Pugh EW - Search Results

1

A genome-wide scan for loci predisposing to non-syndromic cleft lip with or without cleft palate in two large Syrian families.

Wyszynski DF, Albacha-Hejazi H, Aldirani M, Hammod M, Shkair H, Karam A, Alashkar J, Holmes TN, Pugh EW, Doheny KF, McIntosh I, Beaty TH, Bailey-Wilson JE. Wyszynski DF, et al. Among authors: pugh ew. Am J Med Genet A. 2003 Dec 1;123A(2):140-7. doi: 10.1002/ajmg.a.20283. Am J Med Genet A. 2003. PMID: 14598337

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

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

7

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.

8

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

9

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.

10

Results of a high-resolution genome screen of 437 Alzheimer's disease families.

Blacker D, Bertram L, Saunders AJ, Moscarillo TJ, Albert MS, Wiener H, Perry RT, Collins JS, Harrell LE, Go RC, Mahoney A, Beaty T, Fallin MD, Avramopoulos D, Chase GA, Folstein MF, McInnis MG, Bassett SS, Doheny KJ, Pugh EW, Tanzi RE; NIMH Genetics Initiative Alzheimer's Disease Study Group. Blacker D, et al. Among authors: pugh ew. Hum Mol Genet. 2003 Jan 1;12(1):23-32. doi: 10.1093/hmg/ddg007. Hum Mol Genet. 2003. PMID: 12490529

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