-
1
-
-
7444221710
-
Localizing gray matter deficits in lateonset depression using computational cortical pattern matching methods
-
Ballmaier M, Kumar A, Thompson P, Narr K, Lavretsky H, Estanol L, Deluca H, Toga AW. 2004. Localizing gray matter deficits in lateonset depression using computational cortical pattern matching methods. Am J Psychiatry. 161(11):2091-2099.
-
(2004)
Am J Psychiatry
, vol.161
, Issue.11
, pp. 2091-2099
-
-
Ballmaier, M.1
Kumar, A.2
Thompson, P.3
Narr, K.4
Lavretsky, H.5
Estanol, L.6
Deluca, H.7
Toga, A.W.8
-
2
-
-
7244229690
-
Regional brain abnormalities in 22q11.2 deletion syndrome: Association with cognitive abilities and behavioral symptoms
-
Bearden CE, van Erp TG, Monterosso JR, Simon TJ, Glahn DC, Saleh PA, Hill NM, McDonald-McGinn DM, Zackai E, Emanuel BS, et al. 2004. Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms. Neurocase. 10(3):198-206.
-
(2004)
Neurocase
, vol.10
, Issue.3
, pp. 198-206
-
-
Bearden, C.E.1
van Erp, T.G.2
Monterosso, J.R.3
Simon, T.J.4
Glahn, D.C.5
Saleh, P.A.6
Hill, N.M.7
McDonald-McGinn, D.M.8
Zackai, E.9
Emanuel, B.S.10
-
3
-
-
0037043786
-
Williams syndrome cognitive profile also characterizes velocardiofacial/DiGeorge syndrome
-
Bearden CE, Wang PP, Simon TJ. 2002. Williams syndrome cognitive profile also characterizes velocardiofacial/DiGeorge syndrome. Am J Med Genet. 114(6):689-692.
-
(2002)
Am J Med Genet
, vol.114
, Issue.6
, pp. 689-692
-
-
Bearden, C.E.1
Wang, P.P.2
Simon, T.J.3
-
4
-
-
0034873653
-
The neurocognitive phenotype of the 22q11.2 deletion syndrome: Selective deficit in visual-spatial memory
-
Bearden CE, Woodin MF, Wang PP, Moss E, McDonald-McGinn D, Zackai E, Emanuel B, Cannon TD. 2001. The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory. J Clin Exp Neuropsychol. 23(4):447-464.
-
(2001)
J Clin Exp Neuropsychol
, vol.23
, Issue.4
, pp. 447-464
-
-
Bearden, C.E.1
Woodin, M.F.2
Wang, P.P.3
Moss, E.4
McDonald-McGinn, D.5
Zackai, E.6
Emanuel, B.7
Cannon, T.D.8
-
5
-
-
21844461067
-
Genetic bases for endophenotypes in psychiatric disorders
-
Berrettini WH. 2005. Genetic bases for endophenotypes in psychiatric disorders. Dialogues Clin Neurosci. 7(2):95-101.
-
(2005)
Dialogues Clin Neurosci
, vol.7
, Issue.2
, pp. 95-101
-
-
Berrettini, W.H.1
-
6
-
-
0030828882
-
Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11
-
Bingham PM, Zimmerman RA, McDonald-McGinn D, Driscoll D, Emanuel BS, Zackai E. 1997. Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11. Am J Med Genet. 74(5):538-543.
-
(1997)
Am J Med Genet
, vol.74
, Issue.5
, pp. 538-543
-
-
Bingham, P.M.1
Zimmerman, R.A.2
McDonald-McGinn, D.3
Driscoll, D.4
Emanuel, B.S.5
Zackai, E.6
-
7
-
-
0029798254
-
MR of the cerebral operculum: Abnormal opercular formation in infants and children
-
Chen CY, Zimmerman RA, Faro S, Parrish B, Wang Z, Bilaniuk LT, Chou TY. 1996. MR of the cerebral operculum: abnormal opercular formation in infants and children. Am J Neuroradiol. 17(7):1303-1311.
-
(1996)
Am J Neuroradiol
, vol.17
, Issue.7
, pp. 1303-1311
-
-
Chen, C.Y.1
Zimmerman, R.A.2
Faro, S.3
Parrish, B.4
Wang, Z.5
Bilaniuk, L.T.6
Chou, T.Y.7
-
8
-
-
0036468696
-
Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome
-
Chow EW, Zipursky RB, Mikulis DJ, Bassett AS. 2002. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biol Psychiatry. 51(3):208-215.
