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1 lator could lead to the observed decrease in risk taking.
2 modulate longitudinal declines in adolescent risk taking.
3 he PFC disparately contribute to declines in risk taking.
4 t not dorsal, striatum induced a decrease in risk taking.
5 ne self-administration causes alterations in risk taking.
6 t that may help explain seemingly irrational risk taking.
7 ulus correlated significantly with increased risk taking.
8 bility discounting is a measurable aspect of risk taking.
9 ralleling human regulatory focus research on risk taking.
10 ns, aggressive attitudes, and preference for risk taking.
11 he role of the endocrine system in financial risk taking.
12 irection: We found no birth-order effects on risk taking.
13 led a significant effect of ego depletion on risk taking.
14 psychiatric diseases associated with altered risk taking.
15 investigated the effect of ego depletion on risk taking.
16 proach to investigate birth-order effects on risk taking.
17 s before a gambling task increased financial risk taking.
18 ibutes to success in real-world, high-stakes risk taking.
19 (NACs) dopamine dynamics are associated with risk-taking.
20 decision-making captured in impulsivity and risk-taking.
21 nd how this relates to trait impulsivity and risk-taking.
22 ng, alcohol and illicit drug use, and sexual risk-taking.
23 nerability marker for mania and pathological risk-taking.
24 dorsal striatum were associated with greater risk-taking.
25 illuminate effects of population dynamics on risk-taking.
26 in adulthood that negatively correlate with risk-taking.
30 ipitation and seasonal dynamics on pesticide risk taking also concentrations below the limit of quant
32 rstanding factors that are related to sexual risk taking among virologically detectable (VL+) YMSM ca
34 icate that the relationship between elevated risk taking and cocaine self-administration is bi-direct
35 l and hypothetical monetary rewards modulate risk taking and decision making in the same manner remai
38 ability weighting functions underlying their risk taking and found that participants became more risk
40 the mechanisms supporting sex differences in risk taking and may prove useful in understanding sex di
41 interest is dopamine's influence on economic risk taking and on subjective well-being, a quantity kno
43 of errors during set shifting and increased risk taking and reduced FA in uncinate fasciculus correl
44 red formation of long-term memory, increased risk taking and stimulus seeking behavior, enhanced susc
45 d physiological traits--such as impulsivity, risk taking and stress responsivity--as well as a substa
46 ty to emotional faces may contribute to less risk taking and susceptibility to peer influence in adol
48 vides a possible neural mechanism explaining risk-taking and impaired reinforcement learning in BD.
49 re/exploit trade-off encompasses elements of risk-taking and impulsivity-common behaviors in psychiat
50 (GM), and test whether modernization, sexual risk-taking and parity are associated with greater risk
51 utcomes both negatively influence subsequent risk-taking and positively influence the weight put on p
53 ce were hyperactive and showed more frequent risk-taking and repetitive behaviors, less depression-li
54 examined how modernization influences sexual risk-taking and reproductive health early in demographic
56 ongitudinal analysis provides new insight in risk-taking and reward sensitivity in adolescence: (1) c
59 -report and testosterone levels), laboratory risk-taking and self-reported risk-taking tendency; and
60 es, a combination suggested to contribute to risk-taking and susceptibility to peer influence during
63 ciated with impaired set shifting, increased risk taking, and impaired integrity of frontolimbic whit
64 lite levels and measures of decision making, risk taking, and impulsivity in smokers and nonsmokers h
65 e was additionally associated with real-life risk taking, and N1 source activity was reduced in visua
66 al predictor of future excessive aggression, risk taking, and premature death among nonhuman primate
67 for hormonal contraception/pregnancy, sexual risk-taking, and age, metronidazole and Ecologic Femi+ u
68 cuss hypotheses involving "self-medication," risk-taking, and changes in the social climate but concl
69 ate that acute temperature changes influence risk-taking, and could have profound short and long-term
71 s characterised by increased impulsivity and risk-taking, and psychological accounts argue that these
72 levels with neurocognitive, decision-making, risk-taking, and self-reported impulsivity measures were
75 possibility that birth-order differences in risk taking are not reflected in survey responses and la
77 ievement since traits like aggressiveness or risk-taking are not uniformly positive for success in sc
78 lly problematic substance use showed greater risk taking as well as lower striatal activation relativ
79 bility and loss in BD can potentially modify risk-taking attitudes, which have important public healt
80 se of ART might increase sexual or injecting risk-taking, available research suggests that unprotecte
81 vity Scale) and performance-based behavioral risk taking (Balloon Analogue Risk Task) in bipolar diso
82 -report and testosterone levels), laboratory risk-taking (balloon analog risk task; BART), and self-r
86 real versus hypothetical monetary rewards on risk taking behavior and brain activity, suggesting a ca
87 cence might have more predominant effects on risk-taking behavior (indexed by increases in open-arm a
88 tors of mental health disturbance, including risk-taking behavior (suicidality, self-mutilation, and
91 ritical mediator of psychiatric symptoms and risk-taking behavior among sexually abused children.
