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1 effects on these different forms of 'waiting impulsivity'.
2 ial risk and a neuropsychological measure of impulsivity.
3 t," including novelty-induced locomotion and impulsivity.
4 ive-limbic subthalamic nucleus in decisional impulsivity.
5 e levels of inattention and hyperactivity or impulsivity.
6 ing-state functional connectivity (RSFC) and impulsivity.
7 tor urgency and SSRT in proactive control of impulsivity.
8 S modulated different components of temporal impulsivity.
9 nhibition, gambling decisions and reflection impulsivity.
10 ssion were included as a model of disordered impulsivity.
11 2B mutant (Htr2B(-/-)) mice also showed high impulsivity.
12 g during adulthood are involved in mediating impulsivity.
13 mental period associated with an increase in impulsivity.
14 entral striatum and related these changes to impulsivity.
15 red with the baseline level of hyperactivity/impulsivity.
16 n fail to improve cognitive problems such as impulsivity.
17 relationship between the accumbal volume and impulsivity.
18 ssion and sex were significant covariates of impulsivity.
19 s and striatum was associated with increased impulsivity.
20 the tendency toward negative affect-provoked impulsivity.
21 CB1Rs reversed and prevented cocaine-induced impulsivity.
22 sive-compulsive spectrum disorders with high impulsivity.
23 ionally implicate the Nrg3 candidate gene in impulsivity.
24 yrus thickness mediated the association with impulsivity.
25 ence and underlie enhanced susceptibility to impulsivity.
26 manifest relatively high levels of cognitive impulsivity.
27 ed by intermediate behavioral traits such as impulsivity.
28 rating lithium's effects to reduce cognitive impulsivity.
29 ts in reducing psychostimulant-induced motor impulsivity.
30 ms by which OXR blockade may influence motor impulsivity.
31 nd delay discounting are forms of decisional impulsivity.
32 ric disorders, which present with disordered impulsivity.
33 ntagonists to attenuate acute cocaine-evoked impulsivity.
34 ventral SN network was associated with motor impulsivity.
35 ociated with better neurocognition and lower impulsivity.
36 exhibited poorer decision making and greater impulsivity.
37 otentially has implications for disorders of impulsivity.
38 sses, which include effects on attention and impulsivity, a mechanism that may contribute to the addi
41 accommodates the commonalities of apathy and impulsivity across disorders and reveals their cognitive
42 of institutionalization with inattention and impulsivity; additionally, supramarginal gyrus thickness
43 uding (i) the assessment of either apathy or impulsivity alone, despite their frequent co-existence;
46 There are well-established links between impulsivity and alcohol use in humans and animal models;
48 s support a developmental imbalance model of impulsivity and are consistent with the idea that negati
49 in the context of measures of aggression and impulsivity and as a function of intermittent explosive
50 and non-binge drinkers were tested for motor impulsivity and attentional abilities in a human version
51 on training, we observed reduced aggression, impulsivity and behavioral approach tendencies, as well
52 tonin-sensitive period affecting aggression, impulsivity and behavioral response to psychostimulants.