-
(2002)
Biol Psychiatry
, vol.51
, Issue.3
, pp. 208-215
-
-
Chow, E.W.1
Zipursky, R.B.2
Mikulis, D.J.3
Bassett, A.S.4
-
9
-
-
0034287039
-
Language and calculation within the parietal lobe: A combined cognitive, anatomical and fMRI study
-
Cohen L, Dehaene S, Chochon F, Lehericy S, Naccache L. 2000. Language and calculation within the parietal lobe: a combined cognitive, anatomical and fMRI study. Neuropsychologia. 38(10):1426-1440.
-
(2000)
Neuropsychologia
, vol.38
, Issue.10
, pp. 1426-1440
-
-
Cohen, L.1
Dehaene, S.2
Chochon, F.3
Lehericy, S.4
Naccache, L.5
-
10
-
-
0028287162
-
Automatic 3D intersubject registration of MR volumetric data into standardized Talairach space
-
Collins DL, Neelin P, Peters TM, Evans AC. 1994. Automatic 3D intersubject registration of MR volumetric data into standardized Talairach space. J Comput Assist Tomogr. 18(2):192-205.
-
(1994)
J Comput Assist Tomogr
, vol.18
, Issue.2
, pp. 192-205
-
-
Collins, D.L.1
Neelin, P.2
Peters, T.M.3
Evans, A.C.4
-
11
-
-
0025649549
-
Temporal lobe asymmetries as the key to the etiology of schizophrenia
-
Crow TJ. 1990. Temporal lobe asymmetries as the key to the etiology of schizophrenia. Schizophr Bull. 16(3):433-443.
-
(1990)
Schizophr Bull
, vol.16
, Issue.3
, pp. 433-443
-
-
Crow, T.J.1
-
12
-
-
0033213393
-
Form and content: Dissociating syntax and semantics in sentence comprehension
-
Dapretto M, Bookheimer SY. 1999. Form and content: dissociating syntax and semantics in sentence comprehension. Neuron. 24(2):427-432.
-
(1999)
Neuron
, vol.24
, Issue.2
, pp. 427-432
-
-
Dapretto, M.1
Bookheimer, S.Y.2
-
13
-
-
0034064651
-
Children and adolescents with velocardiofacial syndrome: A volumetric MRI study
-
Eliez S, Schmitt JE, White CD, Reiss AL. 2000. Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. Am J Psychiatry. 157(3):409-415.
-
(2000)
Am J Psychiatry
, vol.157
, Issue.3
, pp. 409-415
-
-
Eliez, S.1
Schmitt, J.E.2
White, C.D.3
Reiss, A.L.4
-
14
-
-
0035869620
-
A quantitative MRI study of posterior fossa development in velocardiofacial syndrome
-
Eliez S, Schmitt JE, White CD, Wellis VG, Reiss AL. 2001. A quantitative MRI study of posterior fossa development in velocardiofacial syndrome. Biol Psychiatry. 49(6):540-546.
-
(2001)
Biol Psychiatry
, vol.49
, Issue.6
, pp. 540-546
-
-
Eliez, S.1
Schmitt, J.E.2
White, C.D.3
Wellis, V.G.4
Reiss, A.L.5
-
16
-
-
0032721892
-
The genetic basis of cognition
-
Flint J. 1999. The genetic basis of cognition. Brain. 122(Pt 11):2015-2032.
-
(1999)
Brain
, vol.122
, Issue.PART 11
, pp. 2015-2032
-
-
Flint, J.1
-
17
-
-
0019741981
-
Anatomical asymmetries in the adult and developing brain and their implications for function
-
Galaburda AM, Geschwind N. 1981. Anatomical asymmetries in the adult and developing brain and their implications for function. Adv Pediatr. 28:271-292.
-
(1981)
Adv Pediatr
, vol.28
, pp. 271-292
-
-
Galaburda, A.M.1
Geschwind, N.2
-
18
-
-
0018163034
-
Human brain. Cytoarchitectonic left-right asymmetries in the temporal speech region
-
Galaburda AM, Sanides F, Geschwind N. 1978. Human brain. Cytoarchitectonic left-right asymmetries in the temporal speech region. Arch Neurol. 35(12):812-817.
