Pugh EW - Search Results

1

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.

Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I. Zeiger JS, et al. Among authors: pugh ew. Eur J Hum Genet. 2003 Nov;11(11):835-9. doi: 10.1038/sj.ejhg.5201052. Eur J Hum Genet. 2003. PMID: 14571267

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

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

5

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

6

Environmental covariates: effects on the power of sib-pair linkage methods.

Mandal DM, Sorant AJ, Pugh EW, Marcus SE, Klein AP, Mathias RA, O'Neill J, Temiyakarn LF, Wilson AF, Bailey-Wilson JE. Mandal DM, et al. Among authors: pugh ew. Genet Epidemiol. 1999;17 Suppl 1:S643-8. doi: 10.1002/gepi.13701707105. Genet Epidemiol. 1999. PMID: 10597507

7

Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13.

Kelley MJ, Jawien W, Lin A, Hoffmeister K, Pugh EW, Doheny KF, Korczak JF. Kelley MJ, et al. Among authors: pugh ew. Hum Genet. 2000 May;106(5):557-64. doi: 10.1007/s004390000294. Hum Genet. 2000. PMID: 10914687

8

Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3.

Wang K, Pugh EW, Griffen S, Doheny KF, Mostafa WZ, al-Aboosi MM, el-Shanti H, Gitschier J. Wang K, et al. Among authors: pugh ew. Am J Hum Genet. 2001 Apr;68(4):1055-60. doi: 10.1086/319514. Epub 2001 Mar 12. Am J Hum Genet. 2001. PMID: 11254458 Free PMC article.

9

Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data.

Bailey-Wilson JE, Sorant AJ, Malley JD, Presciuttini S, Redner RA, Severini TA, Badner JA, Pajevic S, Jufer R, Baffoe-Bonnie A, Kao L, Doan BQ, Goldstein JL, Holmes TN, Behneman D, Mandal DM, Turley TN, Weissbecker KA, O'Neill J, Pugh EW. Bailey-Wilson JE, et al. Among authors: pugh ew. Genet Epidemiol. 2001;21 Suppl 1:S378-83. doi: 10.1002/gepi.2001.21.s1.s378. Genet Epidemiol. 2001. PMID: 11793703

10

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. Piao X, et al. Among authors: pugh ew. Am J Hum Genet. 2002 Apr;70(4):1028-33. doi: 10.1086/339552. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845408 Free PMC article.

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