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

1 phenotypically and genetically heterogeneous neurodevelopmental disorder.

2 eterious CDK19 variants underlie a syndromic neurodevelopmental disorder.

3 velopmental syndrome, termed syt1-associated neurodevelopmental disorder.

4 in neonatal populations at increased risk of neurodevelopmental disorder.

5 ntial treatment approach for syt1-associated neurodevelopmental disorder.

6 provide clues to the pathophysiology of this neurodevelopmental disorder.

7 it has not previously been associated with a neurodevelopmental disorder.

8 ed that insufficiency of DLL1 causes a human neurodevelopmental disorder.

9 r association to Rett Syndrome (RTT), a rare neurodevelopmental disorder.

10 CDH2 has not yet been linked to a Mendelian neurodevelopmental disorder.

11 usination of eIF5A and are associated with a neurodevelopmental disorder.

12 nting, causes Angelman syndrome (AS), a rare neurodevelopmental disorder.

13 disruptions of this gene in a characteristic neurodevelopmental disorder.

14 ions for the diagnosis and treatment of this neurodevelopmental disorder.

15 critical role in the pathogenicity of human neurodevelopmental disorder.

16 disease-modifying treatment for a syndromic neurodevelopmental disorder.

17 Schizophrenia (SCZ) is a neurodevelopmental disorder.

18 s besides cancer, including lung, renal, and neurodevelopmental disorders.

19 ons toward understanding the pathogenesis of neurodevelopmental disorders.

20 including benign and malignant neoplasia and neurodevelopmental disorders.

21 g these genes in COS as well as in pediatric neurodevelopmental disorders.

22 cardiac anomalies, limb dysmorphologies and neurodevelopmental disorders.

23 PTCHD1-AS in genetic risk for ASD and other neurodevelopmental disorders.

24 synaptic pruning is associated with several neurodevelopmental disorders.

25 nvolved in proteostasis is a common cause of neurodevelopmental disorders.

26 nervous system causing neurodegeneration to neurodevelopmental disorders.

27 over-representation of left-handers in some neurodevelopmental disorders.

28 er called "transcriptome reversal" for these neurodevelopmental disorders.

29 tated in many patients with autism and other neurodevelopmental disorders.

30 nts affected genes which are associated with neurodevelopmental disorders.

31 al period, features that may be disrupted in neurodevelopmental disorders.

32 SR leads to maternal inflammation-associated neurodevelopmental disorders.

33 underlie aberrant sensory processing in some neurodevelopmental disorders.

34 periods, is hypothesized to be disrupted in neurodevelopmental disorders.

35 on of this regulatory pathway contributes to neurodevelopmental disorders.

36 represent a contributing factor in multiple neurodevelopmental disorders.

37 ine the origin of abnormal gamma activity in neurodevelopmental disorders.

38 on channel family are linked to epilepsy and neurodevelopmental disorders.

39 of de novo mutations associated with complex neurodevelopmental disorders.

40 ears of age is important in the detection of neurodevelopmental disorders.

41 or overlapped with genes identified in other neurodevelopmental disorders.

42 opicalis as a model system for understanding neurodevelopmental disorders.

43 s the mechanism underlying GABRB2-associated neurodevelopmental disorders.

44 MECP2 is involved in two severe and complex neurodevelopmental disorders.

45 ants (CNVs) have a higher risk of developing neurodevelopmental disorders.

46 ic etiologies of ASD and, more generally, of neurodevelopmental disorders.

47 be more pronounced in patients with comorbid neurodevelopmental disorders.

48 ed biphenyls (PCBs) has been associated with neurodevelopmental disorders.

49 promotes social behavior in mouse models of neurodevelopmental disorders.

50 d an association between prenatal stress and neurodevelopmental disorders.

51 vo mutations in SLC12A2 in six children with neurodevelopmental disorders.

52 cidence of a large number of psychiatric and neurodevelopmental disorders.

53 neural networks and circuit abnormalities in neurodevelopmental disorders.

54 ved in synaptic function and the etiology of neurodevelopmental disorders.

55 health related adverse events in people with neurodevelopmental disorders.

56 f mature neurons will help better understand neurodevelopmental disorders.

57 pathogenic variants in NSUN2 being linked to neurodevelopmental disorders.

