuliani, N. R., Flournoy, J. C., & Pfeifer, J. H. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2017.02.003 · Cited by 26

The role of cognitive reappraisal in placebo analgesia: an fMRI study

van der Meulen, M., Kamping, S., & Anton, F. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx033 · Cited by 27

Amygdala–midbrain connectivity indicates a role for the mammalian parental care system in human altruism

Brethel-Haurwitz, K. M., O’Connell, K., Cardinale, E. M., Stoianova, M., Stoycos, S. A., Lozier, L. M., VanMeter, J. W., & Marsh, A. A. (2017) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.1731 · Cited by 25

Enhanced Amygdala-Striatal Functional Connectivity during the Processing of Cocaine Cues in Male Cocaine Users with a History of Childhood Trauma

Kaag, A. M., Reneman, L., Homberg, J. R., van den Brink, W., & van Wingen, G. A. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00070 · Cited by 26

Distinct neural substrates for visual short‐term memory of actions

Cai, Y., Urgolites, Z. J., Wood, J. N., Chen, C., Li, S., Chen, A., & Xue, G. (2018) · Human Brain Mapping · doi:10.1002/hbm.24236 · Cited by 24

Time-resolved effective connectivity in task fMRI: Psychophysiological interactions of Co-Activation patterns

Freitas, L. G. A., Bolton, T. A. W., Krikler, B. E., Jochaut, D., Giraud, A., Hüppi, P. S., & Ville, D. V. D. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116635 · Cited by 24

Clarifying the Link Between Amygdala Functioning During Emotion Processing and Antisocial Behaviors Versus Callous-Unemotional Traits Within a Population-Based Community Sample

Dotterer, H. L., Waller, R. E., Hein, T. C., Pardon, A., Mitchell, C. M., Lopez‐Duran, N. L., Monk, C. S., & Hyde, L. W. (2020) · Clinical Psychological Science · doi:10.1177/2167702620922829 · Cited by 25

Gamma-band synchronisation in a frontotemporal auditory information processing network

Leicht, G., Björklund, J., Vauth, S., Mußmann, M., Haaf, M., Steinmann, S., Rauh, J., & Mulert, C. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118307 · Cited by 27

Probing neurodynamics of experienced emotions—a Hitchhiker’s guide to film fMRI

Morgenroth, E., Vilaclara, L., Muszyński, M., Gaviria, J., Vuilleumier, P. O., & Ville, D. V. D. (2023) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsad063 · Cited by 24

Multiple insular-prefrontal pathways underlie perception to execution during response inhibition in humans

Osada, T., Nakajima, K., Shirokoshi, T., Ogawa, A., Oka, S., Kamagata, K., Aoki, S., Oshima, Y., Tanaka, S., & Konishi, S. (2024) · Nature Communications · doi:10.1038/s41467-024-54564-9 · Cited by 26

Amygdala functional connectivity during socioemotional processing prospectively predicts increases in internalizing symptoms in a sample of low-income, urban, young men

Gard, A. M., Waller, R. E., Swartz, J. R., Shaw, D. S., Forbes, E. E., & Hyde, L. W. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.05.079 · Cited by 26

Loneliness and depression dissociated on parietal-centered networks in cognitive and resting states

Shao, R., Liu, H., Huang, C., Chen, Y.-L., Gao, M., Lee, S., Lin, C., & Lee, T. M. C. (2019) · Psychological Medicine · doi:10.1017/s0033291719002782 · Cited by 25

Fronto-parietal engagement in response inhibition is inversely scaled with attention-deficit/hyperactivity disorder symptom severity

Kolodny, T., Mevorach, C., Stern, P., Biderman, N., Ankaoua, M., Tsafrir, S., & Shalev, L. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.102119 · Cited by 28

Systemic inflammation is associated with differential neural reactivity and connectivity to affective images

Alvarez, G., Hackman, D. A., Miller, A. B., & Muscatell, K. A. (2020) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaa065 · Cited by 27

Childhood Maltreatment Alters the Neural Processing of Chemosensory Stress Signals

