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References
100
[1]
Karayiorgou M, Simon TJ, Gogos JA . 22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia. Nat Rev Neurosci 2010; 11: 402–416. 10.1038/nrn2841
[2]
Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J et al. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry 2011; 168: 302–316. 10.1176/appi.ajp.2010.10060876
[3]
Karayiorgou M, Morris MA, Morrow B, Shprintzen RJ, Goldberg R, Borrow J et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci USA 1995; 92: 7612–7616. 10.1073/pnas.92.17.7612
[4]
Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M . Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet 2008; 40: 880–885. 10.1038/ng.162
[5]
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T et al. Strong association of de novo copy number mutations with autism. Science 2007; 316: 445–449. 10.1126/science.1138659
[6]
Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron 2011; 72: 951–963. 10.1016/j.neuron.2011.11.007
[7]
Stark KL, Xu B, Bagchi A, Lai W-S, Liu H, Hsu R et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat Genet 2008; 40: 751–760. 10.1038/ng.138
[8]
Mukai J, Dhilla A, Drew LJ, Stark KL, Cao L, Macdermott AB et al. Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion. Nat Neurosci 2008; 11: 1302–1310. 10.1038/nn.2204
[9]
Sigurdsson T, Stark KL, Karayiorgou M, Gogos JA, Gordon JA . Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia. Nature 2010; 464: 763–767. 10.1038/nature08855
[10]
Fénelon K, Mukai J, Xu B, Hsu P-K, Drew LJ, Karayiorgou M et al. Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex. Proc Natl Acad Sci USA 2011; 108: 4447–4452. 10.1073/pnas.1101219108
[11]
Drew LJ, Stark KL, Fénelon K, Karayiorgou M, Macdermott AB, Gogos JA . Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion. Mol Cell Neurosci 2011; 47: 293–305. 10.1016/j.mcn.2011.05.008
[12]
Xu B, Ionita-Laza I, Roos JL, Boone B, Woodrick S, Sun Y et al. De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia. Nat Genet 2012; 44: 1365–1369. 10.1038/ng.2446
[13]
Drew LJ, Crabtree GW, Markx S, Stark KL, Chaverneff F, Xu B et al. The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders. Int J Dev Neurosci 2011; 29: 259–281. 10.1016/j.ijdevneu.2010.09.007
[14]
Modeling Madness in Mice: One Piece at a Time

P. Alexander Arguello, Joseph A. Gogos

Neuron 2006 10.1016/j.neuron.2006.09.023
[15]
Zhang J, Peng Q, Li Q, Jahanshad N, Hou Z, Jiang M et al. Longitudinal characterization of brain atrophy of a Huntington's disease mouse model by automated morphological analyses of magnetic resonance images. Neuroimage 2010; 49: 2340–2351. 10.1016/j.neuroimage.2009.10.027
[16]
Cramer PE, Cirrito JR, Wesson DW, Lee CYD, Karlo JC, Zinn AE et al. ApoE-directed therapeutics rapidly clear β-amyloid and reverse deficits in AD mouse models. Science 2012; 335: 1503–1506. 10.1126/science.1217697
[17]
Goldberg MS, Pisani A, Haburcak M, Vortherms TA, Kitada T, Costa C et al. Nigrostriatal dopaminergic deficits and hypokinesia caused by inactivation of the familial Parkinsonism-linked gene DJ-1. Neuron 2005; 45: 489–496. 10.1016/j.neuron.2005.01.041
[18]
Lerch JP, Yiu AP, Martinez-Canabal A, Pekar T, Bohbot VD, Frankland PW et al. Maze training in mice induces MRI-detectable brain shape changes specific to the type of learning. Neuroimage 2011; 54: 2086–2095. 10.1016/j.neuroimage.2010.09.086
[19]
Nieman BJ, Wong MD, Henkelman RM . Genes into geometry: imaging for mouse development in 3D. Curr Opini Genet Dev 2011; 21: 638–646. 10.1016/j.gde.2011.08.009
[20]
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. 10.1002/hbm.20408
[21]
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. 10.1016/j.neuroimage.2010.03.038
[22]
Horev G, Ellegood J, Lerch JP, Son Y-EE, Muthuswamy L, Vogel H et al. Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism. Proc Natl Acad Sci USA 2011; 108: 17076–17081. 10.1073/pnas.1114042108
[23]
Ellegood J, Lerch JP, Henkelman RM . Brain abnormalities in a Neuroligin3 R451C knocking mouse model associated with autism. Autism Res 2011; 4: 368–376. 10.1002/aur.215
[24]
Tan GM, Arnone D, McIntosh AM, Ebmeier KP . Meta-analysis of magnetic resonance imaging studies in chromosome 22q11.2 deletion syndrome (velocardiofacial syndrome). Schizophrenia Res 2009; 115: 173–181. 10.1016/j.schres.2009.09.010
[25]
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. 10.1002/jmri.10175
[26]
Lerch JP, Sled JG, Henkelman RM . MRI phenotyping of genetically altered mice. Methods Mol Biol 2011; 711: 349–361. 10.1007/978-1-61737-992-5_17
[27]
Dazai J, Spring S, Cahill LS, Henkelman RM . Multiple-mouse neuroanatomical magnetic resonance imaging. J Vis Exp 2011; 48: 2497.
[28]
Thomas DL, De Vita E, Roberts S, Turner R, Yousry TA, Ordidge RJ . High-resolution fast spin echo imaging of the human brain at 4.7T: implementation and sequence characteristics. Magn Reson Med 2004; 51: 1254–1264. 10.1002/mrm.20106
[29]
Automatic 3D Intersubject Registration of MR Volumetric Data in Standardized Talairach Space

