-
1
-
-
28544438461
-
Sex differences in cognitive functioning in velocardiofacial syndrome (VCFS)
-
Antshel K.M., AbdulSabur N., Roizen N., Fremont W., and Kates W.R. Sex differences in cognitive functioning in velocardiofacial syndrome (VCFS). Dev. Neuropsychol. 28 3 (2005) 849-869
-
(2005)
Dev. Neuropsychol.
, vol.28
, Issue.3
, pp. 849-869
-
-
Antshel, K.M.1
AbdulSabur, N.2
Roizen, N.3
Fremont, W.4
Kates, W.R.5
-
2
-
-
18044377629
-
Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome)
-
Antshel K.M., Conchelos J., Lanzetta G., Fremont W., and Kates W.R. Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome). Psychiatry Res. 138 3 (2005) 235-245
-
(2005)
Psychiatry Res.
, vol.138
, Issue.3
, pp. 235-245
-
-
Antshel, K.M.1
Conchelos, J.2
Lanzetta, G.3
Fremont, W.4
Kates, W.R.5
-
3
-
-
33751260533
-
Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia
-
Arinami T. Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia. J. Hum. Genet. 51 12 (2006) 1037-1045
-
(2006)
J. Hum. Genet.
, vol.51
, Issue.12
, pp. 1037-1045
-
-
Arinami, T.1
-
4
-
-
53749100863
-
Meta-analysis of magnetic resonance imaging studies of the corpus callosum in bipolar disorder
-
Arnone D., McIntosh A.M., Chandra P., and Ebmeier K.P. Meta-analysis of magnetic resonance imaging studies of the corpus callosum in bipolar disorder. Acta Psychiatr. Scand. 118 5 (2008) 357-362
-
(2008)
Acta Psychiatr. Scand.
, vol.118
, Issue.5
, pp. 357-362
-
-
Arnone, D.1
McIntosh, A.M.2
Chandra, P.3
Ebmeier, K.P.4
-
5
-
-
42749096035
-
Meta-analysis of magnetic resonance imaging studies of the corpus callosum in schizophrenia
-
Arnone D., McIntosh A.M., Tan G.M., and Ebmeier K.P. Meta-analysis of magnetic resonance imaging studies of the corpus callosum in schizophrenia. Schizophr. Res. 101 1-3 (2008) 124-132
-
(2008)
Schizophr. Res.
, vol.101
, Issue.1-3
, pp. 124-132
-
-
Arnone, D.1
McIntosh, A.M.2
Tan, G.M.3
Ebmeier, K.P.4
-
6
-
-
13244261075
-
Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group
-
Baker K.D., and Skuse D.H. Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group. Br. J. Psychiatry 186 (2005) 115-120
-
(2005)
Br. J. Psychiatry
, vol.186
, pp. 115-120
-
-
Baker, K.D.1
Skuse, D.H.2
-
7
-
-
49649124127
-
Schizophrenia and 22q11.2 deletion syndrome
-
Bassett A.S., and Chow W.C. Schizophrenia and 22q11.2 deletion syndrome. Curr. Psychiatry Rep. 10 2 (2008) 148-157
-
(2008)
Curr. Psychiatry Rep.