-
(1978)
Arch Neurol
, vol.35
, Issue.12
, pp. 812-817
-
-
Galaburda, A.M.1
Sanides, F.2
Geschwind, N.3
-
19
-
-
0033066999
-
Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion
-
Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P, Goldmuntz E, Clark BJ 3rd, Driscoll DA, Jawad A, et al. 1999. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet. 85(2):127-133.
-
(1999)
Am J Med Genet
, vol.85
, Issue.2
, pp. 127-133
-
-
Gerdes, M.1
Solot, C.2
Wang, P.P.3
Moss, E.4
LaRossa, D.5
Randall, P.6
Goldmuntz, E.7
Clark 3rd, B.J.8
Driscoll, D.A.9
Jawad, A.10
-
20
-
-
0032948179
-
The gene encoding proline dehydrogenase modulates sensorimotor gating in mice
-
Gogos JA, Santha M, Takacs Z, Beck KD, Luine V, Lucas LR, Nadler JV, Karayiorgou M. 1999. The gene encoding proline dehydrogenase modulates sensorimotor gating in mice. Nat Genet. 21(4):434-439.
-
(1999)
Nat Genet
, vol.21
, Issue.4
, pp. 434-439
-
-
Gogos, J.A.1
Santha, M.2
Takacs, Z.3
Beck, K.D.4
Luine, V.5
Lucas, L.R.6
Nadler, J.V.7
Karayiorgou, M.8
-
21
-
-
2542597718
-
Dynamic mapping of human cortical development during childhood through early adulthood
-
Gogtay N, Giedd JN, Lusk L, Hayashi KM, Greenstein D, Vaituzis AC, Nugent TF 3rd, Herman DH, Clasen LS, Toga AW, et al. 2004. Dynamic mapping of human cortical development during childhood through early adulthood. Proc Natl Acad Sci USA. 101(21):8174-8179.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, Issue.21
, pp. 8174-8179
-
-
Gogtay, N.1
Giedd, J.N.2
Lusk, L.3
Hayashi, K.M.4
Greenstein, D.5
Vaituzis, A.C.6
Nugent 3rd, T.F.7
Herman, D.H.8
Clasen, L.S.9
Toga, A.W.10
-
22
-
-
0032924127
-
The neuropathology of schizophrenia. A critical review of the data and their interpretation
-
Harrison PJ. 1999. The neuropathology of schizophrenia. A critical review of the data and their interpretation. Brain. 122(Pt 4):593-624.
-
(1999)
Brain
, vol.122
, Issue.PART 4
, pp. 593-624
-
-
Harrison, P.J.1
-
23
-
-
0032768204
-
Schizophrenia and temporal lobe asymmetry. A post-mortem stereological study of tissue volume
-
Highley JR, McDonald B, Walker MA, Esiri MM, Crow TJ. 1999. Schizophrenia and temporal lobe asymmetry. A post-mortem stereological study of tissue volume. Br J Psychiatry. 175:127-134.
-
(1999)
Br J Psychiatry
, vol.175
, pp. 127-134
-
-
Highley, J.R.1
McDonald, B.2
Walker, M.A.3
Esiri, M.M.4
Crow, T.J.5
-
24
-
-
20044363089
-
Interactions between number and space in parietal cortex
-
Hubbard EM, Piazza M, Pinel P, Dehaene S. 2005. Interactions between number and space in parietal cortex. Nat Rev Neurosci. 6(6):435-448.
-
(2005)
Nat Rev Neurosci
, vol.6
, Issue.6
, pp. 435-448
-
-
Hubbard, E.M.1
Piazza, M.2
Pinel, P.3
Dehaene, S.4
-
25
-
-
3042704489
-
Resolving schizophrenia's CATCH22
-
Jablensky A. 2004. Resolving schizophrenia's CATCH22. Nat Genet. 36(7):674-765.
-
(2004)
Nat Genet
, vol.36
, Issue.7
, pp. 674-765
-
-
Jablensky, A.1
-
26
-
-
4544300012
-
Exploring the Williams syndrome face-processing debate: The importance of building developmental trajectories
-
Karmiloff-Smith A, Thomas M, Annaz D, Humphreys K, Ewing S, Brace N, Duuren M, Pike G, Grice S, Campbell R. 2004. Exploring the Williams syndrome face-processing debate: the importance of building developmental trajectories. J Child Psychol Psychiatry. 45(7):1258-1274.
