No association of the LRRK2 genetic variants with Alzheimer's disease in Han Chinese individuals-Reference-Cited by-同舟云学术

No association of the LRRK2 genetic variants with Alzheimer's disease in Han Chinese individuals

Published:2014-02 Issue:2 Volume:35 Page:444.e5-444.e9
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Bi Rui,Zhao Liansheng,Zhang Chen,Lu Weihong,Feng Jia-Qi,Wang Yingcheng,Ni Jianliang,Zhang Jiangtao,Li Guo-Dong,Hu Qiu-Xiang,Wang Dong,Yao Yong-Gang,Li Tao

Funder

Ministry of Science and Technology of China

National Natural Science Foundation of China

Strategic Priority Research Program

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

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3. Leucine-rich repeat kinase 2 for beginners: six key questions;Kett;Cold Spring Harb. Perspect. Med.,2012

4. LRRK2 G2019S and I2020T mutations are not common in Alzheimer's disease and vascular dementia;Lee;Am. J. Med. Genet. B Neuropsychiatr. Genet.,2006

5. ApoE genotype in relation to AD and cholesterol: a study of 2,326 Chinese adults;Liu;Neurology,1999

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1. A Comprehensive Analysis of the CaMK2A Gene and Susceptibility to Alzheimer’s Disease in the Han Chinese Population;Frontiers in Aging Neuroscience;2019-04-11

2. A meta-analysis of leucine-rich repeat kinase 2 (LRRK2) polymorphisms in Alzheimer’s disease;Folia Neuropathologica;2019

3. Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses;Experimental Gerontology;2018-07

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