Pugh E - Search Results

1

Identifying rare variants from exome scans: the GAW17 experience.

Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J Jr, Laird N, Pankratz N, Paterson A, Pugh E, Suarez B, Sun Y, Thomas A, Tintle N, Zhu X, Ziegler A, Maccluer JW, Almasy L. Ghosh S, et al. Among authors: pugh e. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S1. doi: 10.1186/1753-6561-5-S9-S1. BMC Proc. 2011. PMID: 22373325 Free PMC article.

2

Effects of marker information on sib-pair linkage analysis of a rare disease.

Korczak JF, Pugh EW, Premkumar S, Guo X, Elston RC, Bailey-Wilson JE. Korczak JF, et al. Among authors: pugh ew. Genet Epidemiol. 1995;12(6):625-30. doi: 10.1002/gepi.1370120617. Genet Epidemiol. 1995. PMID: 8787984 Clinical Trial.

3

Comparison of selected methods used to analyze bipolar disorder.

Wyszynski DF, Doetsch JP, Pugh EW, Bailey-Wilson JE. Wyszynski DF, et al. Among authors: pugh ew. Genet Epidemiol. 1997;14(6):705-10. doi: 10.1002/(SICI)1098-2272(1997)14:6<705::AID-GEPI26>3.0.CO;2-T. Genet Epidemiol. 1997. PMID: 9433567

4

Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data.

Ling H, Hetrick K, Bailey-Wilson JE, Pugh EW. Ling H, et al. Among authors: pugh ew. BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S57. doi: 10.1186/1753-6561-3-s7-s57. BMC Proc. 2009. PMID: 20018050 Free PMC article.

5

Statistical analysis of rare sequence variants: an overview of collapsing methods.

Dering C, Hemmelmann C, Pugh E, Ziegler A. Dering C, et al. Among authors: pugh e. Genet Epidemiol. 2011;35 Suppl 1(Suppl 1):S12-7. doi: 10.1002/gepi.20643. Genet Epidemiol. 2011. PMID: 22128052 Free PMC article. Review.

6

Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17.

Tintle N, Aschard H, Hu I, Nock N, Wang H, Pugh E. Tintle N, et al. Among authors: pugh e. Genet Epidemiol. 2011;35 Suppl 1(Suppl 1):S56-60. doi: 10.1002/gepi.20650. Genet Epidemiol. 2011. PMID: 22128060 Free PMC article.

7

Filtering genetic variants and placing informative priors based on putative biological function.

Friedrichs S, Malzahn D, Pugh EW, Almeida M, Liu XQ, Bailey JN. Friedrichs S, et al. BMC Genet. 2016 Feb 3;17 Suppl 2(Suppl 2):8. doi: 10.1186/s12863-015-0313-x. BMC Genet. 2016. PMID: 26866982 Free PMC article.

8

Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data.

Holzinger ER, Szymczak S, Malley J, Pugh EW, Ling H, Griffith S, Zhang P, Li Q, Cropp CD, Bailey-Wilson JE. Holzinger ER, et al. Among authors: pugh ew. BMC Proc. 2016 Oct 18;10(Suppl 7):147-152. doi: 10.1186/s12919-016-0021-1. eCollection 2016. BMC Proc. 2016. PMID: 27980627 Free PMC article.

9

Comparison of sib-pair and variance-components methods for genomic screening.

Pugh EW, Jaquish CE, Sorant AJ, Doetsch JP, Bailey-Wilson JE, Wilson AF. Pugh EW, et al. Genet Epidemiol. 1997;14(6):867-72. doi: 10.1002/(SICI)1098-2272(1997)14:6<867::AID-GEPI51>3.0.CO;2-K. Genet Epidemiol. 1997. PMID: 9433592

10

Possible linkage of alcoholism, monoamine oxidase activity and P300 amplitude to markers on chromosome 12q24.

Juo SH, Pugh EW, Baffoe-Bonnie A, Kingman A, Sorant AJ, Klein AP, O'Neill J, Mathias RA, Wilson AF, Bailey-Wilson JE. Juo SH, et al. Among authors: pugh ew. Genet Epidemiol. 1999;17 Suppl 1:S193-8. doi: 10.1002/gepi.1370170733. Genet Epidemiol. 1999. PMID: 10597435

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