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A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.一项针对近期全基因组扫描中涉及帕金森病的12个单核苷酸多态性的病例对照关联研究。
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Completing the map of human genetic variation.完成人类基因变异图谱。
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miRNA-mediated relationships between Cis-SNP genotypes and transcript intensities in lymphocyte cell lines.miRNA 介导的顺式单核苷酸多态性基因型与淋巴细胞系转录本强度之间的关系。
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Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease.编码单核苷酸多态性的全基因组调查揭示了帕金森病一种可重复的通路决定因素。
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Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.复制和模拟均不支持轴突导向通路在帕金森病遗传学中发挥作用。
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Genetic variability of histamine receptors in patients with Parkinson's disease.帕金森病患者组胺受体的遗传变异性。
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本文引用的文献

1
High-resolution whole-genome association study of Parkinson disease.帕金森病的高分辨率全基因组关联研究。
Am J Hum Genet. 2005 Nov;77(5):685-93. doi: 10.1086/496902. Epub 2005 Sep 9.
2
Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.帕金森病1号染色体上风险基因和发病年龄相关基因的鉴定
Am J Hum Genet. 2005 Aug;77(2):252-64. doi: 10.1086/432588. Epub 2005 Jun 28.
3
A common LRRK2 mutation in idiopathic Parkinson's disease.特发性帕金森病中一种常见的LRRK2突变。
Lancet. 2005;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1.
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Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.迟发性阿尔茨海默病与甘油醛-3-磷酸脱氢酶（GAPD）基因家族多个成员的基因变异之间的关联。
Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15688-93. doi: 10.1073/pnas.0403535101. Epub 2004 Oct 26.
5
Significant linkage of Parkinson disease to chromosome 2q36-37.帕金森病与2号染色体q36 - 37区域存在显著连锁。
Am J Hum Genet. 2003 Apr;72(4):1053-7. doi: 10.1086/374383. Epub 2003 Mar 13.
6
A susceptibility gene for late-onset idiopathic Parkinson's disease.晚发性特发性帕金森病的一个易感基因。
Ann Neurol. 2002 Nov;52(5):549-55. doi: 10.1002/ana.10324.
7
Age at onset in two common neurodegenerative diseases is genetically controlled.两种常见神经退行性疾病的发病年龄受基因控制。
Am J Hum Genet. 2002 Apr;70(4):985-93. doi: 10.1086/339815. Epub 2002 Mar 1.
8
CED-12/ELMO, a novel member of the CrkII/Dock180/Rac pathway, is required for phagocytosis and cell migration.CED-12/ELMO是CrkII/Dock180/Rac信号通路的一个新成员，在吞噬作用和细胞迁移过程中发挥作用。
Cell. 2001 Oct 5;107(1):27-41. doi: 10.1016/s0092-8674(01)00520-7.
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Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.特发性帕金森病临床诊断的准确性：100例临床病理研究
J Neurol Neurosurg Psychiatry. 1992 Mar;55(3):181-4. doi: 10.1136/jnnp.55.3.181.

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.

作者信息

Li Yonghong, Rowland Charles, Schrodi Steven, Laird Walter, Tacey Kristina, Ross David, Leong Diane, Catanese Joseph, Sninsky John, Grupe Andrew

出版信息

Am J Hum Genet. 2006 Jun;78(6):1090-2; author reply 1092-4. doi: 10.1086/504725.

DOI:10.1086/504725
PMID:16685663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1474092/
Abstract
摘要