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Blackinton J, Kumaran R, van der Brug MP, Ahmad R, Olson L, Galter D, et al. Post-transcriptional regulation of mRNA associated with DJ-1 in sporadic Parkinson disease. Neurosci Lett. 2009;452(1):8-11.
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Westerlund M, Carmine Belin A, Anvret A, Håkansson A, Nissbrandt H, Lind C, et al. Association of a polymorphism in the ABCB1 gene with Parkinson's disease. Parkinsonism Relat Disord. 2009;15(6):422-4.
Westerlund M, Carmine Belin A, Anvret A, Håkansson A, Nissbrandt H, Lind C, et al. Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material. FASEB J. 2008;22(10):3509-14.
Terzioglu M, Galter D. Parkinson's disease: genetic versus toxin-induced rodent models. FEBS J. 2008;275(7):1384-91.
Carmine Belin A, Björk BF, Westerlund M, Galter D, Sydow O, Lind C, et al. Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease. Neurosci Lett. 2007;420(3):257-62.
Carmine Belin A, Westerlund M, Bergman O, Nissbrandt H, Lind C, Sydow O, et al. S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden. Parkinsonism Relat Disord. 2007;13(5):295-8.
Ekstrand MI, Terzioglu M, Galter D, Zhu S, Hofstetter C, Lindqvist E, et al. Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons. Proc Natl Acad Sci USA. 2007;104(4):1325-30.
Blackinton JG, Anvret A, Beilina A, Olson L, Cookson MR, Galter D. Expression of PINK1 mRNA in human and rodent brain and in Parkinson's disease. Brain Res. 2007;1184:10-6.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, et al. A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. Arch Neurol. 2005;62(1):74-8.