, vol.10
, Issue.2
, pp. 148-157
-
-
Bassett, A.S.1
Chow, W.C.2
-
8
-
-
7244229690
-
Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms
-
Bearden C.E., van Erp T.G., Monterosso J.R., Simon T.J., Glahn D.C., Saleh P.A., Hill N.M., McDonald-McGinn D.M., Zackai E., Emanuel B.S., and Cannon T.D. Regional brain abnormalities in 22q11.2 deletion syndrome: association with cognitive abilities and behavioral symptoms. Neurocase 10 3 (2004) 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
Cannon, T.D.11
-
9
-
-
34547665010
-
Mapping cortical thickness in children with 22q11.2 deletions
-
Bearden C.E., van Erp T.G., Dutton R.A., Tran H., Zimmermann L., Sun D., Geaga J.A., Simon T.J., Glahn D.C., Cannon T.D., Emanuel B.S., Toga A.W., and Thompson P.M. Mapping cortical thickness in children with 22q11.2 deletions. Cereb. Cortex 17 8 (2007) 1889-1898
-
(2007)
Cereb. Cortex
, vol.17
, Issue.8
, pp. 1889-1898
-
-
Bearden, C.E.1
van Erp, T.G.2
Dutton, R.A.3
Tran, H.4
Zimmermann, L.5
Sun, D.6
Geaga, J.A.7
Simon, T.J.8
Glahn, D.C.9
Cannon, T.D.10
Emanuel, B.S.11
Toga, A.W.12
Thompson, P.M.13
-
10
-
-
42049110960
-
Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome
-
Boot E., Booij J., Zinkstok J., Abeling N., de Haan L., Baas F., Linszen D., and van Amelsvoort T. Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome. Neuropsychopharmacology 33 6 (2008) 1252-1258
-
(2008)
Neuropsychopharmacology
, vol.33
, Issue.6
, pp. 1252-1258
-
-
Boot, E.1
Booij, J.2
Zinkstok, J.3
Abeling, N.4
de Haan, L.5
Baas, F.6
Linszen, D.7
van Amelsvoort, T.8
-
11
-
-
34247629010
-
Regional gray matter volume abnormalities in the at risk mental state
-
Borgwardt S.J., Riecher-Rossler A., Dazzan P., Chitnis X., Aston J., Drewe M., Gschwandtner U., Haller S., Pfluger M., Rechsteiner E., D'Souza M., Stieglitz R.D., Radu E.W., and McGuire P.K. Regional gray matter volume abnormalities in the at risk mental state. Biol. Psychiatry 61 (2007) 1148-1156
-
(2007)
Biol. Psychiatry
, vol.61
, pp. 1148-1156
-
-
Borgwardt, S.J.1
Riecher-Rossler, A.2
Dazzan, P.3
Chitnis, X.4
Aston, J.5
Drewe, M.6
Gschwandtner, U.7
Haller, S.8
Pfluger, M.9
Rechsteiner, E.10
D'Souza, M.11
Stieglitz, R.D.12
Radu, E.W.13
McGuire, P.K.14
-
12
-
-
33646263842
-
Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study
-
Campbell L.E., Daly E., Toal F., Stevens A., Azuma R., Catani M., Ng V., van Amelsvoort T., Chitnis X., Cutter W., Murphy D.G., and Murphy K.C. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study. Brain 129 Pt 5 (2006) 1218-1228
-
(2006)
Brain
, vol.129
, Issue.PART 5
, pp. 1218-1228
-
-
Campbell, L.E.1
Daly, E.2
Toal, F.3
Stevens, A.4
Azuma, R.5
Catani, M.6
Ng, V.7
van Amelsvoort, T.8
Chitnis, X.9
Cutter, W.10
Murphy, D.G.11
Murphy, K.C.12
-
13
-
-
0036468696
-
Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome
-
Chow E.W., Zipursky R.B., Mikulis D.J., and Bassett A.S. Structural brain abnormalities in patients with schizophrenia and 22q11 deletion syndrome. Biol. Psychiatry 51 3 (2002) 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
-
14
-
-
33746123033
-
Hippocampal volume reduction in 22q11.2 deletion syndrome
-
Debbane M., Schaer M., Farhoumand R., Glaser B., and Eliez S. Hippocampal volume reduction in 22q11.2 deletion syndrome. Neuropsychologia 44 12 (2006) 2360-2365
-
(2006)
Neuropsychologia
, vol.44
, Issue.12
, pp. 2360-2365
-
-
Debbane, M.1
Schaer, M.2
Farhoumand, R.3
Glaser, B.4
Eliez, S.5
-
15
-
-
37849038398
-
Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment
-
Deboer T., Wu Z., Lee A., and Simon T.J. Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behav. Brain Funct. 3 (2007) 54
-
(2007)
Behav. Brain Funct.
