deletion
Terms related to the query
Term Similarity Weight in brain map N In query
fusiform
0.003037829940496871
1.0
4278 In expansion
white matter
0.005977855749593193
0.9777996487712902
4236 In expansion
matter
0.005087156983108484
0.7425682035308091
6324 In expansion
brainstem
0.002596564446727745
0.7321645401610339
1502 In expansion
white
0.004727606319626989
0.5918351564399792
6774 In expansion
amygdala
0.001866418128334104
0.570858741385999
4540 In expansion
parietal
0.001315859987053389
0.5599959602165686
10159 In expansion
thalamus
0.0013387318373269974
0.43501470014147076
4891 In expansion
default
0.003018300140048561
0.4090985254179039
3687 In expansion
face
0.0018161717432615013
0.4050751527638795
4405 In expansion
frontal
0.0025697699938863564
0.3604924345963825
11471 In expansion
motor
0.0011066835020909372
0.35395382784968776
7928 In expansion
fusiform gyrus
0.0019212655500148322
0.3137665448737798
3445 In expansion
default mode
0.003597324560733168
0.30042915765838984
2555 In expansion
cingulate
0.0009890366437346914
0.2880282091319752
9501 In expansion
prefrontal
0.0013136058092857786
0.2603808538296953
10017 In expansion
working
0.0022334100949000873
0.1960651092648859
5201 In expansion
left
0.001865326993219185
0.19551063291794954
12782 In expansion
temporal
0.0007735118560158013
0.16918113588807945
11897 In expansion
occipital
0.0005628979041472382
0.16221655539798158
6796 In expansion
callosum
0.0033774133249965537
0.15823235579030093
895 In expansion
visual
0.0004813075363515908
0.15210163300827598
10448 In expansion
motion
0.0005438883864935827
0.14232094512521865
9061 In expansion
corpus
0.003182823193607312
0.1263530954167284
1153 In expansion
working memory
0.0024616085931455233
0.1173254068587943
4424 In expansion
precuneus
0.0004776075000623794
0.11567942252983453
5186 In expansion
fa
0.0005092470804702118
0.10006339271481222
1796 In expansion
parahippocampal
0.0005212931681947741
0.09992013646670564
3512 In expansion
insula
0.0002323454760315843
0.09695180882458418
7050 In expansion
inferior
0.0010549059050571784
0.09472592239384729
10215 In expansion
memory
0.0020788805446979
0.07983961142514952
8405 In expansion
superior
0.0008017081876381296
0.07514372742224219
9978 In expansion
ffa
0.0005325703637807183
0.07462927316909436
407 In expansion
corpus callosum
0.0032048219834894497
0.06387781686193322
740 In expansion
auditory
0.00016176923830842259
0.06203886384683543
4009 In expansion
task
0.0008407764910133713
0.057017278592513626
12194 In expansion
stg
0.0005302901734747939
0.0547889298376967
1459 In expansion
dlpfc
0.00047927799829949874
0.05475606212676851
2726 In expansion
cerebellum
0.00014262661946085623
0.054169500336346946
5578 In expansion
putamen
0.00036396887252957983
0.04328462168387766
3208 In expansion
patient
0.004260683582316846
0.0
7859 In expansion
psychosis
0.014520778148432485
0.0
833 In expansion
psychotic
0.00477564622942325
0.0
1078 In expansion
mental fatigue
0.004521706962356044
0.0
36 In expansion
tourette
0.02882347623520314
0.0
135 In expansion
tourette syndrome
0.025969283013740838
0.0
116 In expansion
tic
0.01051340827537723
0.0
77 In expansion
tics
0.01220946847355522
0.0
57 In expansion
symptom
0.007768382446115494
0.0
4491 In expansion
syndrome
0.0743901318902018
0.0
2020 In expansion
visceral
0.004370937781113479
0.0
508 In expansion
x
0.004463900450387674
0.0
5864 In expansion
turner
0.00742162475929892
0.0
93 In expansion
schizophrenia
0.023654778851244996
0.0
2513 In expansion
severity
0.004482294948657489
0.0
2888 In expansion
sibling
0.006558224697140207
0.0
273 In expansion
cognitive
0.013169379961476789
0.0
11288 In expansion
chronic fatigue syndrome
0.005837982836769993
0.0
41 In expansion
chromosome
0.005329299259249227
0.0
154 In expansion
children
0.027041310485962953
0.0
2616 In expansion
deletion
1.0
0.0
146 In query
deficit
0.0043300741846092105
0.0
5820 In expansion
disorder
0.004411369999203083
0.0
8378 In expansion
developmental dyslexia
0.005708028121452146
0.0
113 In expansion
control
0.0050001266168293226
0.0
12606 In expansion
abnormal
0.007194054512843743
0.0
4726 In expansion
brain
0.0046021607309732725
0.0
13395 In expansion
irritable
0.00757220921157276
0.0
135 In expansion
ds
0.00440498465383844
0.0
112 In expansion
dyslexia
0.027135836395722653
0.0
346 In expansion
fragile
0.005220529024875833
0.0
139 In expansion
group
0.008369495073410557
0.0
12268 In expansion
gender
0.006065968070340871
0.0
4280 In expansion
gene
0.004553944667155482
0.0
899 In expansion
fatigue
0.021739027703536733
0.0
687 In expansion
facial
0.0075719339773696525
0.0
2184 In expansion
facial expression
0.004335975273407481
0.0
1402 In expansion
Predicted distribution of activations in the literature
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Publications related to the query
Copy number deletion burden is associated with cognitive, structural, and resting-state network differences in patients with schizophrenia
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
Impaired Activation of Face Processing Networks Revealed by Functional Magnetic Resonance Imaging in 22q11.2 Deletion Syndrome
Atypical functional connectivity in resting-state networks of individuals with 22q11.2 deletion syndrome: associations with neurocognitive and psychiatric functioning
Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study
From the Cover: A genetic variation of the noradrenergic system is related to differential amygdala activation during encoding of emotional memories
An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome
The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)
Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome
Genetic Subtype Differences in Neural Circuitry of Food Motivation in Prader-Willi Syndrome
Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
The effects of gender and Catechol O-Methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in Velo-Cardio-Facial Syndrome (22q11.2 Deletion Syndrome): a fMRI study
Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome
Neural Substrates of Inhibitory Control Deficits in 22q11.2 Deletion Syndrome
Disrupted working memory circuitry and psychotic symptoms in 22q11.2 deletion syndrome
Resting-state networks in adolescents with 22q11.2 deletion syndrome: Associations with prodromal symptoms and executive functions
Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study
White matter abnormalities in adults with 22q11 deletion syndrome with and without schizophrenia
Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome
The D-allele of ACE insertion/deletion polymorphism is associated with regional white matter volume changes and cognitive impairment in remitted geriatric depression
The DCDC2/intron 2 deletion and white matter disorganization: Focus on developmental dyslexia
Neural mechanisms of response inhibition and impulsivity in 22q11.2 deletion carriers and idiopathic attention deficit hyperactivity disorder
Brain activation during executive processes in schizophrenia
Neural correlates of task switching in paternal 15q11–q13 deletion Prader–Willi syndrome
Cognitive and structural neuroimaging characteristics of schizophrenia patients with large, rare copy number deletions
Reduced Cortical Complexity in Children with Prader-Willi Syndrome and Its Association with Cognitive Impairment and Developmental Delay
Pattern of Increased Cerebral FDG Uptake in Down Syndrome Patients
Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content
Violence: heightened brain attentional network response is selectively muted in Down syndrome