-
(2004)
J Child Psychol Psychiatry
, vol.45
, Issue.7
, pp. 1258-1274
-
-
Karmiloff-Smith, A.1
Thomas, M.2
Annaz, D.3
Humphreys, K.4
Ewing, S.5
Brace, N.6
Duuren, M.7
Pike, G.8
Grice, S.9
Campbell, R.10
-
27
-
-
0035871350
-
Regional cortical white matter reductions in velocardiofacial syndrome: A volumetric MRI analysis
-
Kates WR, Burnette CP, Jabs EW, Rutberg J, Murphy AM, Grados M, Geraghty M, Kaufmann WE, Pearlson GD. 2001. Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis. Biol Psychiatry. 49(8):677-684.
-
(2001)
Biol Psychiatry
, vol.49
, Issue.8
, pp. 677-684
-
-
Kates, W.R.1
Burnette, C.P.2
Jabs, E.W.3
Rutberg, J.4
Murphy, A.M.5
Grados, M.6
Geraghty, M.7
Kaufmann, W.E.8
Pearlson, G.D.9
-
28
-
-
34247138229
-
Normal developmental changes in inferior frontal gray matter are associated with improvement in phonological processing: A longitudinal MRI analysis
-
June 6, 10.1093/cercor/bhl019
-
Lu LH, Leonard CM, Thompson PM, Kan E, Jolley J, Welcome SE, Toga AW, Sowell ER. June 6, 2006. Normal developmental changes in inferior frontal gray matter are associated with improvement in phonological processing: a longitudinal MRI analysis. Cereb Cortex. 10.1093/cercor/bhl019.
-
(2006)
Cereb Cortex
-
-
Lu, L.H.1
Leonard, C.M.2
Thompson, P.M.3
Kan, E.4
Jolley, J.5
Welcome, S.E.6
Toga, A.W.7
Sowell, E.R.8
-
29
-
-
33745769023
-
Hemispheric asymmetries in cortical thickness
-
Luders E, Narr KL, Thompson PM, Rex DE, Jancke L, Toga AW. 2006. Hemispheric asymmetries in cortical thickness. Cereb Cortex. 16(8):1232-1238.
-
(2006)
Cereb Cortex
, vol.16
, Issue.8
, pp. 1232-1238
-
-
Luders, E.1
Narr, K.L.2
Thompson, P.M.3
Rex, D.E.4
Jancke, L.5
Toga, A.W.6
-
30
-
-
33749765551
-
Multiple surface identification and matching in magnetic resonance imaging
-
MacDonald D, Avis D, Evans A. 1994. Multiple surface identification and matching in magnetic resonance imaging. Proc SPIE. 2359:160-169.
-
(1994)
Proc SPIE
, vol.2359
, pp. 160-169
-
-
MacDonald, D.1
Avis, D.2
Evans, A.3
-
32
-
-
0345060815
-
A comprehensive analysis of 22q11 gene expression in the developing and adult brain
-
Maynard TM, Haskell GT, Peters AZ, Sikich L, Lieberman JA, LaMantia AS. 2003. A comprehensive analysis of 22q11 gene expression in the developing and adult brain. Proc Natl Acad Sci USA. 100(24):14433-14438.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, Issue.24
, pp. 14433-14438
-
-
Maynard, T.M.1
Haskell, G.T.2
Peters, A.Z.3
Sikich, L.4
Lieberman, J.A.5
LaMantia, A.S.6
-
33
-
-
0029043654
-
A probabilistic atlas of the human brain: Theory and rationale for its development. The International Consortium for Brain Mapping (ICBM)
-
Mazziotta JC, Toga AW, Evans A, Fox P, Lancaster J. 1995. A probabilistic atlas of the human brain: theory and rationale for its development. The International Consortium for Brain Mapping (ICBM). Neuroimage. 2(2):89-101.
-
(1995)
Neuroimage
, vol.2
, Issue.2
, pp. 89-101
-
-
Mazziotta, J.C.1
Toga, A.W.2
Evans, A.3
Fox, P.4
Lancaster, J.5
-
34
-
-
0033961703
-
Anomalous asymmetry of fusiform and parahippocampal gyrus gray matter in schizophrenia: A postmortem study
-
McDonald B, Highley JR, Walker MA, Herron BM, Cooper SJ, Esiri MM, Crow TJ. 2000. Anomalous asymmetry of fusiform and parahippocampal gyrus gray matter in schizophrenia: a postmortem study. Am J Psychiatry. 157(1):40-47.
