ライフサイエンスコーパス: neurodevelopmental disorder

1 ght into how DHX30 dysfunction might cause a neurodevelopmental disorder.

2 gene cause Angelman syndrome (AS), a severe neurodevelopmental disorder.

3 ogenesis of Rett Syndrome (RTT), an X-linked neurodevelopmental disorder.

4 potential therapeutic avenues for a complex neurodevelopmental disorder.

5 hyperactivity disorder (ADHD) is a heritable neurodevelopmental disorder.

6 rt of this gene in association with a severe neurodevelopmental disorder.

7 sights into the nature of schizophrenia as a neurodevelopmental disorder.

8 ene develop Angelman syndrome (AS), a severe neurodevelopmental disorder.

9 ost notable characteristics of this group of neurodevelopmental disorders.

10 (ASD) are common, complex and heterogeneous neurodevelopmental disorders.

11 dentified as the genetic basis of congenital neurodevelopmental disorders.

12 of the molecular mechanisms contributing to neurodevelopmental disorders.

13 werful approach to gene discovery in complex neurodevelopmental disorders.

14 part in the etiology of neuropsychiatric and neurodevelopmental disorders.

15 genes for which mutations are known to cause neurodevelopmental disorders.

16 are less genetic risk as compared with other neurodevelopmental disorders.

17 hose mutation is known to cause ASD or other neurodevelopmental disorders.

18 c characteristics of individuals affected by neurodevelopmental disorders.

19 ular and molecular defects underlying ID and neurodevelopmental disorders.

20 uide the search for epigenomic mechanisms in neurodevelopmental disorders.

21 AF subunits and is expected to contribute to neurodevelopmental disorders.

22 associated with a spectrum of epilepsies and neurodevelopmental disorders.

23 e of CASPR2 and possibly other antibodies in neurodevelopmental disorders.

24 2 locus are associated with elevated risk of neurodevelopmental disorders.

25 e novo protein-truncating variants (PTVs) in neurodevelopmental disorders.

26 genetic risk between schizophrenia and other neurodevelopmental disorders.

27 o the role of cell-cycle checkpoint genes in neurodevelopmental disorders.

28 r inflammatory insults increases the risk of neurodevelopmental disorders.

29 orphology has been found in populations with neurodevelopmental disorders.

30 wn as Ube3a that is implicated in cancer and neurodevelopmental disorders.

31 behavioural problems and is associated with neurodevelopmental disorders.

32 ous system, as several are closely linked to neurodevelopmental disorders.

33 quisite for assessing circuit dysfunction in neurodevelopmental disorders.

34 unit, which are relevant to autism and other neurodevelopmental disorders.

35 cal and genetic overlap with other childhood neurodevelopmental disorders.

36 now established as conferring risk of other neurodevelopmental disorders.

37 ing and memory impairments of PNN-associated neurodevelopmental disorders.

38 terodimer) can give rise to severe, sporadic neurodevelopmental disorders.

39 ations found in ASD to develop therapies for neurodevelopmental disorders.

40 responding genes as likely to have a role in neurodevelopmental disorders.

41 with neuronal activation, and is altered in neurodevelopmental disorders.

42 leads to numerous human neurodegenerative or neurodevelopmental disorders.

43 fic behavioral abnormalities associated with neurodevelopmental disorders.

44 normal neuronal oscillations associated with neurodevelopmental disorders.

45 litate therapeutic drug screening for severe neurodevelopmental disorders.

46 imately 0.1% of individuals with unexplained neurodevelopmental disorders.

47 al migration or differentiation may underlie neurodevelopmental disorders.

48 ding contributes to symptoms associated with neurodevelopmental disorders.

49 pacted on the prognosis of the children with neurodevelopmental disorders.

50 ) protein may play a key role in HCMV-caused neurodevelopmental disorders.

51 of sex biased genes in brain development and neurodevelopmental disorders.

52 al growth, is an established risk factor for neurodevelopmental disorders.

53 ct of deleterious variants in EGs on complex neurodevelopmental disorders.

54 henotypic abnormalities likely contribute to neurodevelopmental disorders.

55 nic mechanisms underlie ADHD and these other neurodevelopmental disorders.

56 ained genes are enriched in individuals with neurodevelopmental disorders.

57 ity of cerebral organoids for modeling human neurodevelopmental disorders.

