ライフサイエンスコーパス: IQ

1 IQ motif-containing GTPase-activating protein 1 (IQGAP1)

2 IQ scores are correlated with the morphology and activit

3 IQ was significantly lower for preterm than full-term ch

4 IQ-CSF sensitivity and specificity were evaluated on CSF

5 NAm GrimAge was associated with lower age 11 IQ (beta = -0.11), lower age 73 general cognitive abilit

6 Here, we find that 3515 (18.11%) IQ-TREE-inferred and 1813 (9.34%) RAxML-NG-inferred maxi

7 tructure of Ca(2+)/CaM bound to the Na(V)1.4 IQ domain, which shows a binding mode that would clash w

8 reening would be ~2.5 cm for height and ~2.5 IQ points for cognitive ability.

9 exposure associated with a decrement of 3.70 IQ points (95% confidence interval: 0.83, 6.56).

10 rence was equal to 3.70 (95% CI: 0.49, 6.90) IQ points.

11 al implantation of the PanOptix IOL (AcrySof IQ PanOptixTM; Alcon Research, Fort Worth, Texas, USA) p

12 veral baseline covariates such as adolescent IQ, family background, and educational level.

13 ations (rpart,92 = -.35, p < .001) and adult IQ (rpart,88 = .33, p = .001) even after controlling for

14 es in associative temporal cortices on adult IQ is influenced itself by gyrification abnormalities oc

15 e brain conveys prematurity effects on adult IQ.

16 iation between prematurity and reduced adult IQ (two-path mediation), indicating that aberrant gyrifi

17 All IQ parameters were significantly worse in the KCE cohort

18 , whose rCBF values were elevated across all IQ levels.

19 resulted in a significant improvement in all IQ parameters but they all remained significantly poorer

20 mated algorithm for its calculation (Amyloid(IQ)).

21 Probabilities of having an IQ in the normal (>/=70) or intellectual disability (<70

22 the C-terminal (CT) region, consisting of an IQ domain downstream of an EF-hand domain.

23 ith the reciprocal duplication (n = 27), and IQ-matched control subjects with no large copy number va

24 ciodemographic and perinatal adversities and IQ, psychotic experiences at ages 11-12 predicted receiv

25 en we tested a smaller cohort of 30 age- and IQ-matched autistic children on the same task, we found

26 a diagnosis of ASD and IQ>80 and 17 age- and IQ-matched male typically developing (TD) young adults 1

27 y-one children with ADHD and thirty age- and IQ-matched typically developing (TD) controls underwent

28 without intellectual disability and age- and IQ-matched typically developing control subjects (n = 20

29 ale participants with a diagnosis of ASD and IQ>80 and 17 age- and IQ-matched male typically developi

30 ree (RAxML-, FastTree regular bootstrap- and IQ-Tree regular bootstrap-based) analytical approaches h

31 difference in specificity between PQ-CSF and IQ-CSF, the latter showed a significant improvement in s

32 were also assessed for mental disorders and IQ.

33 of whom 287 and 211 had data for the GCI and IQ analyses, respectively.

34 95% CI -4.12, -0.59) lower offspring GCI and IQ scores, respectively.

35 ve domains of attention, working memory, and IQ were assessed.

36 ed item-level self-report questionnaires and IQ and demographic measures.

37 gene dosage with respect to autism risk and IQ loss.

38 he tail-end deciles of the schizophrenia and IQ polygenic score distributions, 33% versus 9% of indiv

39 tes the positive association between SES and IQ.

40 es the positive relationship between SES and IQ.

41 ounted for documented differences in sex and IQ in affected individuals with de novo mutations by mat

42 dicated and unmedicated; and 26 age, sex and IQ matched control subjects.

43 ort and 53 controls matched for age, sex and IQ, on the Cambridge Neuropsychological Test Automated B

44 residualised for the effects of age, sex and IQ.

45 with the two groups matched in age, sex, and IQ as assessed with Raven's Advanced Progressive matrice

46 ting influences of participant age, sex, and IQ on our findings and the correlations of rCBF with N-a

47 Finally, age, sex, and IQ were important sources of cerebellar volume variabili

48 atypical moderating effects of age, sex, and IQ.

49 d avoided assessing effects of age, sex, and IQ.

50 n metabolites, as moderated by age, sex, and IQ.

51 ositive association between birth weight and IQ was observed, and 88% of the association was direct.

52 en conditional height at 11, 15, or 18 y and IQ.

