-
2
-
-
84856239145
-
Diagnostic evaluation of autism spectrum disorders
-
PID: 22284796
-
Huerta M, Lord C. Diagnostic evaluation of autism spectrum disorders. Pediatr Clin North Am 2012;59:103–111.
-
(2012)
Pediatr Clin North Am
, vol.59
, pp. 103-111
-
-
Huerta, M.1
Lord, C.2
-
3
-
-
84898828281
-
A comparison of DSM-IV pervasive developmental disorder and DSM-5 autism spectrum disorder prevalence in an epidemiologic sample
-
PID: 24745950
-
Kim YS, Fombonne E, Koh YJ, Kim SJ. A comparison of DSM-IV pervasive developmental disorder and DSM-5 autism spectrum disorder prevalence in an epidemiologic sample. J Am Acad Child Adolesc Psychiatry 2014;53:500–508.
-
(2014)
J Am Acad Child Adolesc Psychiatry
, vol.53
, pp. 500-508
-
-
Kim, Y.S.1
Fombonne, E.2
Koh, Y.J.3
Kim, S.J.4
-
4
-
-
84884338166
-
The genetic landscapes of autism spectrum disorders
-
COI: 1:CAS:528:DC%2BC3sXhslSmsrjK, PID: 23875794
-
Huguet G, Ey E, Bourgeron T. The genetic landscapes of autism spectrum disorders. Annu Rev Genomics Hum Genet 2013;14:191–213.
-
(2013)
Annu Rev Genomics Hum Genet
, vol.14
, pp. 191-213
-
-
Huguet, G.1
Ey, E.2
Bourgeron, T.3
-
5
-
-
84893844183
-
Disentangling the heterogeneity of autism spectrum disorder through genetic findings
-
PID: 24468882
-
Jeste SS, Geschwind DH. Disentangling the heterogeneity of autism spectrum disorder through genetic findings. Nat Rev Neurol 2014;10:74–81.
-
(2014)
Nat Rev Neurol
, vol.10
, pp. 74-81
-
-
Jeste, S.S.1
Geschwind, D.H.2
-
6
-
-
77953800799
-
Behavioural phenotyping assays for mouse models of autism
-
COI: 1:CAS:528:DC%2BC3cXns1Gis7k%3D, PID: 20559336
-
Silverman JL, Yang M, Lord C, Crawley JN. Behavioural phenotyping assays for mouse models of autism. Nat Rev Neurosci 2010;11:490–502.
-
(2010)
Nat Rev Neurosci
, vol.11
, pp. 490-502
-
-
Silverman, J.L.1
Yang, M.2
Lord, C.3
Crawley, J.N.4
-
7
-
-
84869213888
-
Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders
-
COI: 1:CAS:528:DC%2BC38XhsFCns7jP
-
Spooren W, Lindemann L, Ghosh A. Synapse dysfunction in autism: a molecular medicine approach to drug discovery in neurodevelopmental disorders. Trends Pharmacological Sci 2012;33:669–684.
-
(2012)
Trends Pharmacological Sci
, vol.33
, pp. 669-684
-
-
Spooren, W.1
Lindemann, L.2
Ghosh, A.3
-
8
-
-
13444250843
-
Designing mouse behavioral tasks relevant to autistic-like behaviors
-
Crawley JN. Designing mouse behavioral tasks relevant to autistic-like behaviors. Ment Retard Dev Disabil Res Rev 2005;10:248–258.
-
(2005)
Ment Retard Dev Disabil Res Rev
, vol.10
, pp. 248-258
-
-
Crawley, J.N.1
-
9
-
-
4644373224
-
Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice
-
COI: 1:STN:280:DC%2BD2cvjvFektQ%3D%3D, PID: 15344922
-
Moy SS, Nadler JJ, Perez A, Barbaro RP. Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice. Genes Brain Behav 2004;3:287–302.
-
(2004)
Genes Brain Behav
, vol.3
, pp. 287-302
-
-
Moy, S.S.1
Nadler, J.J.2
Perez, A.3
Barbaro, R.P.4
-
10
-
-
40349093351
-
Autism-like behavioral phenotypes in BTBR T + tf/J mice
-
COI: 1:CAS:528:DC%2BD1cXks1Sqtrk%3D, PID: 17559418
-
McFarlane HG, Kusek GK, Yang M, Phoenix JL, Bolivar VJ, Crawley JN. Autism-like behavioral phenotypes in BTBR T + tf/J mice. Genes Brain Behav 2008;7:152–163.
-
(2008)
Genes Brain Behav
, vol.7
, pp. 152-163
-
-
McFarlane, H.G.1
Kusek, G.K.2
Yang, M.3
Phoenix, J.L.4
Bolivar, V.J.5
Crawley, J.N.6
-
11
-
-
78751692683
-
Unusual repertoire of vocalizations in adult BTBR T + tf/J mice during three types of social encounters
-
COI: 1:STN:280:DC%2BC3M7isVWruw%3D%3D, PID: 20618443
-
Scattoni ML, Ricceri L, Crawley JN. Unusual repertoire of vocalizations in adult BTBR T + tf/J mice during three types of social encounters. Genes Brain Behav 2011;10:44–56.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 44-56
-
-
Scattoni, M.L.1
Ricceri, L.2
Crawley, J.N.3
-
12
-
-
78751697098
-
Reduced scent marking and ultrasonic vocalizations in the BTBR T + tf/J mouse model of autism
-
PID: 20345893
-
Wöhr M, Roullet FI, Crawley JN. Reduced scent marking and ultrasonic vocalizations in the BTBR T + tf/J mouse model of autism. Genes Brain Behav 2011;10:35–43.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 35-43
-
-
Wöhr, M.1
Roullet, F.I.2
Crawley, J.N.3
-
13
-
-
84255209293
-
Crawley JN. Automated three-chambered social approach task for mice. Curr Protoc Neurosci
-
Yang M, Silverman JL, Crawley JN. Automated three-chambered social approach task for mice. Curr Protoc Neurosci 2011;Chapter 8: Unit 8.26.
-
(2011)
Chapter 8: Unit
, vol.8
, pp. 26
-
-
Yang, M.1
Silverman, J.L.2
-
14
-
-
84875825504
-
Translational animal models of autism and neurodevelopmental disorders
-
PID: 23226954
-
Crawley JN. Translational animal models of autism and neurodevelopmental disorders. Dialogues Clin Neurosci 2012;14:293–305.
-
(2012)
Dialogues Clin Neurosci
, vol.14
, pp. 293-305
-
-
Crawley, J.N.1
-
15
-
-
79955536349
-
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction
-
PID: 21423165
-
Peça J, Feliciano C, Ting JT, et al. Shank3 mutant mice display autistic-like behaviours and striatal dysfunction. Nature 2011;472:437–442.
-
(2011)
Nature
, vol.472
, pp. 437-442
-
-
Peça, J.1
Feliciano, C.2
Ting, J.T.3
-
16
-
-
84860678815
-
Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice
-
COI: 1:CAS:528:DC%2BC38XntFOqtr4%3D, PID: 22573675
-
Yang M, Bozdagi O, Scattoni ML, et al. Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice. J Neurosci 2012;32: 6525–6541.
-
(2012)
J Neurosci
, vol.32
, pp. 6525-6541
-
-
Yang, M.1
Bozdagi, O.2
Scattoni, M.L.3
-
17
-
-
80053540965
-
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
-
PID: 21962519
-
Peñagarikano O, Abrahams BS, Herman EI, et al. Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits. Cell 2011;147:235–246.
-
(2011)
Cell
, vol.147
, pp. 235-246
-
-
Peñagarikano, O.1
Abrahams, B.S.2
Herman, E.I.3
-
18
-
-
84902344967
-
Pten haploinsufficient mice show broad brain overgrowth but selective impairments in autism-relevant behavioral tests
-
COI: 1:CAS:528:DC%2BC2cXpvV2rtrg%3D, PID: 24497577
-
Clipperton-Allen AE, Page DT. Pten haploinsufficient mice show broad brain overgrowth but selective impairments in autism-relevant behavioral tests. Hum Mol Genet 2014;23:3490–3505.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 3490-3505
-
-
Clipperton-Allen, A.E.1
Page, D.T.2
-
19
-
-
84865508373
-
Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
-
COI: 1:CAS:528:DC%2BC38XhtFWmsL%2FO, PID: 22763451
-
Tsai PT, Hull C, Chu Y, et al. Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice. Nature 2012;488:647–651.
-
(2012)
Nature
, vol.488
, pp. 647-651
-
-
Tsai, P.T.1
Hull, C.2
Chu, Y.3
-
20
-
-
84864027269
-
Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice
-
COI: 1:CAS:528:DC%2BC38XhtFSksLfN, PID: 22829897
-
Brielmaier J, Matteson PG, Silverman JL, et al. Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice. PLoS ONE 2012;7:e40914.
-
(2012)
PLoS ONE
, vol.7
, pp. e40914
-
-
Brielmaier, J.1
Matteson, P.G.2
Silverman, J.L.3
-
21
-
-
38049013294
-
Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder
-
COI: 1:CAS:528:DC%2BD1cXotlOrtA%3D%3D, PID: 17983671
-
DeLorey TM, Sahbaie P, Hashemi E, Homanics GE, Clark JD. Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder. Behavioural Brain Research 2008;187:207–220.
-
(2008)
Behavioural Brain Research
, vol.187
, pp. 207-220
-
-
DeLorey, T.M.1
Sahbaie, P.2
Hashemi, E.3
Homanics, G.E.4
Clark, J.D.5
-
22
-
-
80053626726
-
Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice
-
PID: 21974935
-
Smith SEP, Zhou Y-D, Zhang G, Jin Z, Stoppel DC, Anderson MP. Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice. Sci Transl Med 2011;3:103ra97.
-
(2011)
Sci Transl Med
, vol.3
, pp. 103ra97
-
-
Smith, S.E.P.1
Zhou, Y.-D.2
Zhang, G.3
Jin, Z.4
Stoppel, D.C.5
Anderson, M.P.6
-
23
-
-
84858748792
-
Oxytocin receptor knockout mice display deficits in the expression of autism-related behaviors
-
COI: 1:CAS:528:DC%2BC38XktlGktbo%3D, PID: 22100185
-
Pobbe RLH, Pearson BL, Defensor EB, et al. Oxytocin receptor knockout mice display deficits in the expression of autism-related behaviors. Horm Behav 2012;61:436–444.
-
(2012)
Horm Behav
, vol.61
, pp. 436-444
-
-
Pobbe, R.L.H.1
Pearson, B.L.2
Defensor, E.B.3
-
24
-
-
34247632952
-
Social approach behaviors in oxytocin knockout mice: comparison of two independent lines tested in different laboratory environments
-
COI: 1:CAS:528:DC%2BD2sXkvFOmu7Y%3D, PID: 17420046
-
Crawley JN, Chen T, Puri A, et al. Social approach behaviors in oxytocin knockout mice: comparison of two independent lines tested in different laboratory environments. Neuropeptides 2007;41:145–163.
