Haynes C - Search Results

1

Genome-wide autozygosity mapping in human populations.

Wang S, Haynes C, Barany F, Ott J. Wang S, et al. Among authors: haynes c. Genet Epidemiol. 2009 Feb;33(2):172-80. doi: 10.1002/gepi.20344. Genet Epidemiol. 2009. PMID: 18814273 Free PMC article.

2

Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata.

Martinez-Mir A, Zlotogorski A, Gordon D, Petukhova L, Mo J, Gilliam TC, Londono D, Haynes C, Ott J, Hordinsky M, Nanova K, Norris D, Price V, Duvic M, Christiano AM. Martinez-Mir A, et al. Among authors: haynes c. Am J Hum Genet. 2007 Feb;80(2):316-28. doi: 10.1086/511442. Epub 2007 Jan 5. Am J Hum Genet. 2007. PMID: 17236136 Free PMC article.

3

Collapsing SNP genotypes in case-control genome-wide association studies increases the type I error rate and power.

Matthews AG, Haynes C, Liu C, Ott J. Matthews AG, et al. Among authors: haynes c. Stat Appl Genet Mol Biol. 2008;7(1):Article23. doi: 10.2202/1544-6115.1325. Epub 2008 Jul 25. Stat Appl Genet Mol Biol. 2008. PMID: 18673292 Free PMC article.

4

Expanded genome scan in extended families with age-related macular degeneration.

Barral S, Francis PJ, Schultz DW, Schain MB, Haynes C, Majewski J, Ott J, Acott T, Weleber RG, Klein ML. Barral S, et al. Among authors: haynes c. Invest Ophthalmol Vis Sci. 2006 Dec;47(12):5453-9. doi: 10.1167/iovs.06-0655. Invest Ophthalmol Vis Sci. 2006. PMID: 17122136

5

Complement factor H polymorphism in age-related macular degeneration.

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J. Klein RJ, et al. Among authors: haynes c. Science. 2005 Apr 15;308(5720):385-9. doi: 10.1126/science.1109557. Epub 2005 Mar 10. Science. 2005. PMID: 15761122 Free PMC article.

6

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. Among authors: haynes c. 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.

7

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.

Petukhova L, Sousa EC Jr, Martinez-Mir A, Vitebsky A, Dos Santos LG, Shapiro L, Haynes C, Gordon D, Shimomura Y, Christiano AM. Petukhova L, et al. Among authors: haynes c. Genomics. 2008 Nov;92(5):273-8. doi: 10.1016/j.ygeno.2008.06.009. Epub 2008 Sep 13. Genomics. 2008. PMID: 18692127 Free PMC article.

8

Linear trend tests for case-control genetic association that incorporate random phenotype and genotype misclassification error.

Gordon D, Haynes C, Yang Y, Kramer PL, Finch SJ. Gordon D, et al. Among authors: haynes c. Genet Epidemiol. 2007 Dec;31(8):853-70. doi: 10.1002/gepi.20246. Genet Epidemiol. 2007. PMID: 17565750

9

Precision and type I error rate in the presence of genotype errors and missing parental data: a comparison between the original transmission disequilibrium test (TDT) and TDTae statistics.

Barral S, Haynes C, Levenstien MA, Gordon D. Barral S, et al. Among authors: haynes c. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S150. doi: 10.1186/1471-2156-6-S1-S150. BMC Genet. 2005. PMID: 16451611 Free PMC article.

10

Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies.

Kang SJ, Finch SJ, Haynes C, Gordon D. Kang SJ, et al. Among authors: haynes c. Hum Hered. 2004;58(3-4):139-44. doi: 10.1159/000083540. Hum Hered. 2004. PMID: 15812170

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