58 t are known to harbor syndromic mutations in neurodevelopmental disorders.

59 rug targets for malignancies, autoimmune and neurodevelopmental disorders.

60 or schizophrenia, epilepsy, and other common neurodevelopmental disorders.

61 including autism spectrum disorder and other neurodevelopmental disorders.

62 unomodulation, irritable bowel syndrome, and neurodevelopmental disorders.

63 nd enhancers involved in NSC maintenance and neurodevelopmental disorders.

64 CBLH and DWM are often features of monogenic neurodevelopmental disorders.

65 dies in mouse models of neuropsychiatric and neurodevelopmental disorders.

66 erstanding may help us design treatments for neurodevelopmental disorders.

67 rformed exome sequencing in individuals with neurodevelopmental disorders.

68 oxidative stress as a therapeutic target in neurodevelopmental disorders.

69 eptor subunits have been found in a range of neurodevelopmental disorders.

70 uch, mutations in either protein can lead to neurodevelopmental disorders.

71 tasks, even though these are very different neurodevelopmental disorders.

72 mutations had been associated with syndromic neurodevelopmental disorders.

73 nesis whose orthologs include risk genes for neurodevelopmental disorders.

74 n social dynamics and is impaired in several neurodevelopmental disorders.

75 ield a broad range of behavioral deficits in neurodevelopmental disorders.

76 tial opportunities for precision medicine in neurodevelopmental disorders.

77 em a potential key point of vulnerability in neurodevelopmental disorders.

78 ranscriptional dysregulation in co-occurring neurodevelopmental disorders.

79 these behaviors in many neuropsychiatric and neurodevelopmental disorders.

80 ure to endocrine disruptors and incidence of neurodevelopmental disorders.

81 n histone-modifying enzymes may cause severe neurodevelopmental disorders.

82 hypofunction has been implicated in several neurodevelopmental disorders.

83 o determine the genetic aetiology underlying neurodevelopmental disorders.

84 tic capacity are known to cause a variety of neurodevelopmental disorders.

85 y-based vaccine preservative and the risk of neurodevelopmental disorders; (3) vaccine-induced Guilla

86 eficit and sleep disturbance across multiple neurodevelopmental disorders(6-9).

87 gnancy are associated with increased risk of neurodevelopmental disorders, although the precise mecha

88 A2 de novo mutations as the cause of a novel neurodevelopmental disorder and bilateral non-syndromic

89 confirm that persistent ADHD in adults is a neurodevelopmental disorder and extend the existing hypo

90 dysfunction in Down ayndrome (trisomy 21), a neurodevelopmental disorder and form of early onset AD,

91 ted de novo variants from 6753 patients with neurodevelopmental disorders and 1911 unaffected sibling

92 ), a pro-inflammatory cytokine implicated in neurodevelopmental disorders and gestational disease.

93 Nevertheless, the etiology of these neurodevelopmental disorders and histamine's role in the

94 ive Pol III mutations have been described in neurodevelopmental disorders and hypersensitivity to vir

95 TOR pathway genes are linked to a variety of neurodevelopmental disorders and malformations of cortic

96 sm spectrum disorder (ASD) is a continuum of neurodevelopmental disorders and needs new therapeutic a

97 inked to synapse pathologies associated with neurodevelopmental disorders and neurodegenerative disea

98 omosomal locus are associated with syndromic neurodevelopmental disorders and reciprocal physiologica

99 It is a prevalent neurodevelopmental disorder, and available treatments of

100 Down syndrome (DS) is a common neurodevelopmental disorder, and cognitive defects in DS

101 hedding light on the genetic architecture of neurodevelopmental disorders, and new approaches are rev

102 bellum is a key brain region in a variety of neurodevelopmental disorders, and the adult cerebellum h

103 ose loss from the maternal allele causes the neurodevelopmental disorder Angelman syndrome (AS).