Maier, A., Heinen-Ludwig, L., Güntürkün, O., Hurlemann, R., & Scheele, D. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00783 · Cited by 27

Restricting Visual Exploration Directly Impedes Neural Activity, Functional Connectivity, and Memory

Liu, Z., Rosenbaum, R. S., & Ryan, J. D. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa054 · Cited by 28

Neural correlates of conscious tactile perception: An analysis of BOLD activation patterns and graph metrics

Grund, M., Forschack, N., Nierhaus, T., & Villringer, A. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117384 · Cited by 26

Prevent breaking bad: A proof of concept study of rebalancing the brain's rumination circuit with real‐time fMRI functional connectivity neurofeedback

Tsuchiyagaito, A., Misaki, M., Zoubi, O. A., Tulsa 1000 Investigators, Paulus, M. P., & Bodurka, J. (2020) · Human Brain Mapping · doi:10.1002/hbm.25268 · Cited by 23

Reach-relevant somatosensory signals modulate activity in the tactile suppression network

Arikan, B. E., Voudouris, D., Voudouri-Gertz, H., Sommer, J. B., & Fiehler, K. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118000 · Cited by 24

Human brain activity and functional connectivity as memories age from one hour to one month

Tallman, C. W., Clark, R. E., & Smith, C. N. (2022) · Cognitive Neuroscience · doi:10.1080/17588928.2021.2021164 · Cited by 24

Changes in working memory brain activity and task-based connectivity after long-duration spaceflight

Salazar, A. P., McGregor, H. R., Hupfeld, K. E., Beltran, N. E., Kofman, I. S., Dios, Y. E. D., Riascos, R., Reuter‐Lorenz, P. A., Bloomberg, J. J., Mulavara, A. P., et al. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac232 · Cited by 26

Consider the pons: bridging the gap on sensory prediction abnormalities in schizophrenia

Abram, S. V., Hua, J. P. Y., & Ford, J. M. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.08.008 · Cited by 22

Angiotensin II Regulates the Neural Expression of Subjective Fear in Humans: A Precision Pharmaco-Neuroimaging Approach

Zhang, R., Zhao, W., Qi, Z., Xu, T., Zhou, F., & Becker, B. (2022) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2022.09.008 · Cited by 21

Disentangling the neural correlates of agency, ownership and multisensory processing

Harduf, A., Shaked, A., Ulmer-Yaniv, A., & Salomon, R. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120255 · Cited by 26

Distinct fronto-striatal couplings reveal the double-faced nature of response–outcome relations in instruction-based learning

Ruge, H., & Wolfensteller, U. (2014) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-014-0325-4 · Cited by 24

The origins of metamodality in visual object area LO: Bodily topographical biases and increased functional connectivity to S1

Tal, Z., Geva, R., & Amedi, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.058 · Cited by 25

GABA Concentrations in the Anterior Cingulate Cortex Are Associated with Fear Network Function and Fear Recovery in Humans

Levar, N., van Leeuwen, J. M. C., Puts, N. A. J., Denys, D. A. J. P., & van Wingen, G. A. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00202 · Cited by 23

Neural - hormonal responses to negative affective stimuli: Impact of dysphoric mood and sex

Marečková, K., Holsen, L. M., Admon, R., Whitfield, S., Seidman, L. J., Buka, S. L., Klibanski, A., & Goldstein, J. M. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.06.050 · Cited by 25

Identification of a Neurocognitive Mechanism Underpinning Awareness of Chronic Tinnitus

Trevis, K. J., Tailby, C., Grayden, D. B., McLachlan, N. M., Jackson, G. D., & Wilson, S. J. (2017) · Scientific Reports · doi:10.1038/s41598-017-15574-4 · Cited by 24

The Role of the Cerebellum in Skin-Picking Disorder

Wabnegger, A., & Schienle, A. (2018) · The Cerebellum · doi:10.1007/s12311-018-0957-y · Cited by 24

Cerebellar neural markers of susceptibility to social isolation and positive affective processing