53 -dependent cocaine-seeking habits or whether impulsivity and cocaine-induced intrastriatal shifts are
54 Converging evidence has long identified both impulsivity and compulsivity as key psychological constr
55 ever, the precise nature of the link between impulsivity and compulsivity in anxiety-related compulsi
56 ide insight into the reciprocal influence of impulsivity and compulsivity in compulsive disorders and
58 o relationship between the effects of MPH on impulsivity and D2/3 receptor availability in any of the
59 reased impulsivity in LI rats, and modulated impulsivity and D2/3 receptor availability in the dorsal
60 nverse relationships with baseline levels of impulsivity and D2/3 receptor availability, respectively
61 dala connectivity, a neural "switch" between impulsivity and deliberation, further underscores the ph
63 borderline personality disorder (BPD), with impulsivity and emotional dysregulation as core symptoms
67 al mechanism may underlie obesity-associated impulsivity and increased consumption of high-calorie fo
69 of the physiological mechanisms involved in impulsivity and may suggest potential targets for therap
71 ms enact functionally unique effects on food impulsivity and motivation relative to PFC-based monoami
72 e in young adults is associated with greater impulsivity and neurobiological alterations in executive
73 benefit from focusing on characterizing how impulsivity and other addiction-related features relate
74 lies on a continuum in which both extremes (impulsivity and overcontrol) contribute to psychopatholo
78 ch, we mapped the relationship between trait impulsivity and reward-related brain activity in a large
81 in NAC than in PFC, which may contribute to impulsivity and risk-taking exhibited by adolescents [5,
82 l cortex was inversely associated with trait impulsivity and risk-taking in the bipolar disorder grou
85 striatum, and that stimulant drugs modulate impulsivity and striatal D2/3 receptor availability thro
86 We investigated the relationship between impulsivity and the development of a compulsive behavior
87 onmental determinants, and propelled by both impulsivity and the responsivity to cocaine-linked cues
88 lity to measure the components of apathy and impulsivity and their associated neural correlates acros
92 EVANCE-Altered paralimbic reward signals and impulsivity and/or carelessness may facilitate unplanned
94 knockout mice show increased aggression and impulsivity, and 5-HT1BR polymorphisms are associated wi
95 positive emotion enhancement and behavioral impulsivity, and another associated with negative emotio
96 ke phenotype with typical high risk seeking, impulsivity, and augmented drug and nondrug reward sensi
97 eeking, increased peer interaction, enhanced impulsivity, and augmented reward sensitivity for drug a
99 ding family history of alcoholism, male sex, impulsivity, and low level of response to alcohol, would
100 nt informants for inattention, hyperactivity-impulsivity, and oppositional defiant disorder, and a co
101 nt informants for inattention, hyperactivity-impulsivity, and oppositional defiant disorder, and a co
102 dimensions of normal behavior, such as human impulsivity, and psychopathology, particularly behaviora
103 (LH) stimulation, eliminates cocaine-induced impulsivity, and reduces cocaine self-administration.
104 characteristics of patients, such as gender, impulsivity, and severity of cannabis use, when selectin
105 ration provides new insights into apathy and impulsivity, and the need for a joint therapeutic strate
106 escents may be causal, whereas hyperactivity-impulsivity appears to act indirectly, through shared pr
112 tress and problem alcohol use is mediated by impulsivity, as reflected in monetary delay discounting
113 sures and parental reports of aggression and impulsivity, as well as structural and diffusion MRI, fr
115 symptoms of inattention, hyperactivity, and impulsivity associated with clinically significant impai
116 current study seeks to examine self-reported impulsivity (Barratt Impulsivity Scale) and performance-
117 xpressions, as well as empathy, risk taking, impulsivity, behavior change, and attentional focus.
118 on-related deficits include distractibility, impulsivity, behavioral rigidity, and reduced habituatio
122 show lines selected for different levels of impulsivity: Border Collies (herding work) and Labrador
123 orsal anterior cingulate connectivity; trait impulsivity, both a risk factor for and a consequence of
124 in 1B receptors (5-HT1BRs) in aggression and impulsivity, but this has never been evaluated in humans
125 -off encompasses elements of risk-taking and impulsivity-common behaviors in psychiatric disorders-an
126 tive control and decision-making and reduced impulsivity, components of behavior mediated in part by
130 ajectories, functional network activity, and impulsivity/compulsivity-related features may lend furth
134 /J (D2) mice (alcohol averse); the degree of impulsivity correlated with subsequent alcohol consumpti
135 dividual variation in the degree of inherent impulsivity could play a role in the generation or exace
136 ty to predict adaptive outcomes may activate impulsivity, delay discounting, and reward seeking.