D. Louis Collins, Peter Neelin, Terrence M. Peters et al.

Journal of Computer Assisted Tomography 1994 10.1097/00004728-199403000-00005
[30]
Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain

B AVANTS, C EPSTEIN, M GROSSMAN et al.

Medical Image Analysis 2008 10.1016/j.media.2007.06.004
[31]
A reproducible evaluation of ANTs similarity metric performance in brain image registration

Brian B. Avants, Nicholas J. Tustison, Gang Song et al.

NeuroImage 2011 10.1016/j.neuroimage.2010.09.025
[32]
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. 10.1152/physiolgenomics.00217.2005
[33]
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. 10.1016/j.neuroimage.2008.03.037
[34]
Thresholding of Statistical Maps in Functional Neuroimaging Using the False Discovery Rate

Christopher R. Genovese, Nicole A. Lazar, Thomas Nichols

NeuroImage 2002 10.1006/nimg.2001.1037
[36]
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. 10.1186/1744-9081-3-54
[37]
Gothelf D, Michaelovsky E, Frisch A, Zohar AH, Presburger G, Burg M 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. 10.1017/s1461145706006699
[38]
Kates WR, Burnette CP, Bessette BA, Folley BS, Strunge L, Jabs EW et al. Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). J Child Neurol 2004; 19: 337–342. 10.1177/088307380401900506
[39]
Eliez S, Barnea-Goraly N, Schmitt JE, Liu Y, Reiss AL . Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2). BPS 2002; 52: 68–70.
[40]
Kates WR, Bansal R, Fremont W, Antshel KM, Hao X, Higgins AM et al. Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome. J Am Acad Child Adolesc Psychiatry 2011; 50: e272. 10.1016/j.jaac.2010.12.002
[41]
Chow EWC, Zipursky RB, Mikulis DJ, Bassett AS . Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. BPS 2002; 51: 208–215.
[42]
Eliez S, Schmitt JE, White CD, Reiss AL . Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. Am J Psychiatry 2000; 157: 409–415. 10.1176/appi.ajp.157.3.409
[43]
van Amelsvoort T, Daly E, Robertson D, Suckling J, Ng V, Critchley H et al. Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome. Br J Psychiatry 2001; 178: 412–419. 10.1192/bjp.178.5.412
[44]
Chow EW, Mikulis DJ, Zipursky RB, Scutt LE, Weksberg R, Bassett AS . Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. BPS 1999; 46: 1436–1442.
[45]
Sugama S, Bingham PM, Wang PP, Moss EM, Kobayashi H, Eto Y . Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2). Acta Paediatr 2000; 89: 546–549. 10.1080/080352500750027826
[46]
Giedd JN, Rapoport JL, Garvey MA, Perlmutter S, Swedo SE . MRI assessment of children with obsessive-compulsive disorder or tics associated with streptococcal infection. Am J Psychiatry 2000; 157: 281–283. 10.1176/appi.ajp.157.2.281
[47]
Karayiorgou M, Sobin C, Blundell ML, Galke BL, Malinova L, Goldberg P et al. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder. BPS 1999; 45: 1178–1189.
[48]
Garrett A, Penniman L, Epstein JN, Casey BJ, Hinshaw SP, Glover G et al. Neuroanatomical abnormalities in adolescents with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2008; 47: 1321–1328. 10.1097/chi.0b013e318185d285
[49]
Sobin C, Kiley-Brabeck K, Daniels S, Khuri J, Taylor L, Blundell M et al. Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis. Child Neuropsychol 2005; 11: 39–53. 10.1080/09297040590911167
[50]
Shenton ME, Dickey CC, Frumin M, McCarley RW . A review of MRI findings in schizophrenia. Schizophrenia Res 2001; 49: 1–52. 10.1016/s0920-9964(01)00163-3

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Published
Sep 03, 2013
Vol/Issue
19(1)
Pages
99-107
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J Ellegood, S Markx, J P Lerch, et al. (2013). Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion. Molecular Psychiatry, 19(1), 99-107. https://doi.org/10.1038/mp.2013.112