Wong, N. M. L., Shao, R., Wu, J., Tao, J., Chen, L., & Lee, T. M. C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01965-y · Cited by 24

Pain and reward circuits antagonistically modulate alcohol expectancy to regulate drinking

Le, T. M., Zhornitsky, S., Zhang, S., & Li, C. R. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-00909-z · Cited by 25

Neuroimaging evidence for a network sampling theory of individual differences in human intelligence test performance

Soreq, E., Violante, I. R., Daws, R. E., & Hampshire, A. (2021) · Nature Communications · doi:10.1038/s41467-021-22199-9 · Cited by 23

Effects of internal and external vividness on hippocampal connectivity during memory retrieval

Ford, J. H., & Kensinger, E. A. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.12.007 · Cited by 23

Neural correlates of autobiographical problem-solving deficits associated with rumination in depression

Jones, N. P., Fournier, J. C. J., & Stone, L. B. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2017.04.069 · Cited by 23

Dorsolateral Prefrontal Cortex Enables Updating of Established Memories

Kluen, L. M., Dandolo, L., Jocham, G., & Schwabe, L. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy298 · Cited by 26

Fear conditioning and extinction in anxious youth, offspring at-risk for anxiety and healthy comparisons: An fMRI study

Chauret, M., Suffren, S., Pine, D. S., Nassim, M., Saint‐Amour, D., & Maheu, F. S. (2019) · Biological Psychology · doi:10.1016/j.biopsycho.2019.107744 · Cited by 22

Abnormal distraction and load‐specific connectivity during working memory in cognitively normal Parkinson's disease

Harrington, D. L., Shen, Q., Filoteo, J. V., Litvan, I., Huang, M., Castillo, G. N., Lee, R. R., & Bayram, E. (2019) · Human Brain Mapping · doi:10.1002/hbm.24868 · Cited by 23

An fMRI study of English and Spanish word reading in bilingual adults

Brignoni‐Pérez, E., Jamal, N. I., & Eden, G. F. (2020) · Brain and Language · doi:10.1016/j.bandl.2019.104725 · Cited by 29

Neurocomputational mechanisms underlying immoral decisions benefiting self or others

Qu, C., Hu, Y., Tang, Z., Derrington, E. A., & Dreher, J. (2020) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaa029 · Cited by 23

Stable inhibition-related inferior frontal hypoactivation and fronto-limbic hyperconnectivity in obsessive–compulsive disorder after concentrated exposure therapy

Thorsen, A. L., de Wit, S. J., Hagland, P., Ousdal, O. T., Hansen, B. K. A., Hagen, K., Kvale, G., & van den Heuvel, O. A. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102460 · Cited by 23

Reported maternal childhood maltreatment experiences, amygdala activation and functional connectivity to infant cry

Olsavsky, A. K., Stoddard, J., Erhart, A., Tribble, R. C., & Kim, P. (2021) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsab005 · Cited by 21

Working memory, cortical dopamine tone, and frontoparietal brain recruitment in post-traumatic stress disorder: a randomized controlled trial

Westphal, A. J., Ballard, M. E., Rodriguez, N., Vega, T. A., D’Esposito, M., & Kayser, A. S. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01512-6 · Cited by 23

A Mechanism-Based Approach to Anti-Aggression Psychotherapy in Borderline Personality Disorder: Group Treatment Affects Amygdala Activation and Connectivity

Neukel, C., Bertsch, K., Wenigmann, M., Spieß, K., Krauch, M., Steinmann, S., & Herpertz, S. C. (2021) · Brain Sciences · doi:10.3390/brainsci11121627 · Cited by 24

Precentral gyrus and insula responses to stress vary with duration to diagnosis in functional seizures

Goodman, A. M., Allendorfer, J. B., LaFrance, W. C., Jr., & Szaflarski, J. P. (2022) · Epilepsia · doi:10.1111/epi.17179 · Cited by 23