53 The mean school grades at age 16 years and IQ test scores at military conscription at age 18 years.

54 indexed by school grades at age 16 years and IQ test scores at military conscription.

55 hydroisoquinoline (THIQ) or fully aromatized IQ natural products.

56 Intellectual disability (ID), defined as IQ<70, occurs in 2.5% of individuals.

57 sess homologous CaM-binding motifs, known as IQ motifs in their C termini, which associate with calmo

58 ein kinase (MAPK) scaffold proteins, such as IQ motif containing GTPase activating protein 1 (IQGAP1)

59 n a substudy in which psychologists assessed IQ using the Wechsler Primary and Preschool Scales of In

60 neural network for image quality assessment (IQ-DCNN) was designed, trained, optimized, and cross-val

61 Persistence, above and beyond IQ, is associated with long-term academic outcomes.

62 ferred by duplications is less influenced by IQ compared with deletions.

63 hippocampal volumes, possibly influenced by IQ.

64 l urinary DAP concentrations and lower child IQ scores at 6 y of age was not observed.

65 of life was associated with higher childhood IQ whereas greater weight gain after the first year of l

66 r childhood self-control and lower childhood IQ than self-only harmers.

67 To evaluate the impact of the Clarity IQ technology on reducing radiation risk in patients und

68 Here, we present compact IQ modulators with an active section occupying a footpri

69 episodic memory ( r = .26), and crystallized IQ ( r = .18).

70 the difference between premorbid and current IQ estimates, in a logistic regression analysis.

71 rived from patterns of premorbid and current IQ showed different premorbid and clinical characteristi

72 sis using estimates of premorbid and current IQ.

73 Heterogeneity in the DAP-IQ association by PON1 gene allele status was not observ

74 gression models were fit to estimate the DAP-IQ associations and PON1 interactions.

75 d performance were self-reported daringness, IQ and self-reported cognitive complexity.

76 Deleting 1 point of pLI decreases IQ by 2.6 points in autism and unselected populations.

77 fic decreases in metabolites with decreasing IQ occurred in several brain areas.

78 ht chains (PfELC and MTIP) by two degenerate IQ motifs.

79 rmance of a new PET/CT system, the Discovery IQ with 5-ring detector blocks.

80 inly for estrogen receptor-positive disease (IQ-OR, 1.44; 95% CI, 1.16 to 1.79; P for heterogeneity =

81 by US public health insurance had estimated IQs that were significantly lower ( P < .001) than those

82 de polymorphism heritability for the extreme IQ trait was 0.33 (0.02), which is the highest so far fo

83 Here we identify one such factor, IQ motif containing GTPase activating protein-1 (IQGAP1)

84 Fluid IQ measured with the Kaufman Brief Intelligence Test, no

85 prevents 0.39 x 10(-2) points for per-foetus IQ decrements and 194 deaths from fatal heart attacks.

86 GWAS data for IQ (N = 78,308) were meta-analyzed with a study comparin

87 elated with the neural transition frequency, IQ scores of individuals with ASD are instead predicted

88 ers and cognitive and behavioral scores from IQ testing, and parental measures of development were te

89 es of attention, memory, executive function, IQ, and processing speed.

90 tive evaluation of intellectual functioning (IQ), working memory, and processing speed (PS) was condu

91 nalyses included the moderators age, gender, IQ, and scan site.

92 of the first (PQ-CSF) and second generation (IQ-CSF) RT-QuIC assays, and investigated the diagnostic

93 up exhibited a significant decline in global IQ, working memory, and processing speed (all P < .05).

94 lin via its N-terminal isoleucine-glutamine (IQ) motif.

95 Thus, maleness, a high IQ or self-reported cognitive complexity, and self-repor

96 ontribute to ASD cases with lower and higher IQ phenotypes, respectively.

97 ated to both fewer sleep problems and higher IQ scores.

98 ntry with free access to health care, higher IQ was seen with greater size at birth and greater weigh

99 dose-response relationship indicated higher IQ scores in children who always (4.80 points) or someti

100 had 8.02 (95% CI 1.46, 14.59) points higher IQ in adolescence versus the declining trajectory group.

101 ower maternal PTSD symptoms predicted higher IQ in preterm children.

102 fractional anisotropy associated with higher IQ.