, vol.3
, pp. 54
-
-
Deboer, T.1
Wu, Z.2
Lee, A.3
Simon, T.J.4
-
16
-
-
0022992740
-
Meta-analysis in clinical trials
-
DerSimonian R., and Laird N. Meta-analysis in clinical trials. Control. Clin. Trials 7 3 (1986) 177-188
-
(1986)
Control. Clin. Trials
, vol.7
, Issue.3
, pp. 177-188
-
-
DerSimonian, R.1
Laird, N.2
-
17
-
-
0030922816
-
Bias in meta-analysis detected by a simple, graphical test
-
Egger M., Davey Smith G., Schneider M., and Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ 315 (1997) 629-634
-
(1997)
BMJ
, vol.315
, pp. 629-634
-
-
Egger, M.1
Davey Smith, G.2
Schneider, M.3
Minder, C.4
-
18
-
-
0034064651
-
Children and adolescents with velocardiofacial syndrome: a volumetric MRI study
-
Eliez S., Schmitt J.E., White C.D., and Reiss A.L. Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. Am. J. Psychiatry 157 3 (2000) 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
-
19
-
-
0035176185
-
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study
-
Eliez S., Antonarakis S.E., Morris M.A., Dahoun S.P., and Reiss A.L. Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study. Arch. Gen. Psychiatry 58 1 (2001) 64-68
-
(2001)
Arch. Gen. Psychiatry
, vol.58
, Issue.1
, pp. 64-68
-
-
Eliez, S.1
Antonarakis, S.E.2
Morris, M.A.3
Dahoun, S.P.4
Reiss, A.L.5
-
20
-
-
0035095617
-
Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?
-
Eliez S., Blasey C.M., Schmitt E.J., White C.D., Hu D., and Reiss A.L. Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?. Am. J. Psychiatry 158 3 (2001) 447-453
-
(2001)
Am. J. Psychiatry
, vol.158
, Issue.3
, pp. 447-453
-
-
Eliez, S.1
Blasey, C.M.2
Schmitt, E.J.3
White, C.D.4
Hu, D.5
Reiss, A.L.6
-
21
-
-
0035869620
-
A quantitative MRI study of posterior fossa development in velocardiofacial syndrome
-
Eliez S., Schmitt J.E., White C.D., Wellis V.G., and Reiss A.L. A quantitative MRI study of posterior fossa development in velocardiofacial syndrome. Biol. Psychiatry 49 6 (2001) 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
-
22
-
-
0036641248
-
Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2)
-
Eliez S., Barnea-Goraly N., Schmitt J.E., Liu Y., and Reiss A.L. Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2). Biol. Psychiatry 52 1 (2002) 68-70
-
(2002)
Biol. Psychiatry
, vol.52
, Issue.1
, pp. 68-70
-
-
Eliez, S.1
Barnea-Goraly, N.2
Schmitt, J.E.3
Liu, Y.4
Reiss, A.L.5
-
23
-
-
60249093730
-
Meta-analysis of diffusion tensor imaging studies in schizophrenia
-
Ellison-Wright I., and Bullmore E. Meta-analysis of diffusion tensor imaging studies in schizophrenia. Schizophr. Res. 108 1-3 (2009) 3-10
-
(2009)
Schizophr. Res.
, vol.108
, Issue.1-3
, pp. 3-10
-
-
Ellison-Wright, I.1
Bullmore, E.2
-
24
-
-
48949087605
-
The anatomy of first-episode and chronic schizophrenia: an anatomical likelihood estimation meta-analysis
-
Ellison-Wright I., Glahn D.C., Laird A.R., Thelen S.M., and Bullmore E. The anatomy of first-episode and chronic schizophrenia: an anatomical likelihood estimation meta-analysis. Am. J. Psychiatry 165 8 (2008) 1015-1023
-
(2008)
Am. J. Psychiatry
, vol.165
, Issue.8
, pp. 1015-1023
-
-
Ellison-Wright, I.1
Glahn, D.C.2
Laird, A.R.3
Thelen, S.M.4
Bullmore, E.5
-
25
-
-
34848921123
-
Structural changes to the fusiform gyrus: a cerebral marker for social impairments in 22q11.2 deletion syndrome?