Development of the neural correlates of self- and other-referential processing across adolescence

van Buuren, M., Sijtsma, H., Lute, N., van Rijn, R., Hollarek, M., Walsh, R. J., Lee, N. C., & Krabbendam, L. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119032 · Cited by 25

Functional lateralization of the medial temporal lobe in novel associative processing during creativity evaluation

Ren, J., Huang, F., Gao, C., Gott, J., Schoch, S. F., Qin, S., Dresler, M., & Luo, J. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac129 · Cited by 23

Effective connectivity during face processing in major depression – distinguishing markers of pathology, risk, and resilience

Sacu, S., Wackerhagen, C., Erk, S., Romanczuk‐Seiferth, N., Schwarz, K., Schweiger, J. I., Tost, H., Meyer‐Lindenberg, A., Heinz, A., Razi, A., et al. (2022) · Psychological Medicine · doi:10.1017/s0033291722000824 · Cited by 24

Analysis of individual differences in neurofeedback training illuminates successful self-regulation of the dopaminergic midbrain

Hellrung, L., Kirschner, M., Sulzer, J. S., Sladky, R., Scharnowski, F., Herdener, M., & Tobler, P. N. (2022) · Communications Biology · doi:10.1038/s42003-022-03756-4 · Cited by 23

Cognitive training enhances growth mindset in children through plasticity of cortico-striatal circuits

Chen, L., Chang, H., Rudoler, J., Arnardóttir, E., Zhang, Y., Angeles, C. D. L., & Menon, V. (2022) · npj Science of Learning · doi:10.1038/s41539-022-00146-7 · Cited by 36

Cannabinoid modulation of corticolimbic activation during extinction learning and fear renewal in adults with posttraumatic stress disorder

Zabik, N. L., Rabinak, C. A., Peters, C. A., & Iadipaolo, A. S. (2023) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2023.107758 · Cited by 22

Neural recruitment and connectivity during emotional memory retrieval across the adult life span

Ford, J. H., Morris, J. A., & Kensinger, E. A. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.05.029 · Cited by 24

Dynamic Coupling Between the Lateral Occipital-Cortex, Default-Mode, and Frontoparietal Networks During Bistable Perception

Karten, A., Pantazatos, S. P., Khalil, D., Zhang, X., & Hirsch, J. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0119 · Cited by 26

Functional connectivity between ventral and dorsal frontoparietal networks underlies stimulus-driven and working memory-driven sources of visual distraction

Greene, C. M., & Soto, D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.060 · Cited by 23

The network architecture of value learning

Mattar, M. G., Thompson‐Schill, S. L., & Bassett, D. S. (2017) · Network Neuroscience · doi:10.1162/netn_a_00021 · Cited by 21

Neural Systems Underlying Individual Differences in Intertemporal Decision-making

Elton, A., Smith, C. T., Parrish, M. H., & Boettiger, C. A. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01069 · Cited by 24

General and emotion‐specific neural effects of ketamine during emotional memory formation

Becker, B., Steffens, M., Zhao, Z.-Y., Kendrick, K., Neumann, C., Weber, B., Schultz, J., Mehta, M., Ettinger, U., & Hurlemann, R. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.02.049 · Cited by 26

Neural substrates of context‐ and person‐dependent altruistic punishment

Wang, L., Lu, X., Gu, R., Zhu, R., Xu, R., Broster, L. S., & Feng, C. (2017) · Human Brain Mapping · doi:10.1002/hbm.23747 · Cited by 22

Preliminary Evidence for Disrupted Nucleus Accumbens Reactivity and Connectivity to Reward in Binge Drinkers

Crane, N. A., Gorka, S. M., Weafer, J. J., Langenecker, S. A., de Wit, H., & Phan, K. L. (2017) · Alcohol and Alcoholism · doi:10.1093/alcalc/agx062 · Cited by 25

Consciously Feeling the Pain of Others Reflects Atypical Functional Connectivity between the Pain Matrix and Frontal-Parietal Regions

Grice-Jackson, T., Critchley, H., Banissy, M. J., & Ward, J. (2017) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2017.00507 · Cited by 25

