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APOE ε4 increases risk for dementia in pure synucleinopathies.
Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Trojanowski JQ, Weintraub D, Chen-Plotkin AS, Irwin DJ, Rick J, Schellenberg GD, Watson GS, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Quinn JF, Chung KA, Yearout D, Mata IF, Wan JY, Edwards KL, Montine TJ, Zabetian CP. Tsuang D, et al. Among authors: edwards kl. JAMA Neurol. 2013 Feb;70(2):223-8. doi: 10.1001/jamaneurol.2013.600. JAMA Neurol. 2013. PMID: 23407718 Free PMC article.
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.
Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, Leis BC, Bird TD, Nutt JG, Higgins DS, Roberts JW, Kay DM, Edwards KL, Samii A, Payami H. Zabetian CP, et al. Among authors: edwards kl. Am J Hum Genet. 2006 Oct;79(4):752-8. doi: 10.1086/508025. Epub 2006 Aug 17. Am J Hum Genet. 2006. PMID: 16960813 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: edwards kl. Ann Neurol. 2007 Jul;62(1):99-101. doi: 10.1002/ana.21149. Ann Neurol. 2007. PMID: 17503507 Free PMC article.
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: edwards kl. Ann Neurol. 2007 Aug;62(2):137-44. doi: 10.1002/ana.21157. Ann Neurol. 2007. PMID: 17514749 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: edwards kl. 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.
Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.
Mata IF, Hutter CM, González-Fernández MC, de Pancorbo MM, Lezcano E, Huerta C, Blazquez M, Ribacoba R, Guisasola LM, Salvador C, Gómez-Esteban JC, Zarranz JJ, Infante J, Jankovic J, Deng H, Edwards KL, Alvarez V, Zabetian CP. Mata IF, et al. Among authors: edwards kl. Neurogenetics. 2009 Oct;10(4):347-53. doi: 10.1007/s10048-009-0187-z. Epub 2009 Mar 24. Neurogenetics. 2009. PMID: 19308469 Free PMC article.
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. Zabetian CP, et al. Among authors: edwards kl. Mov Disord. 2009 May 15;24(7):1034-41. doi: 10.1002/mds.22514. Mov Disord. 2009. PMID: 19343804 Free PMC article.
246 results