104 A large fraction of rare and severe neurodevelopmental disorders are caused by sporadic de n

105 Many neurodevelopmental disorders are characterized by impair

106 However, it is unclear how genetic risks for neurodevelopmental disorders are translated into spatial

107 This question is paramount for neurodevelopmental disorders arising from mutations that

108 These results suggest that neurodevelopmental disorders arising from NMDAR deficien

109 ses understanding of the complex etiology of neurodevelopmental disorders arising from rare missense

110 nces of 101 known de novo variant-associated neurodevelopmental disorders as well as 3106 putative mo

111 Fragile X syndrome is a neurodevelopmental disorder associated with a broad rang

112 e 22q11.2 deletion syndrome (22q11.2DS) is a neurodevelopmental disorder associated with a number of

113 riants in SCAF4 are causative for a variable neurodevelopmental disorder associated with impaired mRN

114 iants as the cause of a characteristic human neurodevelopmental disorder associated with mild facial

115 romatosis type 1 (NF1) is a common monogenic neurodevelopmental disorder associated with physical and

116 ne duplication in KIF21B in individuals with neurodevelopmental disorders associated with brain malfo

117 show that ankyrin-G interacts with Usp9X, a neurodevelopmental-disorder-associated deubiquitinase (D

118 The 41 variants impact 27 neurodevelopmental-disorder-associated genes, thus demon

119 the vast majority of these de novo monogenic neurodevelopmental disorders because of phenotypic heter

120 y has been implicated in the pathogenesis of neurodevelopmental disorders but its contribution to syn

121 ASD is considered to be a heritable neurodevelopmental disorder, but there is limited unders

122 only associated with schizophrenia and other neurodevelopmental disorders, but are also a contributin

123 co-striatal assembloids from patients with a neurodevelopmental disorder caused by a deletion on chro

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

125 Dyslexia is a common neurodevelopmental disorder caused by a significant gene

126 Together, this study defines a neurodevelopmental disorder caused by dominant de novo L

127 Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by either disruptions

128 Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by epigenetic silenci

129 Rett syndrome is an incurable neurodevelopmental disorder caused by mutations in the g

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

131 dependent kinase-like 5 disorder is a severe neurodevelopmental disorder caused by mutations in the X

132 Tuberous Sclerosis Complex (TSC) is a neurodevelopmental disorder caused by mutations in TSC1

133 Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations or delet

134 Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of functi

135 ortical neuroimaging data from patients with neurodevelopmental disorders caused by genomic copy numb

136 it/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder characterized by age-inappro

137 2 in unrelated individuals presenting with a neurodevelopmental disorder characterized by axial hypot

138 Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by glia over-p

139 in CDH2 in nine individuals with a syndromic neurodevelopmental disorder characterized by global deve

140 Autism is a clinically heterogeneous neurodevelopmental disorder characterized by impaired so

141 Loss-of-function SYNGAP1 mutations cause a neurodevelopmental disorder characterized by intellectua

142 ocerebrofacial syndrome (KOS) is a recessive neurodevelopmental disorder characterized by intellectua

143 Angelman syndrome (AS) is a neurodevelopmental disorder characterized by intellectua

144 ift variants in NOVA2 affected with a severe neurodevelopmental disorder characterized by intellectua

145 Affected individuals demonstrated a variable neurodevelopmental disorder characterized by mild intell

146 reminiscent of human ocular motor apraxia, a neurodevelopmental disorder characterized by reduced sac

147 Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by social comm

148 s complex (TSC) is a rare autosomal dominant neurodevelopmental disorder characterized by variable ex

149 ls from six unrelated families, exhibiting a neurodevelopmental disorder characterized with a spectru

150 tual disability disorders (SSRIDDs) are rare neurodevelopmental disorders characterized by developmen

151 ne xeroderma pigmentosum (XP-G) or the fatal neurodevelopmental disorder Cockayne syndrome (XP-G/CS).

152 S signaling pathway components cause diverse neurodevelopmental disorders, collectively called RASopa

153 Tourette syndrome is a neurodevelopmental disorder commonly associated with inv

154 sus NRT for smoking cessation in people with neurodevelopmental disorders, compared to those without,

155 how that de-novo variants in GRIA2 can cause neurodevelopmental disorders, complementing evidence tha

156 ndividuals present with shared features of a neurodevelopmental disorder consisting of global develop

157 functionality, suggesting that PP2A-related neurodevelopmental disorders constitute functionally con

158 ss-of-function variants in this gene cause a neurodevelopmental disorder defined by cognitive impairm

159 of Dravet syndrome (Scn1a+/- mice)-a severe neurodevelopmental disorder defined by temperature-sensi

160 less likely to be prescribed to people with neurodevelopmental disorders despite results suggesting

161 Angelman Syndrome (AS) is a severe neurodevelopmental disorder due to impaired expression o

162 Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder due to pathogenic mutations

163 Individuals with psychiatric and neurodevelopmental disorders exhibited a higher prevalen

164 is in the initial indication of amblyopia, a neurodevelopmental disorder for which available treatmen

165 t of the chapter on mental, behavioural, and neurodevelopmental disorders for ICD-11.

