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Shelley Bull - Publications

Affiliations: 
University of Toronto, Toronto, ON, Canada 
Area:
Statistics, Molecular Biology, Biostatistics Biology
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53 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
2023 Brossard M, Paterson AD, Espin-Garcia O, Craiu RV, Bull SB. Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression. Genetics. PMID 37369448 DOI: 10.1093/genetics/iyad119  0.42
2021 Espin-Garcia O, Craiu RV, Bull SB. Two-phase sample selection strategies for design and analysis in post-genome-wide association fine-mapping studies. Statistics in Medicine. PMID 34596256 DOI: 10.1002/sim.9211  0.3
2020 Romanescu RG, Green J, Andrulis IL, Bull SB. Gene-based and pathway-based testing for rare-variant association in affected sib pairs. Genetic Epidemiology. PMID 32237178 DOI: 10.1002/gepi.22291  0.382
2019 Ah Kim S, Brossard M, Roshandel D, Paterson AD, Bull SB, Yoo YJ. gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks. Bioinformatics (Oxford, England). PMID 31070701 DOI: 10.1093/bioinformatics/btz308  0.346
2018 Lakhal-Chaieb L, Simard J, Bull S. Sequence kernel association test for survival outcomes in the presence of a non-susceptible fraction. Biostatistics (Oxford, England). PMID 30590388 DOI: 10.1093/Biostatistics/Kxy075  0.433
2018 Romanescu RG, Espin-Garcia O, Ma J, Bull SB. Integrating epigenetic, genetic, and phenotypic data to uncover gene-region associations with triglycerides in the GOLDN study. Bmc Proceedings. 12: 57. PMID 30263054 DOI: 10.1186/s12919-018-0142-9  0.31
2017 Espin-Garcia O, Craiu RV, Bull SB. Two-phase designs for joint quantitative-trait-dependent and genotype-dependent sampling in post-GWAS regional sequencing. Genetic Epidemiology. PMID 29239496 DOI: 10.1002/gepi.22099  0.436
2017 Kim SA, Cho CS, Kim SR, Bull SB, Yoo YJ. A new haplotype block detection method for dense genome sequencing data based on interval graph modeling of clusters of highly correlated SNPs. Bioinformatics (Oxford, England). PMID 29028986 DOI: 10.1093/bioinformatics/btx609  0.411
2016 Shin JH, Yi R, Bull SB. Identification of low frequency and rare variants for hypertension using sparse-data methods. Bmc Proceedings. 10: 389-395. PMID 27980667 DOI: 10.1186/s12919-016-0061-6  0.325
2016 Yoo YJ, Sun L, Poirier JG, Paterson AD, Bull SB. Multiple linear combination (MLC) regression tests for common variants adapted to linkage disequilibrium structure. Genetic Epidemiology. PMID 27885705 DOI: 10.1002/gepi.22024  0.307
2016 Brenner DR, Brennan P, Boffetta P, Amos CI, Spitz MR, Chen C, Goodman G, Heinrich J, Bickeböller H, Rosenberger A, Risch A, Muley T, McLaughlin JR, Benhamou S, Bouchardy C, ... ... Bull S, et al. Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Human Genetics. PMID 27264937 DOI: 10.1007/s00439-016-1692-4  0.573
2015 Poirier JG, Faye LL, Dimitromanolakis A, Paterson AD, Sun L, Bull SB. Resampling to Address the Winner's Curse in Genetic Association Analysis of Time to Event. Genetic Epidemiology. PMID 26411674 DOI: 10.1002/Gepi.21920  0.764
2014 Bull SB, Chen Z, Tan KR, Poirier J. An exploration of heterogeneity in genetic analysis of complex pedigrees: linkage and association using whole genome sequencing data in the MAP4 region. Bmc Proceedings. 8: S107. PMID 25519361 DOI: 10.1186/1753-6561-8-S1-S107  0.354
2014 Chen Z, Tan KR, Bull SB. Multiphase analysis by linkage, quantitative transmission disequilibrium, and measured genotype: systolic blood pressure in complex Mexican American pedigrees. Bmc Proceedings. 8: S108. PMID 25519311 DOI: 10.1186/1753-6561-8-S1-S108  0.36
2014 Wang W, Feng Z, Bull SB, Wang Z. A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits. Frontiers in Genetics. 5: 357. PMID 25368629 DOI: 10.3389/fgene.2014.00357  0.384
2014 Chen Z, Craiu RV, Bull SB. A note on the efficiencies of sampling strategies in two-stage Bayesian regional fine mapping of a quantitative trait. Genetic Epidemiology. 38: 599-609. PMID 25132153 DOI: 10.1002/gepi.21845  0.399
2013 Yoo YJ, Sun L, Bull SB. Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis. Frontiers in Genetics. 4: 233. PMID 24273553 DOI: 10.3389/fgene.2013.00233  0.389