137 e trained in one of the two animal models of impulsivity: delay-discounting (DD) or stop-signal react
138 sures (i.e., N2, P300, ERN/Ne, age, sex, IQ, impulsivity, depression, anxiety, motivation for change,
140 with alcoholism demonstrate increased motor impulsivity during abstinence; however, the neuronal mec
141 plasma concentration: it reduced reflection impulsivity during information sampling [adjusted R(2) =
142 ortex (vmPFC) contributes to increased motor impulsivity during protracted abstinence from long-term
143 s to directly investigate these, focusing on impulsivity during response inhibition and decision maki
145 expression of two major genes implicated in impulsivity, encoding the dopamine D2 receptor (DA D2R)
147 ing maladaptive short-lived urges to balance impulsivity, exploration and defiance, while establishin
148 9) = 4.51, P = 0.047] and reduced reflection impulsivity [F(1,9) = 7.86, P = 0.02] and risk taking [F
153 hemical mechanisms contributing to increased impulsivity following long-term alcohol exposure and hig
159 d ratio: 1.74, 95% CI=1.03-2.93), and higher impulsivity (hazard ratio: 1.17, 95% CI=1.00 to 1.37) we
160 ity with substance abuse in humans, and high impulsivity (HI) in rats has been identified as a predic
161 ter variant at rs12765063 is associated with impulsivity, hyperactivity and addiction-related phenoty
162 al manganese (Mn) exposure with inattention, impulsivity, hyperactivity, and oppositional behaviors,
164 ructural correlates of sensation seeking and impulsivity in a large cohort of healthy young adults.
165 HT2 receptor induced head twitch response or impulsivity in a serial reaction time task (SRTT), where
166 in mice, we collected behavioral measures of impulsivity in a single cohort of mice using well-valida
169 the neurocognitive components of apathy and impulsivity in frontotemporal lobar degeneration syndrom
171 on to the tests already available to measure impulsivity in humans in a direct translational analog o
172 e effects were probed regularly by measuring impulsivity in intertemporal choices, i.e., the propensi
176 a functional link that may help explain high impulsivity in methamphetamine-dependent individuals.
177 e negative biases in emotional processing or impulsivity in non-smoking subjects, thereby not support
178 in the context of measures of aggression and impulsivity in physically healthy subjects with intermit
179 These results reveal a novel mechanism of impulsivity in rats involving gamma aminobutyric aciderg
182 re, we investigated a specific form of motor impulsivity in rats, namely premature responding, on a f
184 fied clinical trials of atomoxetine to treat impulsivity in selected patients with Parkinson's diseas
185 tment with lithium or valproate on cognitive impulsivity in selectively bred mice previously shown to
186 easures of decision making, risk taking, and impulsivity in smokers and nonsmokers have not been inve
188 ats, anatomical and functional correlates of impulsivity in the anterior insular (AI) cortex by measu
189 premature responding in the Sx-5CSRTT, trait impulsivity in the BIS-11, and decision making in the TC
190 se (uncorrected P < .046) and elevated trait impulsivity in the CUs (uncorrected P < .012), and an in
191 anatomy predicts sensation seeking and motor impulsivity in the healthy populations, potentially incr
192 that the High-Active line demonstrated motor impulsivity in two different versions of the Go/No-go te
195 luded anxiety, depression, hyperactivity and impulsivity, inattention, conduct problems, and psychoti
197 cies toward increased reward sensitivity and impulsivity, increasing the likelihood of engaging in ri
202 animal models; however, whether exaggerated impulsivity is a premorbid risk factor or a consequence
211 These findings indicate that trait-like impulsivity is associated with decreased D2/3 receptor a
212 e present research tests the hypothesis that impulsivity is associated with higher uric acid in human
215 amphetamine-dependent research participants, impulsivity is correlated negatively with striatal D2-ty
217 airs the inhibition of responses, and whilst impulsivity is mild for some patients, severe impulse co
218 ty for response inhibition, and this form of impulsivity is significantly associated with heightened
220 8, in groups of rats selected for HI and low impulsivity (LI) on a 5-choice serial reaction time task
223 The identification of biological markers of impulsivity may lead to a better understanding of the ph
224 ween uric acid and normal variation in trait impulsivity measured with the Revised NEO Personality In
226 a second approach, we compared one of these impulsivity measures, 5CSRTT performance, in two inbred
227 mixed results in rodents including increased impulsivity, no effect on cognition, impairment or even
228 symptoms, both inattention and hyperactivity-impulsivity, on the development of smoking in male and f