103 ntration in pregnancy were related to higher IQs but this effect was confounded with SES and disappea

104 ICC, 0.992; 95% CI: 0.986, 0.996), and IDEAL IQ and the GE 3.0-T unit (ICC, 0.966; 95% CI: 0.939, 0.9

105 rs (mDIXON Quant [Philips Healthcare], IDEAL IQ [GE Healthcare]).

106 concentration were obtained using the IDEAL-IQ technique for liver imaging.

107 is computational study determined changes in IQ [peak IQ, best focus and depth of focus (DOF)] of 12

108 omic status in adulthood and with changes in IQ and socioeconomic mobility between childhood and midl

109 n greater blood lead levels and a decline in IQ and socioeconomic status from childhood to adulthood

110 he schizophrenia group exhibited declines in IQ and in measures of verbal knowledge and of memory, bu

111 status at age 38 years and with declines in IQ and with downward social mobility.

112 ars at diagnosis are at risk for deficits in IQ and PS in the absence of cranial radiation, regardles

113 about 40% of between-subject variability in IQ.

114 Variance in IQ is associated with a wide range of health outcomes, a

115 t above and beyond accompanying variation in IQ.

116 determinants of health to the discrepancy in IQs, which was 13%.

117 Additionally, the WMD in IQs with NBW were 14, 10 and 7 for ELBW, VLBW, and MLBW

118 The pooled weight mean difference (WMD) in IQs between NBW and LBW individuals was 10 (95% CI 9.26-

119 rCBF declined with increasing IQ in the typically developing group, a correlation that

120 on between low birth weight and individuals' IQ scores (IQs).

121 ting for measures of childhood intelligence (IQ), negative affect, and prior mental health risk and w

122 d a hypomethylated region mapping to Iqgap2 (IQ motif-containing GTPase activating protein 2) and F2r

123 Isoquinolines (IQs) and their derivatives are present in many natural p

124 ia the Wechsler Adult Intelligence Scale IV (IQ range, 40-160, standardized to a mean of 100 [SD, 15]

125 chsler Adult Intelligence Scale-IV (WAIS-IV; IQ range, 40-160).

126 ere matched for age, sex, educational level, IQ, reading abilities (measured by APRA), magnocellular

127 The patients show limited IQ with developmental delay and skewed X-inactivation.

128 hrough-focus analysis performed on the logNS IQ metric over 5 mm pupil diameter following cycloplegia

129 ), characterized by congenital cataract, low IQ, and defective kidney proximal tubule resorption.

130 his is true for individuals with high or low IQ and after removing de novo and known recurrent neurop

131 Healthy individuals with low IQ showed no evidence of decline, suggesting that a decl

132 grades and 0.97% (95% CI, 0.15%-1.78%) lower IQ test scores.

133 o have lower fractional anisotropy and lower IQ than healthy participants, the comparable size of eff

134 associated with lower NAAG levels had lower IQ scores.

135 ng Task (p < 0.05), and had a markedly lower IQ (p < 0.01).

136 ificantly associated with a 2.07-point lower IQ score at age 45 years (95% CI, -3.39 to -0.74; P = .0

137 r had a mean (SE) of 4.4 (0.72) points lower IQ than those without severe disorder (P < .001), and th

138 se had a mean (SE) of 5.6 (1.2) points lower IQ than those without severe disorder (P < .001).

139 h as behavioral and learning problems, lower IQ, hyperactivity, hearing problems, and impaired growth

140 repeat expansions were associated with lower IQ and adaptive ability.

141 of Mn, Pb, and Cr were associated with lower IQ scores, especially at low Cu levels.

142 observed in both CNV groups, with the lowest IQs in deletion carriers.

143 8 individuals from the top 0.0003 ( 170 mean IQ) of the population distribution of intelligence and 8

144 nificantly lower in patients after CSI (mean IQ, 90 [no radiotherapy], v 74 [CSI]; P = .012).

145 of adolescents less than 1 SD below the mean IQ range than those without a disorder.

146 a study comparing 1247 individuals with mean IQ ~170 to 8185 controls.

147 The mean IQs of the extremely low birth weight (ELBW, <1000 g), v

148 ns after delivery and intelligence measures (IQ) in adulthood.

149 subclinical hypothyroidism trial, the median IQ score of the children was 97 (95% confidence interval

150 th IQ [per z-score increase from 5 to 12 mo, IQ increased by 1.53 (95% CI: 0.14; 2.92) points] wherea

151 redictive power was similar to the TC model (IQ-OR, 1.45; 95% CI, 1.21 to 1.73; mC, 0.55), but SNP88

152 PET image quality was assessed using a NEMA IQ phantom.

153 ctyl phthalate (DNOP) exposure and nonverbal IQ.

