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Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.
Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T; Parkinson Study Group-PROGENI Investigators. Simon DK, et al. Among authors: pankratz n. BMC Med Genet. 2010 Apr 1;11:53. doi: 10.1186/1471-2350-11-53. BMC Med Genet. 2010. PMID: 20356410 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.
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T; Parkinson Study Group-PROGENI investigators. Nichols WC, et al. Among authors: pankratz n. Lancet. 2005 Jan 29-Feb 4;365(9457):410-2. doi: 10.1016/S0140-6736(05)17828-3. Lancet. 2005. PMID: 15680455
215 results