229 or other components of choice such as motor impulsivity or loss aversion, suggesting a direct and sp
230 , several regions were found correlated with impulsivity or risky behaviors in AD and RD values, alth
233 poral preferences in animals may not reflect impulsivity, or even mental discounting of future option
235 Delay Discounting Questionnaire, Two-Choice Impulsivity Paradigm (TCIP), Stop Signal Reaction Time,
237 s are observed across subtypes of decisional impulsivity, possibly reflecting uncertainty and the rel
239 readily develop as drug use continues, high impulsivity predicts loss of control over drug seeking a
241 g the second experiment, aimed at preventing impulsivity rather than reversing it, CB1Rs were antagon
242 ighlight that ventral striatal CREM mediates impulsivity related to substance abuse and suggest that
243 ormed a Go/No-Go task during fMRI, completed impulsivity-related assessments, and provided monthly re
247 ociations generalized to self-reported motor impulsivity, replicated in an independent group (n = 219
248 e observed associations generalized to motor impulsivity, replicated in an independent group, and pre
249 een involved in various behaviors, including impulsivity, response to antidepressants, and response t
250 t it is unclear if this is due to changes in impulsivity, risk taking, deliberation or risk adjustmen
252 o examine self-reported impulsivity (Barratt Impulsivity Scale) and performance-based behavioral risk
254 racterized by impaired affective processing, impulsivity, sensation-seeking, poor planning skills and
256 ogical tests included measures of attention, impulsivity, short-term memory, cognitive processing spe
257 uman samples, the emotional aspects of trait impulsivity, specifically impulsiveness and excitement s
258 Here, we aimed to identify genes regulating impulsivity, specifically of impulsive action, in mice.
259 tly with individual differences on the motor impulsivity subscale of the Barratt Impulsivity Scale.
260 psychiatric disorders characterized by high impulsivity, such as attention-deficit/hyperactivity dis
261 dissociable effects on different measures of impulsivity, suggesting considerable specificity in its
262 ders show greater discounting (suggestive of impulsivity), supports the premise that this component o
263 at the developmental course of hyperactivity/impulsivity symptoms followed a sharp linear decrease (m
265 iculties with overactivity, inattention, and impulsivity that are just under the threshold to meet fu
266 a potential therapeutic target for increased impulsivity that may contribute to relapse risk.SIGNIFIC
267 olescence has been associated with increased impulsivity that persists across the lifespan, an effect
268 Premature responding is a form of motor impulsivity that preclinical evidence has shown to predi
270 In this study, we hypothesized that a high impulsivity trait precedes and confers vulnerability for
271 e of bilateral AI cortex lesions on the high impulsivity trait, as measured in the five-choice serial
273 ility to withhold premature responses; motor impulsivity) upon systemic administration or microinfusi
276 ctivation in the anticipation of losses, and impulsivity was associated with increased striatal and i
281 the day confirmed that enhancement of choice impulsivity was related to a specific decrease in the ac
283 ter adult inattention, but not hyperactivity-impulsivity, was associated with significantly lower fra
285 frequency and characteristics of apathy and impulsivity were determined by neuropsychological and be
286 Dopamine levels and resultant variation in impulsivity were likely under differential selection in
288 ion, memory problems, and emotional lability/impulsivity were significantly improved with 50 mg of AZ
289 rences in the linear change in hyperactivity/impulsivity were under strong additive genetic influence
290 overexpression of Nrg3 in the mPFC increased impulsivity, whereas a constitutive Nrg3 loss-of-functio
291 to the left ventral striatum with cognitive impulsivity, whereas a negative relationship was observe
292 ational exposure to a high-fat diet promoted impulsivity, whereas exposure to a low-protein diet led
293 ogies induce fast strategy behaviors such as impulsivity, whereas resource-sufficient and predictable
294 y impair response inhibition and may lead to impulsivity, which can occur even in the presence of pro
295 cortex (dlPFC) are thought to contribute to impulsivity, which is a hallmark of addictive behaviors
296 to be more specific to decisional than motor impulsivity, which might reflect differences in ventral
298 value-coding medial SN network in decisional impulsivity, while the salience-coding ventral SN networ
300 causally implicated in increasing decisional impulsivity with less accumulation of evidence during pr
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