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SNCA variant associated with Parkinson disease and plasma alpha-synuclein level.
Mata IF, Shi M, Agarwal P, Chung KA, Edwards KL, Factor SA, Galasko DR, Ginghina C, Griffith A, Higgins DS, Kay DM, Kim H, Leverenz JB, Quinn JF, Roberts JW, Samii A, Snapinn KW, Tsuang DW, Yearout D, Zhang J, Payami H, Zabetian CP. Mata IF, et al. Among authors: samii a. Arch Neurol. 2010 Nov;67(11):1350-6. doi: 10.1001/archneurol.2010.279. Arch Neurol. 2010. PMID: 21060011 Free PMC article.
Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease.
Hutter CM, Samii A, Factor SA, Nutt JG, Higgins DS, Bird TD, Griffith A, Roberts JW, Leis BC, Montimurro JS, Kay DM, Edwards KL, Payami H, Zabetian CP. Hutter CM, et al. Among authors: samii a. Eur J Neurol. 2008 Feb;15(2):134-9. doi: 10.1111/j.1468-1331.2007.02012.x. Epub 2007 Dec 18. Eur J Neurol. 2008. PMID: 18093156 Free PMC article.
DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.
Chun LS, Samii A, Hutter CM, Griffith A, Roberts JW, Leis BC, Mosley AD, Wander PL, Edwards KL, Payami H, Zabetian CP. Chun LS, et al. Among authors: samii a. Ann Neurol. 2007 Jul;62(1):99-101. doi: 10.1002/ana.21149. Ann Neurol. 2007. PMID: 17503507 Free PMC article.
Parkinson's disease.
Samii A, Nutt JG, Ransom BR. Samii A, et al. Lancet. 2004 May 29;363(9423):1783-93. doi: 10.1016/S0140-6736(04)16305-8. Lancet. 2004. PMID: 15172778 Review.
Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.
Zabetian CP, Hutter CM, Factor SA, Nutt JG, Higgins DS, Griffith A, Roberts JW, Leis BC, Kay DM, Yearout D, Montimurro JS, Edwards KL, Samii A, Payami H. Zabetian CP, et al. Among authors: samii a. Ann Neurol. 2007 Aug;62(2):137-44. doi: 10.1002/ana.21157. Ann Neurol. 2007. PMID: 17514749 Free PMC article.
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, Follett J, Farrer MJ, Trinh J, Gasser T, Goldwurm S, Gustavsson E, Klein C, Lang AE, Langston JW, Latourelle J, Lynch T, Marder K, Marras C, Martin ER, McLean CY, Mejia-Santana H, Molho E, Myers RH, Nuytemans K, Ozelius L, Payami H, Raymond D, Rogaeva E, Rogers MP, Ross OA, Samii A, Saunders-Pullman R, Schüle B, Schulte C, Scott WK, Tanner C, Tolosa E, Tomkins JE, Vilas D, Trojanowski JQ; 23andMe Research Team; Uitti R, Vance JM, Visanji NP, Wszolek ZK, Zabetian CP, Mirelman A, Giladi N, Orr Urtreger A, Cannon P, Fiske B, Foroud T. Lai D, et al. Among authors: samii a. Ann Neurol. 2021 Jul;90(1):76-88. doi: 10.1002/ana.26094. Epub 2021 May 17. Ann Neurol. 2021. PMID: 33938021 Free PMC article.
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
Mata IF, Samii A, Schneer SH, Roberts JW, Griffith A, Leis BC, Schellenberg GD, Sidransky E, Bird TD, Leverenz JB, Tsuang D, Zabetian CP. Mata IF, et al. Among authors: samii a. Arch Neurol. 2008 Mar;65(3):379-82. doi: 10.1001/archneurol.2007.68. Arch Neurol. 2008. PMID: 18332251 Free PMC article.
335 results