SEARCH

SEARCH BY CITATION

References

  • Abbott A. 2010. Mouse megascience. Nature 465:526.
  • Blake JA, Bult CJ, Kadin JA, Richardson JE, Eppig JT; Mouse Genome Database Group. 2011. The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics. Nucleic Acids Res 39:D842D848.
  • Gkoutos GV, Mungall C, Dolken S, Ashburner M, Lewis S, Hancock J, Schofield P, Kohler S, Robinson PN. 2009. Entity/quality-based logical definitions for the human skeletal phenome using PATO. Conf Proc IEEE Eng Med Biol Soc 2009: 70697072
  • Groth P, Pavlova N, Kalev I, Tonov S, Georgiev G, Pohlenz H-D, Weiss B. 2006. PhenomicDB: a new cross-species genotype/phenotype resource. Nucleic Acids Res 35:D696D699.
  • Hoehndorf R, Schofield PN, Gkoutos GV. 2011. PhenomeNET: a whole-phenome approach to disease gene discovery. Nucleic Acids Res 39:e119.
  • Honma Y, Araki T, Gianino S, Bruce A, Heuckeroth R, Johnson E, Milbrandt J. 2002. Artemin is a vascular-derived neurotropic factor for developing sympathetic neurons. Neuron 35:267282.
  • Kitsios GD, Tangri N, Castaldi PJ, Ioannidis JP. 2010. Laboratory mouse models for the human genome-wide associations. PLoS One 5:e13782.
  • Köhler S, Bauer S, Mungall CJ, Carletti G, Smith CL, Schofield P, Gkoutos GV, Robinson PN. 2011. Improving ontologies by automatic reasoning and evaluation of logical definitions. BMC Bioinformatics 12:418.
  • Meehan TF, Carr CJ, Jay JJ, Bult CJ, Chesler EJ, Blake JA. 2011. Autism candidate genes via mouse phenomics. J Biomed Inform. 44:S5S11.
  • Mungall C., Gkoutos G, Smith C, Haendel M, Lewis S, Ashburner M. 2010. Integrating phenotype ontologies across multiple species. Genome Biol 11: R2.
  • Quartu M, Serra MP, Boi M, Sestu N, Lai ML, Del Fiacco M. 2007. Tissue distribution of neurturin, persephin and artemin in the human brainstem at fetal, neonatal and adult age. Brain Res 1143:102115.
  • Ringwald M, Iyer V, Mason JC, Stone KR, Tadepally HD, Kadin JA, Bult CJ, Eppig JT, Oakley DJ, Briois S, Stupka E, Maselli V, Smedley D, Liu S, Hansen J, Baldock R, Hicks GG, Skarnes WC. 2011. Nucleic Acids Res 39:D842D848.
  • Robinson PN, Koehler S, Bauer S, Seelow D, Horn D, Mundlos S. 2008. The human phenotype ontology: a tool for annotating and analyzing human hereditary disease. Am J Hum Genet 83:610615.
  • Rosenthal N, Brown S. 2007. The mouse ascending: perspectives for human-disease models. Nat Cell Biol 9:993999.
  • Sardana D, Vasa S, Vepachedu N, Chen J, Gudivada RC, Aronow BJ, Jegga AG. 2010. PhenoHM: human-mouse comparative phenome-genome server. Nucleic Acids Res 38:W165W174.
  • Schofield PN, Gkoutos GV, Gruenberger M, Sundberg JP, Hancock JM. 2010. Phenotype ontologies for mouse and man: bridging the semantic gap. Dis Model Mech 3: 281289.
  • Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A. 2011. A conditional knockout resource for the genome-wide study of mouse gene function. Nature 474:337342.
  • Smith CL, Eppig JT. 2009. The mammalian phenotype ontology: enabling robust annotation and comparative analysis. Wiley Interdiscip Rev Syst Biol Med 1:390399.
  • Sprague J, Bayraktaroglu L, Bradford Y, Conlin T, Dunn N, Fashena D, Frazer K, Haendel M, Howe DG, Knight J, Mani P, Moxon SA, Pich C, Ramachandran S, Schaper K, Segerdell E, Shao X, Singer A, Song P, Sprunger B, Van Slyke CE, Westerfield M. 2008. The zebrafish information network: the zebrafish model organism database provides expanded support for genotypes and phenotypes. Nucleic Acids Res 36:D768D772.
  • Travillian RS, Adamusiak T, Burdett T, Gruenberger M, Hancock J, Mallon AM, Malone J, Schofield P, Parkinson H. 2011. Anatomy ontologies and potential users: bridging the gap. J Biomed Semantics 2(S4):S3.
  • Tweedie S, Ashburner M, Falls K, Leyland P, McQuilton P, Marygold S, Millburn G, Osumi-Sutherland D, Schroeder A, Seal R, Zhang H; FlyBase Consortium. 2009. FlyBase: enhancing Drosophila gene ontology annotations. Nucleic Acids Res 37:D555D559.
  • Twigger, SN, Shimoyama M, Bromberg S, Kwitek AE, Jacob HJ; RGD Team. 2007. The Rat Genome Database, update 2007—easing the path from disease to data and back again. Nucleic Acids Res 35:D658D662.
  • Washington NL, Haendel MA, Mungall CJ, Ashburner M, Westerfield M, Lewis SE. 2009. Linking human diseases to animal models using ontology-based phenotype annotation. PLoS Biol 7: e1000247.