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Association of a polymorphism in the ABCB1 gene with Parkinson's disease.
Westerlund M, Belin AC, Anvret A, Håkansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D. Westerlund M, et al. Among authors: olson l. Parkinsonism Relat Disord. 2009 Jul;15(6):422-4. doi: 10.1016/j.parkreldis.2008.11.010. Epub 2009 Feb 3. Parkinsonism Relat Disord. 2009. PMID: 19196542
The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden.
Ran C, Willows T, Sydow O, Johansson A, Söderkvist P, Dizdar N, Ahmadi A, Olson L, Belin AC. Ran C, et al. Among authors: olson l. Parkinsonism Relat Disord. 2013 Jul;19(7):701-2. doi: 10.1016/j.parkreldis.2013.03.001. Epub 2013 Apr 8. Parkinsonism Relat Disord. 2013. PMID: 23579001 Free article. No abstract available.
Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease.
Håkansson A, Westberg L, Nilsson S, Buervenich S, Carmine A, Holmberg B, Sydow O, Olson L, Johnels B, Eriksson E, Nissbrandt H. Håkansson A, et al. Among authors: olson l. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):88-92. doi: 10.1002/ajmg.b.30136. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635591
Cyclooxygenase-2 polymorphisms in Parkinson's disease.
Håkansson A, Bergman O, Chrapkowska C, Westberg L, Belin AC, Sydow O, Johnels B, Olson L, Holmberg B, Nissbrandt H. Håkansson A, et al. Among authors: olson l. Am J Med Genet B Neuropsychiatr Genet. 2007 Apr 5;144B(3):367-9. doi: 10.1002/ajmg.b.30449. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17171651
Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden.
Ran C, Brodin L, Forsgren L, Westerlund M, Ramezani M, Gellhaar S, Xiang F, Fardell C, Nissbrandt H, Söderkvist P, Puschmann A, Ygland E, Olson L, Willows T, Johansson A, Sydow O, Wirdefeldt K, Galter D, Svenningsson P, Belin AC. Ran C, et al. Among authors: olson l. Neurobiol Aging. 2016 Sep;45:212.e5-212.e11. doi: 10.1016/j.neurobiolaging.2016.04.022. Epub 2016 May 3. Neurobiol Aging. 2016. PMID: 27255555 Free PMC article.
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: olson l. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
2,010 results