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Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13060-5. doi: 10.1073/pnas.93.23.13060.
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本文引用的文献

1
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree.在一个芬兰大家庭中,X染色体q24-q27.1区域存在双相情感障碍易感基因座的证据。
Genome Res. 1995 Sep;5(2):105-15. doi: 10.1101/gr.5.2.105.
2
An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees.一种利用大型哥斯达黎加家系研究双相情感障碍连锁关系的方法。
Am J Med Genet. 1996 May 31;67(3):254-63. doi: 10.1002/(SICI)1096-8628(19960531)67:3<254::AID-AJMG3>3.0.CO;2-N.
3
Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population.运用连锁不平衡方法在哥斯达黎加人群中定位双相情感障碍相关基因。
Am J Med Genet. 1996 May 31;67(3):244-53. doi: 10.1002/(SICI)1096-8628(19960531)67:3<244::AID-AJMG2>3.0.CO;2-N.
4
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.使用单倍型、关联和连锁方法进行的基因定位表明,严重双相情感障碍(BPI)的一个基因座位于18q22 - q23。
Nat Genet. 1996 Apr;12(4):436-41. doi: 10.1038/ng0496-436.
5
Bipolar disorder: evidence for a major locus.双相情感障碍:一个主要基因座的证据。
Am J Med Genet. 1995 Oct 9;60(5):370-6. doi: 10.1002/ajmg.1320600505.
6
Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect.双相情感障碍与18号染色体连锁且存在亲本来源效应的证据。
Am J Hum Genet. 1995 Dec;57(6):1384-94.
7
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees.对三个以色列家系中躁郁症与X染色体标记之间联系的支持减弱。
Nat Genet. 1993 Jan;3(1):49-55. doi: 10.1038/ng0193-49.
8
A microsatellite genetic linkage map of human chromosome 13.人类13号染色体的微卫星遗传连锁图谱。
Genomics. 1993 Jan;15(1):76-85. doi: 10.1006/geno.1993.1012.
9
Mutational processes of simple-sequence repeat loci in human populations.人类群体中简单序列重复位点的突变过程。
Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):3166-70. doi: 10.1073/pnas.91.8.3166.
10
A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).一张具有厘摩密度的综合性人类连锁图谱。人类连锁合作中心(CHLC)。
Science. 1994 Sep 30;265(5181):2049-54. doi: 10.1126/science.8091227.

对两个哥斯达黎加家系中导致严重双相情感障碍的基因进行全基因组筛查。

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

作者信息

McInnes L A, Escamilla M A, Service S K, Reus V I, Leon P, Silva S, Rojas E, Spesny M, Baharloo S, Blankenship K, Peterson A, Tyler D, Shimayoshi N, Tobey C, Batki S, Vinogradov S, Meza L, Gallegos A, Fournier E, Smith L B, Barondes S H, Sandkuijl L A, Freimer N B

机构信息

Neurogenetics Laboratory, University of California, San Francisco 94143, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13060-5. doi: 10.1073/pnas.93.23.13060.

DOI:10.1073/pnas.93.23.13060
PMID:8917544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC24046/
Abstract

Bipolar mood disorder (BP) is a debilitating syndrome characterized by episodes of mania and depression. We designed a multistage study to detect all major loci predisposing to severe BP (termed BP-I) in two pedigrees drawn from the Central Valley of Costa Rica, where the population is largely descended from a few founders in the 16th-18th centuries. We considered only individuals with BP-I as affected and screened the genome for linkage with 473 microsatellite markers. We used a model for linkage analysis that incorporated a high phenocopy rate and a conservative estimate of penetrance. Our goal in this study was not to establish definitive linkage but rather to detect all regions possibly harboring major genes for BP-I in these pedigrees. To facilitate this aim, we evaluated the degree to which markers that were informative in our data set provided coverage of each genome region; we estimate that at least 94% of the genome has been covered, at a predesignated threshold determined through prior linkage simulation analyses. We report here the results of our genome screen for BP-I loci and indicate several regions that merit further study, including segments in 18q, 18p, and 11p, in which suggestive lod scores were observed for two or more contiguous markers. Isolated lod scores that exceeded our thresholds in one or both families also occurred on chromosomes 1, 2, 3, 4, 5, 7, 13, 15, 16, and 17. Interesting regions highlighted in this genome screen will be followed up using linkage disequilibrium (LD) methods.

摘要

双相情感障碍(BP)是一种以躁狂和抑郁发作为特征的使人衰弱的综合征。我们设计了一项多阶段研究,以在来自哥斯达黎加中央山谷的两个家系中检测所有导致严重双相情感障碍(称为BP-I)的主要基因座,该地区的人口主要是16至18世纪少数奠基者的后裔。我们仅将患有BP-I的个体视为受影响个体,并使用473个微卫星标记对基因组进行连锁筛查。我们使用了一种连锁分析模型,该模型纳入了高拟表型率和对 penetrance 的保守估计。我们在这项研究中的目标不是确定明确的连锁关系,而是检测这些家系中所有可能含有BP-I主要基因的区域。为了实现这一目标,我们评估了数据集中信息丰富的标记对每个基因组区域的覆盖程度;我们估计,通过先前的连锁模拟分析确定的预定义阈值下,至少94%的基因组已被覆盖。我们在此报告我们对BP-I基因座进行基因组筛查的结果,并指出几个值得进一步研究的区域,包括18q、18p和11p中的片段,在这些片段中观察到两个或更多相邻标记的暗示性lod分数。在一个或两个家族中超过我们阈值的孤立lod分数也出现在染色体1、2、3、4、5、7、13、15、16和17上。在这个基因组筛查中突出显示的有趣区域将使用连锁不平衡(LD)方法进行后续研究。