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Genetic Epidemiology|January 17, 2002
Use of variable marker density, principal components, and neural networks in the dissection of disease etiologyN Pankratz, S C Kirkwood, L Flury, et al.
Genetic Epidemiology|January 17, 2002
Parametric linkage analysis and disequilibrium methods to identify loci for complex diseaseJ McClintick, D L Koller, N Pankratz, et al.
Neurology|May 12, 2004
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel lociN Pankratz, S K Uniacke, C A Halter, et al.
Neurology|March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson diseaseT Foroud, S K Uniacke, L Liu, et al.
Neurology|July 29, 2009
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutationsN Pankratz, D K Kissell, M W Pauciulo, et al.
Neurology|September 7, 2007
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8W C Nichols, V E Elsaesser, N Pankratz, et al.
Neurology|November 7, 2008
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onsetW C Nichols, N Pankratz, D K Marek, et al.
Neurology|March 13, 2009
Variation in GIGYF2 is not associated with Parkinson diseaseW C Nichols, D K Kissell, N Pankratz, et al.
Neurology|December 29, 2005
A mutation in myotilin causes spheroid body myopathyT Foroud, N Pankratz, A P Batchman, et al.
International Journal of Obesity (2005)|November 22, 2016
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populationsS Yoneyama, J Yao, X Guo, et al.
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