-
(2007)
Neuropeptides
, vol.41
, pp. 145-163
-
-
Crawley, J.N.1
Chen, T.2
Puri, A.3
-
25
-
-
79952314377
-
Sociability and motor functions in Shank1 mutant mice
-
COI: 1:CAS:528:DC%2BC3MXisFGnurw%3D, PID: 20868654
-
Silverman JL, Turner SM, Barkan CL, et al. Sociability and motor functions in Shank1 mutant mice. Brain Res 2011;1380:120–137.
-
(2011)
Brain Res
, vol.1380
, pp. 120-137
-
-
Silverman, J.L.1
Turner, S.M.2
Barkan, C.L.3
-
26
-
-
84880329347
-
Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2
-
PID: 22820233
-
Wöhr M, Silverman JL, Scattoni ML, et al. Developmental delays and reduced pup ultrasonic vocalizations but normal sociability in mice lacking the postsynaptic cell adhesion protein neuroligin2. Behav Brain Res 2013;251:50–64.
-
(2013)
Behav Brain Res
, vol.251
, pp. 50-64
-
-
Wöhr, M.1
Silverman, J.L.2
Scattoni, M.L.3
-
27
-
-
84908671161
-
Repetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum Disorders
-
Wurzman R, Forcelli PA, Griffey CJ, Kromer LF. Repetitive grooming and sensorimotor abnormalities in an ephrin-A knockout model for Autism Spectrum Disorders. Behav Brain Res 2014;278C:115–128.
-
(2014)
Behav Brain Res
, vol.278C
, pp. 115-128
-
-
Wurzman, R.1
Forcelli, P.A.2
Griffey, C.J.3
Kromer, L.F.4
-
28
-
-
84901286741
-
Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome
-
COI: 1:CAS:528:DC%2BC2cXnsVWku74%3D, PID: 24794428
-
Portmann T, Yang M, Mao R, et al. Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome. Cell Rep 2014;7:1077–1092.
-
(2014)
Cell Rep
, vol.7
, pp. 1077-1092
-
-
Portmann, T.1
Yang, M.2
Mao, R.3
-
29
-
-
61449217094
-
Social approach in genetically engineered mouse lines relevant to autism
-
COI: 1:CAS:528:DC%2BD1MXktlKkur8%3D, PID: 19016890
-
Moy SS, Nadler JJ, Young NB, et al. Social approach in genetically engineered mouse lines relevant to autism. Genes Brain Behav 2009;8:129–142.
-
(2009)
Genes Brain Behav
, vol.8
, pp. 129-142
-
-
Moy, S.S.1
Nadler, J.J.2
Young, N.B.3
-
30
-
-
79951567150
-
Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses
-
PID: 21268289
-
Spencer CM, Alekseyenko O, Hamilton SM, et al. Modifying behavioral phenotypes in Fmr1KO mice: genetic background differences reveal autistic-like responses. Autism Res 2011;4:40–56.
-
(2011)
Autism Res
, vol.4
, pp. 40-56
-
-
Spencer, C.M.1
Alekseyenko, O.2
Hamilton, S.M.3
-
31
-
-
35148858044
-
A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice
-
COI: 1:CAS:528:DC%2BD2sXhtFWitbrK, PID: 17823315
-
Tabuchi K, Blundell J, Etherton MR, et al. A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice. Science 2007;318:71–76.
-
(2007)
Science
, vol.318
, pp. 71-76
-
-
Tabuchi, K.1
Blundell, J.2
Etherton, M.R.3
-
32
-
-
64849084164
-
Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice
-
PID: 19360662
-
Chadman KK, Gong S, Scattoni ML, et al. Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice. Autism Res 2008;1:147–158.
-
(2008)
Autism Res
, vol.1
, pp. 147-158
-
-
Chadman, K.K.1
Gong, S.2
Scattoni, M.L.3
-
33
-
-
80051998693
-
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
-
COI: 1:CAS:528:DC%2BC3MXhtV2ms7bL, PID: 21808020
-
Etherton M, Földy C, Sharma M, et al. Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function. Proc Natl Acad Sci USA 2011;108:13764–13769.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 13764-13769
-
-
Etherton, M.1
Földy, C.2
Sharma, M.3
-
34
-
-
84898917488
-
Autism-related neuroligin-3 mutation alters social behavior and spatial learning
-
PID: 24619977
-
Jaramillo TC, Liu S, Pettersen A, Birnbaum SG, Powell CM. Autism-related neuroligin-3 mutation alters social behavior and spatial learning. Autism Res 2014;7:264–272.
-
(2014)
Autism Res
, vol.7
, pp. 264-272
-
-
Jaramillo, T.C.1
Liu, S.2
Pettersen, A.3
Birnbaum, S.G.4
Powell, C.M.5
-
35
-
-
84877003420
-
-
Ey E, Yang M, Katz AM, et al. Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4. Genes Brain Behav 2012 Sep 18 [Epub ahead of print].
-
Ey E, Yang M, Katz AM, et al. Absence of deficits in social behaviors and ultrasonic vocalizations in later generations of mice lacking neuroligin4. Genes Brain Behav 2012 Sep 18 [Epub ahead of print].
-
-
-
-
36
-
-
84878665879
-
Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism
-
COI: 1:CAS:528:DC%2BC38XhvVCrs7zF, PID: 23183221
-
El-Kordi A, Winkler D, Hammerschmidt K, et al. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism. Behav Brain Res 2013;251:41–49.
-
(2013)
Behav Brain Res
, vol.251
, pp. 41-49
-
-
El-Kordi, A.1
Winkler, D.2
Hammerschmidt, K.3
-
37
-
-
33845336461
-
Assessing autism-like behavior in mice: variations in social interactions among inbred strains
-
PID: 17097158
-
Bolivar VJ, Walters SR, Phoenix JL. Assessing autism-like behavior in mice: variations in social interactions among inbred strains. Behav Brain Res 2007;176:21–26.
-
(2007)
Behav Brain Res
, vol.176
, pp. 21-26
-
-
Bolivar, V.J.1
Walters, S.R.2
Phoenix, J.L.3
-
38
-
-
33845284824
-
Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains
-
PID: 16971002
-
Moy SS, Nadler JJ, Young NB, et al. Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains. Behav Brain Res 2007;176:4–20.
-
(2007)
Behav Brain Res
, vol.176
, pp. 4-20
-
-
Moy, S.S.1
Nadler, J.J.2
Young, N.B.3
-
39
-
-
64849113070
-
Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability
-
PID: 19419429
-
Yang M, Clarke AM, Crawley JN. Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability. Eur J Neurosci 2009;29:1663–1677.
-
(2009)
Eur J Neurosci
, vol.29
, pp. 1663-1677
-
-
Yang, M.1
Clarke, A.M.2
Crawley, J.N.3
-
40
-
-
77955270892
-
Expression of social behaviors of C57BL/6J versus BTBR inbred mouse strains in the visible burrow system
-
PID: 20600340
-
Pobbe RLH, Pearson BL, Defensor EB, Bolivar VJ, Blanchard DC, Blanchard RJ. Expression of social behaviors of C57BL/6J versus BTBR inbred mouse strains in the visible burrow system. Behav Brain Res 2010;214:443–449.
-
(2010)
Behav Brain Res
, vol.214
, pp. 443-449
-
-
Pobbe, R.L.H.1
Pearson, B.L.2
Defensor, E.B.3
Bolivar, V.J.4
Blanchard, D.C.5
Blanchard, R.J.6
-
41
-
-
84875218222
-
Influence of stimulant-induced hyperactivity on social approach in the BTBR mouse model of autism
-
COI: 1:CAS:528:DC%2BC38Xht1GksrnK, PID: 22968082
-
Silverman JL, Babineau BA, Oliver CF, Karras MN, Crawley JN. Influence of stimulant-induced hyperactivity on social approach in the BTBR mouse model of autism. Neuropharmacology 2013;68:210–222.
-
(2013)
Neuropharmacology
, vol.68
, pp. 210-222
-
-
Silverman, J.L.1
Babineau, B.A.2
Oliver, C.F.3
Karras, M.N.4
Crawley, J.N.5
-
42
-
-
84866352950
-
Low sociability in BTBR T + tf/J mice is independent of partner strain
-
COI: 1:CAS:528:DC%2BC38XhslKqsLzO, PID: 22245067
-
Yang M, Abrams DN, Zhang JY, et al. Low sociability in BTBR T + tf/J mice is independent of partner strain. Physiol Behav 2012;107:649–662.
-
(2012)
Physiol Behav
, vol.107
, pp. 649-662
-
-
Yang, M.1
Abrams, D.N.2
Zhang, J.Y.3
-
43
-
-
84878804982
-
D-Cycloserine improves sociability in the BTBR T+ Itpr3tf/J mouse model of autism spectrum disorders with altered Ras/Raf/ERK1/2 signaling
-
COI: 1:CAS:528:DC%2BC3sXhtVOrt7zK, PID: 23685206
-
Burket JA, Benson AD, Tang AH, Deutsch SI. D-Cycloserine improves sociability in the BTBR T+ Itpr3tf/J mouse model of autism spectrum disorders with altered Ras/Raf/ERK1/2 signaling. Brain Res Bull 2013;96:62–70.
-
(2013)
Brain Res Bull
, vol.96
, pp. 62-70
-
-
Burket, J.A.1
Benson, A.D.2
Tang, A.H.3
Deutsch, S.I.4
-
44
-
-
84896279364
-
Enhancement of inhibitory neurotransmission by GABAA receptors having α2,3-subunits ameliorates behavioral deficits in a mouse model of autism
-
COI: 1:CAS:528:DC%2BC2cXks1Oqurk%3D, PID: 24656250
-
Han S, Tai C, Jones CJ, Scheuer T, Catterall WA. Enhancement of inhibitory neurotransmission by GABAA receptors having α2,3-subunits ameliorates behavioral deficits in a mouse model of autism. Neuron 2014;81:1282–1289.
-
(2014)
Neuron
, vol.81
, pp. 1282-1289
-
-
Han, S.1
Tai, C.2
Jones, C.J.3
Scheuer, T.4
Catterall, W.A.5
-
45
-
-
34748889986
-
Social reward among juvenile mice
-
COI: 1:STN:280:DC%2BD2srms1Wkug%3D%3D, PID: 17212648
-
Panksepp JB, Lahvis GP. Social reward among juvenile mice. Genes Brain Behav 2007;6:661–671.