58 n maturation and predispose the offspring to neurodevelopmental disorders.

59 n utero exposure to some antidepressants and neurodevelopmental disorders.

60 essed and have been implicated in a range of neurodevelopmental disorders.

61 on and for genes known to be associated with neurodevelopmental disorders.

62 for pathogenic variation related to complex neurodevelopmental disorders.

63 derlying the E/I imbalance hypothesis across neurodevelopmental disorders.

64 d an important role for de novo variation in neurodevelopmental disorders.

65 dentified in individuals affected by various neurodevelopmental disorders.

66 ve been tightly associated with the onset of neurodevelopmental disorders.

67 tional domain (TRIO) protein associated with neurodevelopmental disorders.

68 1A2 have recently been found to give rise to neurodevelopmental disorders.

69 rhaps consistent with their association with neurodevelopmental disorders.

70 ies to neuronal proteins may be one cause of neurodevelopmental disorders.

71 s impacted by genetic risk factors linked to neurodevelopmental disorders.

72 isoform 2 causes phenotypes translatable to neurodevelopmental disorders.

73 possible contribution to pathophysiology in neurodevelopmental disorders.

74 s concentrated in risk genes associated with neurodevelopmental disorders.

75 ral growth, delayed cerebral maturation, and neurodevelopmental disorders.

76 as a recurring mechanism in the etiology of neurodevelopmental disorders.

77 take into account the strong overlap across neurodevelopmental disorders.

78 variants in 50 genes already established in neurodevelopmental disorders (46 autosomal recessive, 2

79 After excluding known risk genes for neurodevelopmental disorders, a significant rare variant

80 1 sibling diagnosed with any psychiatric or neurodevelopmental disorder (adjusted RR, 2.5; 95% CI, 2

81 bout the clustering of other psychiatric and neurodevelopmental disorders among siblings of persons w

82 adjusted risk ratio (RR) for psychiatric and neurodevelopmental disorders among siblings of probands

83 work implicates BCL11A haploinsufficiency in neurodevelopmental disorders and defines additional targ

84 -LOF to a set of 1142 de novo vari3ants from neurodevelopmental disorders and find enrichment of path

85 e high level of heterogeneity and overlap in neurodevelopmental disorders and for research to link mo

86 Females with neurodevelopmental disorders and in the general populati

87 have implicated hundreds of genetic loci in neurodevelopmental disorders and neurodegeneration, but

88 dynamics may also underlie or contribute to neurodevelopmental disorders and neurodegeneration.

89 ng evidence that these regions contribute to neurodevelopmental disorders and outline strategies for

90 tions (PMMs) have been implicated in several neurodevelopmental disorders and overgrowth syndromes.

91 Because autism spectrum disorders are neurodevelopmental disorders and patients typically disp

92 gene variant identification for undiagnosed neurodevelopmental disorders and provided insights into

93 Comorbidity with childhood-onset neurodevelopmental disorders and psychiatric disorders i

94 the effects of experience in the context of neurodevelopmental disorders and typical neural developm

95 disorder (ADHD) is the most common childhood neurodevelopmental disorder, and boys are two to three t

96 unction is the cause of Angelman syndrome, a neurodevelopmental disorder, and increased expression of

97 States, one in six children are affected by neurodevelopmental disorders, and polybrominated dipheny

98 ant to the onset and diagnosis of a range of neurodevelopmental disorders, and that NRXN1 expression

99 cy is correlated with increased frequency of neurodevelopmental disorders, and this is studied in mic

100 dendritic spine densities are common in the neurodevelopmental disorder Angelman syndrome (AS).

101 This likely explains why certain neurodevelopmental disorders are characterized by weak g

102 Autosomal recessive inherited neurodevelopmental disorders are highly heterogeneous, a

103 Neurodevelopmental disorders are marked by inappropriate

104 Neurodevelopmental disorders are the most common and dis

105 ngoing efforts to understand the etiology of neurodevelopmental disorders arising from Ptchd1 deficie

106 We also argue the importance of viewing neurodevelopmental disorders as traits but highlight tha

107 ntial to uncover altered topologies in other neurodevelopmental disorders, as well.