93 pmental time point associated with increased risk-taking behavior and experimentation with drugs of a
94 ike receptor availability is correlated with risk-taking behavior and sensitivity of prefrontal activ
95 indings suggest dopaminergic augmentation of risk-taking behavior as a potential contributing mechani
97 at right anodal/left cathodal would decrease risk-taking behavior compared with left anodal/right cat
98 opmental period marked by steep increases in risk-taking behavior coupled with dramatic brain changes
101 novel neural mechanism underlying heightened risk-taking behavior in alcohol-dependent individuals an
102 ired for maintaining sex-typical profiles of risk-taking behavior in both males and females, and that
104 , we assessed the role of agonist therapy on risk-taking behavior in PD patients with (n = 22) and wi
109 ty correlated with individual differences in risk-taking behavior observed after monetary losses, whe
110 sociated with changes in sexual or injecting risk-taking behavior or diagnosis of sexually transmitte
111 = .003), lower human immunodeficiency virus risk-taking behavior scores (P < .001), and lower rates
112 that adolescent alcohol use results in adult risk-taking behavior that positively correlates with pha
113 pharmacological approach to the reversal of risk-taking behavior through normalization of this patte
114 dual differences in pubertal development and risk-taking behavior were contributors to longitudinal c
116 owever, there was no difference in injecting risk-taking behavior with antiretroviral use (OR, 0.90;
118 Dopaminergic drugs are known to increase risk-taking behavior, but the underlying mechanisms for
119 terns were reliably predictive of subsequent risk-taking behavior, including a number of regions know
121 oding of reward outcomes was correlated with risk-taking behavior, with safe-preferring and risk-pref
128 animals exhibited individual differences in risk-taking behavior; some displayed a preference for th
130 the present study was to investigate whether risk-taking behaviors could be decreased using concurren
131 he risk of violence and other antisocial and risk-taking behaviors in adulthood has not been studied
132 isk for serious adverse events by increasing risk-taking behaviors in intoxicated or impaired persons
133 a critical developmental phase during which risk-taking behaviors increase across a variety of speci
135 ors suggests that populations with boundless risk-taking behaviors leading to negative real-life cons
137 levant to numerous psychiatric disorders and risk-taking behaviors, and different lines of evidence h
139 d ethanol has been associated with increased risk-taking behaviors, harm to adolescent users, impaire
140 abnormalities, including self-injurious and risk-taking behaviors, hyperactivity, and learning and m
141 ameliorated PPI deficits, hyperactivity, and risk-taking behaviors, in a fashion akin to the antipsyc
143 ts, indoor tanning was associated with other risk-taking behaviors, such as binge drinking (P < .001
149 DLPFC by itself did not significantly change risk-taking behaviors; however, when the contralateral D
150 onsistency in, as well as average levels of, risk taking behaviour (i.e. boldness) when individuals w
151 role in financial markets through increased risk taking behaviour, acting via different behavioural
153 maternal effects will influence age-specific risk-taking behaviour in Trinidadian guppies, Poecilia r
155 sess the extent of sexual dimorphism in four risk-taking behaviour traits in the Trinidadian guppy, P
156 aradigm, patients were found to show genuine risk-taking behaviour with increased deliberation times
157 ing Task to characterize decision-making and risk-taking behaviour, outside of a learning context, in
162 s provide electrophysiological evidence that risk-taking bias is a lateralized push-pull neural syste
163 Voxel-based morphometry showed that greater risk-taking bias was also associated with and partially
168 ional bias to reward that potentially drives risk taking by priming approach behavior and elevating r
170 individuals exerted an overriding effect on risk-taking by the entire group, for reasons independent
172 sistency, independently of average levels of risk-taking, can be advantageous: more consistent indivi
173 tudy to examine how neural activation during risk taking changes over time and contributes to adolesc
174 ssociated with impulsive decision making and risk taking, characteristics that may arise from hyperse
176 lesions, OFC lesions significantly decreased risk-taking compared with sham controls, but did not imp
177 ed choice of the large risky reward (greater risk-taking) compared to both prelesion performance and
180 on examined whether insula activation during risk-taking decisions-a process shown to be disrupted in
181 ar if this is due to changes in impulsivity, risk taking, deliberation or risk adjustment, and how th
185 o controls suggesting increased activity and risk taking, diminished short term memory, and decreased
187 determine whether individual differences in risk taking during adolescence predict later propensity
188 rom these experiments indicated that greater risk taking during adolescence predicted greater intake
190 to better understand the root causes of MSM risk-taking (e.g., poverty, sex work, substance abuse, m
191 tabolic traits, including physical activity, risk-taking, educational attainment, alcohol and cannabi
192 PFC, which may contribute to impulsivity and risk-taking exhibited by adolescents [5, 6, 10-12].
193 on impulsivity [F(1,9) = 7.86, P = 0.02] and risk taking [F(1,9) = 9.2, P = 0.01] in the context of g
194 ect theory, i.e., that ego depletion reduces risk taking for gains, increases risk taking for losses,
195 ion reduces risk taking for gains, increases risk taking for losses, and increases loss aversion.