-
(2007)
Genes Brain Behav
, vol.6
, pp. 661-671
-
-
Panksepp, J.B.1
Lahvis, G.P.2
-
46
-
-
84862777834
-
Sociability and brain development in BALB/cJ and C57BL/6J mice
-
PID: 22178318
-
Fairless AH, Dow HC, Kreibich AS, et al. Sociability and brain development in BALB/cJ and C57BL/6J mice. Behav Brain Res 2012;228:299–310.
-
(2012)
Behav Brain Res
, vol.228
, pp. 299-310
-
-
Fairless, A.H.1
Dow, H.C.2
Kreibich, A.S.3
-
47
-
-
79960111638
-
Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3
-
COI: 1:CAS:528:DC%2BC3MXos1KmsLg%3D, PID: 21558424
-
Wang X, McCoy PA, Rodriguiz RM, et al. Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3. Hum Mol Genet 2011;20:3093–3108.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3093-3108
-
-
Wang, X.1
McCoy, P.A.2
Rodriguiz, R.M.3
-
48
-
-
79957543879
-
Enhanced polyubiquitination of Shank3 and NMDA receptor in a mouse model of autism
-
COI: 1:CAS:528:DC%2BC3MXmvFWhtLs%3D, PID: 21565394
-
Bangash MA, Park JM, Melnikova T, et al. Enhanced polyubiquitination of Shank3 and NMDA receptor in a mouse model of autism. Cell 2011;145:758–772.
-
(2011)
Cell
, vol.145
, pp. 758-772
-
-
Bangash, M.A.1
Park, J.M.2
Melnikova, T.3
-
49
-
-
33749254952
-
En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder
-
COI: 1:CAS:528:DC%2BD28XhtVGis7vL, PID: 16935268
-
Cheh MA, Millonig JH, Roselli LM, et al. En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder. Brain Res 2006;1116:166–176.
-
(2006)
Brain Res
, vol.1116
, pp. 166-176
-
-
Cheh, M.A.1
Millonig, J.H.2
Roselli, L.M.3
-
50
-
-
84879201185
-
Letting a typical mouse judge whether mouse social interactions are atypical
-
PID: 23436806
-
Shah CR, Forsberg CG, Kang J-Q, Veenstra-VanderWeele J. Letting a typical mouse judge whether mouse social interactions are atypical. Autism Res 2013;6:212–220.
-
(2013)
Autism Res
, vol.6
, pp. 212-220
-
-
Shah, C.R.1
Forsberg, C.G.2
Kang, J.-Q.3
Veenstra-VanderWeele, J.4
-
51
-
-
33646142995
-
Pten regulates neuronal arborization and social interaction in mice
-
COI: 1:CAS:528:DC%2BD28XkvFSgsb8%3D, PID: 16675393
-
Kwon C-H, Luikart BW, Powell CM, et al. Pten regulates neuronal arborization and social interaction in mice. Neuron 2006;50:377–388.
-
(2006)
Neuron
, vol.50
, pp. 377-388
-
-
Kwon, C.-H.1
Luikart, B.W.2
Powell, C.M.3
-
52
-
-
84860358233
-
Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism
-
PID: 22539775
-
Silverman JL, Smith DG, Rizzo SJS, et al. Negative allosteric modulation of the mGluR5 receptor reduces repetitive behaviors and rescues social deficits in mouse models of autism. Sci Transl Med 2012;4:131ra51.
-
(2012)
Sci Transl Med
, vol.4
, pp. 131ra51
-
-
Silverman, J.L.1
Smith, D.G.2
Rizzo, S.J.S.3
-
53
-
-
80053273580
-
Complex effects of mGluR5 antagonism on sociability and stereotypic behaviors in mice: possible implications for the pharmacotherapy of autism spectrum disorders
-
COI: 1:CAS:528:DC%2BC3MXht1WqurzL, PID: 21840381
-
Burket JA, Herndon AL, Winebarger EE, Jacome LF, Deutsch SI. Complex effects of mGluR5 antagonism on sociability and stereotypic behaviors in mice: possible implications for the pharmacotherapy of autism spectrum disorders. Brain Res Bull 2011;86:152–158.
-
(2011)
Brain Res Bull
, vol.86
, pp. 152-158
-
-
Burket, J.A.1
Herndon, A.L.2
Winebarger, E.E.3
Jacome, L.F.4
Deutsch, S.I.5
-
54
-
-
80054754473
-
Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism
-
PID: 21969575
-
Horev G, Ellegood J, Lerch JP, et al. Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism. Proc Natl Acad Sci U S A 2011;108:17076–17081.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 17076-17081
-
-
Horev, G.1
Ellegood, J.2
Lerch, J.P.3
-
55
-
-
79951782035
-
Motor and cognitive stereotypies in the BTBR T + tf/J mouse model of autism
-
COI: 1:STN:280:DC%2BC3M3gs1ertQ%3D%3D, PID: 21040460
-
Pearson BL, Pobbe RLH, Defensor EB, et al. Motor and cognitive stereotypies in the BTBR T + tf/J mouse model of autism. Genes Brain Behav 2011;10:228–235.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 228-235
-
-
Pearson, B.L.1
Pobbe, R.L.H.2
Defensor, E.B.3
-
56
-
-
84875139890
-
Maternal immune activation and strain specific interactions in the development of autism-like behaviors in mice
-
COI: 1:CAS:528:DC%2BC3sXhtFSqsrrK, PID: 23481627
-
Schwartzer JJ, Careaga M, Onore CE, Rushakoff JA, Berman RF, Ashwood P. Maternal immune activation and strain specific interactions in the development of autism-like behaviors in mice. Transl Psychiatry 2013;3:e240.
-
(2013)
Transl Psychiatry
, vol.3
, pp. e240
-
-
Schwartzer, J.J.1
Careaga, M.2
Onore, C.E.3
Rushakoff, J.A.4
Berman, R.F.5
Ashwood, P.6
-
58
-
-
77951907483
-
Social deficits, stereotypy and early emergence of repetitive behavior in the C58/J inbred mouse strain
-
PID: 19941908
-
Ryan BC, Young NB, Crawley JN, Bodfish JW, Moy SS. Social deficits, stereotypy and early emergence of repetitive behavior in the C58/J inbred mouse strain. Behav Brain Res 2010;208:178–188.
-
(2010)
Behav Brain Res
, vol.208
, pp. 178-188
-
-
Ryan, B.C.1
Young, N.B.2
Crawley, J.N.3
Bodfish, J.W.4
Moy, S.S.5
-
60
-
-
34250626014
-
A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival
-
COI: 1:CAS:528:DC%2BD2sXmsVWnsrs%3D, PID: 17522300
-
Meikle L, Talos DM, Onda H, et al. A mouse model of tuberous sclerosis: neuronal loss of Tsc1 causes dysplastic and ectopic neurons, reduced myelination, seizure activity, and limited survival. J Neurosci 2007;27:5546–5558.
-
(2007)
J Neurosci
, vol.27
, pp. 5546-5558
-
-
Meikle, L.1
Talos, D.M.2
Onda, H.3
-
61
-
-
35348950503
-
Abnormal glutamate homeostasis and impaired synaptic plasticity and learning in a mouse model of tuberous sclerosis complex
-
COI: 1:CAS:528:DC%2BD2sXht1aktr%2FN, PID: 17714952
-
Zeng L-H, Ouyang Y, Gazit V, et al. Abnormal glutamate homeostasis and impaired synaptic plasticity and learning in a mouse model of tuberous sclerosis complex. Neurobiol Dis 2007;28:184–196.
-
(2007)
Neurobiol Dis
, vol.28
, pp. 184-196
-
-
Zeng, L.-H.1
Ouyang, Y.2
Gazit, V.3
-
62
-
-
12644290240
-
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
-
COI: 1:CAS:528:DyaK2sXis1amsLk%3D, PID: 9108119
-
Homanics GE, DeLorey TM, Firestone LL, et al. Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proc Natl Acad Sci U S A 1997;94:4143–4148.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 4143-4148
-
-
Homanics, G.E.1
DeLorey, T.M.2
Firestone, L.L.3
-
63
-
-
37049032616
-
Correction of fragile X syndrome in mice
-
COI: 1:CAS:528:DC%2BD1cXksFGmsQ%3D%3D, PID: 18093519
-
Dolen G, Osterweil E, Rao BSS, et al. Correction of fragile X syndrome in mice. Neuron 2007;56:955–962.
-
(2007)
Neuron
, vol.56
, pp. 955-962
-
-
Dolen, G.1
Osterweil, E.2
Rao, B.S.S.3
-
64
-
-
79951574616
-
Veenstra-Van der Weele
-
Carter MD, Shah CR, Muller CL, Crawley JN, Carneiro AMD, Veenstra-Van der Weele J. Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions. Autism Res 2011;4:57–67.
-
(2011)
J. Absence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions. Autism Res
, vol.4
, pp. 57-67
-
-
Carter, M.D.1
Shah, C.R.2
Muller, C.L.3
Crawley, J.N.4
Carneiro, A.M.D.5
-
65
-
-
59149088359
-
Increased anxiety-like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2
-
COI: 1:STN:280:DC%2BD1M7ktlKhug%3D%3D, PID: 19016888
-
Blundell, J., Tabuchi, K., Bolliger, M. F., et al. Increased anxiety-like behavior in mice lacking the inhibitory synapse cell adhesion molecule neuroligin 2. Genes Brain Behav 2009;8:114–126.
-
(2009)
Genes Brain Behav
, vol.8
, pp. 114-126
-
-
Blundell, J.1
Tabuchi, K.2
Bolliger, M.F.3
-
66
-
-
79958232386
-
Increased levels of anxiety-related behaviors in a Tsc2 dominant negative transgenic mouse model of tuberous sclerosis
-
PID: 20882401
-
Ehninger D, Silva AJ. Increased levels of anxiety-related behaviors in a Tsc2 dominant negative transgenic mouse model of tuberous sclerosis. Behav Genet 2011;41:357–363.
-
(2011)
Behav Genet
, vol.41
, pp. 357-363
-
-
Ehninger, D.1
Silva, A.J.2
-
67
-
-
84856286525
-
Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome
-
COI: 1:CAS:528:DC%2BC38XlsFyktg%3D%3D, PID: 22231481
-
Samaco RC, Mandel-Brehm C, McGraw CM, Shaw CA, McGill BE, Zoghbi HY. Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome. Nat Genet 2012;44:206–211.
