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PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.
Beecham GW, Dickson DW, Scott WK, Martin ER, Schellenberg G, Nuytemans K, Larson EB, Buxbaum JD, Trojanowski JQ, Van Deerlin VM, Hurtig HI, Mash DC, Beach TG, Troncoso JC, Pletnikova O, Frosch MP, Ghetti B, Foroud TM, Honig LS, Marder K, Vonsattel JP, Goldman SM, Vinters HV, Ross OA, Wszolek ZK, Wang L, Dykxhoorn DM, Pericak-Vance MA, Montine TJ, Leverenz JB, Dawson TM, Vance JM. Beecham GW, et al. Among authors: foroud tm. Neurology. 2015 Mar 10;84(10):972-80. doi: 10.1212/WNL.0000000000001332. Epub 2015 Feb 6. Neurology. 2015. PMID: 25663231 Free PMC article.
Significant linkage of Parkinson disease to chromosome 2q36-37.
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T; Parkinson Study Group. Pankratz N, et al. Am J Hum Genet. 2003 Apr;72(4):1053-7. doi: 10.1086/374383. Epub 2003 Mar 13. Am J Hum Genet. 2003. PMID: 12638082 Free PMC article.
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.
Chromosome 5 and Parkinson disease.
Foroud T, Pankratz N, Martinez M; PROGENI/GSPD-European Consortium. Foroud T, et al. Eur J Hum Genet. 2006 Oct;14(10):1106-10. doi: 10.1038/sj.ejhg.5201666. Epub 2006 May 31. Eur J Hum Genet. 2006. PMID: 16736031
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Ishihara L, Warren L, Gibson R, Amouri R, Lesage S, Dürr A, Tazir M, Wszolek ZK, Uitti RJ, Nichols WC, Griffith A, Hattori N, Leppert D, Watts R, Zabetian CP, Foroud TM, Farrer MJ, Brice A, Middleton L, Hentati F. Ishihara L, et al. Among authors: foroud tm. Arch Neurol. 2006 Sep;63(9):1250-4. doi: 10.1001/archneur.63.9.1250. Arch Neurol. 2006. PMID: 16966502
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.
Variation in GIGYF2 is not associated with Parkinson disease.
Nichols WC, Kissell DK, Pankratz N, Pauciulo MW, Elsaesser VE, Clark KA, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T; Parkinson Study Group-PROGENI Investigators. Nichols WC, et al. Neurology. 2009 Jun 2;72(22):1886-92. doi: 10.1212/01.wnl.0000346517.98982.1b. Epub 2009 Mar 11. Neurology. 2009. PMID: 19279319 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.
622 results