166 and therefore represents a strong candidate neurodevelopmental disorder gene.

167 ng LoF or deletion DNVs in LoF-intolerant or neurodevelopmental disorder genes had significantly less

168 Within these neurodevelopmental disorder genes, SLC6A1, which encodes

169 te cerebral palsy risk genes overlapped with neurodevelopmental disorder genes.

170 with adults with CP alone, those with CP and neurodevelopmental disorders had similar or higher age-s

171 genomic variants in schizophrenia and other neurodevelopmental disorders has so far not yielded ther

172 Neurodevelopmental disorders have a heritable component

173 A variety of syndromic and non-syndromic neurodevelopmental disorders have been connected to alte

174 tation being the primary cause of the severe neurodevelopmental disorder in carriers.

175 t variants in CAPZA2 lead to a non-syndromic neurodevelopmental disorder in children.

176 pectrum Disorder (ASD) is the most prevalent neurodevelopmental disorder in the United States and oft

177 Angelman syndrome (AS) is a neurodevelopmental disorder in which epilepsy is common

178 Some of them were candidates for neurodevelopmental disorders in humans including Nrg3, N

179 enicity of 44 USP9X variants associated with neurodevelopmental disorders in males.

180 mmation during pregnancy are associated with neurodevelopmental disorders in offspring, but little is

181 We compared an environmental model of neurodevelopmental disorders in which mice were exposed

182 pport a neuroimmune mechanism that underlies neurodevelopmental disorders in which the production of

183 ife may be associated with increased risk of neurodevelopmental disorders including ASD.

184 measuring imitative deficits in the study of neurodevelopmental disorders including FXS.

185 Males are more susceptible to neurodevelopmental disorders including intellectual disa

186 STXBP1 are among the most frequent causes of neurodevelopmental disorders including intellectual disa

187 tion factor eEF1A2, have been shown to cause neurodevelopmental disorders including often severe epil

188 twork connectivity, which has been linked to neurodevelopmental disorders, including autism spectrum

189 ion of interneurons is implicated in several neurodevelopmental disorders, including autism spectrum

190 Neurodevelopmental disorders, including autism spectrum

191 Models of neurodevelopmental disorders, including autism spectrum

192 genetic locus are associated with a range of neurodevelopmental disorders, including autism spectrum

193 ild speech and language delay to intractable neurodevelopmental disorders, including but not limited

194 gene encoding ankyrin-G are associated with neurodevelopmental disorders, including intellectual dis

195 ss are implicated in the etiology of complex neurodevelopmental disorders, including schizophrenia, a

196 It has also been implicated in several neurodevelopmental disorders, including schizophrenia.

197 r and among de novo variants associated with neurodevelopmental disorders, including schizophrenia.

198 ion areas may underlie cognitive deficits in neurodevelopmental disorders, including the 22q11.2 dele

199 xperiments are critical because a variety of neurodevelopmental disorders, including those characteri

200 ATEMENT Down syndrome (trisomy 21) (DS) is a neurodevelopmental disorder invariably leading to early-

201 enes DDX3X and DHX30 in an emerging class of neurodevelopmental disorders involving RNA helicases.

202 PPP2R5D-related neurodevelopmental disorder is characterized by a range

203 The prevalence of neurodevelopmental disorders is biased toward male indiv

204 tudy of sexual dimorphism in psychiatric and neurodevelopmental disorders is challenging due to the c

205 of microglia in the onset and progression of neurodevelopmental disorders is less clear.

