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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: cantor r. 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 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. Among authors: cantor rm. 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.
Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals.
Engelman CD, Greenwood CM, Bailey JN, Cantor RM, Kent JW Jr, König IR, Bermejo JL, Melton PE, Santorico SA, Schillert A, Wijsman EM, MacCluer JW, Almasy L. Engelman CD, et al. Among authors: cantor rm. BMC Proc. 2016 Oct 18;10(Suppl 7):67-70. doi: 10.1186/s12919-016-0007-z. eCollection 2016. BMC Proc. 2016. PMID: 27980613 Free PMC article.
Proceedings of the Genetic Analysis Workshop 13: analysis of longitudinal family data for complex diseases and related risk factors. November 11-14, 2002. New Orleans, Louisiana, USA.
Almasy L, Amos CI, Bailey-Wilson JE, Cantor RM, Jaquish CE, Martinez M, Neuman RJ, Olson JM, Palmer LJ, Rich SS, Spence MA, MacCluer JW. Almasy L, et al. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S1-106. doi: 10.1186/1471-2156-4-S1-S1. BMC Genet. 2003. PMID: 14975069 Free PMC article. No abstract available.
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M, Debette S, Shulman JM, Schmidt H, Srikanth V, Schuur M, Yu L, Choi SH, Sigurdsson S, Verhaaren BF, DeStefano AL, Lambert JC, Jack CR Jr, Struchalin M, Stankovich J, Ibrahim-Verbaas CA, Fleischman D, Zijdenbos A, den Heijer T, Mazoyer B, Coker LH, Enzinger C, Danoy P, Amin N, Arfanakis K, van Buchem MA, de Bruijn RF, Beiser A, Dufouil C, Huang J, Cavalieri M, Thomson R, Niessen WJ, Chibnik LB, Gislason GK, Hofman A, Pikula A, Amouyel P, Freeman KB, Phan TG, Oostra BA, Stein JL, Medland SE, Vasquez AA, Hibar DP, Wright MJ, Franke B, Martin NG, Thompson PM; Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium; Nalls MA, Uitterlinden AG, Au R, Elbaz A, Beare RJ, van Swieten JC, Lopez OL, Harris TB, Chouraki V, Breteler MM, De Jager PL, Becker JT, Vernooij MW, Knopman D, Fazekas F, Wolf PA, van der Lugt A, Gudnason V, Longstreth WT Jr, Brown MA, Bennett DA, van Duijn CM, Mosley TH, Schmidt R, Tzourio C, Launer LJ, Ikram MA, Seshadri S; Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. Bis JC, et al. Nat Genet. 2012 Apr 15;44(5):545-51. doi: 10.1038/ng.2237. Nat Genet. 2012. PMID: 22504421 Free PMC article.
Identifying fenofibrate responsive CpG sites.
Cantor R, Navarro L, Pan C. Cantor R, et al. BMC Proc. 2018 Sep 17;12(Suppl 9):43. doi: 10.1186/s12919-018-0148-3. eCollection 2018. BMC Proc. 2018. PMID: 30275892 Free PMC article.
492 results