-
(2000)
Am J Psychiatry
, vol.157
, Issue.1
, pp. 40-47
-
-
McDonald, B.1
Highley, J.R.2
Walker, M.A.3
Herron, B.M.4
Cooper, S.J.5
Esiri, M.M.6
Crow, T.J.7
-
35
-
-
0031291657
-
The 22q11.2 deletion: Screening, diagnostic workup, and outcome of results; report on 181 patients
-
McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, et al. 1997. The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients. Genet Test. 1(2):99-108.
-
(1997)
Genet Test
, vol.1
, Issue.2
, pp. 99-108
-
-
McDonald-McGinn, D.M.1
LaRossa, D.2
Goldmuntz, E.3
Sullivan, K.4
Eicher, P.5
Gerdes, M.6
Moss, E.7
Wang, P.8
Solot, C.9
Schultz, P.10
-
36
-
-
4444331998
-
Neural basis of genetically determined visuospatial construction deficit in Williams syndrome
-
Meyer-Lindenberg A, Mervis CB, Kippenhan JS, Olsen RK, Morris CA, Berman KF. 2004. Neural basis of genetically determined visuospatial construction deficit in Williams syndrome. Neuron. 43(5):623-631.
-
(2004)
Neuron
, vol.43
, Issue.5
, pp. 623-631
-
-
Meyer-Lindenberg, A.1
Mervis, C.B.2
Kippenhan, J.S.3
Olsen, R.K.4
Morris, C.A.5
Berman, K.F.6
-
37
-
-
18044379146
-
Selective reduction in amygdala volume in pediatric anxiety disorders: A voxel-based morphometry investigation
-
Milham MP, Nugent AC, Drevets WC, Dickstein DP, Leibenluft E, Ernst M, Charney D, Pine DS. 2005. Selective reduction in amygdala volume in pediatric anxiety disorders: a voxel-based morphometry investigation. Biol Psychiatry. 57(9):961-966.
-
(2005)
Biol Psychiatry
, vol.57
, Issue.9
, pp. 961-966
-
-
Milham, M.P.1
Nugent, A.C.2
Drevets, W.C.3
Dickstein, D.P.4
Leibenluft, E.5
Ernst, M.6
Charney, D.7
Pine, D.S.8
-
38
-
-
14844331054
-
DiGeorge syndrome, a review of 52 patients]
-
Minier F, Carles D, Pelluard F, Alberti EM, Stern L, Saura R. 2005. [DiGeorge syndrome, a review of 52 patients]. Arch Pediatr. 12(3):254-257.
-
(2005)
Arch Pediatr
, vol.12
, Issue.3
, pp. 254-257
-
-
Minier, F.1
Carles, D.2
Pelluard, F.3
Alberti, E.M.4
Stern, L.5
Saura, R.6
-
39
-
-
0033063788
-
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern [see comments]
-
Moss EM, Batshaw ML, Solot CB, Gerdes M, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH, Wang PP. 1999. Psychoeducational profile of the 22q11.2 microdeletion: a complex pattern [see comments]. J Pediatr. 134(2):193-198.
-
(1999)
J Pediatr
, vol.134
, Issue.2
, pp. 193-198
-
-
Moss, E.M.1
Batshaw, M.L.2
Solot, C.B.3
Gerdes, M.4
McDonald-McGinn, D.M.5
Driscoll, D.A.6
Emanuel, B.S.7
Zackai, E.H.8
Wang, P.P.9
-
40
-
-
3042804077
-
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia
-
Mukai J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M, Gogos JA. 2004. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat Genet. 36(7):725-731.
-
(2004)
Nat Genet
, vol.36
, Issue.7
, pp. 725-731
-
-
Mukai, J.1
Liu, H.2
Burt, R.A.3
Swor, D.E.4
Lai, W.S.5
Karayiorgou, M.6
Gogos, J.A.7
-
41
-
-
0037006412
-
Schizophrenia and velo-cardio-facial syndrome
-
Murphy KC. 2002. Schizophrenia and velo-cardio-facial syndrome. Lancet. 359(9304):426-430.
