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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