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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 12 (of 12 Records)

Query Trace: Amyotrophic Lateral Sclerosis and MAF[original query]
An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Oct 21 (10): 1337-43.
Guo X-Y, Chen Y-P, Song W, Zhao B, Cao B, Wei Q-Q, Ou R-W, Yang Y, Yuan L-X, Shang H
Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
PloS one 2015 10 (7): e0133776.
Chen YongPing, Wei Qian-Qian, Ou RuWei, Cao Bei, Chen XuePing, Zhao Bi, Guo XiaoYan, Yang Yuan, Chen Ke, Wu Ying, Song Wei, Shang Hui-Fa
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
Acta neuropathologica communications 2015 3 68.
Janssens Jonathan, Philtjens Stéphanie, Kleinberger Gernot, Van Mossevelde Sara, van der Zee Julie, Cacace Rita, Engelborghs Sebastiaan, Sieben Anne, Banzhaf-Strathmann Julia, Dillen Lubina, Merlin Céline, Cuijt Ivy, Robberecht Caroline, Schmid Bettina, Santens Patrick, Ivanoiu Adrian, Vandenbulcke Mathieu, Vandenberghe Rik, Cras Patrick, De Deyn Peter P, Martin Jean-Jacques, Maudsley Stuart, Haass Christian, Cruts Marc, Van Broeckhoven Christine,
Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
Neuroscience letters 2017 Nov .
Yuan XiaoQin, Cao Bei, Wu Ying, Chen YongPing, Wei QianQian, Ou RuWei, Yang Jing, Chen XuePing, Zhao Bi, Song Wei, Shang HuiFa
Mutation screening of NEK1 in Chinese ALS patients.
Neurobiology of aging 2018 Jun .
Shu Shi, Lei Xingxing, Liu Fang, Cui Bo, Liu Qing, Ding Qingyun, Liu Ming Sheng, Li Xiao Guang, Cui Liying, Zhang X
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 10 108.
Xu Lianping, Li Jiao, Tian Danyang, Chen Lu, Tang Lu, Fan Dongshe
Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients.
Neurogenetics 2019 8 20 (4): 197-208.
Narain Priyam, Padhi Aditya K, Dave Upma, Mishra Dibyakanti, Bhatia Rohit, Vivekanandan Perumal, Gomes Jam
Rare, low-frequency and common coding variants of ARHGEF28 gene and their association with sporadic amyotrophic lateral sclerosis.
Neurobiology of aging 2019 Mar .
Song Yang, Lin Feng, Ye Cheng-Hui, Huang Huaping, Li Xuying, Yao Xiaoli, Xu Yanming, Wang Chaodo
Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis.
Neurogenetics 2020 Aug .
Naruse Hiroya, Ishiura Hiroyuki, Mitsui Jun, Takahashi Yuji, Matsukawa Takashi, Sakuishi Kaori, Nakamagoe Kiyotaka, Miyake Zenshi, Tamaoka Akira, Goto Jun, Yoshimura Jun, Doi Koichiro, Morishita Shinichi, Toda Tatsushi, Tsuji Sho
Minor Allele Frequencies and Molecular Pathways Differences for SNPs Associated with Amyotrophic Lateral Sclerosis in Subjects Participating in the UKBB and 1000 Genomes Project.
Journal of clinical medicine 2021 Jul 10 (15): .
D'Antona Salvatore, Bertoli Gloria, Castiglioni Isabella, Cava Claud
Systematic Review and Meta-Analyses of Aminopeptidases as Prognostic Biomarkers in Amyotrophic Lateral Sclerosis.
International journal of molecular sciences 2023 4 24 (8): .
Bárbara Teruel-Peña, José Luís Gómez-Urquiza, Nora Suleiman-Martos, Isabel Prieto, Francisco José García-Cózar, Manuel Ramírez-Sánchez, Carmen Fernández-Martos, Germán Domínguez-Ví
Rare DNAJC7 Variants May Play a Minor Role in Chinese Patients with ALS.
Molecular neurobiology 2023 10 .
Shichan Wang, Xiaoting Zheng, Qianqian Wei, Junyu Lin, Tianmi Yang, Yi Xiao, Qirui Jiang, Chunyu Li, Huifang Sha
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