-
(2012)
Nat Genet
, vol.44
, pp. 206-211
-
-
Samaco, R.C.1
Mandel-Brehm, C.2
McGraw, C.M.3
Shaw, C.A.4
McGill, B.E.5
Zoghbi, H.Y.6
-
68
-
-
84925355681
-
Deletion of α-neurexin II results in autism-related behaviors in mice
-
COI: 1:CAS:528:DC%2BC2cXhvF2msr%2FM, PID: 25423136
-
Dachtler J, Glasper J, Cohen RN, et al. Deletion of α-neurexin II results in autism-related behaviors in mice. Transl Psychiatry 2014;4:e484.
-
(2014)
Transl Psychiatry
, vol.4
, pp. e484
-
-
Dachtler, J.1
Glasper, J.2
Cohen, R.N.3
-
69
-
-
26444548563
-
Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome
-
COI: 1:CAS:528:DC%2BD2MXhtFOqt7vE, PID: 16176388
-
Spencer CM, Alekseyenko O, Serysheva E, Yuva-Paylor LA, Paylor R. Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome. Genes Brain Behav 2005;4:420–430.
-
(2005)
Genes Brain Behav
, vol.4
, pp. 420-430
-
-
Spencer, C.M.1
Alekseyenko, O.2
Serysheva, E.3
Yuva-Paylor, L.A.4
Paylor, R.5
-
70
-
-
0031018226
-
A mouse model for the learning and memory deficits associated with neurofibromatosis type I
-
COI: 1:CAS:528:DyaK2sXhsVGrtrw%3D, PID: 9054942
-
Silva AJ, Frankland PW, Marowitz Z, et al. A mouse model for the learning and memory deficits associated with neurofibromatosis type I. Nat Genet 1997;15:281–284.
-
(1997)
Nat Genet
, vol.15
, pp. 281-284
-
-
Silva, A.J.1
Frankland, P.W.2
Marowitz, Z.3
-
71
-
-
84880918470
-
GluN2B in corticostriatal circuits governs choice learning and choice shifting
-
COI: 1:CAS:528:DC%2BC3sXhtVKhu7rF, PID: 23831965
-
Brigman JL, Daut RA, Wright T, et al. GluN2B in corticostriatal circuits governs choice learning and choice shifting. Nat Neurosci 2013;16:1101–1110.
-
(2013)
Nat Neurosci
, vol.16
, pp. 1101-1110
-
-
Brigman, J.L.1
Daut, R.A.2
Wright, T.3
-
72
-
-
84923146057
-
Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex
-
PID: 25193243
-
Bissonette GB, Schoenbaum G, Roesch MR, Powell EM. Interneurons are necessary for coordinated activity during reversal learning in orbitofrontal cortex. Biol Psychiatry 2015;77:454–464.
-
(2015)
Biol Psychiatry
, vol.77
, pp. 454-464
-
-
Bissonette, G.B.1
Schoenbaum, G.2
Roesch, M.R.3
Powell, E.M.4
-
73
-
-
70350571202
-
A meta-analysis of the corpus callosum in autism
-
PID: 19748080
-
Frazier TW, Hardan AY. A meta-analysis of the corpus callosum in autism. Biol Psychiatry 2009;66:935–941.
-
(2009)
Biol Psychiatry
, vol.66
, pp. 935-941
-
-
Frazier, T.W.1
Hardan, A.Y.2
-
74
-
-
79953766804
-
Meta-analysis of gray matter abnormalities in autism spectrum disorder: should Asperger disorder be subsumed under a broader umbrella of autistic spectrum disorder?
-
PID: 21464365
-
Via E, Radua J, Cardoner N, Happé F, Mataix-Cols D. Meta-analysis of gray matter abnormalities in autism spectrum disorder: should Asperger disorder be subsumed under a broader umbrella of autistic spectrum disorder? Arch Gen Psychiatry 2011;68:409–418.
-
(2011)
Arch Gen Psychiatry
, vol.68
, pp. 409-418
-
-
Via, E.1
Radua, J.2
Cardoner, N.3
Happé, F.4
Mataix-Cols, D.5
-
75
-
-
79958807384
-
Voxel-based meta-analysis of regional white-matter volume differences in autism spectrum disorder versus healthy controls
-
PID: 21078227
-
Radua J, Via E, Catani M, Mataix-Cols D. Voxel-based meta-analysis of regional white-matter volume differences in autism spectrum disorder versus healthy controls. Psychol Med 2010;41:1539–1550.
-
(2010)
Psychol Med
, vol.41
, pp. 1539-1550
-
-
Radua, J.1
Via, E.2
Catani, M.3
Mataix-Cols, D.4
-
76
-
-
46649092318
-
Towards a neuroanatomy of autism: a systematic review and meta-analysis of structural magnetic resonance imaging studies
-
PID: 17765485
-
Stanfield AC, McIntosh AM, Spencer MD, Philip R, Gaur S, Lawrie SM. Towards a neuroanatomy of autism: a systematic review and meta-analysis of structural magnetic resonance imaging studies. Eur Psychiatry 2008;23:289–299.
-
(2008)
Eur Psychiatry
, vol.23
, pp. 289-299
-
-
Stanfield, A.C.1
McIntosh, A.M.2
Spencer, M.D.3
Philip, R.4
Gaur, S.5
Lawrie, S.M.6
-
77
-
-
33748295575
-
Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP
-
PID: 16700053
-
Hatton DD, Sideris J, Skinner M, et al. Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP. Am J Med Genet A 2006;140A:1804–1813.
-
(2006)
Am J Med Genet A
, vol.140A
, pp. 1804-1813
-
-
Hatton, D.D.1
Sideris, J.2
Skinner, M.3
-
78
-
-
34147129139
-
Autism spectrum phenotype in males and females with fragile X full mutation and premutation
-
PID: 17031449
-
Clifford S, Dissanayake C, Bui QM, Huggins R, Taylor AK, Loesch DZ. Autism spectrum phenotype in males and females with fragile X full mutation and premutation. J Autism Dev Disord 2007;37:738–747.
-
(2007)
J Autism Dev Disord
, vol.37
, pp. 738-747
-
-
Clifford, S.1
Dissanayake, C.2
Bui, Q.M.3
Huggins, R.4
Taylor, A.K.5
Loesch, D.Z.6
-
79
-
-
56649106246
-
Autism profiles of males with fragile X syndrome
-
PID: 19127654
-
Harris SW, Hessl D, Goodlin-Jones B, et al. Autism profiles of males with fragile X syndrome. Am J Ment Retard 2008;113:427–438.
-
(2008)
Am J Ment Retard
, vol.113
, pp. 427-438
-
-
Harris, S.W.1
Hessl, D.2
Goodlin-Jones, B.3
-
80
-
-
0028246435
-
Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium
-
No authors listed. Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium. Cell 1994;78:23–33.
-
(1994)
Cell
, vol.78
, pp. 23-33
-
-
-
81
-
-
0030986183
-
Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
-
COI: 1:CAS:528:DyaK2sXjtleitr0%3D, PID: 9144249
-
Comery TA, Harris JB, Willems PJ, et al. Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits. Proc Natl Acad Sci U S A 1997;94:5401–5404.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 5401-5404
-
-
Comery, T.A.1
Harris, J.B.2
Willems, P.J.3
-
82
-
-
0033797832
-
Dendritic spine structural anomalies in fragile-X mental retardation syndrome
-
COI: 1:STN:280:DC%2BD3M%2FgvV2lsw%3D%3D, PID: 11007554
-
Irwin SA, Galvez R, Greenough WT. Dendritic spine structural anomalies in fragile-X mental retardation syndrome. Cereb. Cortex 2000;10:1038–1044.
-
(2000)
Cereb. Cortex
, vol.10
, pp. 1038-1044
-
-
Irwin, S.A.1
Galvez, R.2
Greenough, W.T.3
-
83
-
-
0035863624
-
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination
-
COI: 1:STN:280:DC%2BD3M3itlKitA%3D%3D, PID: 11223852
-
Irwin SA, Patel B, Idupulapati M, et al. Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination. Am J Med Genet 2001;98:161–167.
-
(2001)
Am J Med Genet
, vol.98
, pp. 161-167
-
-
Irwin, S.A.1
Patel, B.2
Idupulapati, M.3
-
84
-
-
0035094767
-
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
-
COI: 1:CAS:528:DC%2BD3MXhslOisLc%3D, PID: 11242117
-
Guy J, Hendrich B, Holmes M, Martin JE, Bird A. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet 2001;27:322–326.
-
(2001)
Nat Genet
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
Martin, J.E.4
Bird, A.5
-
85
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
COI: 1:CAS:528:DC%2BD3MXhslOisbo%3D, PID: 11242118
-
Chen RZ, Akbarian S, Tudor M, Jaenisch R. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet 2001;27:327–331.
-
(2001)
Nat Genet
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
Jaenisch, R.4
-
86
-
-
0037081840
-
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
-
COI: 1:CAS:528:DC%2BD38XhtlKmsrY%3D, PID: 11809720
-
Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY. Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Hum Mol Genet 2002;11:115–124.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 115-124
-
-
Shahbazian, M.D.1
Antalffy, B.2
Armstrong, D.L.3
Zoghbi, H.Y.4
-
87
-
-
0345376666
-
Abnormal serotonergic development in a mouse model for the Smith–Lemli–Opitz syndrome: implications for autism
-
COI: 1:CAS:528:DC%2BD3sXps1Onu7w%3D, PID: 14659996
-
Waage-Baudet H, Lauder JM, Dehart DB. Abnormal serotonergic development in a mouse model for the Smith–Lemli–Opitz syndrome: implications for autism. Int J Dev Neurosci 2003;21:451–459.
-
(2003)
Int J Dev Neurosci
, vol.21
, pp. 451-459
-
-
Waage-Baudet, H.1
Lauder, J.M.2
Dehart, D.B.3
-
88
-
-
0019980473
-
Clinical neurochemistry of autism and associated disorders
-
COI: 1:STN:280:DyaL3s%2Fot1Gkug%3D%3D, PID: 6184361
-
Young JG, Kavanagh ME, Anderson GM, Shaywitz BA, Cohen DJ. Clinical neurochemistry of autism and associated disorders. J Autism Dev Disord 1982;12:147–165.
-
(1982)
J Autism Dev Disord
, vol.12
, pp. 147-165
-
-
Young, J.G.1
Kavanagh, M.E.2
Anderson, G.M.3
Shaywitz, B.A.4
Cohen, D.J.5
-
89
-
-
10544234621
-
The serotonin system in autism
-
COI: 1:STN:280:DyaK2s7pslCqtQ%3D%3D, PID: 9053096
-
Cook EH, Leventhal BL. The serotonin system in autism. Curr Opin Pediatr 1996;8:348–354.
