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Genetics of Parkinson disease.
Pankratz N, Foroud T. Pankratz N, et al. NeuroRx. 2004 Apr;1(2):235-42. doi: 10.1602/neurorx.1.2.235. NeuroRx. 2004. PMID: 15717024 Free PMC article. Review.
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T; Parkinson Study Group - PROGENI Investigators. Nichols WC, et al. Among authors: pankratz n. Mov Disord. 2007 Jan 15;22(2):254-7. doi: 10.1002/mds.21233. Mov Disord. 2007. PMID: 17149721
Genetics of Parkinson disease.
Pankratz N, Foroud T. Pankratz N, et al. Genet Med. 2007 Dec;9(12):801-11. doi: 10.1097/gim.0b013e31815bf97c. Genet Med. 2007. PMID: 18091429 Free article. Review.
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH; PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories. Pankratz N, et al. Hum Genet. 2009 Jan;124(6):593-605. doi: 10.1007/s00439-008-0582-9. Epub 2008 Nov 6. Hum Genet. 2009. PMID: 18985386 Free PMC article.
Alpha-synuclein and familial Parkinson's disease.
Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T; Parkinson Study Group - PROGENI Investigators. Pankratz N, et al. Mov Disord. 2009 Jun 15;24(8):1125-31. doi: 10.1002/mds.22524. Mov Disord. 2009. PMID: 19412953 Free PMC article.
Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.
Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T; PSG-Progeni GenePD Investigators, Coordinators, and Molecular Genetic Laboratories. Latourelle JC, et al. Among authors: pankratz n. Mov Disord. 2011 Sep;26(11):2039-44. doi: 10.1002/mds.23781. Epub 2011 Jun 9. Mov Disord. 2011. PMID: 21661047 Free PMC article.
215 results