197 established that dopaminergic drugs modulate risk-taking; however, little is known about how differen
199 g emotional expressions, as well as empathy, risk taking, impulsivity, behavior change, and attention
202 ng behavioral and neurobiological studies of risk taking in anxious youth and conclude by identifying
206 e relationship between dopamine agonists and risk taking in patients with Parkinson's disease with an
209 he risky decision-making task (RDT) measures risk-taking in a rat model by assessing preference betwe
210 food intake, glucose response to insulin and risk-taking in adulthood whereas the small RNA fraction
213 otherapies for disorders involving excessive risk-taking in humans, such as pathological gambling.
217 paper applies the theory of the evolution of risk-taking in the presence of idiosyncratic and environ
218 ing disorder in obesity with similarities in risk-taking in the reward domain to substance use disord
219 ciated with a growth-mortality trade-off via risk-taking in the wild in two subpopulations of juvenil
220 ifferent dopamine receptor subtypes modulate risk-taking in young adult rats, using a "Risky Decision
222 ses to spatial locations and their levels of risk-taking, indicated by betting, and impulsivity, meas
226 ing geographically distinct clusters at high risk, taking into account realistic logistical constrain
228 k and benefit are inherently subjective, and risk taking is best understood as the interplay between
230 mputational modeling, we show that increased risk taking is explained by enhanced phasic responses to
231 addition, the RDT was used to determine how risk taking is modulated by dopamine signaling, particul
232 s and risky decision-making, suggesting that risk-taking is associated with elevated dopamine sensiti
233 preparing to engage in one, suggesting that risk taking may be due, in part, to a failure of the con
235 se anxiety manipulations; and (ii) decreased risk-taking may be specific to pathological anxiety.
236 esults suggest behavioural traits related to risk-taking may lack the sex-specific genetic architectu
238 ase (ORs of two to three), strong for sexual risk taking, mental ill health, and problematic alcohol
239 apeutic target for alleviating the excessive risk-taking observed across multiple forms of psychopath
240 is finding suggests that the higher level of risk-taking observed among adolescents may reflect a hig
241 learning allows animals to capitalize on the risk-taking of others, and avoid endangering themselves,
244 nts approach more robust incentives (such as risk taking or drug experimentation) to recruit this cir
245 erences in different choice domains, such as risk taking or saving, and how preferences in different
246 00047, pFDR = 0.0053), but not self-reported risk-taking or psychiatric disorder status, predicted be
248 is trade-off is mediated through exploration/risk-taking personality, but empirical support for this
249 g behavior are mild enough to encourage some risk taking, predecision PMC activation by a reward/risk
252 is often described as a period of increased risk taking relative to both childhood and adulthood.
253 eater levels of novelty-seeking behavior and risk-taking relative to adults, behaviors associated in
255 ernization is associated with greater sexual risk-taking, report prevalence of gynecological morbidit
257 ulant addiction is often linked to excessive risk taking, sensation seeking, and impulsivity, but in
258 , might not result in substantial changes in risk-taking sexual behaviour by heterosexual couples.
262 g a pharmacological manipulation and a novel risk taking task while performing functional magnetic re
264 f healthy subjects performing a naturalistic risk-taking task and used a classification analysis appr
265 program during early abstinence completed a risk-taking task during functional magnetic resonance im
266 activation decreased during an experimental risk-taking task over time, with greater declines in VLP
267 k) and the balloon analog risk task (BART; a risk-taking task), and we measured their chronotype in t
271 n analog risk task; BART), and self-reported risk-taking tendency (Behavior Inhibition System/Behavio
273 s), laboratory risk-taking and self-reported risk-taking tendency; and (2) to test whether individual
274 self-administration in turn caused elevated risk taking that was present following 6 weeks of abstin
276 al cortex is thought to influence adolescent risk taking, the specific ways in which it functions are
277 rontal cortex (PFC) may influence adolescent risk taking, the specific ways in which it functions rem
279 Specifically, the stress response calibrates risk taking to our circumstances, reducing it in times o
283 Humanity's fossil-fuel use, if unabated, risks taking us, by the middle of the twenty-first centu
284 tal health problems are related to increased risk taking via inconsistent condom use, multiple partne
285 whereas the medial PFC influences adolescent risk taking via its functional neural coupling with rewa
293 ndicating that lesion-induced alterations in risk-taking were not secondary to changes in appetitive
294 ral PFC are linked to declines in adolescent risk taking, whereas the medial PFC influences adolescen
295 ion of D2-like receptors robustly attenuated risk-taking, whereas drugs acting on D1-like receptors h
296 decreasing the left, might lead to decreased risk taking, which could hold clinical relevance as exce
297 lighted adolescence as a period of increased risk-taking, which is postulated to result from an overa
298 nsular cortex was positively associated with risk-taking, while D2 mRNA expression in orbitofrontal a
299 ivity (FRN) in response to money loss during risk taking with real rewards compared to those with hyp