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1 omated brainmapping database [of over 10,000 functional MRI (fMRI) studies], we performed quantitativ
2 etened beverages daily for 21 d, underwent 2 functional MRI sessions, and completed behavioral and ex
4 eld 7T structural MRI and high-resolution 3T functional MRI (hr-fMRI), we evaluated MTL subfield thic
5 s of orientation, we used high-resolution 7T functional MRI as 16 subjects compared their subjective
7 ron emission tomography scan 4 days before a functional MRI fear conditioning and extinction paradigm
9 underpinnings of revenge and forgiveness: a functional MRI (fMRI) approach aiming at integrating for
10 tially 11-15 years of age) participated in a functional MRI paradigm that elicited threat-related amy
11 levels of lifetime trauma participated in a functional MRI task involving passive viewing of threate
17 rolled 15 deaf and 15 hearing adults into an functional MRI experiment during which they discriminate
19 t that volumetric analyses on anatomical and functional MRI contain clinically valuable information.
22 This model accounts for both behavioral and functional MRI (fMRI) responses during inhibitory contro
24 te heart allograft rejection by cellular and functional MRI with selectively depleted systemic macrop
25 an substantia nigra (SN) using diffusion and functional MRI data from the Human Connectome Project.
26 G) to measure neuronal activity directly and functional MRI (fMRI) to measure hemodynamic activity du
27 onship between the three symptom domains and functional MRI neural reactivity during passive viewing
28 lly, we include studies that combine DTI and functional MRI (fMRI) to investigate brain connectivity
30 ate D2DR availability were interrelated, and functional MRI-based resting-state functional connectivi
31 avioral methods, magnetoencephalography, and functional MRI to investigate how human listeners discov
32 tional neurophysiology, pathway mapping, and functional MRI, implicating multiple brain regions inclu
34 MR spectroscopy, diffusion weighted MRI and functional MRI are being studied as potentially useful i
36 hted magnetic resonance imaging (DW-MRI) and functional MRI (fMRI) in humans and macaques to infer an
37 ants had blood sampling, structural MRI, and functional MRI during associative memory encoding and re
38 y stimulus repeats, neuronal firing rate and functional MRI blood oxygen level-dependent responses ty
39 l local field potential (LFP) recordings and functional MRI (fMRI), we study local changes in neurona
40 ried out a series of tests of structural and functional MRI (fMRI) data in 25 group-living macaques.
41 Cross-sectional measures of structural and functional MRI and plasma Abeta assays were assessed in
42 cture and function applied to structural and functional MRI data may provide insights into systems-le
44 connectivity analyses in both structural and functional MRI to further our understanding of the relat
46 sensitivity to the number of syllables, and functional MRI confirmed that the cortical stimulation s
47 combined diffusion imaging tractography and functional MRI to study whether the strength of anatomic
49 in older adults by performing structural and functional MRIs while older participants engage in tasks
50 methods for presurgical language mapping are functional MRI (fMRI) and direct cortical stimulation (D
51 e TT genotype was associated with attenuated functional MRI prefrontal activity, reduced prefrontal c
52 gical interaction (PPI) analyses of auditory functional MRI data, to compare functional connectivity
55 ranial magnetic stimulation with model-based functional MRI, we show that disrupting neural excitabil
57 ine the state of data sharing for task-based functional MRI (fMRI) data, with a focus on various form
59 simulation to create a registration between functional MRI retinotopic mapping data of visual areas
60 ng state blood oxygen level-dependent (BOLD) functional MRI is widely used for noninvasively studying
65 lly implanted microwire electrodes guided by functional MRI targeting, we obtained distinct profiles
73 h experience-induced plasticity, we combined functional MRI with a preclinical drug vs. food self-adm
74 l networks underlying attention by comparing functional MRI data from macaques and humans performing
75 tigated this question directly by conducting functional MRI on two patients with rare bilateral amygd
77 using a large (n = 69) distortion-corrected functional MRI (fMRI) dataset, spanning a range of seman