154 e for an inverse relation of child nonverbal IQ and late pregnancy urinary DAPs, but the estimated as

155 verall, associations between child nonverbal IQ and maternal DAP concentrations were small and imprec

156 re inversely associated with child nonverbal IQ at 6 y of age and to examine potential effect measure

157 y were associated with lower child nonverbal IQ score [e.g., B per 10-fold increase in summed low-mol

158 gestation samples, adjusted child nonverbal IQ was 3.9 points lower (95% CI: [Formula: see text], [F

159 Child nonverbal IQ was measured at 6 y of age using the Mosaics and Cate

160 Child nonverbal IQ was measured at 6 years of age using the Snijders-Oom

161 ols were not associated with child nonverbal IQ.

162 regnancy are associated with lower nonverbal IQ scores in children.

163 henol exposure are associated with nonverbal IQ.

164 arting age for IBI and in achieving a normal IQ based on starting age.

165 dulators may pave the way for application of IQ modulators in long-haul and short-haul communications

166 zed that some of the missing heritability of IQ might lie hidden in the human leukocyte antigen (HLA)

167 sults strongly support the implementation of IQ-CSF in clinical practice.

168 Our results confirm the high sensitivity of IQ-CSF for detecting human prions with a sub-optimal sen

169 ys, and investigated the diagnostic value of IQ-CSF across the broad spectrum of human prions.

170 attractive branch point for the synthesis of IQs, but because of their innate reactivity, they have r

171 t" (pLI) best explains the effect of CNVs on IQ and autism risk.

172 The effect of duplications on IQ is threefold smaller.

173 When CNV effects on IQ are accounted for, autism susceptibility remains most

174 ompassed in CNVs to explain their effects on IQ, autism susceptibility, and behavioral domains.

175 their total, indirect, and direct effects on IQ.

176 healthy comparison subjects group-matched on IQ, gender, and age performed a passive avoidance task w

177 ated the causal effect of DNA methylation on IQ using the offspring genotype at sites close to the me

178 stical models to estimate the effect size on IQ of all CNVs, including undocumented ones.

179 y associated with OCI, and premorbid IQ (one IQ point increase: OR, 0.91; 95%CI, 0.82-0.98; p = 3.8 *

180 d movement, antipsychotics, cannabis use, or IQ, and is not found in other frequency bands.

181 Controlling for parental IQ or socioeconomic status substantially attenuated or e

182 nfluenced by environmental factors, parental IQs and other factors contribute to residual confounding

183 ling trends of association between patients' IQ and affective psychotic symptoms with the local effic

184 ational study determined changes in IQ [peak IQ, best focus and depth of focus (DOF)] of 12 subjects

185 the DOF range were inversely related to peak IQ in these eyes (r = 0.85; p < 0.001).

186 l intelligence quotient (IQ) and performance IQ scores over a period of 5 years were significantly su

187 54) were analysed for verbal and performance IQ with WPPSI-III and 315 (iodine group, n=159; placebo

188 two of these sites on childhood performance IQ which was replicated for one of the sites.

189 Lower performance IQ, male sex, and higher intra-individual variability in

190 a measure of general cognitive performance, IQ, in patients with schizophrenia and healthy participa

191 consumption and verbal, but not performance, IQ.

192 ere 1.4, 0.9, 1.7 and 1.3 ng g(-1) for PhIP, IQ, MeIQ and MeIQx, respectively.

193 ion was observed with treatment arm (placebo IQ-OR, 1.46; 95% CI, 1.13 to 1.87; tamoxifen IQ-OR, 1.25

194 cational attainment and 0.86 with population IQ.

195 ositively associated with OCI, and premorbid IQ (one IQ point increase: OR, 0.91; 95%CI, 0.82-0.98; p

196 not associated with TRS; however, premorbid IQ in males and schizophrenia family history were signif

197 In males, a decrease of premorbid IQ of one standard deviation was significantly associate

198 These findings hold independent of proband IQ.

199 The proposed IQ-DCNN was trained to mimic expert visual image quality

200 cell migration through the scaffold protein IQ motif-containing GTPase-activating protein 1(IQGAP1).

