Similar articles for PMID: 18442140

Year	Number of Results
2002	1
2003	2
2004	5
2005	8
2006	6
2007	2
2008	3
2009	2
2010	1
2011	2
2013	4
2014	2
2015	5
2016	3
2017	1
2018	1
2024	0

1

Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genes.

Soma H, Yabe I, Takei A, Fujiki N, Yanagihara T, Sasaki H. Soma H, et al. Mov Disord. 2008 Jun 15;23(8):1161-7. doi: 10.1002/mds.22046. Mov Disord. 2008. PMID: 18442140

2

Evaluation of the role of the SQSTM1 gene in sporadic Belgian patients with Paget's disease.

Beyens G, Van Hul E, Van Driessche K, Fransen E, Devogelaer JP, Vanhoenacker F, Van Offel J, Verbruggen L, De Clerck L, Westhovens R, Van Hul W. Beyens G, et al. Calcif Tissue Int. 2004 Aug;75(2):144-52. doi: 10.1007/s00223-004-0244-4. Epub 2004 May 20. Calcif Tissue Int. 2004. PMID: 15164150

3

MAPT haplotype diversity in multiple system atrophy.

Labbé C, Heckman MG, Lorenzo-Betancor O, Murray ME, Ogaki K, Soto-Ortolaza AI, Walton RL, Fujioka S, Koga S, Uitti RJ, van Gerpen JA, Petersen RC, Graff-Radford NR, Younkin SG, Boeve BF, Cheshire WP Jr, Low PA, Sandroni P, Coon EA, Singer W, Wszolek ZK, Dickson DW, Ross OA. Labbé C, et al. Parkinsonism Relat Disord. 2016 Sep;30:40-5. doi: 10.1016/j.parkreldis.2016.06.010. Epub 2016 Jun 16. Parkinsonism Relat Disord. 2016. PMID: 27374978 Free PMC article.

4

Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.

Dickel DE, Veenstra-VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL. Dickel DE, et al. Arch Gen Psychiatry. 2006 Jul;63(7):778-85. doi: 10.1001/archpsyc.63.7.778. Arch Gen Psychiatry. 2006. PMID: 16818867

5

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. Hu T, et al. J Neurol Sci. 2017 Jun 15;377:65-71. doi: 10.1016/j.jns.2017.03.028. Epub 2017 Mar 21. J Neurol Sci. 2017. PMID: 28477711

6

Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descent.

Lucas GJ, Hocking LJ, Daroszewska A, Cundy T, Nicholson GC, Walsh JP, Fraser WD, Meier C, Hooper MJ, Ralston SH. Lucas GJ, et al. J Bone Miner Res. 2005 Feb;20(2):227-31. doi: 10.1359/JBMR.041106. Epub 2004 Nov 16. J Bone Miner Res. 2005. PMID: 15647816 Free article.

7

Association study of polymorphisms in the excitatory amino acid transporter 2 gene (SLC1A2) with schizophrenia.

Deng X, Shibata H, Ninomiya H, Tashiro N, Iwata N, Ozaki N, Fukumaki Y. Deng X, et al. BMC Psychiatry. 2004 Aug 6;4:21. doi: 10.1186/1471-244X-4-21. BMC Psychiatry. 2004. PMID: 15296513 Free PMC article.

8

Liang L, Sun C, Liao XP, Xiao F, Chen XD, Huang SX, Tang XL, Wen GQ, Long ZG, Wang XY, Liu GX, Cheng S, Cai WW. Liang L, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):316-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767673 Chinese.

9

Genetic variation at the perilipin locus is associated with changes in serum free fatty acids and abdominal fat following mild weight loss.

Jang Y, Kim OY, Lee JH, Koh SJ, Chae JS, Kim JY, Park S, Cho H, Lee JE, Ordovas JM. Jang Y, et al. Int J Obes (Lond). 2006 Nov;30(11):1601-8. doi: 10.1038/sj.ijo.0803312. Epub 2006 Apr 4. Int J Obes (Lond). 2006. PMID: 16585946

10

Genetic polymorphisms of the HCR gene and a genomic segment in close proximity to HLA-C are associated with patients with psoriasis in Taiwan.

Chang YT, Shiao YM, Chin PJ, Liu YL, Chou FC, Wu S, Lin YF, Li LH, Lin MW, Liu HN, Tsai SF. Chang YT, et al. Br J Dermatol. 2004 Jun;150(6):1104-11. doi: 10.1111/j.1365-2133.2004.05972.x. Br J Dermatol. 2004. PMID: 15214895

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