-
(2002)
Lancet
, vol.359
, Issue.9304
, pp. 426-430
-
-
Murphy, K.C.1
-
42
-
-
12844255141
-
Cortical thickness of the frontopolar area in typically developing children and adolescents
-
O'Donnell S, Noseworthy MD, Levine B, Dennis M. 2005. Cortical thickness of the frontopolar area in typically developing children and adolescents. Neuroimage. 24(4):948-954.
-
(2005)
Neuroimage
, vol.24
, Issue.4
, pp. 948-954
-
-
O'Donnell, S.1
Noseworthy, M.D.2
Levine, B.3
Dennis, M.4
-
43
-
-
34547682618
-
-
Ono M, Kubik S, Abernathey C. 1990. Atlas of the cerebral sulci. Stuttgart (Germany): Thieme. Paterlini M, Zakharenko SS, Lai WS, Qin J, Zhang H, Mukai J, Westphal KG, Olivier B, Sulzer D, Pavlidis P, et al. 2005. Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice. Nat Neurosci. 8(11):1586-1594.
-
Ono M, Kubik S, Abernathey C. 1990. Atlas of the cerebral sulci. Stuttgart (Germany): Thieme. Paterlini M, Zakharenko SS, Lai WS, Qin J, Zhang H, Mukai J, Westphal KG, Olivier B, Sulzer D, Pavlidis P, et al. 2005. Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice. Nat Neurosci. 8(11):1586-1594.
-
-
-
-
44
-
-
0029905766
-
Brain development, gender and IQ in children. A volumetric imaging study
-
Reiss AL, Abrams MT, Singer HS, Ross JL, Denckla MB. 1996. Brain development, gender and IQ in children. A volumetric imaging study. Brain. 119(Pt 5):1763-1774.
-
(1996)
Brain
, vol.119
, Issue.PART 5
, pp. 1763-1774
-
-
Reiss, A.L.1
Abrams, M.T.2
Singer, H.S.3
Ross, J.L.4
Denckla, M.B.5
-
45
-
-
0031040868
-
Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome
-
Roberts C, Daw SC, Halford S, Scambler PJ. 1997. Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome. Hum Mol Genet. 6(2):237-245.
-
(1997)
Hum Mol Genet
, vol.6
, Issue.2
, pp. 237-245
-
-
Roberts, C.1
Daw, S.C.2
Halford, S.3
Scambler, P.J.4
-
46
-
-
0033753819
-
The 22q11 deletion syndromes
-
Scambler PJ. 2000. The 22q11 deletion syndromes. Hum Mol Genet. 9(16):2421-2426.
-
(2000)
Hum Mol Genet
, vol.9
, Issue.16
, pp. 2421-2426
-
-
Scambler, P.J.1
-
47
-
-
0036624329
-
BrainSuite: An automated cortical surface identification tool
-
Shattuck DW, Leahy RM. 2002. BrainSuite: an automated cortical surface identification tool. Med Image Anal. 6(2):129-142.
-
(2002)
Med Image Anal
, vol.6
, Issue.2
, pp. 129-142
-
-
Shattuck, D.W.1
Leahy, R.M.2
-
48
-
-
33645453807
-
Intellectual ability and cortical development in children and adolescents
-
Shaw P, Greenstein D, Lerch J, Clasen L, Lenroot R, Gogtay N, Evans A, Rapoport J, Giedd J. 2006. Intellectual ability and cortical development in children and adolescents. Nature. 440(7084):676-679.
-
(2006)
Nature
, vol.440
, Issue.7084
, pp. 676-679
-
-
Shaw, P.1
Greenstein, D.2
Lerch, J.3
Clasen, L.4
Lenroot, R.5
Gogtay, N.6
Evans, A.7
Rapoport, J.8
Giedd, J.9
-
49
-
-
0036066303
-
Cognitive development in velocardiofacial syndrome
-
Simon T, Bearden C, Moss E, Zackai E, Wang P. 2002. Cognitive development in velocardiofacial syndrome. Prog Pediatr Cardiol. 15(2):109-117.
-
(2002)
Prog Pediatr Cardiol
, vol.15
, Issue.2
, pp. 109-117
-
-
Simon, T.1
Bearden, C.2
Moss, E.3
Zackai, E.4
Wang, P.5
-
50
-
-
33645921626
-
A multiple levels analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children
-
Simon T, Bish J, Bearden C, Ding L, Ferrante S, Nguyen V, Gee J, McDonald-McGinn D, Zackai E, Emanuel BS. 2005. A multiple levels analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children. Dev Psychopathol. 17(3):753-784.