80 The reliance of blood-oxygen-level-dependent functional MRI on a contrast between events and baseline
81 ent advances in blood oxygen level-dependent-functional MRI (BOLD-fMRI)-based neurofeedback reveal th
85 e, then verbally described the events during functional MRI, producing unguided detailed descriptions
86 serve/imitate task of emotional faces during functional MRI in 28 healthy adults, with final analyses
87 this environment by moving within it during functional MRI (fMRI) scanning while we tracked their ev
88 erwent a neuroimaging reward paradigm during functional MRI scanning, structural scanning, and comple
90 essment for simultaneous PET scanning during functional MRI studies was performed with a spiral in-an
91 acking and modeling the arousal state during functional MRI (fMRI) typically precludes the assessment
99 dvent of neuroimaging techniques, especially functional MRI (fMRI), studies have mapped brain regions
103 e correlation to derive visual features from functional MRI patterns elicited by a large set of homog
104 llations and neuronal spiking responses from functional MRI (fMRI)-localized voice-sensitive cortex i
107 methotrexate was also associated with higher functional MRI activity, with thicker cortices in dorsol
109 rmation-based multivariate analyses of human functional MRI data typically find evidence for the temp
110 ltivariate (pattern-based) analyses to human functional MRI data acquired during a noninstrumental ou
113 icipants underwent consecutive and identical functional MRI recordings, during which they performed a
114 isation transfer, diffusion tension imaging, functional MRI, and proton magnetic resonance spectrosco
117 iver perfusion with fresh blood (% change in functional MRI signal intensity due to hyperoxia was 16%
118 on the analysis of temporal fluctuations in functional MRI signal, representing a small fraction of
119 le reviews the current state of knowledge in functional MRI (fMRI) research related to pain with prim
120 Functional connectivity (FC) patterns in functional MRI exhibit dynamic behavior on the scale of
122 ailable that are used to localize the STh in functional MRI studies and clinical procedures such as d
123 ructural MRI data are thus far inconsistent, functional MRI evidence in trans persons suggests change
124 d CBF should be considered when interpreting functional MRI studies comparing activation responses be
125 arameters, we used an arterial-spin-labeling functional MRI stress paradigm in 36 MS patients and 21
126 with epilepsy were identified with language functional MRI (fMRI) and diffusion MRI acquisition.
134 show, using a multivoxel pattern analysis of functional MRI (fMRI) data, that the preparatory activit
135 n strategy and graph theoretical analysis of functional MRI data in human patients with the laryngeal
137 retic framework is used to guide analysis of functional MRI resting-state data and describe systems-l
138 life speaking using a multimodal analysis of functional MRI, intracranial EEG recordings, and large-s
140 oss the cortex using voxel-wise modelling of functional MRI (fMRI) data collected while subjects list
141 humans, researchers have relied primarily on functional MRI (fMRI), but technological and methodologi
146 placebo-controlled, within-subject, pharmaco-functional MRI experiment with 20 heterosexual pair-bond
151 t of shock paradigm was used while recording functional MRI in humans to measure how activation and f
152 are restricted to specific cortical regions, functional MRI has also shown involvement of subcortical
157 s; 637 women) who completed a reward-related functional MRI task to assay VS activity and provided se
162 mporal (magnetoencephalography) and spatial (functional MRI) visual brain representations with repres
167 ighted, diffusion weighted and resting state functional MRI data were acquired at 3 T for 12 asymptom
169 ients underwent structural and resting state functional MRI scans, and spatial neglect was measured u
171 hed healthy controls underwent resting state functional MRI, and rumination about pain was assessed t
173 stimulation (tACS) [8-12] with resting-state functional MRI (fMRI) [13] to follow both changes in loc
175 reward network, assessed using resting-state functional MRI (fMRI), to predict the onset of depressio
177 usion tensor imaging (DTI) and resting-state functional MRI (rfMRI) data were acquired from 38 indivi
178 stituents of the rat DMN using resting-state functional MRI (rs-fMRI) and diffusion tensor imaging.
