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相似文献

1
Covariate-dependent age-at-onset distributions for Huntington disease.亨廷顿舞蹈症的发病年龄分布与协变量有关。
Am J Hum Genet. 1991 Oct;49(4):735-45.
2
Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting.亨廷顿舞蹈症发病年龄与父亲年龄之间的负相关关系提示基因印记的参与。
Am J Hum Genet. 1992 Mar;50(3):528-35.
3
Validation and aplication of an interval factor in estimating age at onset of Huntington's disease.一种间隔因素在估计亨廷顿舞蹈病发病年龄中的验证与应用
J Med Genet. 1978 Feb;15(1):23-6. doi: 10.1136/jmg.15.1.23.
4
Does the omission of missing information bias the estimates of age-at-onset distributions?遗漏缺失信息是否会使发病年龄分布的估计产生偏差?
Am J Hum Genet. 1992 Mar;50(3):652-4.
5
Huntington disease in Georgia: age at onset.佐治亚州的亨廷顿舞蹈症:发病年龄
Am J Hum Genet. 1988 Nov;43(5):695-704.
6
Maternal factors in onset of Huntington disease.亨廷顿病发病中的母体因素。
Am J Hum Genet. 1985 May;37(3):511-23.
7
Predictability of age at onset in Huntington disease in the Dutch population.荷兰人群中亨廷顿舞蹈病发病年龄的可预测性。
Medicine (Baltimore). 2002 Jul;81(4):251-9. doi: 10.1097/00005792-200207000-00001.
8
Age at onset and life table risks in genetic counselling for Huntington's disease.亨廷顿舞蹈病遗传咨询中的发病年龄与生命表风险
J Med Genet. 1992 Apr;29(4):239-42. doi: 10.1136/jmg.29.4.239.
9
Juvenile Huntington disease.青少年型亨廷顿病
Hum Genet. 1986 Jul;73(3):235-9. doi: 10.1007/BF00401235.
10
Factors related to onset age of Huntington disease.与亨廷顿舞蹈症发病年龄相关的因素。
Am J Hum Genet. 1982 May;34(3):481-8.

引用本文的文献

1
Genetic characterization of Spinocerebellar ataxia 1 in a South Indian cohort.南印度人群中脊髓小脑共济失调1型的遗传学特征分析
BMC Med Genet. 2014 Oct 25;15:114. doi: 10.1186/s12881-014-0114-5.
2
Estimating decreased risks for Huntington disease without a test.在不进行检测的情况下估计亨廷顿病风险的降低情况。
Eur J Epidemiol. 2008;23(4):281-7. doi: 10.1007/s10654-008-9224-8. Epub 2008 Jan 30.
3
Unraveling a role for dopamine in Huntington's disease: the dual role of reactive oxygen species and D2 receptor stimulation.揭示多巴胺在亨廷顿舞蹈病中的作用:活性氧和D2受体刺激的双重作用
Proc Natl Acad Sci U S A. 2005 Aug 23;102(34):12218-23. doi: 10.1073/pnas.0502698102. Epub 2005 Aug 15.
4
Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length.亨廷顿病的发病年龄:载脂蛋白E基因型和正常CAG重复长度的性别特异性影响
J Med Genet. 1999 Feb;36(2):108-11.
5
Age at onset in Huntington's disease and methylation at D4S95.亨廷顿舞蹈症的发病年龄与D4S95位点的甲基化
J Med Genet. 1993 Mar;30(3):185-8. doi: 10.1136/jmg.30.3.185.
6
The fragile X premutation in carriers and its effect on mutation size in offspring.携带者中的脆性X前突变及其对后代突变大小的影响。
Am J Hum Genet. 1995 May;56(5):1147-55.

本文引用的文献

1
[Age of onset in Huntington's chorea].
Acta Genet Stat Med. 1959;9(1):18-32.
2
Huntington's chorea in Michigan. I. Demography and genetics.密歇根州的亨廷顿舞蹈症。一、人口统计学与遗传学。
Am J Hum Genet. 1958 Jun;10(2):201-25.
3
A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.
4
Factors influencing age at onset and duration of survival in Huntington's chorea.
Ann Hum Genet. 1981 Oct;45(4):387-96. doi: 10.1111/j.1469-1809.1981.tb00352.x.
5
A life table for onset of Huntington's chorea.亨廷顿舞蹈症发病情况生命表。
Ann Hum Genet. 1981 Oct;45(4):375-85. doi: 10.1111/j.1469-1809.1981.tb00351.x.
6
Factors related to onset age of Huntington disease.与亨廷顿舞蹈症发病年龄相关的因素。
Am J Hum Genet. 1982 May;34(3):481-8.
7
The relation of sex of affected parent to the age at onset of Huntington's disease.患病亲本的性别与亨廷顿舞蹈症发病年龄的关系。
J Med Genet. 1973 Dec;10(4):333-6.
8
Regressive logistic models for familial disease and other binary traits.用于家族性疾病和其他二元性状的回归逻辑模型。
Biometrics. 1986 Sep;42(3):611-25.
9
Maternal factors in onset of Huntington disease.亨廷顿病发病中的母体因素。
Am J Hum Genet. 1985 May;37(3):511-23.
10
Huntington disease in Georgia: age at onset.佐治亚州的亨廷顿舞蹈症:发病年龄
Am J Hum Genet. 1988 Nov;43(5):695-704.

亨廷顿舞蹈症的发病年龄分布与协变量有关。

Covariate-dependent age-at-onset distributions for Huntington disease.

作者信息

Krawczak M, Bockel B, Sandkuijl L, Thies U, Fenton I, Harper P S

机构信息

Institute of Human Genetics, Göttingen, Germany.

出版信息

Am J Hum Genet. 1991 Oct;49(4):735-45.

PMID:1832816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1683183/
Abstract

A combined logistic regression and life-table analysis is presented on age-at-onset data for Huntington disease. Covariates included in the analysis were sex of the at-risk individual, parental age at onset, and sex of transmitting parent. Parental age at onset and parental sex were found to be significant covariates for age at onset in the offspring, and the appropriate logistic regression functions are calculated by maximum likelihood methods. These regression functions permit a more precise evaluation of carrier risks and likelihoods than hitherto was possible by simple computational means. We further introduce a novel method to account for sibship correlations in the significance assessment, using log-likelihood differences between different models.

摘要

本文针对亨廷顿舞蹈病的发病年龄数据进行了逻辑回归和生命表分析相结合的研究。分析中纳入的协变量包括高危个体的性别、发病时父母的年龄以及传递父母的性别。研究发现,发病时父母的年龄和父母的性别是后代发病年龄的显著协变量,并通过最大似然法计算了合适的逻辑回归函数。与以往简单的计算方法相比,这些回归函数能更精确地评估携带者风险和可能性。我们还引入了一种新方法,利用不同模型之间的对数似然差异来考虑在显著性评估中的同胞相关性。