2013 Faye LL, Machiela MJ, Kraft P, Bull SB, Sun L. Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification. Plos Genetics. 9: e1003609. PMID 23950724 DOI: 10.1371/Journal.Pgen.1003609  0.757
2013 Brenner DR, Brennan P, Boffetta P, Amos CI, Spitz MR, Chen C, Goodman G, Heinrich J, Bickeböller H, Rosenberger A, Risch A, Muley T, McLaughlin JR, Benhamou S, Bouchardy C, ... ... Bull S, et al. Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Human Genetics. 132: 579-89. PMID 23370545 DOI: 10.1007/S00439-013-1270-Y  0.671
2012 Rotondi MA, Bull SB. Cumulative meta-analysis for genetic association: when is a new study worthwhile? Human Heredity. 74: 61-70. PMID 23258221 DOI: 10.1159/000345604  0.427
2012 Sandholm N, Salem RM, McKnight AJ, Brennan EP, Forsblom C, Isakova T, McKay GJ, Williams WW, Sadlier DM, Mäkinen VP, Swan EJ, Palmer C, Boright AP, Ahlqvist E, Deshmukh HA, ... ... Bull SB, et al. New susceptibility loci associated with kidney disease in type 1 diabetes. Plos Genetics. 8: e1002921. PMID 23028342 DOI: 10.1371/Journal.Pgen.1002921  0.349
2012 Mirea L, Infante-Rivard C, Sun L, Bull SB. Strategies for genetic association analyses combining unrelated case-control individuals and family trios. American Journal of Epidemiology. 176: 70-9. PMID 22573432 DOI: 10.1093/aje/kwr494  0.308
2012 Chen Z, Craiu RV, Bull SB. Two-phase stratified sampling designs for regional sequencing. Genetic Epidemiology. 36: 320-32. PMID 22460746 DOI: 10.1002/gepi.21624  0.369
2011 Faye LL, Bull SB. Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates. Bmc Proceedings. 5: S64. PMID 22373407 DOI: 10.1186/1753-6561-5-S9-S64  0.772
2011 Yilmaz YE, Bull SB. Are quantitative trait-dependent sampling designs cost-effective for analysis of rare and common variants? Bmc Proceedings. 5: S111. PMID 22373146 DOI: 10.1186/1753-6561-5-S9-S111  0.338
2011 Bailey-Wilson JE, Brennan JS, Bull SB, Culverhouse R, Kim Y, Jiang Y, Jung J, Li Q, Lamina C, Liu Y, Mägi R, Niu YS, Simpson CL, Wang L, Yilmaz YE, et al. Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data. Genetic Epidemiology. 35: S92-100. PMID 22128066 DOI: 10.1002/Gepi.20657  0.346
2011 Faye LL, Sun L, Dimitromanolakis A, Bull SB. A flexible genome-wide bootstrap method that accounts for ranking and threshold-selection bias in GWAS interpretation and replication study design. Statistics in Medicine. 30: 1898-912. PMID 21538984 DOI: 10.1002/Sim.4228  0.769
2011 Böger CA, Chen MH, Tin A, Olden M, Köttgen A, de Boer IH, Fuchsberger C, O'Seaghdha CM, Pattaro C, Teumer A, Liu CT, Glazer NL, Li M, O'Connell JR, Tanaka T, ... ... Bull SB, et al. CUBN is a gene locus for albuminuria. Journal of the American Society of Nephrology : Jasn. 22: 555-70. PMID 21355061 DOI: 10.1681/Asn.2010060598  0.301
2011 Sun L, Dimitromanolakis A, Faye LL, Paterson AD, Waggott D, Bull SB. BR-squared: a practical solution to the winner's curse in genome-wide scans. Human Genetics. 129: 545-52. PMID 21246217 DOI: 10.1007/S00439-011-0948-2  0.758
2010 Yoo YJ, Bull SB, Paterson AD, Waggott D, Sun L. Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies. Genetic Epidemiology. 34: 107-18. PMID 19626703 DOI: 10.1002/gepi.20438  0.385
2009 Paterson AD, Waggott D, Schillert A, Infante-Rivard C, Bull SB, Yoo YJ, Pinnaduwage D. Transmission-ratio distortion in the Framingham Heart Study. Bmc Proceedings. 3: S51. PMID 20018044 DOI: 10.1186/1753-6561-3-S7-S51  0.374
2009 Asimit JL, Yoo YJ, Waggott D, Sun L, Bull SB. Region-based analysis in genome-wide association study of Framingham Heart Study blood lipid phenotypes. Bmc Proceedings. 3: S127. PMID 20017993 DOI: 10.1186/1753-6561-3-S7-S127  0.395
2009 Yoo YJ, Pinnaduwage D, Waggott D, Bull SB, Sun L. Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results. Bmc Proceedings. 3: S103. PMID 20017967 DOI: 10.1186/1753-6561-3-S7-S103  0.389
2008 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, ... ... Bull SB, et al. 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. Diabetes. 57: 218-28. PMID 17914031 DOI: 10.2337/Db07-1059  0.3
