Association of polymorphism of DNA repair gene XRCC1 with sporadic late-onset Alzheimer's disease and age of onset in elderly Han Chinese

2010 ◽  
Vol 295 (1-2) ◽  
pp. 62-65 ◽  
Author(s):  
Yun Qian ◽  
Weixian Chen ◽  
Jianqing Wu ◽  
Tong Tao ◽  
Liqing Bi ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Dna Repair ◽  
Age Of Onset ◽  
Late Onset ◽  
Han Chinese ◽  
Repair Gene ◽  
Dna Repair Gene

The Arg194Trp polymorphism in DNA repair gene XRCC1 and the risk for sporadic late-onset Alzheimer's disease

2007 ◽  
Vol 28 (1) ◽  
pp. 31-34 ◽  
Author(s):  
S. Doğru-Abbasoğlu ◽  
G. Aykaç-Toker ◽  
H. A. Hanagasi ◽  
H. Gürvit ◽  
M. Emre ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Dna Repair ◽  
Late Onset ◽  
Repair Gene ◽  
Dna Repair Gene

DNA repair gene OGG1 polymorphism and its relation with oxidative DNA damage in patients with Alzheimer’s disease

2019 ◽  
Vol 709 ◽  
pp. 134362 ◽  
Author(s):  
Yıldız Dinçer ◽  
Çağlayan Akkaya ◽  
Tuba Mutlu ◽  
Serap Yavuzer ◽  
Gökhan Erkol ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Dna Damage ◽  
Dna Repair ◽  
Oxidative Dna Damage ◽  
Repair Gene ◽  
Dna Repair Gene

A Ser326Cys polymorphism in the DNA repair gene hOGG1 is not associated with sporadic Alzheimer's disease

2007 ◽  
Vol 414 (3) ◽  
pp. 282-285 ◽  
Author(s):  
Fabio Coppedè ◽  
Michelangelo Mancuso ◽  
Annalisa Lo Gerfo ◽  
Maria Laura Manca ◽  
Lucia Petrozzi ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Dna Repair ◽  
Sporadic Alzheimer’S Disease ◽  
Repair Gene ◽  
Dna Repair Gene ◽  
Ser326cys Polymorphism

Association of TOMM40 Polymorphisms with Late-Onset Alzheimer’s Disease in a Northern Han Chinese Population

2013 ◽  
Vol 15 (2) ◽  
pp. 279-287 ◽  
Author(s):  
Xiao-Ying Ma ◽  
Jin-Tai Yu ◽  
Wei Wang ◽  
Hui-Fu Wang ◽  
Qiu-Yan Liu ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Chinese Population ◽  
Late Onset ◽  
Han Chinese ◽  
Han Chinese Population

Polymorphisms in the DNA repair genes XPD (ERCC2) and XPF (ERCC4) are not associated with sporadic late-onset Alzheimer's disease

2006 ◽  
Vol 404 (3) ◽  
pp. 258-261 ◽  
Author(s):  
Semra Dogru-Abbasoglu ◽  
Muzeyyen Inceoglu ◽  
Hande Parildar-Karpuzoglu ◽  
Hasmet A. Hanagasi ◽  
Berrin Karadag ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Dna Repair ◽  
Late Onset ◽  
Dna Repair Genes ◽  
Repair Genes

Association of LRRTM3 polymorphisms with late-onset Alzheimer's disease in Han Chinese

2014 ◽  
Vol 52 ◽  
pp. 18-22 ◽  
Author(s):  
Jun Wang ◽  
Jin-Tai Yu ◽  
Teng Jiang ◽  
Meng-Shan Tan ◽  
Hui-Fu Wang ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Late Onset ◽  
Han Chinese

Association of GWAS-linked loci with late-onset Alzheimer's disease in a northern Han Chinese population

2012 ◽  
Vol 9 (5) ◽  
pp. 546-553 ◽  
Author(s):  
Lan Tan ◽  
Jin-Tai Yu ◽  
Wei Zhang ◽  
Zhong-Chen Wu ◽  
Qun Zhang ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Chinese Population ◽  
Late Onset ◽  
Han Chinese ◽  
Han Chinese Population

Lack of Association Between SLC24A4 Polymorphism and Late-onset Alzheimer's Disease in Han Chinese

2016 ◽  
Vol 13 (3) ◽  
pp. 239-243 ◽  
Author(s):  
Huan Lu ◽  
Xi-Chen Zhu ◽  
Hui-Fu Wang ◽  
Lei Cao ◽  
Meng-Shan Tan ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Late Onset ◽  
Han Chinese

Early onset Alzheimer’s disease

2020 ◽  
pp. 75-82
Author(s):  
Ratnavalli Ellajosyula
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Early Onset ◽  
Age Of Onset ◽  
Late Onset ◽  
Geographical Location ◽  
Epidemiological Studies ◽  
Incidence Rates ◽  
Prevalence Rates ◽  
Early Onset Alzheimer’S Disease

The term ‘early onset Alzheimer’s disease’ (EOAD) is used when symptoms of Alzheimer’s disease (AD) occur in patients younger than 65 years. EOAD is an uncommon condition and data on epidemiology is limited. Prevalence rates range from 15 to 200 and incidence rates 2.4–22.6 per 100,000 population. Prevalence rates increase with age similar to that for late onset AD. The prevalence of autosomal dominant EOAD is 5.2 per 100,000. Half of these patients have an underlying mutation in amyloid precursor protein, presenilin 1 or 2 genes. Apolipoprotein E genotype is a risk factor for EOAD and homozygotes have an earlier age of onset. Methodological issues and geographical location make comparisons across epidemiological studies difficult. Further cross-national and cross-cultural studies with standardized methodology are necessary to understand the role of risk and protective factors, as well as to estimate the burden of the disease.

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