Records 1 - 15
| 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
| 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
| 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
| 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
| 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 Xiao Qin, Cao Bei, Wu Ying, Chen Yong Ping, Wei Qian Qian, Ou Ru Wei, Yang Jing, Chen Xue Ping, Zhao Bi, Song Wei, Shang Hui Fa
| Exome Array Analysis of Nuclear Lens Opacity.
Ophthalmic epidemiology 2017 Nov 1-5.
Loomis Stephanie J, Klein Alison P, Lee Kristine E, Chen Fei, Bomotti Samantha, Truitt Barbara, Iyengar Sudha K, Klein Ronald, Klein Barbara E K, Duggal Pri
| 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,
| 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
| Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.
Human molecular genetics 2013 Feb 22 (4): 832-41.
Lee S Hong, Harold Denise, Nyholt Dale R, , , , Goddard Michael E, Zondervan Krina T, Williams Julie, Montgomery Grant W, Wray Naomi R, Visscher Peter
| Lack of association between PRNP M129V polymorphism and multiple sclerosis, mild cognitive impairment, alcoholism and schizophrenia in a Korean population.
Disease markers 2010 28 (5): 315-21.
Choi Ihn-Geun, Woo Sung-Il, Kim Ho Jin, Kim Dai-Jin, Park Byung Lae, Cheong Hyun Sub, Pasaje Charisse Flerida A, Park Tae Joon, Bae Joon Seol, Chai Young Gyu, Shin Hyoung D
| Exhaustive genotyping of the interferon alpha receptor 1 (IFNAR1) gene and association of an IFNAR1 protein variant with AIDS progression or susceptibility to HIV-1 infection in a French AIDS cohort.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 2006 Nov 60 (9): 569-77.
Diop G, Hirtzig T, Do H, Coulonges C, Vasilescu A, Labib T, Spadoni J-L, Therwath A, Lathrop M, Matsuda F, Zagury J
| Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases.
BMC medical genetics 2006 7 (): 20.
Smyth Deborah J, Howson Joanna M M, Payne Felicity, Maier Lisa M, Bailey Rebecca, Holland Kieran, Lowe Christopher E, Cooper Jason D, Hulme John S, Vella Adrian, Dahlman Ingrid, Lam Alex C, Nutland Sarah, Walker Neil M, Twells Rebecca C J, Todd John
| Association of AIRE Polymorphism and the Susceptibility to Multiple Sclerosis in Iranian Population.
Avicenna journal of medical biotechnology 0 10 (2): 110-114.
Sadeghian-Rizi Tahereh, Alsahebfosoul Fereshteh, Kazemi Mohammad, Khanahmad Hossein, Jahanian-Najafabadi A