2007 Sutradhar R, Pinnaduwage D, Bull SB. Application of bivariate mixed counting process models to genetic analysis of rheumatoid arthritis severity. Bmc Proceedings. 1: S120. PMID 18466462  0.308
2007 Ziegler A, DeStefano AL, König IR, Bardel C, Brinza D, Bull S, Cai Z, Glaser B, Jiang W, Lee KE, Li CX, Li J, Li X, Majoram P, Meng Y, et al. Data mining, neural nets, trees--problems 2 and 3 of Genetic Analysis Workshop 15. Genetic Epidemiology. 31: S51-60. PMID 18046765 DOI: 10.1002/Gepi.20280  0.399
2007 Bull SB, Lewinger JP, Lee SS. Confidence intervals for multinomial logistic regression in sparse data. Statistics in Medicine. 26: 903-18. PMID 16489602 DOI: 10.1002/Sim.2518  0.632
2006 Long YW, Sun L, Bull SB. Locus-specific heritability estimation via the bootstrap in linkage scans for quantitative trait loci Human Heredity. 62: 84-96. PMID 17047338 DOI: 10.1159/000096096  0.417
2006 Sun L, Craiu RV, Paterson AD, Bull SB. Stratified false discovery control for large-scale hypothesis testing with application to genome-wide association studies. Genetic Epidemiology. 30: 519-30. PMID 16800000 DOI: 10.1002/gepi.20164  0.35
2006 Lewinger JP, Bull SB. Validity, efficiency, and robustness of a family-based test of association. Genetic Epidemiology. 30: 62-76. PMID 16355403 DOI: 10.1002/Gepi.20125  0.629
2005 Lewinger JP, Lee SS, Biernacka J, Wu LY, Shi HS, Bull SB. Comparison of family-based association tests in chromosome regions selected by linkage-based confidence intervals. Bmc Genetics. 6: S62. PMID 16451675 DOI: 10.1186/1471-2156-6-S1-S62  0.667
2005 Wu LY, Lee SS, Shi HS, Sun L, Bull SB. Resampling methods to reduce the selection bias in genetic effect estimation in genome-wide scans. Bmc Genetics. 6: S24. PMID 16451633 DOI: 10.1186/1471-2156-6-S1-S24  0.43
2005 Biernacka JM, Sun L, Bull SB. Tests for the presence of two linked disease susceptibility genes. Genetic Epidemiology. 29: 389-401. PMID 16193503 DOI: 10.1002/gepi.20094  0.33
2005 Boright AP, Paterson AD, Mirea L, Bull SB, Mowjoodi A, Scherer SW, Zinman B. Genetic variation at the ACE gene is associated with persistent microalbuminuria and severe nephropathy in type 1 diabetes: the DCCT/EDIC Genetics Study. Diabetes. 54: 1238-44. PMID 15793268 DOI: 10.2337/Diabetes.54.4.1238  0.314
2005 Sun L, Bull SB. Reduction of selection bias in genomewide studies by resampling. Genetic Epidemiology. 28: 352-67. PMID 15761913 DOI: 10.1002/gepi.20068  0.389
2004 Mirea L, Briollais L, Bull S. Tests for covariate-associated heterogeneity in IBD allele sharing of affected relatives. Genetic Epidemiology. 26: 44-60. PMID 14691956 DOI: 10.1002/Gepi.10294  0.437
2003 Mirea L, Bull SB, Stafford J. Comparison of Haseman-Elston regression analyses using single, summary, and longitudinal measures of systolic blood pressure. Bmc Genetics. 4: S23. PMID 14975091 DOI: 10.1186/1471-2156-4-S1-S23  0.319
2003 Gauderman WJ, Macgregor S, Briollais L, Scurrah K, Tobin M, Park T, Wang D, Rao S, John S, Bull S. Longitudinal data analysis in pedigree studies. Genetic Epidemiology. 25: S18-28. PMID 14635165 DOI: 10.1002/Gepi.10280  0.42
2002 Bull SB, Greenwood CM, Mirea L, Morgan K. Regression models for allele sharing: analysis of accumulating data in affected sib pair studies. Statistics in Medicine. 21: 431-44. PMID 11813229 DOI: 10.1002/sim.1028  0.371
2001 Biernacka J, Lewinger JP, Chan V, Bull SB. Does simultaneous consideration of multiple regions improve disease gene localization? Genetic Epidemiology. 21: S504-9. PMID 11793727 DOI: 10.1002/Gepi.2001.21.S1.S504  0.635
1998 Rioux JD, Daly MJ, Green T, Stone V, Lander ES, Hudson TJ, Steinhart AH, Bull S, Cohen Z, Greenberg G, Griffiths A, McLeod R, Silverberg M, Williams CN, Siminovitch KA. Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16. Gastroenterology. 115: 1062-5. PMID 9797358 DOI: 10.1016/S0016-5085(98)70074-5  0.355
1984 Donner A, Koval JJ, Bull S. Testing the effect of sex differences on sib-sib correlations Biometrics. 40: 349-356. PMID 6487723 DOI: 10.2307/2531388  0.309
1983 Donner A, Bull S. Inferences concerning a common intraclass correlation coefficient Biometrics. 39: 771-775. PMID 6652207 DOI: 10.2307/2531107  0.357
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