108 ernal UBE3A causes Angelman syndrome (AS), a neurodevelopmental disorder associated with severe epile

109 EMENT Pitt-Hopkins syndrome (PTHS) is a rare neurodevelopmental disorder associated with TCF4 mutatio

110 ht to contribute to cognitive impairments in neurodevelopmental disorders associated with intellectua

111 They suggest that neurodevelopmental disorders associated with preterm bir

112 er and infections has been linked to various neurodevelopmental disorders, but it is not yet known wh

113 spindle orientation defects result in severe neurodevelopmental disorders, but the precise mechanisms

114 ead exposure during early development causes neurodevelopmental disorders by unknown mechanisms.

115 imately 40 mutations are associated with the neurodevelopmental disorder cardio-facio-cutaneous syndr

116 Williams syndrome (WS) is a neurodevelopmental disorder caused by a genomic deletion

117 Autism spectrum disorder (ASD) is a neurodevelopmental disorder caused by genetic variants,

118 Neurofibromatosis type 1 (NF1) is a common neurodevelopmental disorder caused by impaired function

119 Angelman syndrome (AS) is a debilitating neurodevelopmental disorder caused by loss of function o

120 Angelman Syndrome (AS) is a rare neurodevelopmental disorder caused by loss of function o

121 ICANCE STATEMENT Angelman syndrome (AS) is a neurodevelopmental disorder caused by loss or mutation o

122 KEY POINTS: Rett syndrome is a neurodevelopmental disorder caused by loss-of-function m

123 ABSTRACT: Rett syndrome is a neurodevelopmental disorder caused by loss-of-function m

124 Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by mutation or deleti

125 quarter of deaths in Rett Syndrome (RTT), a neurodevelopmental disorder caused by mutations in Methy

126 Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in Methy

127 kinase-like 5 (CDKL5) deficiency is a severe neurodevelopmental disorder caused by mutations in the C

128 Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the g

129 Rett syndrome (RTT) is a debilitating neurodevelopmental disorder caused by mutations in the M

130 Rett syndrome is a severe neurodevelopmental disorder caused by mutations in the m

131 Rett syndrome (RTT) is an X-linked, neurodevelopmental disorder caused primarily by mutation

132 n-deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterised by development

133 l central hypoventilation syndrome (CCHS), a neurodevelopmental disorder characterized by a failure i

134 l-recessive primary microcephaly (MCPH) is a neurodevelopmental disorder characterized by a reduction

135 Autism is a neurodevelopmental disorder characterized by deficits in

136 endent kinase-like 5 (CDKL5) deficiency is a neurodevelopmental disorder characterized by epileptic s

137 re associated with risk for schizophrenia, a neurodevelopmental disorder characterized by excitatory/

138 Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by hypotonia,

139 Fragile X syndrome (FXS) is an undertreated neurodevelopmental disorder characterized by low intelli

140 Here, we describe seven children with a neurodevelopmental disorder characterized by microcephal

141 Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by persistent

142 es who died soon after birth with a profound neurodevelopmental disorder characterized by pontocerebe

143 D) is a childhood-onset neuropsychiatric and neurodevelopmental disorder characterized by the presenc

144 1) is a shared molecular hallmark in several neurodevelopmental disorders characterized by abnormal b

145 udied interneuron subtype in the etiology of neurodevelopmental disorders characterized by NMDA recep

146 adhesion molecule, is implicated in several neurodevelopmental disorders characterized by synaptic d

147 Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by normal pos

148 Psychiatric and neurodevelopmental disorders cluster among siblings of p

149 tism and intellectual disability are complex neurodevelopmental disorders, debilitating millions of p

150 Autism is a neurodevelopmental disorder, diagnosed behaviorally by s

151 particular; they enable the definition of a neurodevelopmental disorder due to PSMD12 variants, expa

152 Intellectual disability (ID) is a common neurodevelopmental disorder exhibiting extreme genetic h

153 tion mutations of USP7 in individuals with a neurodevelopmental disorder, featuring intellectual disa

154 t modify synaptic phenotypes associated with neurodevelopmental disorder gene defects.

155 red to be VOUS to be new candidate genes for neurodevelopmental disorders (GIT1, MVB12B and PPP1R9A)

156 rotein, disrupt brain function and cause the neurodevelopmental disorder, Glut1 deficiency syndrome (

157 8 of the 13 individuals recruited here for a neurodevelopmental disorder have a germline de novo GNB1

158 Neurodevelopmental disorders have a strong genetic compo

159 Because neurodegenerative disease and other neurodevelopmental disorders have been linked to oxidati

160 urther evidence that several psychiatric and neurodevelopmental disorders have common risk factors.

