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XGAP: a uniform and extensible data model and software platform for genotype and phenotype experiments.
Swertz MA, Velde KJ, Tesson BM, Scheltema RA, Arends D, Vera G, Alberts R, Dijkstra M, Schofield P, Schughart K, Hancock JM, Smedley D, Wolstencroft K, Goble C, de Brock EO, Jones AR, Parkinson HE; Coordination of Mouse Informatics Resources (CASIMIR); Genotype-To-Phenotype (GEN2PHEN) Consortiums; Jansen RC. Swertz MA, et al. Among authors: smedley d. Genome Biol. 2010;11(3):R27. doi: 10.1186/gb-2010-11-3-r27. Epub 2010 Mar 9. Genome Biol. 2010. PMID: 20214801 Free PMC article.
Models for financial sustainability of biological databases and resources.
Chandras C, Weaver T, Zouberakis M, Smedley D, Schughart K, Rosenthal N, Hancock JM, Kollias G, Schofield PN, Aidinis V. Chandras C, et al. Among authors: smedley d. Database (Oxford). 2009;2009:bap017. doi: 10.1093/database/bap017. Epub 2009 Oct 23. Database (Oxford). 2009. PMID: 20157490 Free PMC article.
Mouse Resource Browser--a database of mouse databases.
Zouberakis M, Chandras C, Swertz M, Smedley D, Gruenberger M, Bard J, Schughart K, Rosenthal N, Hancock JM, Schofield PN, Kollias G, Aidinis V. Zouberakis M, et al. Among authors: smedley d. Database (Oxford). 2010 Jul 6;2010:baq010. doi: 10.1093/database/baq010. Database (Oxford). 2010. PMID: 20627861 Free PMC article.
Finding and sharing: new approaches to registries of databases and services for the biomedical sciences.
Smedley D, Schofield P, Chen CK, Aidinis V, Ainali C, Bard J, Balling R, Birney E, Blake A, Bongcam-Rudloff E, Brookes AJ, Cesareni G, Chandras C, Eppig J, Flicek P, Gkoutos G, Greenaway S, Gruenberger M, Hériché JK, Lyall A, Mallon AM, Muddyman D, Reisinger F, Ringwald M, Rosenthal N, Schughart K, Swertz M, Thorisson GA, Zouberakis M, Hancock JM. Smedley D, et al. Database (Oxford). 2010 Jul 6;2010:baq014. doi: 10.1093/database/baq014. Database (Oxford). 2010. PMID: 20627863 Free PMC article.
Research funding. Sustaining the data and bioresource commons.
Schofield PN, Eppig J, Huala E, de Angelis MH, Harvey M, Davidson D, Weaver T, Brown S, Smedley D, Rosenthal N, Schughart K, Aidinis V, Tocchini-Valentini G, Hancock JM. Schofield PN, et al. Among authors: smedley d. Science. 2010 Oct 29;330(6004):592-3. doi: 10.1126/science.1191506. Science. 2010. PMID: 21030633 No abstract available.
MouseFinder: Candidate disease genes from mouse phenotype data.
Chen CK, Mungall CJ, Gkoutos GV, Doelken SC, Köhler S, Ruef BJ, Smith C, Westerfield M, Robinson PN, Lewis SE, Schofield PN, Smedley D. Chen CK, et al. Among authors: smedley d. Hum Mutat. 2012 May;33(5):858-66. doi: 10.1002/humu.22051. Epub 2012 Mar 16. Hum Mutat. 2012. PMID: 22331800 Free PMC article.
Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish.
Doelken SC, Köhler S, Mungall CJ, Gkoutos GV, Ruef BJ, Smith C, Smedley D, Bauer S, Klopocki E, Schofield PN, Westerfield M, Robinson PN, Lewis SE. Doelken SC, et al. Among authors: smedley d. Dis Model Mech. 2013 Mar;6(2):358-72. doi: 10.1242/dmm.010322. Epub 2012 Oct 25. Dis Model Mech. 2013. PMID: 23104991 Free PMC article.
Deletions of chromosomal regulatory boundaries are associated with congenital disease.
Ibn-Salem J, Köhler S, Love MI, Chung HR, Huang N, Hurles ME, Haendel M, Washington NL, Smedley D, Mungall CJ, Lewis SE, Ott CE, Bauer S, Schofield PN, Mundlos S, Spielmann M, Robinson PN. Ibn-Salem J, et al. Among authors: smedley d. Genome Biol. 2014 Sep 4;15(9):423. doi: 10.1186/s13059-014-0423-1. Genome Biol. 2014. PMID: 25315429 Free PMC article.
195 results