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本文引用的文献

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Model-free analysis and permutation tests for allelic associations.等位基因关联的无模型分析与置换检验
Hum Hered. 2000 Mar-Apr;50(2):133-9. doi: 10.1159/000022901.
2
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22.家族性精神分裂症一个主要易感基因座位于1号染色体1q21 - q22区域。
Science. 2000 Apr 28;288(5466):678-82. doi: 10.1126/science.288.5466.678.
3
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.芬兰人群中精神分裂症的全基因组扫描:7号染色体q22区域存在一个位点的证据
Hum Mol Genet. 2000 Apr 12;9(7):1049-57. doi: 10.1093/hmg/9.7.1049.
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Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.6号染色体q24.2-q26末端区域的细微重叠缺失:使用荧光原位杂交技术研究的三例病例
Am J Med Genet. 1999 Nov 5;87(1):17-22.
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A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.在芬兰一个孤立亚群体中对精神分裂症基因进行全基因组筛查,提示存在多个易感基因座。
Am J Hum Genet. 1999 Oct;65(4):1114-24. doi: 10.1086/302567.
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Linkage of familial schizophrenia to chromosome 13q32.家族性精神分裂症与13号染色体长臂32区的连锁关系。
Am J Hum Genet. 1999 Oct;65(4):1096-103. doi: 10.1086/302579.
7
Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23.对一个大型瑞典家族的连锁分析为6号染色体p23区域存在精神分裂症易感基因座提供了进一步支持。
Am J Med Genet. 1999 Aug 20;88(4):369-77.
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Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
Am J Med Genet. 1999 Aug 20;88(4):337-43.
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Chromosome 6 workshop report.6号染色体研讨会报告。
Am J Med Genet. 1999 Jun 18;88(3):233-8. doi: 10.1002/(sici)1096-8628(19990618)88:3<233::aid-ajmg5>3.0.co;2-b.
10
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.自闭症易感性基因的全基因组扫描。巴黎国际自闭症研究同胞对研究。
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在一个全球最大的已报道家系中,位于6号染色体长臂25区的一个精神分裂症易感基因座。

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

作者信息

Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E

机构信息

Department of Genetics and Pathology, Uppsala University, S-751, 23 Uppsala, Sweden.

出版信息

Am J Hum Genet. 2001 Jul;69(1):96-105. doi: 10.1086/321288. Epub 2001 May 25.

DOI:10.1086/321288
PMID:11389481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1226052/
Abstract

We have completed a genome scan of a 12-generation, 3,400-member pedigree with schizophrenia. Samples from 210 individuals were collected from the pedigree. We performed an "affecteds-only" genome-scan analysis using 43 members of the pedigree. The affected individuals included 29 patients with schizophrenia, 10 with schizoaffective disorders, and 4 with psychosis not otherwise specified. Two sets of white-European allele frequencies were used-one from a Swedish control population (46 unrelated individuals) and one from the pedigree (210 individuals). All analyses pointed to the same region: D6S264, located at 6q25.2, showed a maximum LOD score of 3.45 when allele frequencies in the Swedish control population were used, compared with a maximum LOD score of 2.59 when the pedigree's allele frequencies were used. We analyzed additional markers in the 6q25 region and found a maximum LOD score of 6.6 with marker D6S253, as well as a 6-cM haplotype (markers D6S253-D6S264) that segregated, after 12 generations, with the majority of the affected individuals. Multipoint analysis was performed with the markers in the 6q25 region, and a maximum LOD score of 7.7 was obtained. To evaluate the significance of the genome scan, we simulated the complete analysis under the assumption of no linkage. The results showed that a LOD score >2.2 should be considered as suggestive of linkage, whereas a LOD score >3.7 should be considered as significant. These results suggest that a common ancestral region was inherited by the affected individuals in this large pedigree.

摘要

我们对一个有精神分裂症的12代、3400名成员的家系进行了全基因组扫描。从该家系中收集了210名个体的样本。我们使用该家系中的43名成员进行了“仅针对患者”的全基因组扫描分析。受影响个体包括29名精神分裂症患者、10名精神分裂症情感障碍患者和4名未另行指定的精神病患者。使用了两组白人欧洲等位基因频率——一组来自瑞典对照人群(46名无亲属关系的个体),另一组来自该家系(210名个体)。所有分析都指向同一区域:位于6q25.2的D6S264,使用瑞典对照人群的等位基因频率时,最大对数优势(LOD)得分为3.45,而使用该家系的等位基因频率时,最大LOD得分为2.59。我们分析了6q25区域的其他标记,发现标记D6S253的最大LOD得分为6.6,以及一个6厘摩(cM)的单倍型(标记D6S253 - D6S264),经过12代后,该单倍型与大多数受影响个体分离。对6q25区域的标记进行了多点分析,获得的最大LOD得分为7.7。为了评估全基因组扫描的显著性,我们在无连锁的假设下模拟了完整分析。结果表明,LOD得分>2.2应被视为提示连锁,而LOD得分>3.7应被视为显著。这些结果表明,这个大型家系中的受影响个体继承了一个共同的祖先区域。