-
(1996)
Curr Opin Pediatr
, vol.8
, pp. 348-354
-
-
Cook, E.H.1
Leventhal, B.L.2
-
90
-
-
84899906322
-
Blood serotonin levels in autism spectrum disorder: a systematic review and meta-analysis
-
COI: 1:CAS:528:DC%2BC2cXjsF2jsr0%3D, PID: 24613076
-
Gabriele S, Sacco R, Persico AM. Blood serotonin levels in autism spectrum disorder: a systematic review and meta-analysis. Eur Neuropsychopharmacol 2014;24:919–929.
-
(2014)
Eur Neuropsychopharmacol
, vol.24
, pp. 919-929
-
-
Gabriele, S.1
Sacco, R.2
Persico, A.M.3
-
91
-
-
19544382872
-
Oxytocin receptors in brain cortical regions are reduced in haploinsufficient (+/−) reeler mice
-
COI: 1:CAS:528:DC%2BD2MXlslemsL4%3D, PID: 15949229
-
Liu W, Pappas GD, Carter CS. Oxytocin receptors in brain cortical regions are reduced in haploinsufficient (+/−) reeler mice. Neurol Res 2005;27:339–345.
-
(2005)
Neurol Res
, vol.27
, pp. 339-345
-
-
Liu, W.1
Pappas, G.D.2
Carter, C.S.3
-
92
-
-
20344405210
-
Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice
-
COI: 1:CAS:528:DC%2BD2MXlvVSgtrk%3D, PID: 15977646
-
Fukuda T, Itoh M, Ichikawa T, Washiyama K, Goto Y-I. Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice. J Neuropathol Exp Neurol 2005;64:537–544.
-
(2005)
J Neuropathol Exp Neurol
, vol.64
, pp. 537-544
-
-
Fukuda, T.1
Itoh, M.2
Ichikawa, T.3
Washiyama, K.4
Goto, Y.-I.5
-
93
-
-
77955639683
-
Systems biology through mouse imaging centers: experience and new directions
-
COI: 1:CAS:528:DC%2BC3cXhtFais7%2FO, PID: 20415591
-
Henkelman RM. Systems biology through mouse imaging centers: experience and new directions. Annu Rev Biomed Eng 2010;12:143–166.
-
(2010)
Annu Rev Biomed Eng
, vol.12
, pp. 143-166
-
-
Henkelman, R.M.1
-
94
-
-
33645798078
-
Anatomical phenotyping in the brain and skull of a mutant mouse by magnetic resonance imaging and computed tomography
-
COI: 1:CAS:528:DC%2BD28XitFersLk%3D, PID: 16410543
-
Nieman BJ, Flenniken AM, Adamson SL, Henkelman RM, Sled JG. Anatomical phenotyping in the brain and skull of a mutant mouse by magnetic resonance imaging and computed tomography. Physiol Genomics 2006;24:154–162.
-
(2006)
Physiol Genomics
, vol.24
, pp. 154-162
-
-
Nieman, B.J.1
Flenniken, A.M.2
Adamson, S.L.3
Henkelman, R.M.4
Sled, J.G.5
-
95
-
-
77957695802
-
Quantitative CT imaging of the spatio-temporal distribution patterns of vasa vasorum in aortas of apoE−/−/LDL−/− double knockout mice
-
COI: 1:CAS:528:DC%2BC3cXht1OgtbfM, PID: 20692662
-
Kampschulte, M., Brinkmann, A., Stieger, P., et al. Quantitative CT imaging of the spatio-temporal distribution patterns of vasa vasorum in aortas of apoE−/−/LDL−/− double knockout mice. Atherosclerosis 2010;212:444–450.
-
(2010)
Atherosclerosis
, vol.212
, pp. 444-450
-
-
Kampschulte, M.1
Brinkmann, A.2
Stieger, P.3
-
96
-
-
77949709936
-
Comparative structural and hemodynamic analysis of vascular trees
-
COI: 1:CAS:528:DC%2BC3cXkvVSjsb0%3D, PID: 20081111
-
Yang J, Yu LX, Rennie MY, Sled JG, Henkelman RM. Comparative structural and hemodynamic analysis of vascular trees. Am J Physiol Heart Circ Physiol 2010;298:H1249-H1259.
-
(2010)
Am J Physiol Heart Circ Physiol
, vol.298
, pp. H1249-H1259
-
-
Yang, J.1
Yu, L.X.2
Rennie, M.Y.3
Sled, J.G.4
Henkelman, R.M.5
-
97
-
-
84864817243
-
A novel 3D mouse embryo atlas based on micro-CT
-
COI: 1:CAS:528:DC%2BC38XhsV2itbjM, PID: 22872090
-
Wong MD, Dorr AE, Walls JR, Lerch JP, Henkelman RM. A novel 3D mouse embryo atlas based on micro-CT. Development 2012;139:3248–3256.
-
(2012)
Development
, vol.139
, pp. 3248-3256
-
-
Wong, M.D.1
Dorr, A.E.2
Walls, J.R.3
Lerch, J.P.4
Henkelman, R.M.5
-
98
-
-
61649124483
-
MicroCT for developmental biology: a versatile tool for high-contrast 3D imaging at histological resolutions
-
PID: 19235724
-
Metscher BD. MicroCT for developmental biology: a versatile tool for high-contrast 3D imaging at histological resolutions. Dev Dyn 2009;238:632–640.
-
(2009)
Dev Dyn
, vol.238
, pp. 632-640
-
-
Metscher, B.D.1
-
99
-
-
77953648269
-
Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining
-
PID: 20190279
-
Degenhardt K, Wright AC, Horng D, Padmanabhan A, Epstein JA. Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining. Circ Cardiovasc Imaging 2010;3:314–322.
-
(2010)
Circ Cardiovasc Imaging
, vol.3
, pp. 314-322
-
-
Degenhardt, K.1
Wright, A.C.2
Horng, D.3
Padmanabhan, A.4
Epstein, J.A.5
-
100
-
-
3142738008
-
Embryonic heart failure in NFATc1−/− mice: novel mechanistic insights from in utero ultrasound biomicroscopy
-
COI: 1:CAS:528:DC%2BD2cXlt1Cru7s%3D, PID: 15166096
-
Phoon CKL, Ji RP, Aristizábal O, et al. Embryonic heart failure in NFATc1−/− mice: novel mechanistic insights from in utero ultrasound biomicroscopy. Circ Res 2004;95:92–99.
-
(2004)
Circ Res
, vol.95
, pp. 92-99
-
-
Phoon, C.K.L.1
Ji, R.P.2
Aristizábal, O.3
-
101
-
-
0042125604
-
Ultrasound biomicroscopy-Doppler in mouse cardiovascular development
-
PID: 12824473
-
Phoon CKL, Turnbull DH. Ultrasound biomicroscopy-Doppler in mouse cardiovascular development. Physiol Genomics 2003;14:3–15.
-
(2003)
Physiol Genomics
, vol.14
, pp. 3-15
-
-
Phoon, C.K.L.1
Turnbull, D.H.2
-
102
-
-
4844226046
-
Comprehensive transthoracic cardiac imaging in mice using ultrasound biomicroscopy with anatomical confirmation by magnetic resonance imaging
-
PID: 15114000
-
Zhou Y-Q, Foster FS, Nieman BJ, Davidson L, Chen XJ, Henkelman RM. Comprehensive transthoracic cardiac imaging in mice using ultrasound biomicroscopy with anatomical confirmation by magnetic resonance imaging. Physiol Genomics 2004;18:232–244.
-
(2004)
Physiol Genomics
, vol.18
, pp. 232-244
-
-
Zhou, Y.-Q.1
Foster, F.S.2
Nieman, B.J.3
Davidson, L.4
Chen, X.J.5
Henkelman, R.M.6
-
103
-
-
0028925939
-
Ultrasound backscatter microscope analysis of early mouse embryonic brain development
-
COI: 1:CAS:528:DyaK2MXksVCqtbs%3D, PID: 7892254
-
Turnbull DH, Bloomfield TS, Baldwin HS, Foster FS, Joyner AL. Ultrasound backscatter microscope analysis of early mouse embryonic brain development. Proc Natl Acad Sci U S A 1995;92:2239–2243.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 2239-2243
-
-
Turnbull, D.H.1
Bloomfield, T.S.2
Baldwin, H.S.3
Foster, F.S.4
Joyner, A.L.5
-
104
-
-
3242789549
-
Optimization and performance evaluation of the microPET II scanner for in vivo small-animal imaging
-
PID: 15272672
-
Yang Y, Tai Y-C, Siegel S, et al. Optimization and performance evaluation of the microPET II scanner for in vivo small-animal imaging. Phys Med Biol 2004;49:2527–2545.
-
(2004)
Phys Med Biol
, vol.49
, pp. 2527-2545
-
-
Yang, Y.1
Tai, Y.-C.2
Siegel, S.3
-
105
-
-
0037318541
-
Optical projection tomography as a new tool for studying embryo anatomy
-
PID: 12647867
-
Sharpe J. Optical projection tomography as a new tool for studying embryo anatomy. J Anat 2003;202:175–181.
-
(2003)
J Anat
, vol.202
, pp. 175-181
-
-
Sharpe, J.1
-
106
-
-
84865625696
-
Neuroanatomical phenotyping of the mouse brain with three-dimensional autofluorescence imaging
-
Gleave,JA, Wong MD, Dazai J, et al. Neuroanatomical phenotyping of the mouse brain with three-dimensional autofluorescence imaging. Physiol Genomics 2012;44:778–785.
-
(2012)
Physiol Genomics
, vol.44
, pp. 778-785
-
-
-
107
-
-
27844562684
-
Magnetic resonance imaging for detection and analysis of mouse phenotypes
-
PID: 16206127
-
Nieman BJ, Bock NA, Bishop J, et al. Magnetic resonance imaging for detection and analysis of mouse phenotypes. NMR Biomed 2005;18:447–468.
-
(2005)
NMR Biomed
, vol.18
, pp. 447-468
-
-
Nieman, B.J.1
Bock, N.A.2
Bishop, J.3
-
108
-
-
0345415035
-
Three-dimensional anatomical characterization of the developing mouse brain by diffusion tensor microimaging
-
PID: 14642474
-
Zhang J, Richards LJ, Yarowsky P, Huang H, van Zijl PCM, Mori S. Three-dimensional anatomical characterization of the developing mouse brain by diffusion tensor microimaging. Neuroimage 2003;20:1639–1648.
-
(2003)
Neuroimage
, vol.20
, pp. 1639-1648
-
-
Zhang, J.1
Richards, L.J.2
Yarowsky, P.3
Huang, H.4
van Zijl, P.C.M.5
Mori, S.6
-
109
-
-
67949103446
-
Magnetic resonance imaging and micro-computed tomography combined atlas of developing and adult mouse brains for stereotaxic surgery
-
COI: 1:CAS:528:DC%2BD1MXps1aiurY%3D, PID: 19490934
-
Aggarwal M, Zhang J, Miller MI, Sidman RL, Mori S. Magnetic resonance imaging and micro-computed tomography combined atlas of developing and adult mouse brains for stereotaxic surgery. Neuroscience 2009;162:1339–1350.