201 ramide signaling on an ERK scaffold protein, IQ motif containing GTPase activating protein 1 (IQGAP1)

202 hat OX40 associated with a scaffold protein, IQ motif-containing GTPase-activating protein 1 (IQGAP1)

203 ctivity depended on the scaffolding proteins IQ motif-containing GTPase-activating protein-1 (IQGAP1)

204 w variations in dimensions of psychometrics, IQ and demographics relate to changes in brain connectiv

205 It relies on so-called in-phase/quadrature (IQ) electro-optic modulators that encode information on

206 t their impact on the retinal image quality (IQ) of these eyes.

207 vity profiles to self-report questionnaires, IQ and demographic data we identified two distinct modes

208 Here, we applied this improved QuIC (IQ-CSF) for highly efficient detection of TSEs prion pro

209 of 2-amino-3-methyl imidazo[4-5-f]quinolone (IQ), 2-amino-3, 8-dimethlylimidazo[4, 5-f]quinolone (MeI

210 zation and both lower intelligence quotient (IQ) and higher levels of attention deficit/hyperactivity

211 n association between Intelligence Quotient (IQ) and PBDEs.

212 full-scale or global intelligence quotient (IQ) and performance IQ scores over a period of 5 years w

213 points of per-foetus intelligence quotient (IQ) decrements and 7,360 deaths from fatal heart attacks

214 d postnatal growth on Intelligence Quotient (IQ) in childhood in term-born children living in high-in

215 xposure and nonverbal intelligence quotient (IQ) in children 6 years of age.

216 sociated with reduced intelligence quotient (IQ) score in offspring.

217 score at 1 y had mean intelligence quotient (IQ) scores at 18 y 4.50 points (95% CI: 1.08, 7.92) high

218 verbal and full scale intelligence quotient (IQ) scores at 5 and 6 y, but these effects disappeared a

219 ce Scale for Children intelligence quotient (IQ) scores.

220 <2500 g) have a lower intelligence quotient (IQ) than those with normal birth weights (NBW, >/=2500 g

221 Intelligence quotient (IQ) was significantly lower in patients after CSI (mean

222 ents [e.g., decreased intelligence quotient (IQ), academic performance] and neurological disease (e.g

223 rm outcomes in global intelligence quotient (IQ), perceptual reasoning, and working memory compared w

224 ups in the domains of intelligence quotient (IQ), processing speed, working memory, executive functio

225 ophrenia and baseline intelligence quotient (IQ), respectively, but schizophrenia polygenic score was

226 orrelates with lower intelligence quotients (IQ) in individuals with DS; however, its contribution to

227 though normal-range, intelligence quotients (IQs) versus their full-term peers.

228 with published GWA analyses of normal-range IQ or educational attainment.

229 isk overall (interquartile range odds ratio [IQ-OR], 1.37; 95% CI, 1.14 to 1.66; mC, 0.55), but mainl

230 ween developmental PBDE exposure and reduced IQ.

231 Measurable cognitive decline (reduced IQ, academic deficits) have been found to occur at level

232 is prospectively associated with children's IQ at 60 months.

233 children were 18 months old, and children's IQ was measured at 11 years old.

234 maging to probe how the multidomain scaffold IQ motif containing GTPase activating protein 1 (IQGAP1)

235 tistic Disorder (age 18-45 years; full scale IQ >70; ABC-Irritability subscale 13).

236 Full scale IQ was lower in both deletion and duplication carriers c

237 Wechsler Adult Intelligence Scale Full Scale IQ.

238 ted with high-functioning autism (full-scale IQ >100).

239 nce interval (CI): -3.9, -0.5] in Full-Scale IQ and 2.9 points (95% CI: -4.4, -1.3) in Verbal Compreh

240 ognitive outcomes (e.g., beta for Full-Scale IQ for boys = - 1.9, 95% CI: - 4.1, 0.3 and - 1.7, 95% C

241 echsler Adult Intelligence Scale, full-scale IQ test.

242 AMC, birth-related variables, and full-scale IQ.

243 reduced cognition as measured by full-scale IQ.

244 adulthood which links with lower full-scale IQ.

245 rol subjects with comparable mean full-scale IQs.

246 low birth weight and individuals' IQ scores (IQs).

247 Lower mean (SE) IQ was observed among adolescents with past-year bipolar

248 echanistically, the introduction of a second IQ domain to the Ca(V)1.3 carboxyl tail switched the app

249 atively, a substantial improvement was seen (IQ-OR, 1.64; 95% CI, 1.36 to 1.97; mC, 0.60).