161 de novo mutations in >7,000 individuals with neurodevelopmental disorders highlighted mutations in PP

162 argeted sequencing of 5,223 individuals with neurodevelopmental disorders (ID primarily) or by target

163 Schizophrenia (SZ) is a neurodevelopmental disorder in which the emergence of co

164 Rett syndrome (RTT) is an X-linked neurodevelopmental disorder in which the MECP2 (methyl C

165 to behavioural abnormalities associated with neurodevelopmental disorders in both primate and rodent

166 sis and interventions characterize childhood neurodevelopmental disorders in Sub-Saharan Africa.

167 tion during pregnancy with increased risk of neurodevelopmental disorders in the offspring are poorly

168 o induce TH17 cells may increase the risk of neurodevelopmental disorders in the offspring of pregnan

169 ion and is associated with increased risk of neurodevelopmental disorders in the offspring.

170 egnancy serves as a risk factor for multiple neurodevelopmental disorders including autism spectrum d

171 sts that common pathways are altered in many neurodevelopmental disorders including autism spectrum d

172 Candidate risk genes for neurodevelopmental disorders including primary microceph

173 PRS) is considered a risk factor for several neurodevelopmental disorders including schizophrenia (SZ

174 evelopment has been implicated in a range of neurodevelopmental disorders including tuberous sclerosi

175 study compliments the emerging concept that neurodevelopmental disorders (including autism, epilepsy

176 isplayed phenotypes consistent with a severe neurodevelopmental disorder, including sudden unexplaine

177 te receptor 5 (mGlu5) has been implicated in neurodevelopmental disorders, including a genetic cause

178 ne abnormalities have been reported for many neurodevelopmental disorders, including Angelman syndrom

179 ent kinase-like 5) is mutated in many severe neurodevelopmental disorders, including atypical Rett sy

180 Neurodevelopmental disorders, including autism spectrum

181 (CNVs) have been implicated in a variety of neurodevelopmental disorders, including autism spectrum

182 y has been associated with increased risk of neurodevelopmental disorders, including autism spectrum

183 y complications that predispose offspring to neurodevelopmental disorders, including autism, attentio

184 cognitive performance and increased risk of neurodevelopmental disorders, including cerebral palsy.

185 n the impact of a genetic lesion linked with neurodevelopmental disorders, including mechanisms of ma

186 d8(+/del5) mice across pathways disrupted in neurodevelopmental disorders, including neurogenesis, sy

187 regnancy predisposes offspring to sex-biased neurodevelopmental disorders, including schizophrenia, a

188 that LoF variants in SETD1A cause a range of neurodevelopmental disorders, including schizophrenia.

189 products implicated in neurodegeneration and neurodevelopmental disorders, including subunits of the

190 A proposed common cause of neurodevelopmental disorders is an imbalance in excitato

191 tellectual disability and in the etiology of neurodevelopmental disorders is increasingly recognized.

192 tic approach in consanguineous families with neurodevelopmental disorders is recommended.

193 fect of virtual corpus callosotomies and the neurodevelopmental disorder itself.

194 ations in the synaptic gene SHANK3 lead to a neurodevelopmental disorder known as Phelan-McDermid syn

195 APK) pathway causes pathology in a family of neurodevelopmental disorders known as 'RASopathies' and

196 ardiovascular disease, and ageing as well as neurodevelopmental disorders like autism.

197 ficantly associated with genes implicated in neurodevelopmental disorders, like autism spectrum disor

198 mechanism of LIS1 haploinsufficiency in the neurodevelopmental disorder lissencephaly.

199 ental Services, the Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, and refer

200 e a common feature in Rett syndrome (RTT), a neurodevelopmental disorder most often caused by mutatio

201 Angelman syndrome (AS) is a genetic neurodevelopmental disorder, most commonly caused by del

202 ilepsies are often a consequence of numerous neurodevelopmental disorders, most of which are proving

203 s correlated with total number of additional neurodevelopmental disorders (multimorbidity) in childho

204 Neurodevelopmental disorders (NDDs) (attention deficit h

205 de novo missense mutations in patients with neurodevelopmental disorders (NDDs) and highlight 35 gen

206 ople with autism spectrum disorder and other neurodevelopmental disorders (NDDs) are behaviorally and

207 d/or sign as potential communicative acts in neurodevelopmental disorders (NDDs), are research questi

208 ptive mutations contribute to the biology of neurodevelopmental disorders (NDDs), but most of the rel

209 Altered dendritic morphology is common in neurodevelopmental disorders (NDDs), many of which show

210 opment and plasticity are implicated in many neurodevelopmental disorders (NDDs).

