Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population-Reference-Cited by-同舟云学术

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Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population

Published:2014-02-04 Issue:7 Volume:35 Page:1089-1095
ISSN:1590-1874
Container-title:Neurological Sciences
language:en
Short-container-title:Neurol Sci

Author:

Chen Xueping,Huang Rui,Chen Yongping,Zheng Zhenzhen,Chen Ke,Song Wei,Zhao Bi,Yang Yuan,Yuan Lixing,Shang Huifang

Publisher

Springer Science and Business Media LLC

Subject

Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s10072-014-1656-1.pdf

Reference38 articles.

1. Rowland LP, Shneider NA (2001) Amyotrophic Lateral Sclerosis. N Engl J Med 344:1688–1700

2. Simpson CL, Al-Chalabi A (2006) Amyotrophic lateral sclerosis as a complex genetic disease. Biochim Biophys Acta 1762(11–12):973–985. doi: 10.1016/j.bbadis.2006.08.001

3. Rosen DR (1993) Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 364(6435):362. doi: 10.1038/364362c0

4. Valdmanis PN, Rouleau GA (2008) Genetics of familial amyotrophic lateral sclerosis. Neurology 70(2):144–152. doi: 10.1212/01.wnl.0000296811.19811.db

5. Van Deerlin VM, Leverenz JB, Bekris LM, Bird TD, Yuan W, Elman LB, Clay D, Wood EM, Chen-Plotkin AS, Martinez-Lage M, Steinbart E, McCluskey L, Grossman M, Neumann M, Wu IL, Yang WS, Kalb R, Galasko DR, Montine TJ, Trojanowski JQ, Lee VM, Schellenberg GD, Yu CE (2008) TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol 7(5):409–416. doi: 10.1016/S1474-4422(08)70071-1

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1. Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients;Journal of Neurology, Neurosurgery & Psychiatry;2023-05-04

2. UNC13Ain amyotrophic lateral sclerosis: from genetic association to therapeutic target;Journal of Neurology, Neurosurgery & Psychiatry;2023-02-03

3. Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis;Frontiers in Aging Neuroscience;2023-02-01

4. UNC13A variant rs12608932 is associated with increased risk of amyotrophic lateral sclerosis and reduced patient survival: a meta-analysis;Neurological Sciences;2019-06-14

5. The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population;Frontiers in Aging Neuroscience;2018-04-12

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