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642 related items for PubMed ID: 30144538
1. The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy. Chen Y, Cao B, Chen X, Ou R, Wei Q, Zhao B, Wu Y, Yuan L, Shang HF. Neurosci Lett; 2018 Nov 01; 686():205-210. PubMed ID: 30144538 [Abstract] [Full Text] [Related]
2. Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy. Hu T, Chen Y, Ou R, Wei Q, Cao B, Zhao B, Wu Y, Song W, Chen X, Shang HF. J Neurol Sci; 2017 Jun 15; 377():65-71. PubMed ID: 28477711 [Abstract] [Full Text] [Related]
3. 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. Chen Y, Wei QQ, Ou R, Cao B, Chen X, Zhao B, Guo X, Yang Y, Chen K, Wu Y, Song W, Shang HF. PLoS One; 2015 Jun 15; 10(7):e0133776. PubMed ID: 26208350 [Abstract] [Full Text] [Related]
4. No association of GPNMB rs156429 polymorphism with Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in Chinese population. Xu Y, Chen Y, Ou R, Wei QQ, Cao B, Chen K, Shang HF. Neurosci Lett; 2016 May 27; 622():113-7. PubMed ID: 27132081 [Abstract] [Full Text] [Related]
5. SLC1A2 rs3794087 are associated with susceptibility to Parkinson's disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population. Xu Y, Cao B, Chen Y, Ou R, Wei Q, Yang J, Zhao B, Song W, Shang HF. J Neurol Sci; 2016 Jun 15; 365():96-100. PubMed ID: 27206883 [Abstract] [Full Text] [Related]
6. Determining the Effect of the HNMT, STK39, and NMD3 Polymorphisms on the Incidence of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations. Chen Y, Cao B, Ou R, Wei Q, Chen X, Zhao B, Wu Y, Song W, Shang HF. J Mol Neurosci; 2018 Apr 15; 64(4):574-580. PubMed ID: 29564728 [Abstract] [Full Text] [Related]
7. An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China. Guo XY, Chen YP, Song W, Zhao B, Cao B, Wei QQ, Ou RW, Yang Y, Yuan LX, Shang HF. Eur J Neurol; 2014 Oct 15; 21(10):1337-43. PubMed ID: 25040112 [Abstract] [Full Text] [Related]
8. Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Yuan X, Cao B, Wu Y, Chen Y, Wei Q, Ou R, Yang J, Chen X, Zhao B, Song W, Shang H. Neurosci Lett; 2018 Jan 18; 664():128-132. PubMed ID: 29128630 [Abstract] [Full Text] [Related]
9. SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Guo XY, Chen YP, Song W, Zhao B, Cao B, Wei QQ, Ou RW, Yang Y, Yuan LX, Shang HF. Neurobiol Aging; 2014 Dec 18; 35(12):2882.e1-2882.e6. PubMed ID: 25129240 [Abstract] [Full Text] [Related]
10. Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis. Wainberg M, Andrews SJ, Tripathy SJ. Alzheimers Res Ther; 2023 Jun 16; 15(1):113. PubMed ID: 37328865 [Abstract] [Full Text] [Related]
11. Association analysis of the GRN rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis. Chen Y, Cao B, Ou R, Chen X, Zhao B, Wei Q, Wu Y, Shang HF. Int J Neurosci; 2016 Oct 16; 126(10):947-54. PubMed ID: 26303052 [Abstract] [Full Text] [Related]
12. Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population. Chen Y, Chen X, Guo X, Song W, Cao B, Wei Q, Ou R, Zhao B, Shang HF. Neurol Sci; 2015 Oct 16; 36(10):1903-6. PubMed ID: 26058955 [Abstract] [Full Text] [Related]
13. Pathway analysis of two amyotrophic lateral sclerosis GWAS highlights shared genetic signals with Alzheimer's disease and Parkinson's disease. Shang H, Liu G, Jiang Y, Fu J, Zhang B, Song R, Wang W. Mol Neurobiol; 2015 Feb 16; 51(1):361-9. PubMed ID: 24647822 [Abstract] [Full Text] [Related]
14. A study of five candidate genes in Parkinson's disease and related neurodegenerative disorders. European Study Group on Atypical Parkinsonism. Nicholl DJ, Bennett P, Hiller L, Bonifati V, Vanacore N, Fabbrini G, Marconi R, Colosimo C, Lamberti P, Stocchi F, Bonuccelli U, Vieregge P, Ramsden DB, Meco G, Williams AC. Neurology; 1999 Oct 22; 53(7):1415-21. PubMed ID: 10534244 [Abstract] [Full Text] [Related]
15. Analysis and meta-analysis of five polymorphisms of the LINGO1 and LINGO2 genes in Parkinson's disease and multiple system atrophy in a Chinese population. Chen Y, Cao B, Yang J, Wei Q, Ou RW, Zhao B, Song W, Guo X, Shang H. J Neurol; 2015 Nov 22; 262(11):2478-83. PubMed ID: 26254004 [Abstract] [Full Text] [Related]
16. Identifying the Association Between Alzheimer's Disease and Parkinson's Disease Using Genome-Wide Association Studies and Protein-Protein Interaction Network. Liu G, Bao X, Jiang Y, Liao M, Jiang Q, Feng R, Zhang L, Ma G, Chen Z, Wang G, Wang R, Zhao B, Li K. Mol Neurobiol; 2015 Dec 22; 52(3):1629-1636. PubMed ID: 25370933 [Abstract] [Full Text] [Related]
17. Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population. Chung SJ, Jung Y, Hong M, Kim MJ, You S, Kim YJ, Kim J, Song K. Neurobiol Aging; 2013 Nov 22; 34(11):2695.e1-7. PubMed ID: 23820587 [Abstract] [Full Text] [Related]
18. Association between NEK1 gene polymorphisms and the potential risk of sporadic Parkinson's disease in the Chinese Northern Han population: A case-control study. He Q, Zhou Y, Jin J, Tian Q, Li H, Hou B, Xie A. Neurosci Lett; 2024 Aug 10; 837():137913. PubMed ID: 39032803 [Abstract] [Full Text] [Related]
19. The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease. Lill CM, Rengmark A, Pihlstrøm L, Fogh I, Shatunov A, Sleiman PM, Wang LS, Liu T, Lassen CF, Meissner E, Alexopoulos P, Calvo A, Chio A, Dizdar N, Faltraco F, Forsgren L, Kirchheiner J, Kurz A, Larsen JP, Liebsch M, Linder J, Morrison KE, Nissbrandt H, Otto M, Pahnke J, Partch A, Restagno G, Rujescu D, Schnack C, Shaw CE, Shaw PJ, Tumani H, Tysnes OB, Valladares O, Silani V, van den Berg LH, van Rheenen W, Veldink JH, Lindenberger U, Steinhagen-Thiessen E, SLAGEN Consortium, Teipel S, Perneczky R, Hakonarson H, Hampel H, von Arnim CAF, Olsen JH, Van Deerlin VM, Al-Chalabi A, Toft M, Ritz B, Bertram L. Alzheimers Dement; 2015 Dec 10; 11(12):1407-1416. PubMed ID: 25936935 [Abstract] [Full Text] [Related]
20. Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese. Yang X, Zhao Q, An R, Zheng J, Tian S, Xu Y. Amyotroph Lateral Scler Frontotemporal Degener; 2015 Dec 10; 17(1-2):142-7. PubMed ID: 26313240 [Abstract] [Full Text] [Related] Page: [Next] [New Search]