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Neuroimaging in psychiatry

Published online by Cambridge University Press:  13 June 2014

Dara M Cannon
Dara M Cannon*
Affiliation:
Department of Psychiatry, 201 Comerford Building, Clinical Sciences Institute, National University of Ireland, Galway, Ireland. E-mail:dara.cannon@nuigalway.ie
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Abstract

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Type
Editorial
Information
Irish Journal of Psychological Medicine , Volume 24 , Issue 3 , September 2007 , pp. 86 - 88
Copyright
Copyright © Cambridge University Press 2007

References

1.Hounsfield, G.N., Computerized transverse axial scanning (tomography). 1. Description of system. Br J Radiol, 1973. 46(552): p. 1016–22.Google Scholar
2.Drevets, VV.G., Ongur, D., and Price, J.L., Neuroimaging abnormalities in the subgenual prefrontal cortex: implications for the pathophysiology of familial mood disorders. Mol Psychiatry, 1998. 3(3): p. 220–6, 190-1.Google Scholar
3.Macmaster, F.P., et al., Amygdala and Hippocampal Volumes in Familial Early Onset Major Depressive Disorder. Biol Psychiatry, 2007.Google Scholar
4.Okugawa, G., Tamagaki, C., and Agartz, I., Frontal and temporal volume size of grey and white matter in patients with schizophrenia: An MRI panellation study. Eur Arch Psychiatry Clin Neurosci, 2007.Google Scholar
5.McDonald, O, et al., Regional volume deviations of brain structure in schizophrenia and psychotic bipolar disorder: computational morphometry study. Br J Psychiatry, 2005. 186: p. 369–77.Google Scholar
6.McDonald, C, et al., Meta-analysis of magnetic resonance imaging brain morphometry studies in bipolar disorder. Biol Psychiatry, 2004. 56(6): p. 411–7.Google Scholar
7.Fornito, A., et al., Surface-based morphometry of the anterior cingulate cortex in first episode schizophrenia. Hum Brain Mapp, 2007.Google Scholar
8.Sanacora, G., et al., Reduced cortical gamma-aminobutyric acid levels in depressed patients determined by proton magnetic resonance spectroscopy. Arch Gen Psychiatry, 1999. 56(11): p. 1043–7.Google Scholar
9.Bhagwagar, Z., et al., Reduction in occipital cortex gamma-aminobutyric acid concentrations in medication-free recovered unipolar depressed and bipolar subjects. Biol Psychiatry, 2007. 61(6): p. 806–12.Google Scholar
10.Yildiz-Yesiloglu, A. and Ankerst, D.P., Review of 1H magnetic resonance spectroscopy findings in major depressive disorder: a meta-analysis. Psychiatry Res, 2006. 147(1): p. 1–25.Google Scholar
11.Yildiz-Yesiloglu, A. and Ankerst, D.P., Neurochemical alterations of the brain in bipolar disorder and their implications for pathophysiology: a systematic review of the in vivo proton magnetic resonance spectroscopy findings. Prog Neuropsychopharmacol Biol Psychiatry, 2006. 30(6): p. 969–95.Google Scholar
12.Basser, P.J., Mattiello, J., and LeBihan, D., Estimation of the effective self-diffusion tensor from the NMR spin echo. J Magn Reson B, 1994. 103(3): p. 247–54.Google Scholar
13.Fujiwara, H., et al., Anterior and posterior cingulum abnormalities and their association with psychopathology in schizophrenia: A diffusion tensor imaging study. Schizophr Res, 2007.Google Scholar
14.Mori, T., et al., Progressive changes of white matter integrity in schizophrenia revealed by diffusion tensor imaging. Psychiatry Res, 2007. 154(2): p. 133–45.Google Scholar
15.Drevets, W., et al., Subgenule prefrontal cortex abnormalities in mood disorders. Nature (Letters to Nature), 1997. 386: p. 824–827.Google Scholar
16.Knutson, B., et al., Dissociation of reward anticipation and outcome with event-related fMRI. Neuroreport, 2001. 12(17): p. 3683–7.Google Scholar
17.Owen, A.M., et al., Detecting awareness in the vegetative state. Science, 2006. 313(5792): p. 1402.Google Scholar
18.Cannon, D.M., et al., Serotonin transporter binding in bipolar disorder assessed using [11C]DASB and positron emission tomography. Biol Psychiatry, 2006. 60(3): p. 207–17.Google Scholar
19.Meyer, J.H., et al., Brain serotonin transporter binding potential measured with carbon 11 -labeled DASB positron emission tomography: effects of major depressive episodes and severity of dysfunctional attitudes. Arch Gen Psychiatry, 2004. 61 (12): p. 1271–9.Google Scholar
20.Drevets, W.C., et al., Serotonin type-1A receptor imaging in depression. Nucl Med Biol, 2000. 27(5): p. 499–507.Google Scholar
21.Montgomery, A.J., et al., Extrastriatal D2 and striatal D2 receptors in depressive illness: pilot PET studies using [11C]FLB 457 and [11C]raclopride. J Affect Disord, 2007. 101(1-3): p. 113–22.Google Scholar
22.Cannon, D.M., et al., Reduced muscarinic type 2 receptor binding in subjects with bipolar disorder. Arch Gen Psychiatry, 2006. 63(7): p. 741–7.Google Scholar
23.Cannon, D.M., et al., Elevated Serotonin Transporter Binding in Major Depressive Disorder Assessed Using Positron Emission Tomography and [(11)C]DASB; Comparison with Bipolar Disorder. Biol Psychiatry, 2007.Google Scholar
24.McMahon, F.J., et al., Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatment. Am J Hum Genet, 2006. 78(5): p. 804–14.Google Scholar
25.Martin-Soelch, C, et al., Lateralized dopaminergic response to reward in the human ventral striatum. Society for Neuroscience Annual Meeting Abstract Book, 2007.Google Scholar
26.Meyer, J.H., et al., Serotonin transporter occupancy of five selective serotonin reuptake inhibitors at different doses: an [11C]DASB positron emission tomography study. Am J Psychiatry, 2004. 161 (5): p. 826–35.Google Scholar
27.Saxena, S., et al., Differential cerebral metabolic changes with paroxetine treatment of obsessive-compulsive disorder vs major depression. Arch Gen Psychiatry, 2002. 59(3): p. 250–61.Google Scholar
28.Hamidi, M., Drevets, W.C., and Price, J.L., Glial reduction in amygdala in major depressive disorder is due to oligodendrocytes. Biol Psychiatry, 2004. 55(6): p. 563–9.Google Scholar
29.Gaughran, F, et al., Hippocampal FGF-2 and FGFR1 mRNA expression in major depression, schizophrenia and bipolar disorder. Brain Res Bull, 2006. 70(3): p. 221–7Google Scholar