-
Glaser B., Schaer M., Berney S., Debbane M., Vuilleumier P., and Eliez S. Structural changes to the fusiform gyrus: a cerebral marker for social impairments in 22q11.2 deletion syndrome?. Schizophr. Res. 96 1-3 (2007) 82-86
-
(2007)
Schizophr. Res.
, vol.96
, Issue.1-3
, pp. 82-86
-
-
Glaser, B.1
Schaer, M.2
Berney, S.3
Debbane, M.4
Vuilleumier, P.5
Eliez, S.6
-
26
-
-
12144290440
-
Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome
-
Gothelf D., Presburger G., Levy D., Nahmani A., Burg M., Berant M., Blieden L.C., Finkelstein Y., Frisch A., Apter A., and Weizman A. Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B 1 (2004) 116-121
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.126 B
, Issue.1
, pp. 116-121
-
-
Gothelf, D.1
Presburger, G.2
Levy, D.3
Nahmani, A.4
Burg, M.5
Berant, M.6
Blieden, L.C.7
Finkelstein, Y.8
Frisch, A.9
Apter, A.10
Weizman, A.11
-
27
-
-
12144289483
-
Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome
-
Gothelf D., Presburger G., Zohar A.H., Burg M., Nahmani A., Frydman M., Shohat M., Inbar D., Aviram-Goldring A., Yeshaya J., Steinberg T., Finkelstein Y., Frisch A., Weizman A., and Apter A. Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B 1 (2004) 99-105
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.126 B
, Issue.1
, pp. 99-105
-
-
Gothelf, D.1
Presburger, G.2
Zohar, A.H.3
Burg, M.4
Nahmani, A.5
Frydman, M.6
Shohat, M.7
Inbar, D.8
Aviram-Goldring, A.9
Yeshaya, J.10
Steinberg, T.11
Finkelstein, Y.12
Frisch, A.13
Weizman, A.14
Apter, A.15
-
28
-
-
27644524899
-
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
-
Gothelf D., Eliez S., Thompson T., Hinard C., Penniman L., Feinstein C., Kwon H., Jin S., Jo B., Antonarakis S.E., Morris MA., and Reiss AL. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome. Nat. Neurosci. 8 11 (2005) 1500-1502
-
(2005)
Nat. Neurosci.
, vol.8
, Issue.11
, pp. 1500-1502
-
-
Gothelf, D.1
Eliez, S.2
Thompson, T.3
Hinard, C.4
Penniman, L.5
Feinstein, C.6
Kwon, H.7
Jin, S.8
Jo, B.9
Antonarakis, S.E.10
Morris, MA.11
Reiss, AL.12
-
29
-
-
34848889944
-
Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study
-
Gothelf D., Penniman L., Gu E., Eliez S., and Reiss A.L. Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study. Schizophr. Res. 96 1-3 (2007) 72-81
-
(2007)
Schizophr. Res.
, vol.96
, Issue.1-3
, pp. 72-81
-
-
Gothelf, D.1
Penniman, L.2
Gu, E.3
Eliez, S.4
Reiss, A.L.5
-
30
-
-
44149125060
-
Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome
-
Gothelf D., Schaer M., and Eliez S. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome. Dev. Disabil. Res. Rev. 14 1 (2008) 59-68
-
(2008)
Dev. Disabil. Res. Rev.