-
(2005)
Dev Psychopathol
, vol.17
, Issue.3
, pp. 753-784
-
-
Simon, T.1
Bish, J.2
Bearden, C.3
Ding, L.4
Ferrante, S.5
Nguyen, V.6
Gee, J.7
McDonald-McGinn, D.8
Zackai, E.9
Emanuel, B.S.10
-
51
-
-
21244445787
-
Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome
-
Sobin C, Kiley-Brabeck K, Karayiorgou M. 2005. Associations between prepulse inhibition and executive visual attention in children with the 22q11 deletion syndrome. Mol Psychiatry. 10(6):553-562.
-
(2005)
Mol Psychiatry
, vol.10
, Issue.6
, pp. 553-562
-
-
Sobin, C.1
Kiley-Brabeck, K.2
Karayiorgou, M.3
-
52
-
-
0033306649
-
In vivo evidence for post-adolescent brain maturation in frontal and striatal regions
-
Sowell ER, Thompson PM, Holmes CJ, Jernigan TL, Toga AW. 1999. In vivo evidence for post-adolescent brain maturation in frontal and striatal regions. Nat Neurosci. 2(10):859-861.
-
(1999)
Nat Neurosci
, vol.2
, Issue.10
, pp. 859-861
-
-
Sowell, E.R.1
Thompson, P.M.2
Holmes, C.J.3
Jernigan, T.L.4
Toga, A.W.5
-
53
-
-
0035890277
-
Mapping continued brain growth and gray matter density reduction in dorsal frontal cortex: Inverse relationships during postadolescent brain maturation
-
Sowell ER, Thompson PM, Tessner KD, Toga AW. 2001. Mapping continued brain growth and gray matter density reduction in dorsal frontal cortex: inverse relationships during postadolescent brain maturation. J Neurosci. 21(22):8819-8829.
-
(2001)
J Neurosci
, vol.21
, Issue.22
, pp. 8819-8829
-
-
Sowell, E.R.1
Thompson, P.M.2
Tessner, K.D.3
Toga, A.W.4
-
54
-
-
20544435515
-
Early asymmetry of gene transcription in embryonic human left and right cerebral cortex
-
Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry TJ, Orkin SH, Geschwind DH, Walsh CA. 2005. Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Science. 308(5729):1794-1798.
-
(2005)
Science
, vol.308
, Issue.5729
, pp. 1794-1798
-
-
Sun, T.1
Patoine, C.2
Abu-Khalil, A.3
Visvader, J.4
Sum, E.5
Cherry, T.J.6
Orkin, S.H.7
Geschwind, D.H.8
Walsh, C.A.9
-
55
-
-
33748109768
-
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): From infancy to adolescence
-
Swillen A, Devriendt K, Legius E, Prinzie P, Vogels A, Ghesquiere P, Fryns JP. 1999. The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genet Couns. 10(1):79-88.
-
(1999)
Genet Couns
, vol.10
, Issue.1
, pp. 79-88
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
Prinzie, P.4
Vogels, A.5
Ghesquiere, P.6
Fryns, J.P.7
-
56
-
-
0037319171
-
Dynamics of gray matter loss in Alzheimer's disease
-
Thompson PM, Hayashi KM, de Zubicaray G, Janke AL, Rose SE, Semple J, Herman D, Hong MS, Dittmer SS, Doddrell DM, et al. 2003. Dynamics of gray matter loss in Alzheimer's disease. J Neurosci. 23(3):994-1005.
-
(2003)
J Neurosci
, vol.23
, Issue.3
, pp. 994-1005
-
-
Thompson, P.M.1
Hayashi, K.M.2
de Zubicaray, G.3
Janke, A.L.4
Rose, S.E.5
Semple, J.6
Herman, D.7
Hong, M.S.8
Dittmer, S.S.9
Doddrell, D.M.10
-
57
-
-
7044253600
-
Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia
-
Thompson PM, Hayashi KM, Sowell ER, Gogtay N, Giedd JN, Rapoport JL, de Zubicaray GI, Janke AL, Rose SE, Semple J, et al. 2004. Mapping cortical change in Alzheimer's disease, brain development, and schizophrenia. Neuroimage. 23(Suppl 1):S2-S18.