Emotion Regulation in Obsessive-Compulsive Disorder, Unaffected Siblings, and Unrelated Healthy Control Participants

Thorsen, A. L., de Wit, S. J., de Vries, F. E., Cath, D. C., Veltman, D. J., van der Werf, Y. D., Mataix‐Cols, D., Hansen, B. K. A., Kvale, G., & van den Heuvel, O. A. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.03.007 · Cited by 23

The Functional Role of Large-scale Brain Network Coordination in Placebo-induced Anxiolysis

Meyer, B., Yuen, K. S. L., Saase, V., & Kalisch, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy188 · Cited by 22

Faster learners transfer their knowledge better: Behavioral, mnemonic, and neural mechanisms of individual differences in children’s learning

Chang, H., Rosenberg‐Lee, M., Qin, S., & Menon, V. (2019) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2019.100719 · Cited by 27

Neural mechanisms underlying heterogeneous expression of threat-related attention in social anxiety

Evans, T. C., Bar‐Haim, Y., Fox, N. A., Pine, D. S., & Britton, J. C. (2020) · Behaviour Research and Therapy · doi:10.1016/j.brat.2020.103657 · Cited by 25

Changes in functional connectivity with cognitive behavioral therapy for social anxiety disorder predict outcomes at follow-up

Sandman, C. F., Young, K. S., Burklund, L. J., Saxbe, D. E., Lieberman, M. D., & Craske, M. G. (2020) · Behaviour Research and Therapy · doi:10.1016/j.brat.2020.103612 · Cited by 22

The neural networks of subjectively evaluated emotional conflicts

Rohr, C. S., Villringer, A., Solms-Baruth, C., van der Meer, E. E., Margulies, D. S., & Okon‐Singer, H. (2016) · Human Brain Mapping · doi:10.1002/hbm.23169 · Cited by 22

Neural Correlates of Evidence and Urgency During Human Perceptual Decision-Making in Dynamically Changing Conditions

Yau, Y. H. C., Dadar, M., Taylor, M., Zeighami, Y., Fellows, L. K., Cisek, P., & Dagher, A. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa129 · Cited by 22

Neural Development of Speech Sensorimotor Learning

Ohashi, H., & Ostry, D. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2884-20.2021 · Cited by 26

Acute neurofunctional effects of escitalopram during emotional processing in pediatric anxiety: a double-blind, placebo-controlled trial

Lu, L., Li, H., Baumel, W. T., Mills, J. A., Cecil, K. M., Schroeder, H. K., Mossman, S. A., Huang, X., Gong, Q., Sweeney, J. A., et al. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01186-0 · Cited by 22

Spatiotemporal Dynamics of Stress-Induced Network Reconfigurations Reflect Negative Affectivity

Kühnel, A., Czisch, M., Sämann, P. G., Brückl, T. M., Spoormaker, V. I., Erhardt, A., Grandi, N. C., Ziebula, J., Elbau, I., Namendorf, T., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.01.008 · Cited by 24

Disorder- and cognitive demand-specific neurofunctional alterations during social emotional working memory in generalized anxiety disorder and major depressive disorder

Xu, X., Xin, F., Liu, C., Chen, Y., Yao, S., Zhou, X., Zhou, F., Huang, Y., Dai, J., Wang, J., et al. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.04.023 · Cited by 28

The Angiotensin Antagonist Losartan Modulates Social Reward Motivation and Punishment Sensitivity via Modulating Midbrain-Striato-Frontal Circuits

Zhou, X., Xu, T., Zeng, Y., Zhang, R., Qi, Z., Zhao, W., Kendrick, K. M., & Becker, B. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1114-22.2022 · Cited by 19

The social transmission of empathy relies on observational reinforcement learning

Zhou, Y., Han, S., Kang, P., Tobler, P. N., & Hein, G. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2313073121 · Cited by 22

Sleep-amount differentially affects fear-processing neural circuitry in pediatric anxiety: A preliminary fMRI investigation