, vol.14
, Issue.1
, pp. 59-68
-
-
Gothelf, D.1
Schaer, M.2
Eliez, S.3
-
31
-
-
0036132265
-
An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS)
-
Henry J.C., van Amelsvoort T., Morris R.G., Owen M.J., Murphy D.G., and Murphy K.C. An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS). Neuropsychologia 40 5 (2002) 471-478
-
(2002)
Neuropsychologia
, vol.40
, Issue.5
, pp. 471-478
-
-
Henry, J.C.1
van Amelsvoort, T.2
Morris, R.G.3
Owen, M.J.4
Murphy, D.G.5
Murphy, K.C.6
-
33
-
-
0035871350
-
Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis
-
Kates W.R., Burnette C.P., Jabs E.W., Rutberg J., Murphy A.M., Grados M., Geraghty M., Kaufmann W.E., and Pearlson G.D. Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis. Biol. Psychiatry 49 8 (2001) 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
-
34
-
-
3042738235
-
Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2)
-
Kates W.R., Burnette C.P., Bessette B.A., Folley B.S., Strunge L., Jabs E.W., and Pearlson G.D. Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). J. Child Neurol. 19 5 (2004) 337-342
-
(2004)
J. Child Neurol.
, vol.19
, Issue.5
, pp. 337-342
-
-
Kates, W.R.1
Burnette, C.P.2
Bessette, B.A.3
Folley, B.S.4
Strunge, L.5
Jabs, E.W.6
Pearlson, G.D.7
-
35
-
-
17144407295
-
Gender-moderated dorsolateral prefrontal reductions in 22q11.2 Deletion Syndrome: implications for risk for schizophrenia
-
Kates W.R., Antshel K., Willhite R., Bessette B.A., AbdulSabur N., and Higgins A.M. Gender-moderated dorsolateral prefrontal reductions in 22q11.2 Deletion Syndrome: implications for risk for schizophrenia. Child Neuropsychol 11 1 (2005) 73-85
-
(2005)
Child Neuropsychol
, vol.11
, Issue.1
, pp. 73-85
-
-
Kates, W.R.1
Antshel, K.2
Willhite, R.3
Bessette, B.A.4
AbdulSabur, N.5
Higgins, A.M.6
-
36
-
-
33646776794
-
Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome
-
Kates W.R., Miller A.M., Abdulsabur N., Antshel K.M., Conchelos J., Fremont W., and Roizen N. Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome. J. Am. Acad. Child Adolesc. Psych. 45 5 (2006) 587-595
-
(2006)
J. Am. Acad. Child Adolesc. Psych.
, vol.45
, Issue.5
, pp. 587-595
-
-
Kates, W.R.1
Miller, A.M.2
Abdulsabur, N.3
Antshel, K.M.4
Conchelos, J.5
Fremont, W.6
Roizen, N.7
-
37
-
-
33845980272
-
Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome
-
Machado A.M., Simon T.J., Nguyen V., McDonald-McGinn D.M., Zackai E.H., and Gee J.C. Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome. Brain Res. 1131 1 (2007) 197-210
-
(2007)
Brain Res.
, vol.1131
, Issue.1
, pp. 197-210
-
-
Machado, A.M.1
Simon, T.J.2
Nguyen, V.3
McDonald-McGinn, D.M.4
Zackai, E.H.5
Gee, J.C.6
-
38
-
-
0033033492
-
The Philadelphia story: the 22q11.2 deletion: report on 250 patients
-
McDonald-McGinn D.M., Kirschner R., Goldmuntz E., Sullivan K., Eicher P., Gerdes M., Moss E., Solot C., Wang P., Jacobs I., Handler S., Knightly C., Heher K., Wilson M., Ming J.E., Grace K., Driscoll D., Pasquariello P., Randall P., Larossa D., Emanuel B.S., and Zackai E.H. The Philadelphia story: the 22q11.2 deletion: report on 250 patients. Genet. Couns. 10 1 (1999) 11-24
-
(1999)
Genet. Couns.
, vol.10
, Issue.1
, pp. 11-24
-
-
McDonald-McGinn, D.M.1
Kirschner, R.2
Goldmuntz, E.3
Sullivan, K.4
Eicher, P.5
Gerdes, M.6
Moss, E.7
Solot, C.8
Wang, P.9
Jacobs, I.10
Handler, S.11
Knightly, C.12
Heher, K.13
Wilson, M.14
Ming, J.E.15
Grace, K.16
Driscoll, D.17
Pasquariello, P.18
Randall, P.19
Larossa, D.20
Emanuel, B.S.21
Zackai, E.H.22
more..