250 Most effects did not depend on age, sex, IQ, severity or medication use.

251 ith and without these genetic events on sex, IQ, and age before comparing them on multiple behavioral

252 Since IQ is inherited and influenced by environmental factors,

253 Suppressor of site IQ electron leak and vehicle were administered during ca

254 phate-buffered saline) or suppressor of site IQ electron leak, an inhibitor of superoxide production

255 en species generation by suppression of site IQ electron leak, decreased myocardial reactive oxygen s

256 targeting this mechanism, suppressor of site IQ electron leak, represents a potential, practical ther

257 Suppressor of site IQ electron leak, which inhibits complex I-dependent rea

258 Such IQ modulators may pave the way for application of IQ mod

259 Ideally, such IQ modulators should offer energy-efficient operation an

260 IQ-OR, 1.46; 95% CI, 1.13 to 1.87; tamoxifen IQ-OR, 1.25; 95% CI, 0.96 to 1.64; P for heterogeneity =

261 mammalian brain and heart, lack a C-terminal IQ motif.

262 The IQ (primary outcome) and indexes of Verbal Comprehension

263 The IQ strata were assigned probabilities of achieving an in

264 reorientation of the EF-hand domain and the IQ domain as a possible conformational switch that under

265 IQGAP1 and CaMKK2, which is mediated by the IQ domain of IQGAP1.

266 th dissociation of calmodulin (CaM) from the IQ motif in Myo1c.

267 The results from the IQ-DCNN were in good agreement with human expert reading

268 noncoding mutations and heterogeneity in the IQ of ASD probands.

269 Deletion of the IQ motif (amino acids 29-58) results in loss of calmodul

270 We solved separate NMR structures of the IQ motif (residues 1,646-1,664) bound to alpha-actinin-1

271 Regression performance of the IQ-DCNN was within the range of human intra- and interob

272 HIV- participants, in PHIV+ participants the IQ score increased significantly more over time (group*t

273 ve in vitro binding assays, we show that the IQ domain of IQGAP1 is both necessary and sufficient for

274 lization to endothelial borders and that the IQ domain, on the same IQGAP1 polypeptide, is required f

275 Recently, we have shown that the IQ motif-containing GTPase-activating protein 1 (IQGAP1)

276 and interobserver agreement and (b) that the IQ-DCNN algorithm may be used to monitor a compressed se

277 Binding of alpha-actinin to the IQ motif of Ca(V) 1.2 supports its surface localization

278 PA specifically binds to the IQ motif-containing guanosine triphosphatase-activating

279 (top 0.0003 of the population equivalent to IQ > 147) and 3,253 unselected population controls.

280 In each trial, IQ scores were missing for 4% of the children.

281 ler discrepancy between nonverbal and verbal IQ and a greater likelihood of having achieved fluent la

282 ociated with decreased full-scale and verbal IQ scores compared with duplication carriers without the

283 nificantly associated with cognitive (verbal IQ) decline and nominally associated with sub-threshold

284 ld not be explained by differences in verbal IQ, intracranial volume, anxiety/depression, or attentio

285 al modelling to predict out-of-sample verbal IQ and depression from cortical metabolism alone.

286 ality were assessed at age 9-11 years, while IQ was assessed at age 12.

287 Moreover, in contrast to the controls whose IQ is correlated with the neural transition frequency, I

288 ence growth in childhood was associated with IQ [per z-score increase from 12 mo to 5 y, IQ increased

289 Weight gain in infancy was associated with IQ [per z-score increase from 5 to 12 mo, IQ increased b

290 n infancy and childhood were associated with IQ at age 5 y in term-born children using path analysis.

291 ontrol analyses and were not associated with IQ or head motion.

292 concentration was positively associated with IQ, but adjustment for confounding cofactors attenuated

293 in from 12 mo to 5 y was not associated with IQ.

294 for group comparisons and correlations with IQ.

295 egative association of mercury exposure with IQ.

296 Here, we show that LGR5 interacts with IQ motif-containing GTPase-activating protein 1 (IQGAP1)

297 imate associations of the metal mixture with IQ.

298 ingulate cortices correlated positively with IQ scores in PM and control boys while negatively in PM

299 ygous for a 2 base pair (bp) deletion within IQ calmodulin-binding motif-containing protein-1 (IQCB1)

300 IQ [per z-score increase from 12 mo to 5 y, IQ increased by 0.98 (95% CI: 0.17; 1.79) and 2.09 (95%