Bull SB - Search Results

1

Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes.

Asimit JL, Yoo YJ, Waggott D, Sun L, Bull SB. Asimit JL, et al. Among authors: bull sb. BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S127. doi: 10.1186/1753-6561-3-s7-s127. BMC Proc. 2009. PMID: 20017993 Free PMC article.

2

Using an age-at-onset phenotype with interval censoring to compare methods of segregation and linkage analysis in a candidate region for elevated systolic blood pressure.

Kopciuk KA, Briollais L, Demenais F, Bull SB. Kopciuk KA, et al. Among authors: bull sb. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S84. doi: 10.1186/1471-2156-4-S1-S84. BMC Genet. 2003. PMID: 14975152 Free PMC article.

3

Simultaneous localization of two linked disease susceptibility genes.

Biernacka JM, Sun L, Bull SB. Biernacka JM, et al. Among authors: bull sb. Genet Epidemiol. 2005 Jan;28(1):33-47. doi: 10.1002/gepi.20033. Genet Epidemiol. 2005. PMID: 15481103

4

Reduction of selection bias in genomewide studies by resampling.

Sun L, Bull SB. Sun L, et al. Among authors: bull sb. Genet Epidemiol. 2005 May;28(4):352-67. doi: 10.1002/gepi.20068. Genet Epidemiol. 2005. PMID: 15761913

5

Tests for the presence of two linked disease susceptibility genes.

Biernacka JM, Sun L, Bull SB. Biernacka JM, et al. Among authors: bull sb. Genet Epidemiol. 2005 Dec;29(4):389-401. doi: 10.1002/gepi.20094. Genet Epidemiol. 2005. PMID: 16193503

6

Resampling methods to reduce the selection bias in genetic effect estimation in genome-wide scans.

Wu LY, Lee SS, Shi HS, Sun L, Bull SB. Wu LY, et al. Among authors: bull sb. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S24. doi: 10.1186/1471-2156-6-S1-S24. BMC Genet. 2005. PMID: 16451633 Free PMC article.

7

Stratified false discovery control for large-scale hypothesis testing with application to genome-wide association studies.

Sun L, Craiu RV, Paterson AD, Bull SB. Sun L, et al. Among authors: bull sb. Genet Epidemiol. 2006 Sep;30(6):519-30. doi: 10.1002/gepi.20164. Genet Epidemiol. 2006. PMID: 16800000

8

Locus-specific heritability estimation via the bootstrap in linkage scans for quantitative trait loci.

Wu LY, Sun L, Bull SB. Wu LY, et al. Among authors: bull sb. Hum Hered. 2006;62(2):84-96. doi: 10.1159/000096096. Epub 2006 Oct 12. Hum Hered. 2006. PMID: 17047338

9

Multiple variants in vascular endothelial growth factor (VEGFA) are risk factors for time to severe retinopathy in type 1 diabetes: the DCCT/EDIC genetics study.

Al-Kateb H, Mirea L, Xie X, Sun L, Liu M, Chen H, Bull SB, Boright AP, Paterson AD; DCCT/EDIC Research Group. Al-Kateb H, et al. Among authors: bull sb. Diabetes. 2007 Aug;56(8):2161-8. doi: 10.2337/db07-0376. Epub 2007 May 18. Diabetes. 2007. PMID: 17513698

10

Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.

Al-Kateb H, Boright AP, Mirea L, Xie X, Sutradhar R, Mowjoodi A, Bharaj B, Liu M, Bucksa JM, Arends VL, Steffes MW, Cleary PA, Sun W, Lachin JM, Thorner PS, Ho M, McKnight AJ, Maxwell AP, Savage DA, Kidd KK, Kidd JR, Speed WC, Orchard TJ, Miller RG, Sun L, Bull SB, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Research Group. Al-Kateb H, et al. Among authors: bull sb. Diabetes. 2008 Jan;57(1):218-28. doi: 10.2337/db07-1059. Epub 2007 Oct 3. Diabetes. 2008. PMID: 17914031 Free PMC article. Clinical Trial.

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