-
(2004)
Neuroimage
, vol.23
, Issue.SUPPL. 1
-
-
Thompson, P.M.1
Hayashi, K.M.2
Sowell, E.R.3
Gogtay, N.4
Giedd, J.N.5
Rapoport, J.L.6
de Zubicaray, G.I.7
Janke, A.L.8
Rose, S.E.9
Semple, J.10
-
58
-
-
20244374988
-
Abnormal cortical complexity and thickness profiles mapped in Williams syndrome
-
Thompson PM, Lee AD, Dutton RA, Geaga JA, Hayashi KM, Eckert MA, Bellugi U, Galaburda AM, Korenberg JR, Mills DL, et al. 2005. Abnormal cortical complexity and thickness profiles mapped in Williams syndrome. J Neurosci. 25(16):4146-4158.
-
(2005)
J Neurosci
, vol.25
, Issue.16
, pp. 4146-4158
-
-
Thompson, P.M.1
Lee, A.D.2
Dutton, R.A.3
Geaga, J.A.4
Hayashi, K.M.5
Eckert, M.A.6
Bellugi, U.7
Galaburda, A.M.8
Korenberg, J.R.9
Mills, D.L.10
-
59
-
-
0035949688
-
Mapping adolescent brain change reveals dynamic wave of accelerated gray matter loss in very earlyonset schizophrenia
-
Thompson PM, Vidal C, Giedd JN, Gochman P, Blumenthal J, Nicolson R, Toga AW, Rapoport JL. 2001. Mapping adolescent brain change reveals dynamic wave of accelerated gray matter loss in very earlyonset schizophrenia. Proc Natl Acad Sci USA. 98(20):11650-11655.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, Issue.20
, pp. 11650-11655
-
-
Thompson, P.M.1
Vidal, C.2
Giedd, J.N.3
Gochman, P.4
Blumenthal, J.5
Nicolson, R.6
Toga, A.W.7
Rapoport, J.L.8
-
60
-
-
7744229511
-
Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: Preliminary results of a structural magnetic resonance imaging study
-
van Amelsvoort T, Daly E, Henry J, Robertson D, Ng V, Owen M, Murphy KC, Murphy DG. 2004. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Arch Gen Psychiatry. 61(11):1085-1096.
-
(2004)
Arch Gen Psychiatry
, vol.61
, Issue.11
, pp. 1085-1096
-
-
van Amelsvoort, T.1
Daly, E.2
Henry, J.3
Robertson, D.4
Ng, V.5
Owen, M.6
Murphy, K.C.7
Murphy, D.G.8
-
61
-
-
0035010976
-
Structural brain abnormalities associated with deletion at chromosome 22q11: Quantitative neuroimaging study of adults with velo-cardio-facial syndrome
-
van Amelsvoort T, Daly E, Robertson D, Suckling J, Ng V, Critchley H, Owen MJ, Henry J, Murphy KC, Murphy DG. 2001. Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome. Br J Psychiatry. 178:412-419.
-
(2001)
Br J Psychiatry
, vol.178
, pp. 412-419
-
-
van Amelsvoort, T.1
Daly, E.2
Robertson, D.3
Suckling, J.4
Ng, V.5
Critchley, H.6
Owen, M.J.7
Henry, J.8
Murphy, K.C.9
Murphy, D.G.10
-
62
-
-
0035746483
-
Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion
-
Woodin M, Wang PP, Aleman D, McDonald-McGinn D, Zackai E, Moss E. 2001. Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion. Genet Med. 3(1):34-39.
-
(2001)
Genet Med
, vol.3
, Issue.1
, pp. 34-39
-
-
Woodin, M.1
Wang, P.P.2
Aleman, D.3
McDonald-McGinn, D.4
Zackai, E.5
Moss, E.6
-
63
-
-
0033961355
-
Meta-analysis of regional brain volumes in schizophrenia
-
Wright I, Rabe-Hesketh S, Woodruff P, David A, Murray R, Bullmore E. 2000. Meta-analysis of regional brain volumes in schizophrenia. Am J Psychiatry. 157:16-25.
-
(2000)
Am J Psychiatry
, vol.157
, pp. 16-25
-
-
Wright, I.1
Rabe-Hesketh, S.2
Woodruff, P.3
David, A.4
Murray, R.5
Bullmore, E.6
|