Abee L. Boyles, Ph.D. - Publications

Affiliations: 
2006 Duke University, Durham, NC 
Area:
Genetics

12 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2009 Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Trung TN, Bille C, Lidral AC, Murray JC. Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. Plos One. 4: e5385. PMID 19401770 DOI: 10.1371/Journal.Pone.0005385  0.308
2009 Boyles AL, Wilcox AJ, Taylor JA, Shi M, Weinberg CR, Meyer K, Fredriksen A, Ueland PM, Johansen AM, Drevon CA, Jugessur A, Trung TN, Gjessing HK, Vollset SE, Murray JC, et al. Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study. Genetic Epidemiology. 33: 247-55. PMID 19048631 DOI: 10.1002/Gepi.20376  0.347
2008 Boyles AL, Wilcox AJ, Taylor JA, Meyer K, Fredriksen A, Ueland PM, Drevon CA, Vollset SE, Lie RT. Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts. American Journal of Medical Genetics. Part A. 146: 440-9. PMID 18203168 DOI: 10.1002/ajmg.a.32162  0.413
2007 O'Grady G, Boyles AL, Speer M, DeRuyter F, Strittmatter W, Worley G. Apolipoprotein E alleles and sensorineural hearing loss International Journal of Audiology. 46: 183-186. PMID 17454231 DOI: 10.1080/14992020601145294  0.546
2006 Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, et al. Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15. American Journal of Medical Genetics. Part A. 140: 2776-85. PMID 17103432 DOI: 10.1002/Ajmg.A.31546  0.566
2006 Boyles AL, Billups AV, Deak KL, Siegel DG, Mehltretter L, Slifer SH, Bassuk AG, Kessler JA, Reed MC, Nijhout HF, George TM, Enterline DS, Gilbert JR, Speer MC. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions. Environmental Health Perspectives. 114: 1547-52. PMID 17035141 DOI: 10.1289/Ehp.9166  0.648
2005 Boyles AL, Scott WK, Martin ER, Schmidt S, Li YJ, Ashley-Koch A, Bass MP, Schmidt M, Pericak-Vance MA, Speer MC, Hauser ER. Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing. Human Heredity. 59: 220-7. PMID 16093727 DOI: 10.1159/000087122  0.559
2005 Deak KL, Boyles AL, Etchevers HC, Melvin EC, Siegel DG, Graham FL, Slifer SH, Enterline DS, George TM, Vekemans M, McClay D, Bassuk AG, Kessler JA, Linney E, Gilbert JR, et al. SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects. Human Genetics. 117: 133-42. PMID 15883837 DOI: 10.1007/S00439-005-1299-7  0.641
2005 Bammler T, Beyer RP, Bhattacharya S, Boorman GA, Boyles A, Bradford BU, Bumgarner RE, Bushel PR, Chaturvedi K, Choi D, Cunningham ML, Deng S, Dressman HK, Fannin RD, Farin FM, et al. Standardizing global gene expression analysis between laboratories and across platforms. Nature Methods. 2: 351-6. PMID 15846362 DOI: 10.1038/Nmeth754  0.522
2005 Boyles AL, Hammock P, Speer MC. Candidate gene analysis in human neural tube defects. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 135: 9-23. PMID 15816061 DOI: 10.1002/Ajmg.C.30048  0.607
2005 Mathias RA, Beaty TH, Bailey-Wilson JE, Bickel C, Stockton ML, Barnes KC, Becker T, Knapp M, Vieland VJ, Wu X, Naiman DQ, Bergemann TL, Clarkson DB, Boyles AL, Scott WK, et al. Contents Vol. 59, 2005 Human Heredity. 59: 241-241. DOI: 10.1159/000087469  0.444
2005 Mathias RA, Beaty TH, Bailey-Wilson JE, Bickel C, Stockton ML, Barnes KC, Becker T, Knapp M, Vieland VJ, Wu X, Naiman DQ, Bergemann TL, Clarkson DB, Boyles AL, Scott WK, et al. Subject Index Vol. 59, 2005 Human Heredity. 59: 240-240. DOI: 10.1159/000087468  0.468
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