206 at DAPLE, a non-GPCR protein linked to human neurodevelopmental disorders, is expressed specifically

207 Sensorimotor deficits are prevalent in many neurodevelopmental disorders like autism, including one

208 5, which is associated with a higher rate of neurodevelopmental disorders like microcephaly, induced

209 iatal pathway and may shed novel insights on neurodevelopmental disorders linked to the corticostriat

210 the ARF activator Efa6 in C. elegans, and by neurodevelopmental disorders linked to the mammalian kin

211 y-use critical period.SIGNIFICANCE STATEMENT Neurodevelopmental disorders manifest symptoms at specif

212 In the full dataset, genes associated with neurodevelopmental disorders (n = 159) were significantl

213 abits are risk factors for the occurrence of neurodevelopmental disorders (NDD).

214 Neurodevelopmental disorders (NDDs) are clinically and g

215 ctivity disorder (ADHD), the entire range of neurodevelopmental disorders (NDDs) has not yet been wel

216 A disproportional large number of neurodevelopmental disorders (NDDs) is caused by variant

217 ediated decay (NMD) has been associated with neurodevelopmental disorders (NDDs) such as autism spect

218 self during childhood, belongs to a group of neurodevelopmental disorders (NDDs) that are clinically

219 KCNB1 variants associated with DEE or other neurodevelopmental disorders (NDDs) to rapidly ascertain

220 ns of the X-chromosome gene UPF3B cause male neurodevelopmental disorders (NDDs) via largely unknown

221 Most genes associated with neurodevelopmental disorders (NDDs) were identified with

222 arge number of genes have been implicated in neurodevelopmental disorders (NDDs), but their contribut

223 iated with increased risk of psychiatric and neurodevelopmental disorders (NDDs).

224 re clinically and biologically heterogeneous neurodevelopmental disorders (NDDs).

225 ses (HMTs) are major contributing factors in neurodevelopmental disorders (NDDs).

226 e SWI/SNF chromatin remodeling complex cause neurodevelopmental disorders (NDDs).

227 elated phenotypes into a broader category of neurodevelopmental disorders (NDDs).

228 syndrome is widely regarded as an archetypal neurodevelopmental disorder of central, motor control.

229 mented and cost-effective screening tool for neurodevelopmental disorders, particularly in cases when

230 ts in OCD are enriched for those reported in neurodevelopmental disorders, particularly Tourette's di

231 set of the data from the Province of Ontario Neurodevelopmental Disorder (POND) Network was used incl

232 Neurodevelopmental disorders present with synaptic alter

233 Rett syndrome (RTT) is a neurodevelopmental disorder primarily caused by mutation

234 ylating enzyme that has been associated with neurodevelopmental disorders primarily in female subject

235 rsely, increased lactate was associated with neurodevelopmental disorders regardless of genotype (p =

236 n contrast, the involvement of USP9X in male neurodevelopmental disorders remains tentative.

237 Rett Syndrome is a devastating neurodevelopmental disorder resulting from mutations in

238 nsight into the possible etiology underlying neurodevelopmental disorders resulting from histamine dy

239 is question and to provide a novel model for neurodevelopmental disorders resulting from mutations in

240 The neurodevelopmental disorder Rett syndrome is caused by m

241 ions in the MECP2 gene cause the progressive neurodevelopmental disorder Rett syndrome(3-5), which is

242 eural cultures lacking MECP2, a model of the neurodevelopmental disorder Rett syndrome, with exosomes

243 epressor protein MeCP2 cause the devastating neurodevelopmental disorder Rett syndrome.

244 or behaviour, it is not surprising that most neurodevelopmental disorders share motor deficits as a c

245 Pathogenic deletions implicated in neurodevelopmental disorders show significantly more ext

246 nding the neural basis of autism and related neurodevelopmental disorders.SIGNIFICANCE STATEMENT The

247 ng health issues, such as epilepsy and other neurodevelopmental disorders, sleep problems, and mental

248 especially when the fetus is known to have a neurodevelopmental disorder such as trisomy.

249 DSM-5 childhood neurodevelopmental disorders such as ADHD, typically ons

250 Dysregulated arousal often accompanies neurodevelopmental disorders such as attention deficit h

251 uitry, and its disruption has been linked to neurodevelopmental disorders such as autism and schizoph

252 s) is linked to increased risk for offspring neurodevelopmental disorders such as autism spectrum dis

253 ious benign and malignant tumors, as well as neurodevelopmental disorders such as autism spectrum dis

254 We ask how this framework can be applied to neurodevelopmental disorders such as autism spectrum dis

255 hether impaired transport is associated with neurodevelopmental disorders such as autism.