Carlisi, C. O., Hilbert, K., Guyer, A. E., & Ernst, M. (2017) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-017-0535-7 · Cited by 22

Studying emotion theories through connectivity analysis: Evidence from generalized psychophysiological interactions and graph theory

Huang, Y., Jastorff, J., den Stock, J. V., de Vliet, L. V., Dupont, P. J., & Vandenbulcke, M. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.01.026 · Cited by 25

Reward anticipation and punishment anticipation are instantiated in the brain via opponent mechanisms

Lake, J. I., Spielberg, J. M., Infantolino, Z. P., Crocker, L. D., Yee, C. M., Heller, W., & Miller, G. A. (2019) · Psychophysiology · doi:10.1111/psyp.13381 · Cited by 21

Impact of exogenous estradiol on task-based and resting-state neural signature during and after fear extinction in healthy women

Wen, Z., Hammoud, M. Z., Scott, J. C., Jimmy, J., Brown, L. A., Marin, M., Asnaani, A., Gur, R. C., Foa, E. B., & Milad, M. R. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01158-4 · Cited by 23

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Turney, I., & Dennis, N. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.005 · Cited by 23

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Cho, C., Smith, D. V., & Delgado, M. R. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00529 · Cited by 22

Oral and dental findings in children with Fanconi anemia.

Tekçiçek, M. U., Tavil, B., Çakar, A., Pinar, A., Ünal, S., & Gümrük, F. (2007) · PubMed · Cited by 22

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Davis, M. M., Miernicki, M. E., Telzer, E. H., & Rudolph, K. D. (2019) · Journal of Abnormal Child Psychology · doi:10.1007/s10802-018-0456-0 · Cited by 20

FDA cigarette warning labels lower craving and elicit frontoinsular activation in adolescent smokers

Do, K. T., & Galván, A. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv038 · Cited by 22

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Functional connections between activated and deactivated brain regions mediate emotional interference during externally directed cognition

Plinio, S. D., Ferri, F., Marzetti, L., Romani, G. L., Northoff, G., & Pizzella, V. (2018) · Human Brain Mapping · doi:10.1002/hbm.24197 · Cited by 20

Neural substrates of subphonemic variation and lexical competition in spoken word recognition

Luthra, S., Guediche, S., Blumstein, S. E., & Myers, E. B. (2018) · Language Cognition and Neuroscience · doi:10.1080/23273798.2018.1531140 · Cited by 20

Modafinil enhances cognitive, but not emotional conflict processing via enhanced inferior frontal gyrus activation and its communication with the dorsomedial prefrontal cortex

Li, J., Yang, X., Zhou, F., Liu, C., Wei, Z., Xin, F., Daumann, B., Daumann, J., Kendrick, K. M., & Becker, B. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0625-z · Cited by 18

Impact of sex and depressed mood on the central regulation of cardiac autonomic function

Garcia, R. G., Marečková, K., Holsen, L. M., Cohen, J. E., Whitfield, S., Napadow, V., Barbieri, R., & Goldstein, J. M. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0651-x · Cited by 21

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Lei, W. I., Chen, J., Yang, C., Guo, Y., Feng, P., Feng, T., & Li, H. (2020) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2020.107502 · Cited by 24

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Xu, S., Li, Y., & Liu, J. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab182 · Cited by 20

The selective contributions of right cerebellar lobules to reading

Li, H., Marks, R. A., Liu, L., Feng, X., Zhang, M., Ai, F., Gao, Y., Tian, M., Yang, X., Zhang, J., et al. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02434-1 · Cited by 22

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Kryza‐Lacombe, M., Palumbo, D., Wakschlag, L. S., Dougherty, L. R., & Wiggins, J. L. (2022) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2022.111483 · Cited by 25

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Di, X., Zhang, Z., & Biswal, B. B. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00304-8 · Cited by 62

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O’Reilly, J. X., Woolrich, M. W., Behrens, T. E. J., Smith, S. M., & Johansen-Berg, H. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss055 · Cited by 765

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