-
39
-
-
0035183495
-
Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia
-
Murphy K.C., and Owen M.J. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. Br. J. Psychiatry 179 (2001) 397-402
-
(2001)
Br. J. Psychiatry
, vol.179
, pp. 397-402
-
-
Murphy, K.C.1
Owen, M.J.2
-
40
-
-
0031992676
-
Chromosome 22q11 deletions: an under recognized cause of idiopathic learning disability
-
Murphy K.C., Jones R.G., Griffiths E., Thompson P.W., and Owen M.J. Chromosome 22q11 deletions: an under recognized cause of idiopathic learning disability. Br. J. Psychiatry 172 (1998) 180-183
-
(1998)
Br. J. Psychiatry
, vol.172
, pp. 180-183
-
-
Murphy, K.C.1
Jones, R.G.2
Griffiths, E.3
Thompson, P.W.4
Owen, M.J.5
-
41
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy K.C., Jones L.A., and Owen M.J. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch. Gen. Psychiatry 56 (1999) 940-945
-
(1999)
Arch. Gen. Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
42
-
-
0031862340
-
Hippocampal volume reduction in schizophrenia as assessed by magnetic resonance imaging: A meta-analytic study
-
Nelson, M.D., Saykin, A.J., Riordan, H.J., 1998. Hippocampal volume reduction in schizophrenia as assessed by magnetic resonance imaging: a meta-analytic study. Arch. Gen. Psychiatry 55 (5), 433-440.
-
(1998)
Arch. Gen. Psychiatry
, vol.55
, Issue.5
, pp. 433-440
-
-
Nelson, M.D.1
Saykin, A.J.2
Riordan, H.J.3
-
43
-
-
0036143742
-
Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects
-
Niklasson L., Rasmussen P., Oskarsdóttir S., and Gillberg C. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects. Dev. Med. Child Neurol. 44 1 (2002) 44-50
-
(2002)
Dev. Med. Child Neurol.
, vol.44
, Issue.1
, pp. 44-50
-
-
Niklasson, L.1
Rasmussen, P.2
Oskarsdóttir, S.3
Gillberg, C.4
-
44
-
-
0037464759
-
Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison
-
Pantelis C., Velakoulis D., McGorry P.D., Wood S.J., Suckling J., Phillips L.J., Yung A.R., Bullmore E.T., Brewer W., Soulsby B., Desmond P., and McGuire P.K. Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison. Lancet 361 9354 (2003) 281-288
-
(2003)
Lancet
, vol.361
, Issue.9354
, pp. 281-288
-
-
Pantelis, C.1
Velakoulis, D.2
McGorry, P.D.3
Wood, S.J.4
Suckling, J.5
Phillips, L.J.6
Yung, A.R.7
Bullmore, E.T.8
Brewer, W.9
Soulsby, B.10
Desmond, P.11
McGuire, P.K.12
-
45
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos D.F., Faedda G.L., Veit S., Goldberg R., Morrow B., Kucherlapati R., and Shprintzen R.J. Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?. Am. J. Psychiatry 153 12 (1996) 1541-1547
-
(1996)
Am. J. Psychiatry
, vol.153
, Issue.12
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
Goldberg, R.4
Morrow, B.5
Kucherlapati, R.6
Shprintzen, R.J.7
-
46
-
-
0026511084
-
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
-
Scambler P.J., Kelly D., Lindsay E., Williamson R., Goldberg R., Shprintzen R., Wilson D.I., Goodship J.A., Cross I.E., and Burn J. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. Lancet 339 8802 (1992) 1138-1139
-
(1992)
Lancet
, vol.339
, Issue.8802
, pp. 1138-1139
-
-
Scambler, P.J.1
Kelly, D.2
Lindsay, E.3
Williamson, R.4
Goldberg, R.5
Shprintzen, R.6
Wilson, D.I.7
Goodship, J.A.8
Cross, I.E.9
Burn, J.10
-
47
-
-
1842587656
-
Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome
-
Shashi V., Muddasani S., Santos C.C., Berry M.N., Kwapil T.R., Lewandowski E., and Keshavan M.S. Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome. NeuroImage 21 4 (2004) 1399-1406
-
(2004)
NeuroImage
, vol.21
, Issue.4
, pp. 1399-1406
-
-
Shashi, V.1
Muddasani, S.2
Santos, C.C.3
Berry, M.N.4
Kwapil, T.R.5
Lewandowski, E.6
Keshavan, M.S.7
-
48
-
-
14244256353
-
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
-
Simon T.J., Ding L., Bish J.P., McDonald-McGinn D.M., Zackai E.H., and Gee J. Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study. NeuroImage 25 1 (2005) 169-180
-
(2005)
NeuroImage
, vol.25
, Issue.1
, pp. 169-180
-
-
Simon, T.J.1
Ding, L.2
Bish, J.P.3
McDonald-McGinn, D.M.4
Zackai, E.H.5
Gee, J.6
-
49
-
-
0031009068
-
-
Swillen A., Devriendt K., Legius E., Eyskens B., Dumoulin M., Gewillig M., and Fryns J.P. J. Med. Genet. 34 6 (1997) 453-458
-
(1997)
J. Med. Genet.
, vol.34
, Issue.6
, pp. 453-458
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
Eyskens, B.4
Dumoulin, M.5
Gewillig, M.6
Fryns, J.P.7
-
50
-
-
64849086184
-
Progressive gray matter reduction of the superior temporal gyrus during transition to psychosis
-
Takahashi T., Wood S.J., Yung A.R., Soulsby B., McGorry P.D., Suzuki M., Kawasaki Y., Phillips L.J., Velakoulis D., and Pantelis C. Progressive gray matter reduction of the superior temporal gyrus during transition to psychosis. Arch. Gen. Psychiatry 66 4 (2009) 366
-
(2009)
Arch. Gen. Psychiatry
, vol.66
, Issue.4
, pp. 366
-
-
Takahashi, T.1
Wood, S.J.2
Yung, A.R.3
Soulsby, B.4
McGorry, P.D.5
Suzuki, M.6
Kawasaki, Y.7
Phillips, L.J.8
Velakoulis, D.9
Pantelis, C.10
-
51
-
-
34547207179
-
Correlations between Diffusion Tensor Imaging (DTI) and Magnetic Resonance Spectroscopy (1H MRS) in schizophrenic patientsmand normal controls
-
Tang C.Y., Friedman J., Shungu D., Chang L., Ernst T., Stewart D., Hajianpour A., Carpenter D., Ng J., Mao X., Hof P.R., Buchsbaum M.S., Davis K., and Gorman J.mM. Correlations between Diffusion Tensor Imaging (DTI) and Magnetic Resonance Spectroscopy (1H MRS) in schizophrenic patientsmand normal controls. BMC Psychiatry 7 (2007) 25
-
(2007)
BMC Psychiatry
, vol.7
, pp. 25
-
-
Tang, C.Y.1
Friedman, J.2
Shungu, D.3
Chang, L.4
Ernst, T.5
Stewart, D.6
Hajianpour, A.7
Carpenter, D.8
Ng, J.9
Mao, X.10
Hof, P.R.11
Buchsbaum, M.S.12
Davis, K.13
Gorman, J.mM.14
-
52
-
-
0029783493
-
Prevalence of 22q11 microdeletion
-
Tézenas Du Montcel S., Mendizabai H., Aymé S., Lévy A., and Philip N. Prevalence of 22q11 microdeletion. J. Med. Genet. 33 8 (1996) 719
-
(1996)
J. Med. Genet.
, vol.33
, Issue.8
, pp. 719
-
-
Tézenas Du Montcel, S.1
Mendizabai, H.2
Aymé, S.3
Lévy, A.4
Philip, N.5
-
53
-
-
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 K.C., and Murphy D.G. 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 (2004) 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
-
54
-
-
37249069369
-
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome
-
van Amelsvoort T., Zinkstok J., Figee M., Daly E., Morris R., Owen M.J., Murphy K.C., De Haan L., Linszen D.H., Glaser B., and Murphy D.G. Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome. Psychol. Med. 38 1 (2008) 89-100
-
(2008)
Psychol. Med.