179 odel of the brain derived from resting-state functional MRI (rs-fMRI) data and investigate the modula
180 investigated DMN activity with resting-state functional MRI (rs-fMRI), alongside its structural and m
181 lying a clustering analysis on resting-state functional MRI (RSfMRI) data from white-matter voxels, i
183 al connectivity analyses using resting-state functional MRI collected in the same participants reveal
184 rain functional networks using resting-state functional MRI data acquired from 18 patients (11 vegeta
186 ology in head-motion-corrected resting-state functional MRI data acquired from 78 patients with bipol
192 using a large multisite study, resting-state functional MRI data were examined in young children with
198 bjects (n = 1,305) underwent a resting-state functional MRI scan and were analyzed by a two-stage app
200 r treatment, subjects received resting-state functional MRI scans and assessments of depressive sympt
202 , we used repeated-measurement resting-state functional MRI to explore intersubject variability in co
204 loping (TD) controls underwent resting-state functional MRI, and functional connectivity of executive
207 -particularly structural MRI, resting--state functional MRI, and diffusion tensor imaging--are highly
212 Furthermore, these findings demonstrate that functional MRI has the potential to reveal the neural ba
217 amined the therapeutic efficacy of real-time functional MRI neurofeedback (rtfMRI-nf) training aimed
218 used whole-brain classifier-based real-time functional MRI to address these issues, because the meth
221 network model of self-directed cognition to functional MRI data from 71 adolescents and young adults
225 onse to continuous sensory stimulation under functional MRI (fMRI) in two unique patient populations-
230 21; mean age, 16.4 years [SD=1.9]) underwent functional MRI (fMRI) before and after treatment; simila
231 jects (N=38) 14 to 29 years of age underwent functional MRI while performing a verbal working memory
232 lial risk of developing depression underwent functional MRI while recalling autobiographical memories
233 METHOD: Individuals with PTSD underwent functional MRI (fMRI) at rest and while completing three
234 METHOD: Individuals with PTSD underwent functional MRI (fMRI) while completing three tasks asses
235 t Response in Clinical Care) study underwent functional MRI during a well-validated reward task.
236 -, and IQ-matched comparison youth underwent functional MRI while performing an emotional conflict ta
238 nd trial with 48 obese participants and used functional MRI to study the effects of lorcaserin on the
242 major studies in bipolar disorder that used functional MRI, volumetric analysis, diffusion imaging,
243 gyrus (IFG) in healthy volunteers, then used functional MRI to investigate acute changes in effective
245 ctivity at the normal time of birth, we used functional MRI (fMRI) to measure blood oxygen level-depe
254 r understand this network in humans, we used functional MRI to measure the responses to moving object
274 oned fear generalization were assessed using functional MRI and behavioral measures in U.S. combat ve
275 oned fear generalization were assessed using functional MRI and behavioral measures in U.S. combat ve
280 ditioning and extinction were measured using functional MRI before and after a manualized CBT program
282 and Neuroscience (Cam-CAN) was scanned using functional MRI during two versions of an experiment: a n
284 ental brain response to infant stimuli using functional MRI, oxytocin, and parenting behavior in thre
287 istration of oxytocin (OT), we measured, via functional MRI, changes in brain activity during judgmen
289 ing provides structural information, whereas functional MRI and electroencephalography provide functi
291 ry incentive delay task (in conjunction with functional MRI) and a probabilistic reward learning task
292 sured dynamical functional connectivity with functional MRI during the resting state in awake and ane
293 ed to map brain functional connectivity with functional MRI, but their source is not well understood.
295 trics, especially connectivity measured with functional MRI, can correlate with differences in motion
297 =47; never affected, N=99) were scanned with functional MRI (fMRI) (N=85), magnetoencephalography (N=
298 ere followed longitudinally and scanned with functional MRI while performing an event-related cued re
299 transcranial magnetic stimulation (TMS) with functional MRI to causally excite or inhibit TMS-accessi
300 atry.SIGNIFICANCE STATEMENT In recent years, functional MRI (fMRI) has revolutionized all fields of n
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