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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: anvret m. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
Alcohol dehydrogenase alleles in Parkinson's disease.
Buervenich S, Sydow O, Carmine A, Zhang Z, Anvret M, Olson L. Buervenich S, et al. Among authors: anvret m. Mov Disord. 2000 Sep;15(5):813-8. doi: 10.1002/1531-8257(200009)15:5<813::aid-mds1008>3.0.co;2-y. Mov Disord. 2000. PMID: 11009184
NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
Carmine A, Buervenich S, Galter D, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Chowdari KV, Nimgaonkar VL, Anvret M, Sydow O, Olson L. Carmine A, et al. Among authors: anvret m. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):51-7. doi: 10.1002/ajmg.b.20033. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12815740
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease.
Belin AC, Ran C, Anvret A, Paddock S, Westerlund M, Håkansson A, Nissbrandt H, Söderkvist P, Dizdar N, Ahmadi A, Anvret M, Willows T, Sydow O, Galter D. Belin AC, et al. Among authors: anvret m. Neurosci Lett. 2012 Jul 26;522(1):30-5. doi: 10.1016/j.neulet.2012.06.007. Epub 2012 Jun 13. Neurosci Lett. 2012. PMID: 22704918
NURR1 mutations in cases of schizophrenia and manic-depressive disorder.
Buervenich S, Carmine A, Arvidsson M, Xiang F, Zhang Z, Sydow O, Jönsson EG, Sedvall GC, Leonard S, Ross RG, Freedman R, Chowdari KV, Nimgaonkar VL, Perlmann T, Anvret M, Olson L. Buervenich S, et al. Among authors: anvret m. Am J Med Genet. 2000 Dec 4;96(6):808-13. doi: 10.1002/1096-8628(20001204)96:6<808::aid-ajmg23>3.0.co;2-e. Am J Med Genet. 2000. PMID: 11121187
Mutation screening in Rett syndrome patients.
Xiang F, Buervenich S, Nicolao P, Bailey ME, Zhang Z, Anvret M. Xiang F, et al. Among authors: anvret m. J Med Genet. 2000 Apr;37(4):250-5. doi: 10.1136/jmg.37.4.250. J Med Genet. 2000. PMID: 10745042 Free PMC article.
146 results