-
(2009)
Neuroscience
, vol.162
, pp. 1339-1350
-
-
Aggarwal, M.1
Zhang, J.2
Miller, M.I.3
Sidman, R.L.4
Mori, S.5
-
110
-
-
18044373435
-
Magnetic resonance imaging at microscopic resolution reveals subtle morphological changes in a mouse model of dopaminergic hyperfunction
-
PID: 15862208
-
Cyr M, Caron MG, Johnson GA, Laakso A. Magnetic resonance imaging at microscopic resolution reveals subtle morphological changes in a mouse model of dopaminergic hyperfunction. Neuroimage 2005;26:83–90.
-
(2005)
Neuroimage
, vol.26
, pp. 83-90
-
-
Cyr, M.1
Caron, M.G.2
Johnson, G.A.3
Laakso, A.4
-
111
-
-
0036793134
-
Magnetic resonance histology for morphologic phenotyping
-
PID: 12353257
-
Johnson GA, Cofer GP, Fubara B, Gewalt SL, Hedlund LW, Maronpot RR. Magnetic resonance histology for morphologic phenotyping. J Magn Reson Imaging 2002;16:423–429.
-
(2002)
J Magn Reson Imaging
, vol.16
, pp. 423-429
-
-
Johnson, G.A.1
Cofer, G.P.2
Fubara, B.3
Gewalt, S.L.4
Hedlund, L.W.5
Maronpot, R.R.6
-
112
-
-
34447577998
-
High-throughput morphologic phenotyping of the mouse brain with magnetic resonance histology
-
PID: 17574443
-
Johnson GA, Ali-Sharief A, Badea A, et al. High-throughput morphologic phenotyping of the mouse brain with magnetic resonance histology. Neuroimage 2007;37:82–89.
-
(2007)
Neuroimage
, vol.37
, pp. 82-89
-
-
Johnson, G.A.1
Ali-Sharief, A.2
Badea, A.3
-
113
-
-
79955480287
-
Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain
-
PID: 21310249
-
Cleary JO, Wiseman FK, Norris FC, et al. Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain. Neuroimage 2011;56:974–983.
-
(2011)
Neuroimage
, vol.56
, pp. 974-983
-
-
Cleary, J.O.1
Wiseman, F.K.2
Norris, F.C.3
-
114
-
-
17744394309
-
A three-dimensional MRI atlas of the mouse brain with estimates of the average and variability
-
PID: 15342433
-
Kovacević N, Henderson JT, Chan E, et al. A three-dimensional MRI atlas of the mouse brain with estimates of the average and variability. Cereb Cortex 2005;15:639–645.
-
(2005)
Cereb Cortex
, vol.15
, pp. 639-645
-
-
Kovacević, N.1
Henderson, J.T.2
Chan, E.3
-
115
-
-
0032803747
-
Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging
-
COI: 1:STN:280:DyaK1MzmvVygsg%3D%3D, PID: 10439957
-
Kooy RF, Reyniers E, Verhoye M, et al. Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging. Eur J Hum Genet 1999;7:526–532.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 526-532
-
-
Kooy, R.F.1
Reyniers, E.2
Verhoye, M.3
-
116
-
-
30144434255
-
Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism
-
COI: 1:CAS:528:DC%2BD28XksVWjsw%3D%3D, PID: 16380085
-
Saywell V, Viola A, Confort-Gouny S, Le Fur Y, Villard L, Cozzone PJ. Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism. Biochem Biophys Res Commun 2006;340:776–783.
-
(2006)
Biochem Biophys Res Commun
, vol.340
, pp. 776-783
-
-
Saywell, V.1
Viola, A.2
Confort-Gouny, S.3
Le Fur, Y.4
Villard, L.5
Cozzone, P.J.6
-
117
-
-
0027308186
-
Neuroanatomy of Rett syndrome: a volumetric imaging study
-
COI: 1:STN:280:DyaK3szjt1eqtw%3D%3D, PID: 8338347
-
Reiss AL, Faruque F, Naidu S, et al. Neuroanatomy of Rett syndrome: a volumetric imaging study. Ann Neurol 1993;34:227–234.
-
(1993)
Ann Neurol
, vol.34
, pp. 227-234
-
-
Reiss, A.L.1
Faruque, F.2
Naidu, S.3
-
118
-
-
0031028124
-
Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa
-
COI: 1:STN:280:DyaK2s7ptlWgtQ%3D%3D, PID: 9040729
-
Subramaniam B, Naidu S, Reiss AL. Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa. Neurology 1997;48:399–407.
-
(1997)
Neurology
, vol.48
, pp. 399-407
-
-
Subramaniam, B.1
Naidu, S.2
Reiss, A.L.3
-
119
-
-
41149136769
-
Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study
-
COI: 1:STN:280:DC%2BD1c7ps1SksA%3D%3D, PID: 18065507
-
Carter JC, Lanham DC, Pham D, Bibat G, Naidu S, Kaufmann WE. Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study. AJNR Am J Neuroradiol 2008;29:436–441.
-
(2008)
AJNR Am J Neuroradiol
, vol.29
, pp. 436-441
-
-
Carter, J.C.1
Lanham, D.C.2
Pham, D.3
Bibat, G.4
Naidu, S.5
Kaufmann, W.E.6
-
120
-
-
44949148164
-
Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline
-
COI: 1:CAS:528:DC%2BD1cXnsF2ltrk%3D, PID: 18571096
-
Ward BC, Agarwal S, Wang K, Berger-Sweeney J, Kolodny NH. Longitudinal brain MRI study in a mouse model of Rett Syndrome and the effects of choline. Neurobiol Dis 2008;31:110–119.
-
(2008)
Neurobiol Dis
, vol.31
, pp. 110-119
-
-
Ward, B.C.1
Agarwal, S.2
Wang, K.3
Berger-Sweeney, J.4
Kolodny, N.H.5
-
121
-
-
56549105433
-
Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp21lox mice
-
PID: 18687363
-
Nag N, Moriuchi JM, Peitzman CGK, Ward BC, Kolodny NH, Berger-Sweeney JE. Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp21lox mice. Behav Brain Res 2009;196:44–48.
-
(2009)
Behav Brain Res
, vol.196
, pp. 44-48
-
-
Nag, N.1
Moriuchi, J.M.2
Peitzman, C.G.K.3
Ward, B.C.4
Kolodny, N.H.5
Berger-Sweeney, J.E.6
-
122
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
COI: 1:CAS:528:DC%2BD3sXjt1Ontrg%3D, PID: 12669065
-
Jamain S, Quach H, Betancur C, et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 2003;34:27–29.
-
(2003)
Nat Genet
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
-
123
-
-
67650750977
-
A synaptic trek to autism
-
COI: 1:CAS:528:DC%2BD1MXptVGktbY%3D, PID: 19545994
-
Bourgeron T. A synaptic trek to autism. Curr Opin Neurobiol 2009;19:231–234.
-
(2009)
Curr Opin Neurobiol
, vol.19
, pp. 231-234
-
-
Bourgeron, T.1
-
124
-
-
65249120231
-
Multiple rare variants in the etiology of autism spectrum disorders
-
PID: 19432386
-
Buxbaum JD. Multiple rare variants in the etiology of autism spectrum disorders. Dialogues Clin Neurosci 2009;11:35–43.
-
(2009)
Dialogues Clin Neurosci
, vol.11
, pp. 35-43
-
-
Buxbaum, J.D.1
-
125
-
-
67149127032
-
Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit
-
COI: 1:STN:280:DC%2BD1MvltlKisQ%3D%3D, PID: 19243448
-
Radyushkin K, Hammerschmidt K, Boretius S, et al. Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit. Genes Brain Behav 2009;8:416–425.
-
(2009)
Genes Brain Behav
, vol.8
, pp. 416-425
-
-
Radyushkin, K.1
Hammerschmidt, K.2
Boretius, S.3
-
126
-
-
37849049287
-
Cognitive deficits in Tsc1+/−mice in the absence of cerebral lesions and seizures
-
PID: 18067135
-
Goorden SMI, van Woerden GM, van der Weerd L, Cheadle JP, Elgersma Y. Cognitive deficits in Tsc1+/−mice in the absence of cerebral lesions and seizures. Ann Neurol 2007;62:648–655.
-
(2007)
Ann Neurol
, vol.62
, pp. 648-655
-
-
Goorden, S.M.I.1
van Woerden, G.M.2
van der Weerd, L.3
Cheadle, J.P.4
Elgersma, Y.5
-
128
-
-
45849094758
-
Longitudinal neuroanatomical changes determined by deformation-based morphometry in a mouse model of Alzheimer's disease
-
PID: 18547819
-
Lau JC, Lerch JP, Sled JG, Henkelman RM, Evans AC, Bedell BJ. Longitudinal neuroanatomical changes determined by deformation-based morphometry in a mouse model of Alzheimer's disease. Neuroimage 2008;42:19–27.
-
(2008)
Neuroimage
, vol.42
, pp. 19-27
-
-
Lau, J.C.1
Lerch, J.P.2
Sled, J.G.3
Henkelman, R.M.4
Evans, A.C.5
Bedell, B.J.6
-
129
-
-
45849093291
-
High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice
-
COI: 1:STN:280:DC%2BD1cvitVChsw%3D%3D, PID: 18502665
-
Dorr AE, Lerch JP, Spring S, Kabani N, Henkelman RM. High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice. Neuroimage 2008;42:60–69.
-
(2008)
Neuroimage
, vol.42
, pp. 60-69
-
-
Dorr, A.E.1
Lerch, J.P.2
Spring, S.3
Kabani, N.4
Henkelman, R.M.5
-
130
-
-
77956211293
-
Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging
-
PID: 20304074
-
Ellegood J, Pacey LK, Hampson DR, Lerch JP, Henkelman RM. Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging. Neuroimage 2010;53:1023–1029.
-
(2010)
Neuroimage
, vol.53
, pp. 1023-1029
-
-
Ellegood, J.1
Pacey, L.K.2
Hampson, D.R.3
Lerch, J.P.4
Henkelman, R.M.5
-
131
-
-
80053913696
-
Brain abnormalities in a Neuroligin3 R451C knockin mouse model associated with autism
-
PID: 21882360
-
Ellegood J, Lerch JP, Henkelman RM. Brain abnormalities in a Neuroligin3 R451C knockin mouse model associated with autism. Autism Res 2011;4:368–376.
