Nichols WC - Search Results

1

Genome-wide scan for a healthy aging phenotype provides support for a locus near D4S1564 promoting healthy aging.

Reed T, Dick DM, Uniacke SK, Foroud T, Nichols WC. Reed T, et al. Among authors: nichols wc. J Gerontol A Biol Sci Med Sci. 2004 Mar;59(3):227-32. doi: 10.1093/gerona/59.3.b227. J Gerontol A Biol Sci Med Sci. 2004. PMID: 15031306

2

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.

Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA 3rd, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Nichols WC, et al. Nat Genet. 1997 Mar;15(3):277-80. doi: 10.1038/ng0397-277. Nat Genet. 1997. PMID: 9054941

3

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.

Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM. Levy GG, et al. Among authors: nichols wc. Nature. 2001 Oct 4;413(6855):488-94. doi: 10.1038/35097008. Nature. 2001. PMID: 11586351 Free article.

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. Among authors: nichols wc. 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. 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

Reliability of reported age at onset for Parkinson's disease.

Reider CR, Halter CA, Castelluccio PF, Oakes D, Nichols WC, Foroud T; and the Parkinson Study Group. Reider CR, et al. Among authors: nichols wc. Mov Disord. 2003 Mar;18(3):275-279. doi: 10.1002/mds.10391. Mov Disord. 2003. PMID: 12621630

7

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: nichols wc. Neurology. 2003 Mar 11;60(5):796-801. doi: 10.1212/01.wnl.0000049470.00180.07. Neurology. 2003. PMID: 12629236

8

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. Among authors: nichols wc. 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.

9

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. Among authors: nichols wc. 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

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. Among authors: nichols wc. Neurology. 2004 May 11;62(9):1616-8. doi: 10.1212/01.wnl.0000123112.51368.10. Neurology. 2004. PMID: 15136695

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