Studies
CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD)
CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD)
Request Access
Overview
Selected Publications (8)
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
W. Nichols, N. Pankratz, D. Hernandez, et al.. (2005). The Lancet. Cited 473 times.
https://doi.org/10.1016/S0140-6736(05)17828-3
Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.
Mei Sun, J. Latourelle, G. F. Wooten, et al.. (2006). Archives of neurology. Cited 149 times.
https://doi.org/10.1001/ARCHNEUR.63.6.826
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
Samer Karamohamed, J. Latourelle, B. Racette, et al.. (2005). Neurology. Cited 76 times.
https://doi.org/10.1212/01.wnl.0000187075.81589.fd
Mutations in DJ-1 are rare in familial Parkinson disease
N. Pankratz, M. Pauciulo, V. E. Elsaesser, et al.. (2006). Neuroscience Letters. Cited 58 times.
https://doi.org/10.1016/j.neulet.2006.09.003
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
William C. Nichols, William C. Nichols, V. E. Elsaesser, et al.. (2007). Neurology. Cited 46 times.
https://doi.org/10.1212/01.wnl.0000278115.50741.4e
Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age
J. Wilk, J. E. Tobin, O. Suchowersky, et al.. (2006). Neurology. Cited 42 times.
https://doi.org/10.1212/01.wnl.0000249149.22407.d1
Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease
N. Pankratz, M. Pauciulo, V. E. Elsaesser, et al.. (2006). Movement Disorders. Cited 38 times.
https://doi.org/10.1002/mds.21162
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ‐1 (T497C) genes in familial Parkinson's disease from the GenePD study
Samer Karamohamed, L. Golbe, M. Mark, et al.. (2005). Movement Disorders. Cited 18 times.
https://doi.org/10.1002/mds.20515