-
(2011)
Autism Res
, vol.4
, pp. 368-376
-
-
Ellegood, J.1
Lerch, J.P.2
Henkelman, R.M.3
-
132
-
-
84907731361
-
High resolution magnetic resonance imaging for characterization of the neuroligin-3 knock-in mouse model associated with autism spectrum disorder
-
PID: 25299583
-
Kumar M, Duda JT, Hwang W-T, et al. High resolution magnetic resonance imaging for characterization of the neuroligin-3 knock-in mouse model associated with autism spectrum disorder. PLoS ONE 2014;9:e109872.
-
(2014)
PLoS ONE
, vol.9
, pp. e109872
-
-
Kumar, M.1
Duda, J.T.2
Hwang, W.-T.3
-
133
-
-
84866842812
-
Neuroanatomical assessment of the integrin β3 mouse model related to autism and the serotonin system using high resolution MRI
-
PID: 22557981
-
Ellegood J, Henkelman RM, Lerch JP. Neuroanatomical assessment of the integrin β3 mouse model related to autism and the serotonin system using high resolution MRI. Front Psychiatry 2012;3:37.
-
(2012)
Front Psychiatry
, vol.3
, pp. 37
-
-
Ellegood, J.1
Henkelman, R.M.2
Lerch, J.P.3
-
134
-
-
84863393507
-
Brain anatomy and its relationship to behavior in adults with autism spectrum disorder: a multicenter magnetic resonance imaging study
-
PID: 22310506
-
Ecker C, Suckling J, Deoni SC, et al. Brain anatomy and its relationship to behavior in adults with autism spectrum disorder: a multicenter magnetic resonance imaging study. Arch Gen Psychiatry 2012;69:195–209.
-
(2012)
Arch Gen Psychiatry
, vol.69
, pp. 195-209
-
-
Ecker, C.1
Suckling, J.2
Deoni, S.C.3
-
135
-
-
33846921789
-
Autism spectrum disorders: developmental disconnection syndromes
-
COI: 1:CAS:528:DC%2BD2sXhvVOqtLo%3D, PID: 17275283
-
Geschwind DH, Levitt P. Autism spectrum disorders: developmental disconnection syndromes. Curr Opin Neurobiol 2007;17:103–111.
-
(2007)
Curr Opin Neurobiol
, vol.17
, pp. 103-111
-
-
Geschwind, D.H.1
Levitt, P.2
-
136
-
-
81755184074
-
Impaired structural connectivity of socio-emotional circuits in autism spectrum disorders: a diffusion tensor imaging study
-
COI: 1:CAS:528:DC%2BC3MXhs1ensLzO, PID: 22132206
-
Ameis SH, Fan J, Rockel C, et al. Impaired structural connectivity of socio-emotional circuits in autism spectrum disorders: a diffusion tensor imaging study. PLoS ONE 2011;6:e28044.
-
(2011)
PLoS ONE
, vol.6
, pp. e28044
-
-
Ameis, S.H.1
Fan, J.2
Rockel, C.3
-
137
-
-
84901284227
-
The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism
-
PID: 23774715
-
Di Martino A, Yan C-G, Li Q, et al. The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism. Mol Psychiatry 2014;19:659–667.
-
(2014)
Mol Psychiatry
, vol.19
, pp. 659-667
-
-
Di Martino, A.1
Yan, C.-G.2
Li, Q.3
-
138
-
-
84857138766
-
Disrupted cortical connectivity theory as an explanatory model for autism spectrum disorders
-
PID: 22018722
-
Kana RK, Libero LE, Moore MS. Disrupted cortical connectivity theory as an explanatory model for autism spectrum disorders. Phys Life Rev 2011;8:410–437.
-
(2011)
Phys Life Rev
, vol.8
, pp. 410-437
-
-
Kana, R.K.1
Libero, L.E.2
Moore, M.S.3
-
139
-
-
37849038398
-
Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment
-
PID: 17956622
-
Deboer T, Wu Z, Lee A, Simon TJ. Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behav Brain Funct 2007;3:54.
-
(2007)
Behav Brain Funct
, vol.3
, pp. 54
-
-
Deboer, T.1
Wu, Z.2
Lee, A.3
Simon, T.J.4
-
140
-
-
34247842799
-
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome
-
COI: 1:CAS:528:DC%2BD2sXkvFWgt70%3D, PID: 16734939
-
Gothelf D, Michaelovsky E, Frisch A, et al. Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome. Int J Neuropsychopharmacol 2007;10:301–308.
-
(2007)
Int J Neuropsychopharmacol
, vol.10
, pp. 301-308
-
-
Gothelf, D.1
Michaelovsky, E.2
Frisch, A.3
-
141
-
-
3042738235
-
Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2)
-
PID: 15224707
-
Kates WR, Burnette CP, Bessette BA, et al. Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). J Child Neurol 2004;19:337–342.
-
(2004)
J Child Neurol
, vol.19
, pp. 337-342
-
-
Kates, W.R.1
Burnette, C.P.2
Bessette, B.A.3
-
142
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
COI: 1:CAS:528:DyaK2sXisFehuro%3D, PID: 9106540
-
Cook EH, Lindgren V, Leventhal BL, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 1997;60:928–934.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 928-934
-
-
Cook, E.H.1
Lindgren, V.2
Leventhal, B.L.3
-
143
-
-
67549083336
-
Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism
-
PID: 19563756
-
Nakatani J, Tamada K, Hatanaka F, et al. Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism. Cell 2009;137:1235–1246.
-
(2009)
Cell
, vol.137
, pp. 1235-1246
-
-
Nakatani, J.1
Tamada, K.2
Hatanaka, F.3
-
144
-
-
84945446962
-
-
Ellegood J, Nakai N, Nakatani J, Henkelman M, Takumi T, Lerch J. Neuroanatomical phenotypes are consistent with autism-like behavioral phenotypes in the 15q11-13 duplication mouse model. Autism Res 2015 Mar 7 [Epub ahead of print].
-
Ellegood J, Nakai N, Nakatani J, Henkelman M, Takumi T, Lerch J. Neuroanatomical phenotypes are consistent with autism-like behavioral phenotypes in the 15q11-13 duplication mouse model. Autism Res 2015 Mar 7 [Epub ahead of print].
-
-
-
-
145
-
-
0035829969
-
The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders
-
COI: 1:STN:280:DC%2BD38%2FnsVOjsw%3D%3D, PID: 11803514
-
Bolton PF, Dennis NR, Browne CE, et al. The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders. Am J Med Genet 2001;105:675–685.
-
(2001)
Am J Med Genet
, vol.105
, pp. 675-685
-
-
Bolton, P.F.1
Dennis, N.R.2
Browne, C.E.3
-
146
-
-
84860225460
-
Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism
-
COI: 1:CAS:528:DC%2BC38XlvFeitbw%3D, PID: 22487857
-
Wegiel J, Schanen NC, Cook EH, et al. Differences between the pattern of developmental abnormalities in autism associated with duplications 15q11.2-q13 and idiopathic autism. J Neuropathol Exp Neurol 2012;71:382–397.
-
(2012)
J Neuropathol Exp Neurol
, vol.71
, pp. 382-397
-
-
Wegiel, J.1
Schanen, N.C.2
Cook, E.H.3
-
147
-
-
33845319742
-
BALB/c mice: low sociability and other phenotypes that may be relevant to autism
-
COI: 1:CAS:528:DC%2BD28Xht12rsLvN, PID: 16890300
-
Brodkin ES. BALB/c mice: low sociability and other phenotypes that may be relevant to autism. Behav Brain Res 2007;176:53–65.
-
(2007)
Behav Brain Res
, vol.176
, pp. 53-65
-
-
Brodkin, E.S.1
-
148
-
-
84887176861
-
Balb/c mice treated with D-cycloserine arouse increased social interest in conspecifics
-
COI: 1:CAS:528:DC%2BC3sXhvFWis7vL, PID: 24157954
-
Benson AD, Burket JA, Deutsch SI. Balb/c mice treated with D-cycloserine arouse increased social interest in conspecifics. Brain Res Bull 2013;99:95–99.
-
(2013)
Brain Res Bull
, vol.99
, pp. 95-99
-
-
Benson, A.D.1
Burket, J.A.2
Deutsch, S.I.3
-
149
-
-
84872714279
-
Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging
-
PID: 23275046
-
Ellegood J, Babineau BA, Henkelman RM, Lerch JP, Crawley JN. Neuroanatomical analysis of the BTBR mouse model of autism using magnetic resonance imaging and diffusion tensor imaging. Neuroimage 2013;70:288–300.
-
(2013)
Neuroimage
, vol.70
, pp. 288-300
-
-
Ellegood, J.1
Babineau, B.A.2
Henkelman, R.M.3
Lerch, J.P.4
Crawley, J.N.5
-
150
-
-
0037414416
-
Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/+ tf/tf has severely reduced hippocampal commissure and absent corpus callosum
-
COI: 1:CAS:528:DC%2BD3sXis12rs7Y%3D, PID: 12691836
-
Wahlsten D, Metten P, Crabbe JC. Survey of 21 inbred mouse strains in two laboratories reveals that BTBR T/+ tf/tf has severely reduced hippocampal commissure and absent corpus callosum. Brain Res 2003;971:47–54.
-
(2003)
Brain Res
, vol.971
, pp. 47-54
-
-
Wahlsten, D.1
Metten, P.2
Crabbe, J.C.3
-
151
-
-
84885761119
-
Neuroimaging evidence of major morpho-anatomical and functional abnormalities in the BTBR T + TF/J mouse model of autism
-
COI: 1:CAS:528:DC%2BC3sXhs1OisLvL, PID: 24146902
-
Dodero L, Damiano M, Galbusera A, et al. Neuroimaging evidence of major morpho-anatomical and functional abnormalities in the BTBR T + TF/J mouse model of autism. PLoS ONE 2013;8:e76655.
-
(2013)
PLoS ONE
, vol.8
, pp. e76655
-
-
Dodero, L.1
Damiano, M.2
Galbusera, A.3
-
152
-
-
84907348224
-
Dysfunctional dopaminergic neurotransmission in asocial BTBR mice
-
COI: 1:CAS:528:DC%2BC2cXhtlKktr%2FO, PID: 25136890
-
Squillace M, Dodero L, Federici M, et al. Dysfunctional dopaminergic neurotransmission in asocial BTBR mice. Transl Psychiatry 2014;4:e427.
-
(2014)
Transl Psychiatry
, vol.4
, pp. e427
-
-
Squillace, M.1
Dodero, L.2
Federici, M.3
-
153
-
-
84855866909
-
Association between sociability and diffusion tensor imaging in BALB/cJ mice
-
PID: 21618305
-
Kim S, Pickup S, Fairless AH, et al. Association between sociability and diffusion tensor imaging in BALB/cJ mice. NMR Biomed 2012;25:104–112.
