Gordon D - Search Results

1

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis.

Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM. Helms C, et al. Among authors: gordon d. Nat Genet. 2003 Dec;35(4):349-56. doi: 10.1038/ng1268. Epub 2003 Nov 9. Nat Genet. 2003. PMID: 14608357

2

Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR.

Helms C, Saccone NL, Cao L, Daw JA, Cao K, Hsu TM, Taillon-Miller P, Duan S, Gordon D, Pierce B, Ott J, Rice J, Fernandez-Vina MA, Kwok PY, Menter A, Bowcock AM. Helms C, et al. Among authors: gordon d. Hum Genet. 2005 Dec;118(3-4):466-76. doi: 10.1007/s00439-005-0048-2. Epub 2005 Oct 19. Hum Genet. 2005. PMID: 16235096

3

Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis.

Gordon D, Ott J. Gordon D, et al. Pac Symp Biocomput. 2001:18-29. doi: 10.1142/9789814447362_0003. Pac Symp Biocomput. 2001. PMID: 11262939 Free article.

4

A transmission disequilibrium test for general pedigrees that is robust to the presence of random genotyping errors and any number of untyped parents.

Gordon D, Haynes C, Johnnidis C, Patel SB, Bowcock AM, Ott J. Gordon D, et al. Eur J Hum Genet. 2004 Sep;12(9):752-61. doi: 10.1038/sj.ejhg.5201219. Eur J Hum Genet. 2004. PMID: 15162128 Free PMC article.

5

Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms.

Gordon D, Finch SJ, Nothnagel M, Ott J. Gordon D, et al. Hum Hered. 2002;54(1):22-33. doi: 10.1159/000066696. Hum Hered. 2002. PMID: 12446984

6

Are molecular haplotypes worth the time and expense? A cost-effective method for applying molecular haplotypes.

Levenstien MA, Ott J, Gordon D. Levenstien MA, et al. Among authors: gordon d. PLoS Genet. 2006 Aug 18;2(8):e127. doi: 10.1371/journal.pgen.0020127. Epub 2006 Jun 28. PLoS Genet. 2006. PMID: 16933998 Free PMC article.

7

CHD7 gene polymorphisms are associated with susceptibility to idiopathic scoliosis.

Gao X, Gordon D, Zhang D, Browne R, Helms C, Gillum J, Weber S, Devroy S, Swaney S, Dobbs M, Morcuende J, Sheffield V, Lovett M, Bowcock A, Herring J, Wise C. Gao X, et al. Among authors: gordon d. Am J Hum Genet. 2007 May;80(5):957-65. doi: 10.1086/513571. Epub 2007 Mar 12. Am J Hum Genet. 2007. PMID: 17436250 Free PMC article.

8

True pedigree errors more frequent than apparent errors for single nucleotide polymorphisms.

Gordon D, Heath SC, Ott J. Gordon D, et al. Hum Hered. 1999 Mar;49(2):65-70. doi: 10.1159/000022846. Hum Hered. 1999. PMID: 10077724

9

An analytic solution to single nucleotide polymorphism error-detection rates in nuclear families: implications for study design.

Gordon D, Leal SM, Heath SC, Ott J. Gordon D, et al. Pac Symp Biocomput. 2000:663-74. doi: 10.1142/9789814447331_0064. Pac Symp Biocomput. 2000. PMID: 10902214 Free PMC article.

10

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.

Gordon D, Heath SC, Liu X, Ott J. Gordon D, et al. Am J Hum Genet. 2001 Aug;69(2):371-80. doi: 10.1086/321981. Epub 2001 Jul 5. Am J Hum Genet. 2001. PMID: 11443542 Free PMC article.

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