Pankratz N - Search Results

1

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

Nichols WC, Elsaesser VE, Pankratz N, Pauciulo MW, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T; Parkinson Study Group-PROGENI Investigators. Nichols WC, et al. Among authors: pankratz n. Neurology. 2007 Oct 30;69(18):1737-44. doi: 10.1212/01.wnl.0000278115.50741.4e. Epub 2007 Sep 5. Neurology. 2007. PMID: 17804834

2

Parametric linkage analysis and disequilibrium methods to identify loci for complex disease.

McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. McClintick J, et al. Among authors: pankratz n. Genet Epidemiol. 2001;21 Suppl 1:S528-33. doi: 10.1002/gepi.2001.21.s1.s528. Genet Epidemiol. 2001. PMID: 11793731

3

Use of variable marker density, principal components, and neural networks in the dissection of disease etiology.

Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Pankratz N, et al. Genet Epidemiol. 2001;21 Suppl 1:S732-7. doi: 10.1002/gepi.2001.21.s1.s732. Genet Epidemiol. 2001. PMID: 11793770

4

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.

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. 2002 Jul;71(1):124-35. doi: 10.1086/341282. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058349 Free PMC article.

5

Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families.

Nichols WC, Pankratz N, Uniacke SK, Pauciulo MW, Halter C, Rudolph A, Conneally PM, Foroud T. Nichols WC, et al. Among authors: pankratz n. J Med Genet. 2002 Jul;39(7):489-92. doi: 10.1136/jmg.39.7.489. J Med Genet. 2002. PMID: 12114481 Free PMC article. No abstract available.

6

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease.

Foroud T, Uniacke SK, Liu L, Pankratz N, Rudolph A, Halter C, Shults C, Marder K, Conneally PM, Nichols WC; Parkinson Study Group. Foroud T, et al. Among authors: pankratz n. Neurology. 2003 Mar 11;60(5):796-801. doi: 10.1212/01.wnl.0000049470.00180.07. Neurology. 2003. PMID: 12629236

7

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.

8

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.

Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T; Parkinson Study Group. Pankratz N, et al. Hum Mol Genet. 2003 Oct 15;12(20):2599-608. doi: 10.1093/hmg/ddg270. Epub 2003 Aug 12. Hum Mol Genet. 2003. PMID: 12925570

9

Identification of genes for complex disease using longitudinal phenotypes.

Pankratz N, Mukhopadhyay N, Huang S, Foroud T, Kirkwood SC. Pankratz N, et al. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S58. doi: 10.1186/1471-2156-4-S1-S58. BMC Genet. 2003. PMID: 14975126 Free PMC article.

10

Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci.

Pankratz N, Uniacke SK, Halter CA, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC; Parkinson Study Group. Pankratz N, et al. Neurology. 2004 May 11;62(9):1616-8. doi: 10.1212/01.wnl.0000123112.51368.10. Neurology. 2004. PMID: 15136695

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