] Filters: Author is Sharma, Manu [Clear All Filters]
Sharma M, Lichtner P, Kruger R, Berg D, Schulte C, Illig T, et al. Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease. Neurobiol Aging. 2009;30(10):1706-9.
Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, et al. Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: Large-scale collaborative study. Am J Med Genet B Neuropsychiatr Genet. 2009.
Scholz SW, Houlden H, Schulte C, Sharma M, Li A, Berg D, et al. SNCA variants are associated with increased risk for multiple system atrophy. Ann Neurol. 2009;65(5):610-4.
Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, et al. The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiol Aging. 2009;30(5):731-8.
Rothfuss O, Fischer H, Hasegawa T, Maisel M, Leitner P, Miesel F, et al. Parkin protects Mitochondrial Genome Integrity and supports Mitochondrial DNA Repair. Hum Mol Genet. 2009.
Prestel J, Sharma M, Leitner P, Zimprich A, Vaughan JR, Dürr A, et al. PARK11 is not linked with Parkinson's disease in European families. Eur J Hum Genet. 2005;13(2):193-7.
Biskup S, Mueller JC, Sharma M, Lichtner P, Zimprich A, Berg D, et al. Common variants of LRRK2 are not associated with sporadic Parkinson's disease. Ann Neurol. 2005;58(6):905-8.
Zimprich A, Müller-Myhsok B, Farrer M, Leitner P, Sharma M, Hulihan M, et al. The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval. Am J Hum Genet. 2004;74(1):11-9.