211 cing focused on congenital heart disease and neurodevelopmental disorders (NDDs).

212 lead to epilepsy and are also implicated in neurodevelopmental disorders, neuropathic pain, and schi

213 Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder of unknown etiology, but ver

214 eimer's disease (AD)-related proteins in the neurodevelopmental disorders of FXS and autism.

215 Neurodevelopmental disorders offer a window to addressin

216 Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder often accompanied by intelle

217 eins, many of which are either implicated in neurodevelopmental disorders or are of unknown function.

218 (ADHD) - prevalent and often highly comorbid neurodevelopmental disorders - others have not different

219 that is strongly associated with the risk of neurodevelopmental disorders, particularly autism and at

220 ing neural and behavioral dysfunction across neurodevelopmental disorders, particularly autism spectr

221 s associated with the DMSs were enriched for neurodevelopmental disorders, particularly for CpG sites

222 tions of microcephalin (MCPH1) can cause the neurodevelopmental disorder primary microcephaly type 1.

223 easing recognition of gene dosage effects in neurodevelopmental disorders prompted us to develop a co

224 trongly implicated in the pathophysiology of neurodevelopmental disorders, raising the question of wh

225 However, human neurodevelopmental disorders related to EBF3 have not be

226 ne regulation in human brain development and neurodevelopmental disorders remains mostly uncharacteri

227 Mutations in the MECP2 gene cause the neurodevelopmental disorder Rett syndrome (RTT).

228 Mutations in MECP2 cause the neurodevelopmental disorder Rett syndrome (RTT).

229 al regulator Mecp2 cause the severe X-linked neurodevelopmental disorder Rett syndrome (RTT).

230 The postnatal neurodevelopmental disorder Rett syndrome, caused by mut

231 cynomolgus monkeys serving as a model for a neurodevelopmental disorder, Rett syndrome (RTT), which

232 However, a subset, including neurodevelopmental disorders, Rett syndrome (RTT), fragi

233 ied in previously implicated high-confidence neurodevelopmental disorder risk genes, such as CHD2, CT

234 lopment and reveal a potential mechanism for neurodevelopmental disorder risk in pregnancies complica

235 icularly those with primary neurological and neurodevelopmental disorders, since coexisting sleep pro

236 e offspring, resulting in increased risk for neurodevelopmental disorders such as ADHD.

237 Neurodevelopmental disorders such as attention deficit h

238 ve and sensorimotor deficits associated with neurodevelopmental disorders such as autism and schizoph

239 tion of early emotional circuits may lead to neurodevelopmental disorders such as autism and schizoph

240 k3 is a postsynaptic protein associated with neurodevelopmental disorders such as autism and schizoph

241 of microglia contributes to the pathology of neurodevelopmental disorders such as autism spectrum dis

242 l as a key player in conditions ranging from neurodevelopmental disorders such as autism to neurodege

243 Numerous genes are associated with neurodevelopmental disorders such as intellectual disabi

244 Neurodevelopmental disorders such as intellectual disabi

245 g from hiPSCs, a cellular model for studying neurodevelopmental disorders such as schizophrenia (SZ).

246 development and when defective, the risk of neurodevelopmental disorders such as schizophrenia is in

247 nction and contribute to the pathogenesis of neurodevelopmental disorders such as schizophrenia.

248 ases, such as Alzheimer disease (AD), and in neurodevelopmental disorders, such as Angelman syndrome

249 in regulating gene networks dysregulated in neurodevelopmental disorders, such as autism or schizoph

250 on as a major contributor in psychiatric and neurodevelopmental disorders, such as cognitive impairme

251 They all increase risk for other neurodevelopmental disorders, such as developmental dela

252 These CNVs also increase the risk for other neurodevelopmental disorders, such as intellectual disab

253 examine how these processes are affected in neurodevelopmental disorders, such as Rett syndrome.

