Linkage analysis of schizophrenia to chromosome 15

被引:42
|
作者
Gejman, PV
Sanders, AR
Badner, JA
Cao, QH
Zhang, J
机构
[1] Univ Chicago, Jules F Knapp Res Ctr, Dept Psychiat, Schizophrenia Genet Res Program, Chicago, IL 60637 USA
[2] NIMH, Unit Mol Clin Invest, Clin Neurogenet Branch, Bethesda, MD 20892 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 2001年 / 105卷 / 08期
关键词
genetic mapping; nonparametric; dominant; recessive; P50 auditory-evoked response;
D O I
10.1002/ajmg.1552
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have mapped a sample of 68 families consisting of one or more affected sibling pairs with schizophrenia or schizoaffective disorder with 20 markers spanning all of chromosome 15 to investigate whether there is a locus on chromosome 15 that confers an increased susceptibility to schizophrenia using parametric and nonparametric linkage analyses. Allele sharing identical by descent and multipoint maximum likelihood score (MLS) statistics were employed. Results show excess allele sharing for multiple markers in 15q11.2-q25, a chromosomal region previously found linked to a decrease in the normal inhibition of the P50 auditory-evoked response to the second of paired stimuli, a decrease associated with schizophrenia. Excess allele sharing was found for markers spanning about 48 cM in 15q11.2q25 (D15S1002-D15S1023). The greatest single point allele sharing was found at D15S659 (62.6%). The multipoint MLS scores were greater than 1.0 in the 30-52 cM interval delimited by ACTC and D15S150, with a maximum value of 2.0 with GENE-HUNTER PLUS near D15S1039. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:789 / 793
页数:5
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