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Identifying rare variants from exome scans: the GAW17 experience.
Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J Jr, Laird N, Pankratz N, Paterson A, Pugh E, Suarez B, Sun Y, Thomas A, Tintle N, Zhu X, Ziegler A, Maccluer JW, Almasy L. Ghosh S, et al. Among authors: bickeboller h. BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S1. doi: 10.1186/1753-6561-5-S9-S1. BMC Proc. 2011. PMID: 22373325 Free PMC article.
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.
Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, Rice J, Satten G, Suarez B, Vieland V, Wilcox M, Zhang H, Ziegler A, MacCluer JW. Bailey-Wilson JE, et al. Among authors: bickeboller h. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S1. doi: 10.1186/1471-2156-6-S1-S1. BMC Genet. 2005. PMID: 16451554 Free PMC article. No abstract available.
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci.
Cordell HJ, de Andrade M, Babron MC, Bartlett CW, Beyene J, Bickeböller H, Culverhouse R, Cupples LA, Daw EW, Dupuis J, Falk CT, Ghosh S, Goddard KA, Goode EL, Hauser ER, Martin LJ, Martinez M, North KE, Saccone NL, Schmidt S, Tapper W, Thomas D, Tritchler D, Vieland VJ, Wijsman EM, Wilcox MA, Witte JS, Yang Q, Ziegler A, Almasy L, Maccluer JW. Cordell HJ, et al. Among authors: bickeboller h. BMC Proc. 2007;1 Suppl 1(Suppl 1):S1. doi: 10.1186/1753-6561-1-s1-s1. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466438 Free PMC article. No abstract available.
Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses.
Cupples LA, Beyene J, Bickeböller H, Daw EW, Fallin MD, Gauderman WJ, Ghosh S, Goode EL, Hauser ER, Hinrichs A, Kent JW Jr, Martin LJ, Martinez M, Neuman RJ, Province M, Szymczak S, Wilcox MA, Ziegler A, Maccluer JW, Almasy L. Cupples LA, et al. Among authors: bickeboller h. BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S1. doi: 10.1186/1753-6561-3-s7-s1. BMC Proc. 2009. PMID: 20017962 Free PMC article.
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees.
Bickeböller H, Bailey JN, Beyene J, Cantor RM, Cordell HJ, Culverhouse RC, Engelman CD, Fardo DW, Ghosh S, König IR, Lorenzo Bermejo J, Melton PE, Santorico SA, Satten GA, Sun L, Tintle NL, Ziegler A, MacCluer JW, Almasy L. Bickeböller H, et al. BMC Proc. 2014 Jun 17;8(Suppl 1):S1. doi: 10.1186/1753-6561-8-S1-S1. eCollection 2014. BMC Proc. 2014. PMID: 25519310 Free PMC article.
Inclusion of a priori information in genome-wide association analysis.
Tintle N, Lantieri F, Lebrec J, Sohns M, Ballard D, Bickeböller H. Tintle N, et al. Among authors: bickeboller h. Genet Epidemiol. 2009;33 Suppl 1(Suppl 1):S74-80. doi: 10.1002/gepi.20476. Genet Epidemiol. 2009. PMID: 19924705 Free PMC article.
Issues in association mapping with high-density SNP data and diverse family structures.
Bickeböller H, Goddard KA, Igo RP Jr, Kraft P, Lozano JP, Pankratz N, Balavarca Y, Bardel C, Charoen P, Croiseau P, Guo CY, Joo J, Köhler K, Madsen A, Malzahn D, Monsees G, Sohns M, Ye Z. Bickeböller H, et al. Genet Epidemiol. 2007;31 Suppl 1:S22-33. doi: 10.1002/gepi.20277. Genet Epidemiol. 2007. PMID: 18046763
176 results