254 rain-specific microRNA, has been observed in neurodevelopmental disorders, such as schizophrenia (SCZ

255 opment, and are altered in several models of neurodevelopmental disorders, such as schizophrenia and

256 its in sensory systems are commonly noted in neurodevelopmental disorders, such as the Rett syndrome

257 Autism spectrum disorder (ASD) is a serious neurodevelopmental disorder that affects one in 45 child

258 Schizophrenia is a neurodevelopmental disorder that affects up to 1% of the

259 Fragile X syndrome (FXS) is a neurodevelopmental disorder that is a leading cause of i

260 Primary microcephaly is a neurodevelopmental disorder that is caused by a reductio

261 s system, we find that in Timothy syndrome-a neurodevelopmental disorder that is caused by mutations

262 are the main causes of Kleefstra syndrome, a neurodevelopmental disorder that is characterized by imp

263 widely acknowledged that schizophrenia is a neurodevelopmental disorder that likely affects the brai

264 Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder that presents with hypotonia

265 Rett syndrome (RS) is a neurodevelopmental disorder that shares many symptomatic

266 ining feature of autism spectrum disorder, a neurodevelopmental disorder that shows a strong male pre

267 hyperactivity disorder (ADHD) is a heritable neurodevelopmental disorder that shows clinical and gene

268 Autism spectrum disorder (ASD) is a common neurodevelopmental disorder that tends to co-occur with

269 lated Vici syndrome defines a novel group of neurodevelopmental disorders that should be considered i

270 While altered cIN development contributes to neurodevelopmental disorders, the inaccessibility of hum

271 nderstand the heterogeneity of ASD and other neurodevelopmental disorders, the relationship between q

272 obing a wide range of cellular phenotypes in neurodevelopmental disorders using patient-derived neura

273 rs of which are mutated in several monogenic neurodevelopmental disorders, was significantly enriched

274 From a cohort of >5,000 families affected by neurodevelopmental disorders, we identified six consangu

275 A receptor have already been associated with neurodevelopmental disorders, we suggest that pathogenic

276 at were not previously reported in regard to neurodevelopmental disorders were identified.

277 iously associated with brain development and neurodevelopmental disorders were prioritized highly wit

278 Neurodevelopmental disorders were the most frequent diag

279 onal morphology and synaptic changes seen in neurodevelopmental disorders, while alteration in astroc

280 Schizophrenia is a devastating neurodevelopmental disorder with a complex genetic etiol

281 Autism is a prevailing neurodevelopmental disorder with a large genetic/genomic

282 ctivity disorder (ADHD) is a childhood-onset neurodevelopmental disorder with a prevalence of 1.4-3.0

283 Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic basis.

284 chizophrenia is increasingly recognized as a neurodevelopmental disorder with altered connectivity am

285 RTT is a 'prototypical' neurodevelopmental disorder with many clinical features

286 ity disorder (ADHD) is a heritable, chronic, neurodevelopmental disorder with serious long-term reper

287 f maternal UBE3A causes Angelman syndrome, a neurodevelopmental disorder with some overlapping neurol

288 Autism spectrum disorder (ASD) is a neurodevelopmental disorder with unclear etiology and im

289 The study of monogenic, neurodevelopmental disorders with a high incidence of au

290 tism spectrum disorders (ASD) are a group of neurodevelopmental disorders with clinical heterogeneity

291 reatments for FASD and conceivably for other neurodevelopmental disorders with cognitive deficits.

292 utical agents, and can be adapted for use in neurodevelopmental disorders with genetic etiologies.

293 spectrum disorder (ASD) describes a group of neurodevelopmental disorders with high heritability, alt

294 m disorder (ASD) represents a set of complex neurodevelopmental disorders with large degrees of herit

295 this domain and the C-terminal likely cause neurodevelopmental disorders with or without seizures.

296 Neurodevelopmental disorders with periventricular nodula

297 hrenia (SCZ) - a heterogeneous collection of neurodevelopmental disorders with unclear pathophysiolog

298 m disorder (ASD) is a heterogeneous group of neurodevelopmental disorders without any defined uniting

299 ntaining 1 (HUWE1) E3 ubiquitin ligase cause neurodevelopmental disorder X-linked intellectual disabi

300 rmal Ras signaling as a major contributor in neurodevelopmental disorders, yet how such signaling cau