, vol.38
, Issue.1
, pp. 89-100
-
-
van Amelsvoort, T.1
Zinkstok, J.2
Figee, M.3
Daly, E.4
Morris, R.5
Owen, M.J.6
Murphy, K.C.7
De Haan, L.8
Linszen, D.H.9
Glaser, B.10
Murphy, D.G.11
-
55
-
-
9144220855
-
A systematic genomewide linkage study in 353 sib pairs with schizophrenia
-
Williams N.M., Norton N., Williams H., Ekholm B., Hamshere M.L., Lindblom Y., Chowdari K.V., Cardno A.G., Zammit S., Jones L.A., Murphy K.C., Sanders R.D., McCarthy G., Gray M.Y., Jones G., Holmans P., Nimgaonkar V., Adolfson R., Osby U., Terenius L., Sedvall G., O'Donovan M.C., and Owen M.J. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. Am. J. Hum. Genet. 73 6 (2003) 1355-1367
-
(2003)
Am. J. Hum. Genet.
, vol.73
, Issue.6
, pp. 1355-1367
-
-
Williams, N.M.1
Norton, N.2
Williams, H.3
Ekholm, B.4
Hamshere, M.L.5
Lindblom, Y.6
Chowdari, K.V.7
Cardno, A.G.8
Zammit, S.9
Jones, L.A.10
Murphy, K.C.11
Sanders, R.D.12
McCarthy, G.13
Gray, M.Y.14
Jones, G.15
Holmans, P.16
Nimgaonkar, V.17
Adolfson, R.18
Osby, U.19
Terenius, L.20
Sedvall, G.21
O'Donovan, M.C.22
Owen, M.J.23
more..
-
56
-
-
68949209644
-
Gray matter abnormalities in subjects at ultra-high risk for schizophrenia and first-episode schizophrenic patients compared to healthy controls
-
Witthaus H., Kaufmann C., Bohner G., Ozgürdal S., Gudlowski Y., Gallinat J., Ruhrmann S., Brüne M., Heinz A., Klingebiel R., Juckel G., 2009. Gray matter abnormalities in subjects at ultra-high risk for schizophrenia and first-episode schizophrenic patients compared to healthy controls. Psychiatry Res. 173, 163-169.
-
(2009)
Psychiatry Res
, vol.173
, pp. 163-169
-
-
Witthaus, H.1
Kaufmann, C.2
Bohner, G.3
Ozgürdal, S.4
Gudlowski, Y.5
Gallinat, J.6
Ruhrmann, S.7
Brüne, M.8
Heinz, A.9
Klingebiel, R.10
Juckel, G.11
-
57
-
-
0007482654
-
Chromosome 22q11.2 interstizial deletions among childhood onset schizophrenics and 'multidimensionally impaired'
-
Yan W., Jacobsen L.K., Krasnewich D.M., Guan X.Y., Lenane M.C., Paul S.P., Dalwadi H.N., Long R.T., Kumra S., Martin B.M., Scrambler P.J., Trent J.M., Sidrandky E., Ginns E.I., and Rapoport J.L. Chromosome 22q11.2 interstizial deletions among childhood onset schizophrenics and 'multidimensionally impaired'. Am. J. Med. Genet. 81 (1998) 41-43
-
(1998)
Am. J. Med. Genet.
, vol.81
, pp. 41-43
-
-
Yan, W.1
Jacobsen, L.K.2
Krasnewich, D.M.3
Guan, X.Y.4
Lenane, M.C.5
Paul, S.P.6
Dalwadi, H.N.7
Long, R.T.8
Kumra, S.9
Martin, B.M.10
Scrambler, P.J.11
Trent, J.M.12
Sidrandky, E.13
Ginns, E.I.14
Rapoport, J.L.15
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