Neural phenotypes of common and rare genetic variants

被引:10
作者
Bearden, Carrie E. [1 ,2 ]
Glahn, David C. [3 ,4 ]
Lee, Agatha D. [5 ]
Chiang, Ming-Chang [5 ]
van Erp, Theo G. M. [2 ]
Cannon, Tyrone D. [1 ,2 ]
Reiss, Allan L. [6 ,7 ]
Toga, Arthur W. [5 ]
Thompson, Paul M. [5 ]
机构
[1] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90095 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Psychiat, San Antonio, TX 78229 USA
[4] Univ Texas Hlth Sci Ctr San Antonio, Res Imaging Ctr, San Antonio, TX 78229 USA
[5] Univ Calif Los Angeles, Dept Neurol, Lab NeuroImaging, Los Angeles, CA 90095 USA
[6] Stanford Univ, Sch Med, Ctr Interdisciplinary Brain Sci Res, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
brain; genetic; neuroimaging; psychosis; chromosome; 22q11.2; fragile X; COMT; velocardiofacial syndrome; Williams syndrome; neurofibromatosis I;
D O I
10.1016/j.biopsycho.2008.02.005
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Neuroimaging methods offer a powerful way to bridge the gaps between genes, neurobiology and behavior. Such investigations may be further empowered by complementary strategies involving chromosomal abnormalities associated with particular neurobehavioral phenotypes, which can help to localize causative genes and better understand the genetics of complex traits in the general population. Here we review the evidence from studies using these convergent approaches to investigate genetic influences on brain structure: (1) studies of common genetic variations associated with particular neuroanatomic phenotypes, and (2) studies of possible 'genetic subtypes' of neuropsychiatric disorders with very high penetrance, with a focus on neuroimaging studies using novel computational brain mapping algorithms. Finally, we discuss the contribution of behavioral neurogenetics research to our understanding of the genetic basis of neuropsychiatric disorders in the broader population. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 57
页数:15
相关论文
共 220 条
[1]  
Akil M, 2003, J NEUROSCI, V23, P2008
[2]   Functional activation of the human brain during mental rotation [J].
Alivisatos, B ;
Petrides, M .
NEUROPSYCHOLOGIA, 1997, 35 (02) :111-118
[3]   Neurofibromatosis type 1: Diffusion weighted imaging findings of brain [J].
Alkan, A ;
Sigirci, A ;
Kutlu, R ;
Ozcan, H ;
Erdem, G ;
Aslan, M ;
Ates, O ;
Yakinci, C ;
Egri, M .
EUROPEAN JOURNAL OF RADIOLOGY, 2005, 56 (02) :229-234
[4]   Proton MR spectroscopy features of normal appearing white matter in neurofibromatosis type 1 [J].
Alkan, A ;
Sarac, K ;
Kutlu, R ;
Yakinci, C ;
Sigirci, A ;
Aslan, M ;
Ozcan, H ;
Yologlu, S .
MAGNETIC RESONANCE IMAGING, 2003, 21 (09) :1049-1053
[5]  
[Anonymous], 2002, CVS
[6]   Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome) [J].
Antshel, KM ;
Conchelos, J ;
Lanzetta, G ;
Fremont, W ;
Kates, WR .
PSYCHIATRY RESEARCH-NEUROIMAGING, 2005, 138 (03) :235-245
[7]   Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders [J].
Arnold, PD ;
Siegel-Bartelt, J ;
Cytrynbaum, C ;
Teshima, I ;
Schachar, R .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (04) :354-362
[8]   Quantitative genetic modeling of variation in human brain morphology [J].
Baaré, WFC ;
Pol, HEH ;
Boomsma, DI ;
Posthuma, D ;
de Geus, EJC ;
Schnack, HG ;
van Haren, NEM ;
van Oel, CJ ;
Kahn, RS .
CEREBRAL CORTEX, 2001, 11 (09) :816-824
[9]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[10]   Arithmetic ability and parietal alterations: A diffusion tensor imaging study in Velocardiofacial syndrome [J].
Barnea-Goraly, N ;
Eliez, S ;
Menon, V ;
Bammer, R ;
Reiss, AL .
COGNITIVE BRAIN RESEARCH, 2005, 25 (03) :735-740