Genetic insights into schizophrenia

被引:21
作者
Bassett, AS
Chow, EWC
Waterworth, DM
Brzustowicz, L
机构
[1] Ctr Addict & Mental Hlth, Queen St Div, Schizophrenia Res Program, Genet Sect, Toronto, ON M6J 1H4, Canada
[2] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[3] Rutgers State Univ, Dept Genet, Piscataway, NJ USA
[4] Univ Med & Dent New Jersey, Dept Genet, Piscataway, NJ 08854 USA
[5] Univ Med & Dent New Jersey, Dept Psychiat, Piscataway, NJ 08854 USA
来源
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE | 2001年 / 46卷 / 02期
关键词
genetics; schizophrenia; linkage; 221 deletion syndrome; psychiatric genetics;
D O I
10.1177/070674370104600203
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To outline new insights into the genetic etiology of schizophrenia. Methods: We discuss several commonly held beliefs about the genetic issues in schizophrenia. Results: The complex genetic nature of the illness poses a challenge for investigators seeking causative genetic mutations. Multiple independent research findings are, however converging to identify a relatively small number of chromosomal locations that appear to contain schizophrenia susceptibility genes. Also, a clinically relevant genetic subtype of schizophrenia (22qDS) has been identified. We are developing a better understanding of how schizophrenia relates to other psychiatric disorders. While investigations into the possible roles of dopaminergic and serotonergic systems continue, other approaches that do not require theories of the mechanism of illness are also being used to identify candidate susceptibility genes. Conclusions: Research to date suggests that our understanding of the pathophysiology of schizophrenia will soon be fundamentally altered by genetic approaches to this complex disease.
引用
收藏
页码:131 / 137
页数:7
相关论文
共 75 条
[1]  
[Anonymous], 1982, SCHIZOPHRENIA EPIGEN
[2]  
[Anonymous], 1986, HUMAN GENETICS PROBL
[3]   Genome scan for susceptibility loci for schizophrenia [J].
Bailer, U ;
Leisch, F ;
Meszaros, K ;
Lenzinger, E ;
Willinger, U ;
Strobl, R ;
Gebhardt, C ;
Gerhard, E ;
Fuchs, K ;
Sieghart, W ;
Kasper, S ;
Hornik, K ;
Aschauer, HN .
NEUROPSYCHOBIOLOGY, 2000, 42 (04) :175-182
[4]   22q11 deletion syndrome: A genetic subtype of schizophrenia [J].
Bassett, AS ;
Chow, EWC .
BIOLOGICAL PSYCHIATRY, 1999, 46 (07) :882-891
[5]  
Bassett AS, 2000, AM J MED GENET, V97, P45, DOI 10.1002/(SICI)1096-8628(200021)97:1<45::AID-AJMG6>3.0.CO
[6]  
2-9
[7]  
Bassett AS, 1998, AM J MED GENET, V81, P328, DOI 10.1002/(SICI)1096-8628(19980710)81:4<328::AID-AJMG10>3.3.CO
[8]  
2-8
[9]   Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 [J].
Blouin, JL ;
Dombroski, BA ;
Nath, SK ;
Lasseter, VK ;
Wolyniec, PS ;
Nestadt, G ;
Thornquist, M ;
Ullrich, G ;
McGrath, J ;
Kasch, L ;
Lamacz, M ;
Thomas, MG ;
Gehrig, C ;
Radhakrishna, U ;
Snyder, SE ;
Balk, KG ;
Neufeld, K ;
Swartz, KL ;
DeMarchi, N ;
Papadimitriou, GN ;
Dikeos, DG ;
Stefanis, CN ;
Chakravarti, A ;
Childs, B ;
Housman, DE ;
Kazazian, HH ;
Antonarakis, SE ;
Pulver, AE .
NATURE GENETICS, 1998, 20 (01) :70-73
[10]   Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 [J].
Bork, JM ;
Peters, LM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, ZM ;
Ness, SL ;
Polomeno, R ;
Ramesh, A ;
Schloss, M ;
Srisailpathy, CRS ;
Wayne, S ;
Bellman, S ;
Desmukh, D ;
Ahmed, Z ;
Khan, SN ;
Kaloustian, VMD ;
Li, XC ;
Lalwani, A ;
Riazuddin, S ;
Bitner-Glindzicz, M ;
Nance, WE ;
Liu, XZ ;
Wistow, G ;
Smith, RJH ;
Griffith, AJ ;
Wilcox, ER ;
Friedman, TB ;
Morell, RJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) :26-37