-
(2012)
NMR Biomed
, vol.25
, pp. 104-112
-
-
Kim, S.1
Pickup, S.2
Fairless, A.H.3
-
154
-
-
84860367629
-
Longitudinal in-vivo diffusion tensor imaging for assessing brain developmental changes in BALB/cJ mice, a model of reduced sociability relevant to autism
-
COI: 1:CAS:528:DC%2BC38Xmt1Cktb8%3D, PID: 22513103
-
Kumar M, Kim S, Pickup S, et al. Longitudinal in-vivo diffusion tensor imaging for assessing brain developmental changes in BALB/cJ mice, a model of reduced sociability relevant to autism. Brain Res 2012;1455:56–67.
-
(2012)
Brain Res
, vol.1455
, pp. 56-67
-
-
Kumar, M.1
Kim, S.2
Pickup, S.3
-
155
-
-
34249793700
-
Sled.JG, Henkelman RM. Mouse behavioral mutants have neuroimaging abnormalities
-
Nieman BJ, Lerch JP, Bock NA, Chen XJ, Sled.JG, Henkelman RM. Mouse behavioral mutants have neuroimaging abnormalities. Hum Brain Mapp 2007;28:567–575.
-
(2007)
Hum Brain Mapp
, vol.28
, pp. 567-575
-
-
Nieman, B.J.1
Lerch, J.P.2
Bock, N.A.3
Chen, X.J.4
-
156
-
-
78650283593
-
Maze training in mice induces MRI-detectable brain shape changes specific to the type of learning
-
PID: 20932918
-
Lerch, J. P., Yiu, A. P., Martinez-Canabal, A., et al. Maze training in mice induces MRI-detectable brain shape changes specific to the type of learning. Neuroimage 2011;54:2086–2095.
-
(2011)
Neuroimage
, vol.54
, pp. 2086-2095
-
-
Lerch, J.P.1
Yiu, A.P.2
Martinez-Canabal, A.3
-
157
-
-
80054997134
-
Shining new light on the brain
-
COI: 1:CAS:528:DC%2BC3MXhtl2hsLfN, PID: 22145158
-
Gross M. Shining new light on the brain. Curr Biol 2011;21:R831-R833.
-
(2011)
Curr Biol
, vol.21
, pp. R831-R833
-
-
Gross, M.1
-
158
-
-
84904391507
-
Optogenetic insights on the relationship between anxiety-related behaviors and social deficits
-
PID: 25076878
-
Allsop SA, Vander Weele CM, Wichmann R, Tye KM. Optogenetic insights on the relationship between anxiety-related behaviors and social deficits. Front Behav Neurosci 2014;8:241.
-
(2014)
Front Behav Neurosci
, vol.8
, pp. 241
-
-
Allsop, S.A.1
Vander Weele, C.M.2
Wichmann, R.3
Tye, K.M.4
-
159
-
-
84891166667
-
Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion
-
COI: 1:CAS:528:DC%2BC2cXltFOi, PID: 23999526
-
Ellegood J, Markx S, Lerch JP, et al. Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion. Mol Psychiatry 2014;19:99–107.
-
(2014)
Mol Psychiatry
, vol.19
, pp. 99-107
-
-
Ellegood, J.1
Markx, S.2
Lerch, J.P.3
-
160
-
-
84864519921
-
Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain
-
COI: 1:CAS:528:DC%2BC38XhtVeiu7rP, PID: 22589251
-
Harper KM, Hiramoto T, Tanigaki K, et al. Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain. Hum Mol Genet 2012;21:3489–3499.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 3489-3499
-
-
Harper, K.M.1
Hiramoto, T.2
Tanigaki, K.3
-
161
-
-
31444443968
-
Social behavior deficits in the Fmr1 mutant mouse
-
COI: 1:CAS:528:DC%2BD28XhtV2ltrg%3D, PID: 16343653
-
Mineur YS, Huynh LX, Crusio WE. Social behavior deficits in the Fmr1 mutant mouse. Behav Brain Res 2006;168:172–175.
-
(2006)
Behav Brain Res
, vol.168
, pp. 172-175
-
-
Mineur, Y.S.1
Huynh, L.X.2
Crusio, W.E.3
-
162
-
-
84888781767
-
Delayed myelination in a mouse model of fragile X syndrome
-
COI: 1:CAS:528:DC%2BC3sXhvVGqu73N, PID: 23740941
-
Pacey LKK, Xuan ICY, Guan S, et al. Delayed myelination in a mouse model of fragile X syndrome. Hum Mol Genet 2013;22:3920–3930.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 3920-3930
-
-
Pacey, L.K.K.1
Xuan, I.C.Y.2
Guan, S.3
-
163
-
-
84922229342
-
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity
-
COI: 1:CAS:528:DC%2BC2cXhsFylsbrK, PID: 25199916
-
Ellegood J, Anagnostou E, Babineau BA, et al. Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity. Mol Psychiatry 2015;20:118–125.
-
(2015)
Mol Psychiatry
, vol.20
, pp. 118-125
-
-
Ellegood, J.1
Anagnostou, E.2
Babineau, B.A.3
-
164
-
-
84870016257
-
Female Mecp2(+/−) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies
-
COI: 1:CAS:528:DC%2BC38XhvVChs7fK, PID: 23026749
-
Samaco RC, McGraw CM, Ward CS, Sun Y, Neul JL, Zoghbi HY. Female Mecp2(+/−) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies. Hum Mol Genet 2013;22:96–109.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 96-109
-
-
Samaco, R.C.1
McGraw, C.M.2
Ward, C.S.3
Sun, Y.4
Neul, J.L.5
Zoghbi, H.Y.6
-
165
-
-
77952291678
-
Cognitive and social functions and growth factors in a mouse model of Rett syndrome
-
COI: 1:CAS:528:DC%2BC3cXlt1Gjtr8%3D, PID: 20045424
-
Schaevitz LR, Moriuchi JM, Nag N, Mellot TJ, Berger-Sweeney J. Cognitive and social functions and growth factors in a mouse model of Rett syndrome. Physiol Behav 2010;100:255–263.
-
(2010)
Physiol Behav
, vol.100
, pp. 255-263
-
-
Schaevitz, L.R.1
Moriuchi, J.M.2
Nag, N.3
Mellot, T.J.4
Berger-Sweeney, J.5
-
166
-
-
84860691547
-
Mecp2 truncation in male mice promotes affiliative social behavior
-
COI: 1:STN:280:DC%2BC383hvVensA%3D%3D, PID: 21909962
-
Pearson BL, Defensor EB, Pobbe RLH, et al. Mecp2 truncation in male mice promotes affiliative social behavior. Behav Genet 2012;42:299–312.
-
(2012)
Behav Genet
, vol.42
, pp. 299-312
-
-
Pearson, B.L.1
Defensor, E.B.2
Pobbe, R.L.H.3
-
167
-
-
84894326125
-
Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas
-
PID: 24151012
-
Steadman PE, Ellegood J, Szulc KU, et al. Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas. Autism Res 2014;7:124–137.
-
(2014)
Autism Res
, vol.7
, pp. 124-137
-
-
Steadman, P.E.1
Ellegood, J.2
Szulc, K.U.3
-
168
-
-
12744261491
-
Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome
-
COI: 1:CAS:528:DC%2BD2MXitFGlug%3D%3D, PID: 15548546
-
Moretti P, Bouwknecht JA, Teague R, Paylor R, Zoghbi HY. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome. Hum Mol Genet 2005;14:205–220.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 205-220
-
-
Moretti, P.1
Bouwknecht, J.A.2
Teague, R.3
Paylor, R.4
Zoghbi, H.Y.5
-
169
-
-
84886380930
-
High resolution whole brain imaging of anatomical variation in XO, XX, and XY mice
-
PID: 23891883
-
Raznahan A, Probst F, Palmert MR, Giedd JN, Lerch JP. High resolution whole brain imaging of anatomical variation in XO, XX, and XY mice. Neuroimage 2013;83:962–968.
-
(2013)
Neuroimage
, vol.83
, pp. 962-968
-
-
Raznahan, A.1
Probst, F.2
Palmert, M.R.3
Giedd, J.N.4
Lerch, J.P.5
-
170
-
-
84871944400
-
Age dependent forebrain structural changes in mice deficient in the autism associated gene Met tyrosine kinase
-
PID: 24179738
-
Smith JM, Xu J, Powell EM. Age dependent forebrain structural changes in mice deficient in the autism associated gene Met tyrosine kinase. Neuroimage Clin 2012;1:66–74.
-
(2012)
Neuroimage Clin
, vol.1
, pp. 66-74
-
-
Smith, J.M.1
Xu, J.2
Powell, E.M.3
-
171
-
-
70449686185
-
Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
-
COI: 1:CAS:528:DC%2BD1MXhtl2qtr7I, PID: 19822762
-
Etherton MR, Blaiss CA, Powell CM, Südhof TC. Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments. Proc Natl Acad Sci U S A 2009;106:17998–18003.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 17998-18003
-
-
Etherton, M.R.1
Blaiss, C.A.2
Powell, C.M.3
Südhof, T.C.4
-
172
-
-
84879522237
-
Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders
-
COI: 1:CAS:528:DC%2BC3sXhtFahsr7M, PID: 23840597
-
Grayton HM, Missler M, Collier DA, Fernandes C. Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders. PLoS ONE 2013;8:e67114.
-
(2013)
PLoS ONE
, vol.8
, pp. e67114
-
-
Grayton, H.M.1
Missler, M.2
Collier, D.A.3
Fernandes, C.4
-
173
-
-
84992437960
-
Mapping pathological phenotypes in reelin mutant mice
-
PID: 25237666
-
Michetti C, Romano E, Altabella L, et al. Mapping pathological phenotypes in reelin mutant mice. Front Pediatr 2014;2:95.
-
(2014)
Front Pediatr
, vol.2
, pp. 95
-
-
Michetti, C.1
Romano, E.2
Altabella, L.3
-
174
-
-
17044378032
-
Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons
-
COI: 1:CAS:528:DC%2BD2MXjtlSisr4%3D, PID: 15814786
-
Roussignol G, Ango F, Romorini S, et al. Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons. J Neurosci 2005;25:3560–3570.
-
(2005)
J Neurosci
, vol.25
, pp. 3560-3570
-
-
Roussignol, G.1
Ango, F.2
Romorini, S.3
-
175
-
-
80054889797
-
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
-
COI: 1:CAS:528:DC%2BC3cXhs1eit7bE, PID: 21167025
-
Bozdagi O, Sakurai T, Papapetrou D, et al. Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Mol Autism 2010;1:15.
-
(2010)
Mol Autism
, vol.1
, pp. 15
-
-
Bozdagi, O.1
Sakurai, T.2
Papapetrou, D.3
|