256 vity is a common and debilitating feature of neurodevelopmental disorders such as Fragile X Syndrome

257 tor of chromatin topology recently linked to neurodevelopmental disorders such as intellectual disabi

258 sal ganglia disorders, including early-onset neurodevelopmental disorders such as obsessive-compulsiv

259 ynapses, and its disruption is implicated in neurodevelopmental disorders such as Phelan-McDermid syn

260 The etiology of major neurodevelopmental disorders such as schizophrenia and a

261 as been linked to complex disease, including neurodevelopmental disorders such as schizophrenia and a

262 the Kanizsa illusory contours is impaired in neurodevelopmental disorders such as schizophrenia, auti

263 functions, especially in working memory and neurodevelopmental disorders such as schizophrenia.

264 lity in humans and have been linked to other neurodevelopmental disorders, such as autism spectrum di

265 behaviors and its dysregulation is linked to neurodevelopmental disorders, such as autism spectrum di

266 l (CBD) as a treatment for mental health and neurodevelopmental disorders, such as autism spectrum di

267 omposition and function modulate the risk of neurodevelopmental disorders, such as schizophrenia.

268 spectrum disorder (ASD) is a multifactorial neurodevelopmental disorder that encompasses a complex a

269 n-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder that is consistently associa

270 nia is still unknown, it is accepted to be a neurodevelopmental disorder that results from the intera

271 sessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur.

272 ironmental insults causes a constellation of neurodevelopmental disorders that manifest as intellectu

273 ormations of cortical development (MCDs) are neurodevelopmental disorders that result from abnormal d

274 grammed microglia or their products in human neurodevelopmental disorders that share this neuropathol

275 l dysphagia-is often associated with several neurodevelopmental disorders that subsequently alter com

276 and penetrant microdeletion associated with neurodevelopmental disorders, the 22q11.2 microdeletion

277 velopment, and the role of EphB receptors in neurodevelopmental disorders, these findings establish a

278 Neurodegenerative and neurodevelopmental disorders, trauma, stroke, and brain

279 campal CA1, using a mouse model of the human neurodevelopmental disorder Type I Lissencephaly.

280 atric comorbidities in adults with these two neurodevelopmental disorders using population-based data

281 (DNMs) are significant risk factors in many neurodevelopmental disorders, whereas schizophrenia (SCZ

282 , as its loss leads to fragile X syndrome, a neurodevelopmental disorder which is the most prevalent

283 variant burden of NCKAP1 in individuals with neurodevelopmental disorders which needs further replica

284 ities to model and test therapies for severe neurodevelopmental disorders, while revealing significan

285 rder (ADHD) is a common and highly heritable neurodevelopmental disorder with a complex pathophysiolo

286 vity disorder (ADHD) is a severely impairing neurodevelopmental disorder with a prevalence of 5% in c

287 Schizophrenia (SCZ) is a neurodevelopmental disorder with a progressive, prolonge

288 st evidence existed for its involvement in a neurodevelopmental disorder with dystonia.

289 de novo variants in MAPK8IP3 as a cause of a neurodevelopmental disorder with intellectual disability

290 Schizophrenia is a neurodevelopmental disorder with many genetic variants o

291 it/Hyperactivity Disorder (ADHD) is a common neurodevelopmental disorder with only symptomatic care a

292 nd female Dravet syndrome (Scn1a+/-) mice, a neurodevelopmental disorder with prominent temperature-s

293 dividuals with HVDAS, adding to the group of neurodevelopmental disorders with an epigenetic signatur

294 or oligodendrocyte and myelin dysfunction in neurodevelopmental disorders with cognitive symptoms.

295 pectrum disorder (ASD) is a constellation of neurodevelopmental disorders with high phenotypic and ge

296 ging data and the male prevalence in various neurodevelopmental disorders with inhibitory dysfunction

297 rum Disorder (ASD) is one of the most common neurodevelopmental disorders with no drugs treating the

298 N2A, have been associated with a spectrum of neurodevelopmental disorders with prominent speech-relat

299 tism spectrum disorders (ASD) are a group of neurodevelopmental disorders with symptoms including soc

300 genes encoding synaptic proteins cause many neurodevelopmental disorders, with the majority affectin