Bailey-Wilson JE - Search Results

1

Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis.

Karban AS, Okazaki T, Panhuysen CI, Gallegos T, Potter JJ, Bailey-Wilson JE, Silverberg MS, Duerr RH, Cho JH, Gregersen PK, Wu Y, Achkar JP, Dassopoulos T, Mezey E, Bayless TM, Nouvet FJ, Brant SR. Karban AS, et al. Hum Mol Genet. 2004 Jan 1;13(1):35-45. doi: 10.1093/hmg/ddh008. Epub 2003 Nov 12. Hum Mol Genet. 2004. PMID: 14613970

2

Localization of a novel melanoma susceptibility locus to 1p22.

Gillanders E, Juo SH, Holland EA, Jones M, Nancarrow D, Freas-Lutz D, Sood R, Park N, Faruque M, Markey C, Kefford RF, Palmer J, Bergman W, Bishop DT, Tucker MA, Bressac-de Paillerets B, Hansson J, Stark M, Gruis N, Bishop JN, Goldstein AM, Bailey-Wilson JE, Mann GJ, Hayward N, Trent J; Lund Melanoma Study Group; Melanoma Genetics Consortium. Gillanders E, et al. Am J Hum Genet. 2003 Aug;73(2):301-13. doi: 10.1086/377140. Epub 2003 Jul 3. Am J Hum Genet. 2003. PMID: 12844286 Free PMC article.

3

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. Eur J Hum Genet. 2003 Nov;11(11):835-9. doi: 10.1038/sj.ejhg.5201052. Eur J Hum Genet. 2003. PMID: 14571267

4

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M. Arcos-Burgos M, et al. Am J Hum Genet. 2004 Dec;75(6):998-1014. doi: 10.1086/426154. Epub 2004 Oct 20. Am J Hum Genet. 2004. PMID: 15497111 Free PMC article.

5

Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36.

Wojciechowski R, Moy C, Ciner E, Ibay G, Reider L, Bailey-Wilson JE, Stambolian D. Wojciechowski R, et al. Hum Genet. 2006 May;119(4):389-99. doi: 10.1007/s00439-006-0153-x. Epub 2006 Feb 24. Hum Genet. 2006. PMID: 16501916 Free PMC article.

6

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH Jr, Brant SR. Panhuysen CI, et al. Hum Genet. 2006 Aug;120(1):31-41. doi: 10.1007/s00439-006-0163-8. Epub 2006 May 30. Hum Genet. 2006. PMID: 16733713

7

Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis.

Simpson CL, Cropp CD, Wahlfors T, George A, Jones MS, Harper U, Ponciano-Jackson D, Tammela T, Schleutker J, Bailey-Wilson JE. Simpson CL, et al. Eur J Hum Genet. 2013 Apr;21(4):437-43. doi: 10.1038/ejhg.2012.185. Epub 2012 Sep 5. Eur J Hum Genet. 2013. PMID: 22948022 Free PMC article.

8

Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33.

Musolf AM, Simpson CL, Alexander TA, Portas L, Murgia F, Ciner EB, Stambolian D, Bailey-Wilson JE. Musolf AM, et al. Hum Genet. 2019 Apr;138(4):339-354. doi: 10.1007/s00439-019-01991-0. Epub 2019 Mar 2. Hum Genet. 2019. PMID: 30826882 Free PMC article.

9

Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3.

Pollin TI, Dobyns WB, Crowe CA, Ledbetter DH, Bailey-Wilson JE, Smith AC. Pollin TI, et al. Am J Med Genet. 1999 Aug 6;85(4):369-75. Am J Med Genet. 1999. PMID: 10398263

10

Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia.

Ibay G, Doan B, Reider L, Dana D, Schlifka M, Hu H, Holmes T, O'Neill J, Owens R, Ciner E, Bailey-Wilson JE, Stambolian D. Ibay G, et al. BMC Med Genet. 2004 Aug 3;5:20. doi: 10.1186/1471-2350-5-20. BMC Med Genet. 2004. PMID: 15291966 Free PMC article.

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